NZ748812B2 - New fluorescent dyes and their uses as biomarkers - Google Patents

Abstract

The present application relates to benzopyran fluorescent dyes of formula (I) and (V) and their uses as fluorescent labels. The compounds may be used as fluorescent labels for nucleotides in nucleic acid sequencing applications.

Description

/074880 NEW FLUORESCENT DYES AND THEIR USES AS BIOMARKERS INCORPORATION BY REFERENCE TO ANY PRIORITY APPLICATIONS This application claims the benefit ofUS. Provisional Application No. 62/402635, entitled New Fluorescent Dyes and Their Uses as Biomarkers, filed September 30, 2016, the disclosure of which is orated herein by reference in its ty.

BACKGROUND Field The present application s to new benzopyran derivatives for use as fluorescent dyes. The compounds may be used as cent labels, particularly for nucleotide labeling in nucleic acid sequencing applications.

Background Non-radioactive detection of c acids utilizing fluorescent labels is an important technology in molecular biology. Many procedures ed in recombinant DNA technology previously relied heavily on the use of nucleotides or polynucleotides radioactively d with, for example 32P. Radioactive compounds permit sensitive ion of nucleic acids and other molecules of interest. However, there are serious limitations in the use ofradioactive isotopes such as their expense, limited shelf life and more importantly safety considerations. Eliminating the need for radioactive labels enhances safety whilst ng the environmental impact and costs associated with, for example, reagent disposal. Methods amenable to non-radioactive fluorescent detection include by way ofnon-limiting example, automated DNA sequencing, hybridization methods, real-time detection of polymerase-chain-reaction products and immunoassays.

For many applications it is desirable to employ multiple spectrally distinguishable fluorescent labels in order to achieve independent detection of a plurality of lly overlapping analytes. In such multiplex methods the number of reaction vessels may be reduced fying experimental protocols and facilitating the production of application-specific reagent kits. In multi- color automated DNA sequencing for example, multiplex fluorescent detection allows for the analysis of multiple nucleotide bases in a single electrophoresis lane thereby increasing throughput over single- color methods and reducing uncertainties associated with inter-lane electrophoretic mobility variations.

However, multiplex fluorescent detection can be problematic and there are a number of important factors which constrain selection of fluorescent labels. First, it is difficult to find dye compounds whose absorption and emission spectra are suitably spectrally ed. In addition when several fluorescent dyes are used together, simultaneous excitation may be difficult because the absorption bands of the dyes for different spectral regions are usually widely separated. Many excitation s use high power lasers and therefore the dye must have sufficient photo-stability to withstand such laser excitation. A final consideration of particular importance in molecular y methods is that the fluorescent dyes must be compatible with the reagent chemistries used such as for example DNA synthesis solvents and reagents, buffers, polymerase enzymes and ligase enzymes.

As sequencing technology advances a need has developed for further fluorescent dye compounds, their nucleic acid conjugates and dye sets which satisfy all of the above constraints and which are amenable particularly to high throughput molecular methods such as solid phase sequencing and the like.

PCT Publication No. WC 2007/135368 bes a class of rhodamine compounds suitable for use as fluorescent labels. The compounds bed therein are suitable for use in solid phase nucleic acid sequencing protocols. Advances in the logy and throughput of solid phase nucleic acid sequencing have led to fithher developments and ements to the molecular design of fluorescent labels, particularly in the context ofthe interaction n the fluorescent reagents and particular nucleic acid sequences.

Fluorescent dye molecules with improved fluorescence ties (such as Stokes shift, fluorescence intensity, position of fluorescence maximum and shape of fluorescence band) can improve the speed and accuracy of nucleic acid sequencing. Stokes Shift is a key aspect in the identifying of the fluorescent signals in biological applications. For example, the detection ted light can be lt to guish from the excitation light when using fluorophores with absorption and fluorescence max very close to each other (i.e., small Stokes shift), because the excitation and emission bands greatly p. In contrast, fluorophores with large Stokes shifts are easy to distinguish because of the r separation n the excitation and emission wavelengths. The Stokes shift is especially critical in multiplex fluorescence ations, because the emission wavelength of one fluorophore may overlap, and therefore excite, another fluorophore in the same sample. In addition, fluorescence signal intensity is especially important when measurements are made in water based biological buffers and/or at higher temperature as fluorescence of most dyes is cantly lower at such conditions. Moreover, the nature of the base to which a dye is attached also affects the cence maximum, fluorescence intensity and other spectral dye properties. The sequence specific interactions n the fluorescent dye and the nucleobase can be tailored by ic design of the fluorescent dyes. Optimization of the ure of the fluorescent dyes can improve their fluorescent properties and also e the efficiency of nucleotide incorporation, reduce the level of sequencing errors and decrease the usage of reagents in, and therefore the costs of, nucleic acid sequencing.

Described herein are novel benzopyran derivatives and their use as bio-molecule labels, particularly as labels for nucleotides used in nucleic acid cing. The improvements can be seen in the greater Stokes shifts of such dyes when ed as lecule conjugates and in the length, intensity and quality of sequencing read obtainable using the new fluorescent compounds.

SUMMARY Some embodiments described herein are related to new benzopyran derivatives of Formula (I) or mesomeric forms thereof: R4 (1) wherein each R1, R2, and R1, is independently selected from the group consisting of H, alkyl, substituted alkyl, alkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, alkoxyalkyl, amino, aminoalkyl, aminosulfonyl, halo, cyano, hydroxy, hydroxyalkyl, hetero alkyl, C-carboxy, O-carboxy, C-amido, N- amido, nitro, sulfonyl, sulfo, sulfino, sulfonate, yl halide, S-sulfonamido, N-sulfonamido, optionally substituted carbocyclyl, optionally substituted aryl, optionally substituted heteroaryl and optionally substituted heterocyclyl; alternatively, R1 and R1, er and with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally substituted carbocyclyl, optionally substituted aryl, ally tuted heteroaryl, and optionally substituted heterocyclyl; each R3 and R4 is independently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, alkynyl, aminoalkyl, haloalkyl, heteroalkyl, alkoxyalkyl, yl hydroxide, optionally substituted aryl, optionally substituted aryl, optionally substituted carbocyclyl, and optionally substituted heterocyclyl; atively, R1 and R3 together with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally substituted 5-10 ed heteroaryl or optionally substituted 5-10 membered heterocyclyl; alternatively, R2 and R4 together with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally substituted 5-10 ed heteroaryl and optionally substituted 5-10 membered heterocyclyl; R5 and R6 is independently selected from the group consisting of alkyl, substituted alkyl, alkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, alkoxyalkyl, amino, aminoalkyl, aminosulfonyl, halo, cyano, y, hydroxyalkyl, alkyl, C-carboxy, O-carboxy, C-amido, N—amido, nitro, sulfonyl, sulfo, sulfino, sulfonate, sulfonyl , onamido, N-sulfonamido, optionally substituted carbocyclyl, optionally substituted aryl, optionally substituted heteroaryl and optionally substituted heterocyclyl; R is selected from -OR7 or -NR8R9; R7 is selected from the group consisting of H, alkyl, substituted alkyl, optionally tuted aryl, optionally substituted heteroaryl, optionally substituted carbocyclyl, and optionally substituted heterocyclyl; each R8 and R9 is independently selected from the group ting of H, alkyl, substituted alkyl, alkenyl, alkynyl, aminoalkyl, carboxyalkyl, sulfonatoalkyl, haloalkyl, heteroalkyl, alkoxyalkyl, sulfo, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted carbo cyclyl, and ally substituted heterocyclyl; X is selected from the group consisting of O, S, NR”, and Se; R10 is ed from the group consisting of H, alkyl, tuted alkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted yclyl, and optionally substituted heterocyclyl; m is an integer selected from 0 to 4; and n is an integer selected from 0 to 4; provided that when each R1, R17 and R2 is H; each R3 and R4 is ethyl; each m and n is 0; R is - NHCH(CH3)CH20H; then X is selected from O, S or Se; when each R1, R1’ and R2 is H; each R3 and R4 is ethyl; each m and n is 0; R is-OH; then X is selected from S or Se; when each R1, RF and R2 is H; each R3 and R4 is ethyl; m is l and R5 is methyl; n is 0; R is - OH or -OEt; then X is selected from S, NR10 or Se; and when each R1, R17 and R2 is H; each R3 and R4 is ethyl; m is l and R5 is -S(02)Et; n is 0; R is -OH or -OEt; then X is selected from S, NR10 or Se.

Some additional embodiments described herein are related to a fluorescent compound of Formula (V) with a Stokes shift ranging from about 60 nm to about 100 nm: wherein each R1, R1, and R2 is independently selected from the group consisting of H, alkyl, substituted alkyl, alkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, alkoxyalkyl, amino, aminoalkyl, aminosulfonyl, halo, cyano, hydroxy, hydroxyalkyl, heteroalkyl, C-carboxy, O-carboxy, C-amido, N- amido, nitro, yl, sulfo, sulfino, sulfonate, sulfonyl halide, S-sulfonamido, N-sulfonamido, ally substituted carbocyclyl, optionally substituted aryl, optionally substituted heteroaryl and optionally substituted heterocyclyl; alternatively, R1 and R1, together and with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally substituted carbocyclyl, ally substituted aryl, optionally substituted heteroaryl, and optionally substituted heterocyclyl; each R3 and R4 is independently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, alkynyl, aminoalkyl, haloalkyl, alkyl, alkoxyalkyl, sulfo, optionally substituted aryl, ally substituted heteroaryl, ally substituted carbocyclyl, and ally substituted heterocyclyl; alternatively, R1 and R3 together with the atoms to which they are attached form a ring or ring system selected from the group consisting of ally tuted 5-10 membered heteroaryl or optionally substituted 5-10 membered heterocyclyl; alternatively, R2 and R4 together with the atoms to which they are attached form a ring or ring system ed from the group consisting of optionally substituted 5-10 ed aryl and optionally substituted 5-10 membered heterocyclyl; RHEt is a aryl optionally substituted with one or more R5; each R5 and R6 is independently selected from the group consisting of alkyl, substituted alkyl, alkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, alkoxyalkyl, amino, aminoalkyl, aminosulfonyl, halo, cyano, hydroxy, hydroxyalkyl, heteroalkyl, C-carboxy, O-carboxy, C-amido, N—amido, nitro, sulfonyl, WO 60482 sulfo, sulfino, sulfonate, sulfonyl halide, S-sulfonamido, N-sulfonamido, optionally substituted yclyl, optionally substituted aryl, optionally substituted heteroaryl and optionally substituted cyclyl; R is selected from -OR7 or -NR8R9; Y is selected from O or NH; R7 is selected from the group consisting of H, alkyl, substituted alkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted carbocyclyl, and optionally substituted heterocyclyl; each R8 and R9 is independently ed from the group consisting of H, alkyl, substituted alkyl, alkenyl, alkynyl, aminoalkyl, carboxyalkyl, sulfonatoalkyl, haloalkyl, alkyl, alkoxyalkyl, sulfo, ally tuted aryl, optionally substituted heteroaryl, optionally substituted carbocyclyl, and optionally substituted heterocyclyl; and n is an r of0 to 4.

Some embodiments described herein are related to nucleotide or oligonucleotide labeled with a compound of Formula (I) or (V).

Some embodiments described herein are related to kits containing one or more nucleotides Where at least one nucleotide is a nucleotide labeled with a cent dye described herein.

Some filrther embodiments described herein are related to methods of sequencing including incorporating a labeled nucleotide described herein in a sequencing assay, and detecting the labeled tide.

Some additional embodiments described herein are related to a method ofpreparing a compound of Formula (Ia), the methods include reacting a compound of Formula (Ila) N R" N CHZCN (Ila) or Formula (IIb) (”b) with a compound of Formula (111) to form Where the variables R1, R1,, R2, R3, R4, R5, R6, X, m and n are defined above in the disclosure of compounds ofFormula (I), and R” is ed from the group consisting of H, optionally substituted alkyl, alkenyl, alkynyl, aminoalkyl, haloalkyl, hetero alkyl, alkoxyalkyl, sulfo, optionally substituted aryl; ally substituted heteroaryl, ally substituted carbocyclyl, and optionally substituted heterocyclyl.

Some additional embodiments described herein are related to a method ofpreparing a compound of Formula (la’), the methods include reacting a compound of Formula (Ila) N CH2002R" N CHZCN (Ila) or Formula (llb) (”b) with a compound of Formula (Illa) (Illa) to form where the variables R], R1,, R2, R3, R4, R5, R6, R7, R”, X, m and n are defined above.

Some additional embodiments described herein are related to a method ofpreparing a nd of Formula (la’), the method includes converting a compound of Formula (Ia) to a compound of Formula (la’) h ylic acid activation: R6( n) \ X 0R7 activation 5Q 0 o u’ R2 R4 Ga) Ga) Where the variables R1, R1,, R2, R3, R4, R5, R6, R7, R8, R9, X, m and n are defined above in the disclosure of compounds ofFormula (I).

Some additional embodiments bed herein are related to a method ofpreparing a compound of a (lb), the method includes converting a compound of Formula (Ia) to a compound of Formula (la’) through carboxylic acid activation: (Ia) (Ia') and reacting the compound of Formula (Ia’) With a primary or secondary amine of Formula (IV), R6\(n ) 5X / x R2 R4 (IV) (Ia') (I b) Where the variables R1, R1,, R2, R3, R4, R5, R6, R7, R8, R9, X, m and n are defined above in the disclosure of compounds ofFormula (I).

Some additional embodiments described herein are related to a method ofpreparing a compound of Formula (1b), the methods include reacting a compound of a (Ila) N CHZCOZR" N CHZCN (”3) or Formula (Ilb) (”b) with a compound of a (IIIb) (IIIb) to form where the variables R], R1,, R2, R3, R4, R5, R6, R7, R”, X, m and n are defined above.

WO 60482 BRIEF DESCRIPTION OF THE DRAWINGS is a line graph that illustrates the fluorescent spectra of the benzopyran fluorescent dyes as bed herein as compared to commercial dyes with absorption in the same spectral region.

FIGS. 2A and 2B are plots that illustrate the usability of the C-nucleotide labeled with the new fluorescent new dyes as described herein (as shown in black) for sequencing analysis. is a bar chart that rates the fluorescent intensity of the C- tide d with the new fluorescent dyes as described herein when these dyes were excited with Blue (460 nm) or Green (530 nm) light. is a bar chart that illustrates the cent intensity of the C-nucleotide labeled with a new fluorescent dye as bed herein as compared to a commercial dye at two different temperatures.

DETAILED DESCRIPTION Embodiments bed herein relate to new benzopyran derivatives of the structure of Formula (I) or (V) for use as fluorescent dyes. These new fluorescent dyes have greater Stokes shifts and may be used as fluorescent labels, particularly for nucleotide labeling in nucleic acid sequencing applications. Methods of preparing these fluorescent dyes and downstream sequencing applications utilizing these dyes are also exemplified.

Some embodiments described herein are related to new benzopyran derivatives of Formula (I) or mesomeric forms f: R4 (1) wherein each R1, R2 and R1, is independently selected from the group consisting of H, alkyl, substituted alkyl, alkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, alkoxyalkyl, amino, aminoalkyl, aminosulfonyl, halo, cyano, hydroxy, hydroxyalkyl, heteroalkyl, C-carboxy, O- carboxy, C—amido, N-amido, nitro, sulfonyl, sulfo, sulfino, sulfonate, sulfonyl halide, S- sulfonamido, N-sulfonamido, optionally substituted carbocyclyl, optionally substituted aryl, optionally substituted heteroaryl and optionally substituted heterocyclyl; alternatively, R1 and R17 together and with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally substituted carbocyclyl, optionally substituted aryl, optionally substituted heteroaryl, and ally substituted heterocyclyl; each R3 and R4 is independently selected from the group consisting of H, alkyl, substituted alkyl, l, alkynyl, aminoalkyl, haloalkyl, heteroalkyl, alkoxyalkyl, sulfo, optionally substituted aryl, ally substituted heteroaryl, optionally substituted carbocyclyl, and optionally substituted cyclyl; alternatively, R1 and R3 er with the atoms to which they are attached form a ring or ring system selected from the group ting of ally substituted 5-10 membered heteroaryl or optionally substituted 5-10 membered heterocyclyl; alternatively, R2 and R4 together with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally substituted 5-10 membered hetero aryl and optionally substituted 5-10 membered heterocyclyl; R5 and R6 is independently selected from the group consisting of alkyl, substituted alkyl, alkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, alkoxyalkyl, amino, aminoalkyl, aminosulfonyl, halo, cyano, hydroxy, hydroxyalkyl, heteroalkyl, C-carboxy, O-carboxy, C— amido, N-amido, nitro, sulfonyl, sulfo, sulfino, sulfonate, sulfonyl halide, S-sulfonamido, N- sulfonamido, optionally substituted carbocyclyl, optionally substituted aryl, ally substituted heteroaryl and optionally substituted heterocyclyl; R is selected from -OR7 or -NR8R9; R7 is selected from the group consisting of H, alkyl, substituted alkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted carbocyclyl, and optionally substituted heterocyclyl; each R8 and R9 is independently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, l, aminoalkyl, carboxyalkyl, sulfonatoalkyl, haloalkyl, heteroalkyl, alkoxyalkyl, sulfo, optionally substituted aryl, optionally tuted heteroaryl, optionally substituted carbocyclyl, and ally substituted cyclyl; X is selected from the group ting of O, S, NR“), and Se; R10 is selected from the group consisting of H, alkyl, substituted alkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted carbocyclyl, and optionally substituted heterocyclyl; m is an r selected from 0 to 4; and n is an integer selected from 0 to 4; provided that when each R1, R17 and R2 is H; each R3 and R4 is ethyl; each m and n is 0; R is - NHCH(CH3)CH20H; then X is selected from O, S or Se; when each R1, R17 and R2 is H; each R3 and R4 is ethyl; each m and n is 0; R is-OH; then X is selected from S or Se; when each R1, R17 and R2 is H; each R3 and R4 is ethyl; m is l and R5 is methyl; n is 0; R is -OH or -OEt; then X is selected from S, NR10 or Se; and when each R1, R1’ and R2 is H; each R3 and R4 is ethyl; m is l and R5 is -S(02)Et; n is 0; R is -OH or -OEt; then X is selected from S, NR10 or Se.

In some embodiments of the compounds of a (I), when each R1, R1, and R2 is H; each R3 and R4 is ethyl; m is l; R5 is Cl; then X is ed from S, O, or Se, preferably 0.

In some ments of the compounds of Formula (I), the optionally substituted aryl disclosed herein is optionally substituted C610 aryl, for example, phenyl. In some embodiments, the optionally substituted heteroaryl disclosed herein is optionally substituted 5—10 ed heteroaryl; more preferably, ally tuted 5-6 ed heteroaryl. In some embodiments, the optionally substituted carbocyclyl disclosed herein is optionally substituted 3—7 membered carbocyclyl, in particular 3-7 membered cycloalkyl. In some embodiments, optionally substituted heterocyclyl disclosed herein are optionally substituted 3-7 membered heterocyclyl, more preferably -6 membered heterocyclyl.

In some embodiments of the compounds of Formula (I), R is -OR7 and the compound of Formula (I) is also represented by Formula (Ia’): ('8') . In one embodiment, R7 is H and the compound of a (I) is also represented by Formula (Ia): In some embodiments of the compounds of Formula (I), R is -NR8R9 and the nd of Formula (I) is also represented by Formula (Ib): (lb) . In one embodiment, each R8 and R9 is H. In some other embodiments, R8 is H and R9 is substituted alkyl. In some further embodiments, both R8 and R9 are substituted alkyl. In some such embodiments, the substituted alkyl is selected from alkyl substituted with carboxyl (-C(=O)OH), sulfo (-SOgH) or sulfonate (-SO3' ). In some other embodiments, the tuted alkyl is selected from alkyl substituted with o group.

In some embodiments ofthe compounds ofFormula (I), (la), (Ia’), or (Ib), each R], R17 and R2 is H. In some other embodiments, at least one of R1, R1, and R2 is an alkyl.

In some embodiments of the compounds of Formula (I), (la), (Ia’), or (Ib), each R3 and R4 is an alkyl. In some such embodiments, R3 and/or R4 can be selected from methyl or ethyl. In some other embodiments, R3 is H and R4is an alkyl. In some embodiments, R3 and R4 are ethyl.

In some other embodiments of the compounds ula (I), (Ia), (Ia’), or (Ib), R1 and R3 er with the atoms to which they are attached form an optionally substituted 3-7 membered heterocyclyl, for example, an optionally substituted 6 membered heterocyclyl. In some embodiments, the heterocyclyl ring has one heteroatom (i.e., nitrogen). In some other embodiments, the heterocyclyl ring may have two or more heteroatoms. In one embodiment, the optionally substituted 6-membered heterocyclyl has the structure R4 where the : represents either a single bond or a double bond, such that each of the carbon atoms in the ring is neutral and not charged. In some such embodiments, R4 is selected from H or alkyl. In one embodiment, R4 is ethyl. In some such embodiments, at least one of RF and R2 is H. In one embodiment, both R1, and R2 are H.

In some other embodiments of the compounds ofFormula (I), (la), (Ia’), or (Ib), R2 and R4together with the atoms to which they are attached form an optionally tuted 3-7 membered heterocyclyl, for example, an optionally substituted 6 membered heterocyclyl. In some embodiments, the heterocyclyl ring has one heteroatom (i.e., nitrogen). In some other embodiments, the heterocyclyl ring may have two or more heteroatoms. In one embodiment, the ally substituted ered cyclyl has the structure r r where the : represents either a single bond or a double bond, such that each of the carbon atoms in the ring is neutral and not d. In some such embodiments, R3 is selected from H or alkyl. In one ment, R3 is ethyl. In some such embodiments, at least one of R1, and R1 is H. In one embodiment, both R1, and R1 are H.

In some alternative embodiments of the compounds of Formula (I), (la), (Ia’), or (Ib), R1 and R3 together with the atoms to which they are attached form an optionally substituted 3-7 membered heterocyclyl, for example, an optionally substituted 6 membered heterocyclyl; and R2 and R4 together with the atoms to which they are attached form an optionally substituted 3-7 membered heterocyclyl, for example, an optionally substituted 6 membered heterocyclyl. In some ments, the resulting fiJsed heterocyclyl ring system has one heteroatom (i.e., nitrogen). In some other embodiments, the resulting fused heterocyclyl ring system may have two or more heteroatoms. In one embodiment, the resulting fused heterocyclyl ring system has the structure where the : represents either a single bond or a double bond, such that each ofthe carbon atoms in the ring is neutral and not charged. In one embodiment, R1, is H.

In some embodiments of the nds of Formula (I), (la), (Ia’), or (1b), the 3-7 membered heterocyclyl ring formed by R1 / R3 and/or R2/ R4 are unsubstituted. In some other embodiments, such 3-7 membered heterocyclyl is substituted with one or more alkyl, for example, methyl.

In some ments of the compounds of Formula (I), (la), (Ia’), or (Ib), m is 0.

In some other embodiments, m is 1. In some such embodiments, R5 is selected from sulfo, sulfonyl halide, for example, sulfonyl chloride, or aminosulfonyl. In some embodiments, R5 is halogen. In some ments, R5 is chlorine.

In some embodiments of Formula (I), (Ia), (Ia’), or (Ib), n is 0.

In any one of the embodiments ofthe nds ofFormula (I), (la), (Ia’), or (Ib) disclosed herein, X can be S (sulfur). In any one of the embodiments of the compounds of Formula (I), (Ia), (Ia’), or (Ib) disclosed herein, X can be 0 (oxygen). In some such embodiment, the compounds of Formula (Ia), (Ia’) and (lb) can also be represented by Formula (Ic), (Ic’) and (Id) respectively: WO 60482 K (1-1 1), (1—12), K (1—13), WO 60482 302m 0 S02NH2 Q SQ (1'14), K (1-15), and (1-16), or mesomeric forms thereof.

In some embodiments ofthe compounds ofFormula (I), the compound is ntly attached to a nucleotide or oligonucleotide via C(=O)R, wherein R is -OR7, and wherein R7 is a substituted alkyl.

In some alternative embodiments, the compound is covalently attached to a nucleotide or oligonucleotide via , n R is -NR8R9, and wherein at least one of R8 or R9 comprises at least one functional group that may be used for attachment to the biomolecules, for example, one ofR8 or R9 is a substituted alkyl comprising at least one carboxyl group.

In some embodiments, the compound of Formula (I) is present in one or more mesomeric forms (I-A), (LB) or (I-C): Some embodiments disclosed herein are d to a fluorescent nd of Formula (V) with a Stokes shift ranging from about 60 nm to about 100 nm: wherein each R1, R1, and R2 is independently selected from the group consisting of H, alkyl, substituted alkyl, alkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, alkoxyalkyl, amino, aminoalkyl, aminosulfonyl, halo, cyano, hydroxy, hydroxyalkyl, alkyl, C-carboxy, O- carboxy, C-amido, N—amido, nitro, sulfonyl, sulfo, sulfino, sulfonate, sulfonyl halide, S- sulfonamido, N—sulfonamido, optionally substituted carbocyclyl, ally substituted aryl, optionally substituted heteroaryl and optionally substituted heterocyclyl; alternatively, R1 and RP together and with the atoms to which they are attached form a ring or ring system ed from the group consisting of optionally substituted carbocyclyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted heterocyclyl; each R3 and R4 is independently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, alkynyl, aminoalkyl, kyl, heteroalkyl, alkoxyalkyl, sulfo, optionally substituted aryl, optionally substituted heteroaryl, ally substituted carbocyclyl, and optionally substituted cyclyl; alternatively, R1 and R3 together with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally substituted 5-10 membered heteroaryl or optionally substituted 5-10 membered cyclyl; alternatively, R2 and R4 together with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally substituted 5-10 membered hetero aryl and optionally substituted 5-10 membered heterocyclyl; RH‘:t is a heteroaryl optionally substituted with one or more R5; each R5 and R6 is independently selected from the group consisting of alkyl, substituted alkyl, alkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, alkoxyalkyl, amino, lkyl, aminosulfonyl, halo, cyano, hydroxy, hydroxyalkyl, heteroalkyl, C-carboxy, O-carboxy, C- amido, N—amido, nitro, yl, sulfo, , sulfonate, sulfonyl halide, S-sulfonamido, N- 2017/074880 sulfonamido, optionally substituted carbocyclyl, optionally substituted aryl, optionally substituted heteroaryl and optionally substituted cyclyl; R is selected from -OR7 or -NR8R9; Y is selected from O or NH; R7 is selected from the group consisting of H, alkyl, substituted alkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted carbocyclyl, and optionally substituted cyclyl; each R8 and R9 is independently ed from the group consisting of H, alkyl, substituted alkyl, alkenyl, alkynyl, lkyl, carboxyalkyl, sulfonatoalkyl, haloalkyl, heteroalkyl, alkoxyalkyl, sulfo, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted carbocyclyl, and optionally substituted heterocyclyl; and n is an integer ofO to 4.

In some embodiments of Formula (V), RHat is selected from optionally substituted -10 membered heteroaryl. In some such embodiments, RHet is selected from optionally substituted 9 ed heteroaryl, for example, optionally substituted benzothiazole. In one embodiment, RH6t is :2 i optionally substituted 2-benzothiazolyl: 9i. In one embodiment, RH“ is optionally substituted 2-benzoxazolyl with the structureQ»;. In some such embodiments, RHet is substituted with one or more substituents selected from sulfo, sulfonyl halide or aminosulfonyl. In some such ments, RHet is substituted with one or more halogen. In some such embodiments, RH‘Et is substituted with a chlorine.

In some embodiments, R is —OR7 and the compounds of Formula (V) are also ented by Formula (Va): R4 (Va). In one embodiment, R7 is H. In another embodiment, R7 is substituted alkyl.

In some embodiments, R is -NR8R9 and the compounds of Formula (V) are also represented by Formula (Vb): R4 (Vb). In one embodiment, each R8 and R9 is H. In some other embodiments, R8 is H and R9 is substituted alkyl. In some fiuther embodiments, both R8 and R9 are substituted alkyl. In some such embodiments, the substituted alkyl is selected from alkyl substituted with carboxyl (-C(=O)OH) or sulfo (-SOgH) or sulfonate (-SO3_ ). In some other embodiments, the substituted alkyl is selected from alkyl tuted with C-amido group.

In some embodiments of the compounds of a (V), (Va) or (Vb), Y is O.

In some embodiments ofthe compounds ofFormula (V), (Va) or (Vb), each R1, R1, and R2 is H. In some other embodiments, at least one of R1, R17 and R2 is an alkyl.

In some embodiments ofthe compounds ofFormula (V), (Va) or (Vb), each R3 and R4 is an alkyl. In some such embodiments, R3 and/or R4 can be selected from methyl or ethyl. In some other embodiments, R3 is H and R4 is an alkyl.

In some other embodiments of the compounds of Formula (V), (Va) or (Vb), R1 and R3 together with the atoms to which they are attached form an optionally substituted 3—7 membered cyclyl, for example, an optionally substituted 6 ed heterocyclyl. In some ments, the heterocyclyl ring has one heteroatom (i.e., nitrogen). In some other embodiments, the heterocyclyl ring may have two or more atoms. In one embodiment, the optionally substituted ered heterocyclyl has the structure R4 where the : represents either a single bond or a double bond, such that each of the carbon atoms in the ring is neutral and not charged. In some such embodiments, R4 is selected from H or alkyl. In one embodiment, R4 is ethyl. In some fithher embodiments, at least one of RF and R2 is H. In one embodiment, both R11 and R2 are H.

In some other embodiments of the compounds of Formula (V), (Va) or (Vb), R2 and R4together with the atoms to which they are attached form an optionally substituted 3-7 membered heterocyclyl, for e, an optionally substituted 6 membered heterocyclyl. In some embodiments, the heterocyclyl ring has one atom (i.e., nitrogen). In some other embodiments, the heterocyclyl ring may have two or more heteroatoms. In one embodiment, the optionally substituted 6-membered heterocyclyl has the structure ’ , where the : ents either a single bond or a double bond, such that each of the carbon atoms in the ring is neutral and not charged. In some such embodiments, R3 is selected from H or alkyl. In one embodiment, R3 is ethyl. In some fithher embodiments, at least one of R17 and R1 is H. In one embodiment, both R1, and R1 are H.

In some alternative embodiments of the compounds of Formula (V), (Va) or (Vb), R1 and R3 together with the atoms to which they are attached form an optionally substituted 3-7 membered heterocyclyl, for example, an optionally substituted 6 membered heterocyclyl; and R2 and R4 together with the atoms to which they are attached form an optionally substituted 3-7 membered heterocyclyl, for example, an optionally substituted 6 membered heterocyclyl. In some embodiments, the resulting fiJsed heterocyclyl ring system has one heteroatom (i.e., nitrogen). In some other embodiments, the resulting fused cyclyl ring system may have two or more heteroatoms. In one embodiment, the resulting fused heterocyclyl ring system has the ure where the : ents either a single bond or a double bond, such that each ofthe carbon atoms in the ring is neutral and not charged. In one embodiment, R1, is H.

In some ments of the compounds of a (V), (Va) or (Vb), the 3-7 membered heterocyclyl ring formed by R1 / R3 and/or R2/ R4 are tituted. In some other embodiments, such 3-7 membered heterocyclyl is substituted with one or more alkyl, for example, In some embodiments of the compounds of Formula (V), (Va) or (Vb), n is 0.

In some specific embodiments ofFormula (V), (Va) or (Vb), exemplary compounds of Formula (V) include compounds I-1 through I-15 as disclosed herein.

In some embodiments, the fluorescent compound of Formula (V) is covalently attached to a nucleotide or oligonucleotide via C(=O)R, wherein R is -OR7, and wherein R7 is a tuted alkyl.

In some alternative embodiments, the fluorescent compound of Formula (V) is covalently attached to a nucleotide or oligonucleotide via , wherein R is -NR8R9, and wherein at least one of R8 or R9 is a substituted alkyl. 2017/074880 Definition The section headings used herein are for organizational purposes only and are not to be construed as limiting the subject matter described.

Unless defined otherwise, all technical and ific terms used herein have the same meaning as is commonly understood by one of ordinary skill in the art. The use of the term “including” as well as other forms, such as “include”, “includes,” and “included,” is not limiting. The use of the term “having” as well as other forms, such as , “has,” and “had,” is not limiting. As used in this specification, whether in a tional phrase or in the body of the claim, the terms “comprise(s)” and “comprising” are to be interpreted as having an open-ended meaning. That is, the above terms are to be interpreted synonymously with the phrases “having at least” or “including at least.” For example, when used in the context of a s, the term “comprising” means that the process includes at least the recited steps, but may include additional steps. When used in the context ofa compound, composition, or device, the term “comprising” means that the compound, composition, or device includes at least the recited features or ents, but may also include onal features or components.

As used herein, common organic abbreviations are defined as follows: Ac Acetyl AC2O Acetic anhydride aq. Aqueous BOC or Boc tert—Butoxycarbonyl BOP triazol-l -yloxy)tris(dimethylamino)phosphonium hexafluorophosphate cat. Catalytic c’C Temperature in degrees Centigrade dATP Deoxyadenosine triphosphate dCTP Deoxycytidine triphosphate dGTP Deoxyguanosine triphosphate dTTP Deoxythymidine triphosphate ddNTP(s) Dideoxynucleotide(s) DCM Methylene chloride DMA ylacetamide DMF Dimethylformamide Et Ethyl EtOAc Ethyl acetate ffl\l Fully fianctional Nucleotide Conjugate ffC Fully fimctional Cytidine Conjugate g Gram(s) h or hr Hour(s) IPA pyl Alcohol LCMS Liquid chromatography-mass spectrometry MeCN Acetonitrile mL Milliliter(s) PG Protecting group Ph Phenyl ppt Precipitate PyBOP (Benzotriazol-l -yloxy)tripyrrolidinophosphonium hexafluorophosphate rt Room temperature SBS Sequencing by sis TEA Triethylamine TEAB Tetraethylammonium bicarbonate TFA Trifluoroacetic acid Tert, t tertiary THF Tetrahydrofuran TLC Thin Layer tography TSTU O-(N—Succinimidyl)—N,N,N',N’-tetramethyluronium tetrafluoroborate uL Micro liter(s) As used herein, the term “covalently ed” or “covalently ” refers to the forming ofa chemical bonding that is characterized by the sharing of pairs of electrons between atoms.

For example, a covalently attached polymer coating refers to a polymer coating that forms chemical bonds With a fimctionalized e of a substrate, as compared to ment to the surface via other means, for example, adhesion or electrostatic interaction. It will be iated that polymers that are attached covalently to a surface can also be bonded Via means in addition to covalent attachment.

The term “halogen” or “halo,” as used herein, means any one of the radio-stable atoms of column 7 of the Periodic Table of the Elements, e.g., fluorine, chlorine, bromine, or iodine, with fluorine and chlorine being preferred.

As used herein, “alkyl” refers to a straight or branched hydrocarbon chain that is fully saturated (i.e., contains no double or triple bonds). The alkyl group may have 1 to 20 carbon atoms (whenever it appears herein, a numerical range such as “l to 20” refers to each integer in the given range; e.g., “l to 20 carbon atoms” means that the alkyl group may consist of 1 carbon atom, 2 carbon atoms, 3 carbon atoms, eta, up to and including 20 carbon atoms, although the t definition also covers the occurrence ofthe term “alkyl” where no numerical range is designated). The alkyl group may also be a medium size alkyl having 1 to 9 carbon atoms. The alkyl group could also be a lower alkyl having 1 to 6 carbon atoms. The alkyl group may be designated as “C1_4 alkyl” or similar designations. By way of example only, “C1_5 alkyl” indicates that there are one to six carbon atoms in the alkyl chain, i.e., the alkyl chain is ed from the group ting of methyl, ethyl, propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, and l. Typical alkyl groups include, but are in no way limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tertiary butyl, pentyl, hexyl, and the like.

As used herein, “alkoxy” refers to the formula —OR wherein R is an alkyl as is defined above, such as “C1.9 alkoxy”, including but not limited to y, ethoxy, n-propoxy, 1- methylethoxy (isopropoxy), n-butoxy, iso-butoxy, sec-butoxy, and tert—butoxy, and the like.

As used herein, “alkenyl” refers to a straight or branched hydrocarbon chain containing one or more double bonds. The l group may have 2 to 20 carbon atoms, although the present definition also covers the occurrence of the term “alkenyl” where no numerical range is designated. The alkenyl group may also be a medium size alkenyl having 2 to 9 carbon atoms. The alkenyl group could also be a lower alkenyl having 2 to 6 carbon atoms. The l group may be designated as “C25 l” or similar designations. By way ofexample only, “C2—6 alkenyl” indicates that there are two to six carbon atoms in the alkenyl chain, i.e., the alkenyl chain is selected from the group consisting of ethenyl, propen-l -yl, propenyl, propenyl, buten-l-yl, butenyl, buten yl, buten—4-yl, 1—methy1-propen—l-yl, yl—propenyl, l-ethyl—ethen—l-yl, 2-methyl-propen—3- yl, buta—l,3-dienyl, buta—l ,2,-dienyl, and buta-l,2-dienyl. Typical l groups include, but are in no way limited to, ethenyl, propenyl, l, pentenyl, and hexenyl, and the like.

As used herein, “alkynyl” refers to a straight or branched hydrocarbon chain containing one or more triple bonds. The alkynyl group may have 2 to 20 carbon atoms, although the present definition also covers the occurrence of the term “alkynyl” where no numerical range is designated. The alkynyl group may also be a medium size alkynyl having 2 to 9 carbon atoms. The alkynyl group could also be a lower alkynyl having 2 to 6 carbon atoms. The alkynyl group may be ated as “C245 l” or similar designations. By way ofexample only, “C26 alkynyl” indicates that there are two to six carbon atoms in the alkynyl chain, i.e., the alkynyl chain is selected from the group consisting of ethynyl, propyn-l-yl, propynyl, butyn-l-yl, butynyl, butynyl, and 2- l. Typical alkynyl groups include, but are in no way limited to, ethynyl, propynyl, butynyl, pentynyl, and hexynyl, and the like.

As used , “heteroalkyl” refers to a straight or branched hydrocarbon chain containing one or more atoms, that is, an element other than carbon, including but not limited to, nitrogen, oxygen and sulfur, in the chain backbone. The heteroalkyl group may have 1 to 20 carbon atom, although the t definition also covers the occurrence of the term “heteroalkyl” where no numerical range is designated. The heteroalkyl group may also be a medium size heteroalkyl having 1 to 9 carbon atoms. The heteroalkyl group could also be a lower heteroalkyl having 1 to 6 carbon atoms. The heteroalkyl group may be designated as “C16 heteroalkyl” or similar designations. The heteroalkyl group may contain one or more heteroatoms. By way of example only, “C1-6 heteroalkyl” indicates that there are one to six carbon atoms in the heteroalkyl chain and additionally one or more heteroatoms in the backbone ofthe chain.

The term “aromatic” refers to a ring or ring system haVing a conjugated pi electron system and es both yclic aromatic (e. g., ) and heterocyclic aromatic groups (e. g., pyridine). The term includes monocyclic or fused-ring polycyclic (i.e., rings which share adjacent pairs of atoms) groups provided that the entire ring system is aromatic.

As used herein, “aryl” refers to an aromatic ring or ring system (i.e., two or more fused rings that share two adjacent carbon atoms) containing only carbon in the ring backbone. When the aryl is a ring system, every ring in the system is aromatic. The aryl group may have 6 to 18 carbon atoms, although the t definition also covers the occurrence of the term “aryl” where no numerical range is designated. In some embodiments, the aryl group has 6 to 10 carbon atoms. The aryl group may be designated as “C640 aryl,” “C6 or C10 aryl,” or r designations. Examples of aryl groups include, but are not limited to, phenyl, naphthyl, azulenyl, and anthracenyl.

An “aralkyl” or “arylalkyl” is an aryl group connected, as a substituent, Via an alkylene group, such as “C744 aralkyl” and the like, including but not limited to benzyl, ylethyl, 3-phenylpropyl, and naphthylalkyl. In some cases, the alkylene group is a lower alkylene group (i.e., a C1_6 ne group).

As used herein, “heteroaryl” refers to an aromatic ring or ring system (i.e., two or more fiJsed rings that share two adjacent atoms) that contain(s) one or more heteroatoms, that is, an element other than carbon, including but not limited to, en, oxygen and sulfur, in the ring backbone. When the heteroaryl is a ring , every ring in the system is aromatic. The heteroaryl group may have 5-18 ring members (i.e., the number of atoms making up the ring backbone, including carbon atoms and heteroatoms), although the present definition also covers the occurrence ofthe term “heteroaryl” Where no numerical range is designated. In some embodiments, the heteroaryl group has to 10 ring members or 5 to 7 ring members. The heteroaryl group may be designated as “5-7 membered heteroaryl,” “5-10 membered heteroaryl,” or similar ations. Examples ofheteroaryl rings include, but are not limited to, furyl, thienyl, phthalazinyl, pyrrolyl, oxazolyl, thiazolyl, olyl, pyrazolyl, isoxazolyl, isothiazolyl, triazolyl, thiadiazolyl, nyl, pyridazinyl, pyrimidinyl, pyrazinyl, triazinyl, quinolinyl, isoquinlinyl, benzimidazolyl, benzoxazolyl, hiazolyl, indolyl, isoindolyl, and hienyl.

A “heteroaralkyl” or “heteroarylalkyl” is heteroaryl group connected, as a substituent, via an alkylene group. Examples include but are not limited to 2-thienylmethyl, 3- thienylmethyl, ethyl, thienylethyl, pyrrolylalkyl, pyridylalkyl, isoxazollylalkyl, and imidazolylalkyl. In some cases, the alkylene group is a lower alkylene group (i.e., a (31-6 ne As used herein, “carbocyclyl” means a non-aromatic cyclic ring or ring system containing only carbon atoms in the ring system backbone. When the carbocyclyl is a ring system, two or more rings may bejoined to gether in a filSCd, bridged or Spiro-connected fashion. Carbocyclyls may have any degree of saturation provided that at least one ring in a ring system is not aromatic.

Thus, yclyls include cycloalkyls, cycloalkenyls, and lkynyls. The carbocyclyl group may have 3 to 20 carbon atoms, although the present definition also covers the occurrence of the term “carbocyclyl” Where no numerical range is designated. The yclyl group may also be a medium size carbocyclyl having 3 to 10 carbon atoms. The carbocyclyl group could also be a yclyl having 3 to 6 carbon atoms. The carbocyclyl group may be designated as “C345 carbocyclyl” or similar designations. Examples of carbocyclyl rings include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclohexenyl, 2,3-dihydro—indene, bicycle[2.2.2]octanyl, adamantyl, and spiro[4.4]nonanyl.

As used herein, “cycloalkyl” means a fully ted carbocyclyl ring or ring system. Examples include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.

As used herein, “heterocyclyl” means a omatic cyclic ring or ring system containing at least one heteroatom in the ring backbone. Heterocyclyls may be joined together in a fused, bridged or Spiro-connected fashion. Heterocyclyls may have any degree of saturation provided that at least one ring in the ring system is not aromatic. The heteroatom(s) may be present in either a non-aromatic or aromatic ring in the ring system. The heterocyclyl group may have 3 to 20 ring members (i.e., the number of atoms making up the ring backbone, including carbon atoms and heteroatoms), although the present definition also covers the occurrence of the term ocyclyl” where no numerical range is designated. The heterocyclyl group may also be a medium size MmmwdflhmmgfloflhmgmmwflsTmmdflmyfidgmmmmMaMflwamwmwdflhwmg 3 to 6 ring members. The heterocyclyl group may be designated as “3-6 membered heterocyclyl” or similar designations. In preferred six membered monocyclic heterocyclyls, the heteroatom(s) are selected from one up to three of O, N or S, and in preferred five membered monocyclic heterocyclyls, the heteroatom(s) are selected from one or two heteroatoms selected from O, N, or S. Examples of heterocyclyl rings include, but are not limited to, yl, acridinyl, olyl, cinnolinyl, dioxolanyl, imidazolinyl, imidazolidinyl, morpholinyl, oxiranyl, oxepanyl, thiepanyl, piperidinyl, piperazinyl, dioxopiperazinyl, pyrrolidinyl, pyrrolidonyl, pyrrolidionyl, 4-piperidonyl, pyrazolinyl, pyrazolidinyl, 1,3-dioxinyl, 1,3-dioxanyl, oxinyl, oxanyl, 1,3-oxathianyl, l,4-oxathiinyl, 1,4-oxathianyl, 2H-l,2-oxazinyl, trioxanyl, hexahydro-l,3,5-triazinyl, 1,3-dioxolyl, 1,3-dioxolanyl, 1,3-dithiolyl, 1,3-dithiolanyl, isoxazolinyl, isoxazolidinyl, oxazolinyl, oxazolidinyl, oxazolidinonyl, thiazolinyl, thiazolidinyl, 1,3-oxathiolanyl, indolinyl, isoindolinyl, tetrahydrofiJranyl, tetrahydropyranyl, tetrahydrothiophenyl, tetrahydrothiopyranyl, ydro—l ,4-thiazinyl, thiamorpholinyl, obenzofuranyl, benzimidazolidinyl, and tetrahydroquinoline.

An “O-carboxy” group refers to a “-OC(=O)R” group in which R is selected from hydrogen, C1_6 alkyl, C2_6 alkenyl, C2_6 l, C3.7 carbocyclyl, C640 aryl, 5-10 membered heteroaryl, and 3-10 membered cyclyl, as defined herein.

A “C-carboxy” group refers to a “-C(=O)OR” group in which R is selected from hydrogen, C1—6 alkyl, C2—6 alkenyl, C2—6 alkynyl, C3-7 yclyl, C6—10 aryl, 5-10 membered heteroaryl, and 3-10 membered cyclyl, as defined herein. A non-limiting example includes yl (i.e., -C(=O)OH).

A “cyano” group refers to a “-CN” group.

A “sulfonyl” group refers to an “-S02R” group in which R is selected from hydrogen, C1_6 alkyl, C2_6 l, C2_6 alkynyl, C3.7 carbocyclyl, C640 aryl, 5-10 membered heteroaryl, and 3-10 membered heterocyclyl, as defined herein.

A “sulfonyl hydroxide” or “sulfo” group refers to a “-S(=O)2-OH” group.

A “sulfino” group refers to a “—S(=O)OH” group.

A “sulfonate” group refers to -S03_.

A “sulfonyl halide” group refers to a )2-X” group, wherein X is a halide.

An “S-sulfonamido” group refers to a “-S02NRARB” group in which RA and R3 are each independently selected from hydrogen, C1-6 alkyl, C2—6 alkenyl, C2—6 alkynyl, C3.7 carbocyclyl, C6— aryl, 5-10 ed heteroaryl, and 3-10 membered heterocyclyl, as defined herein.

An “N-sulfonamido” group refers to a “-N(RA)S02RB” group in which RA and Rb are each independently selected from hydrogen, C1_6 alkyl, C2_6 alkenyl, C2_6 alkynyl, C3_7 carbocyclyl, C640 aryl, 5-10 membered heteroaryl, and 3-10 membered heterocyclyl, as defined herein.

A “C-amido” group refers to a “-C(=O)NRARB” group in which RA and R3 are each independently selected from hydrogen, C1_6 alkyl, C26 l, C2_6 alkynyl, C3_7 yclyl, C640 aryl, 5-10 membered heteroaryl, and 3-10 membered heterocyclyl, as defined herein.

An “N-amido” group refers to a )C(=O)RB” group in which RA and R3 are each independently selected from hydrogen, C16 alkyl, C2-6 alkenyl, C26 alkynyl, C34 carbocyclyl, C6- aryl, 5-10 ed heteroaryl, and 3-10 membered heterocyclyl, as defined herein.

An “amino” group refers to a “-NRARB” group in which RA and R3 are each independently selected from hydrogen, C1_6 alkyl, C2_6 alkenyl, C2_6 alkynyl, C3_7 carbocyclyl, C640 aryl, 5-10 membered heteroaryl, and 3-10 membered heterocyclyl, as d herein. A non-limiting example es free amino (i.e., -NH2).

An “aminoalkyl” group refers to an amino group connected Via an ne group.

An “aminosulfonyl” group refers to a “-S(=O)2NH2” group.

An “alkoxyalkyl” group refers to an alkoxy group connected Via an ne group, such as a “C24; alkoxyalkyl” and the like.

As used herein, a substituted group is derived from the unsubstituted parent group in which there has been an exchange ofone or more hydrogen atoms for another atom or group. Unless otherwise indicated, when a group is deemed to be ituted,” it is meant that the group is substituted with one or more substituents ndently selected from C1-C6 alkyl, C1-C6 alkenyl, C1- C6 alkynyl, C1-C6 heteroalkyl, C3-C7 carbocyclyl (optionally substituted with halo, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 haloalkoxy), C3-C7-carbocyclyl-C1-C6-alkyl (optionally substituted with halo, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 haloalkoxy), 3-10 membered heterocyclyl (optionally substituted with halo, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 haloalkoxy), 3-10 membered heterocyclyl-C1-C6-alkyl (optionally substituted with halo, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 koxy), aryl nally substituted with halo, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 haloalkoxy), aryl(C1-C6)alkyl nally substituted with halo, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 haloalkoxy), 5-10 membered heteroaryl (optionally substituted with halo, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 haloalkoxy), 5-10 membered heteroaryl(C1-C6)alkyl (optionally substituted with halo, C1- C6 alkyl, C1-C6 alkoxy, C1-C6 haloalkyl, and C1-C6 haloalkoxy), halo, cyano, hydroxy, C1-C6 , C1-C6 alkoxy(C1-C6)alkyl (i.e., ether), aryloxy, sulfhydryl (mercapto), 1-C6)alkyl (e.g., —CF3), halo(C1-C6)a1koxy (e.g., , C1-C6 hio, arylthio, amino, amino(C1-C6)alkyl, nitro, O- carbamyl, amyl, O-thiocarbamyl, carbamyl, C-amido, N-amido, S-sulfonamido, N- sulfonamido, C-carboxy, O-carboxy, acyl, cyanato, isocyanato, thiocyanato, isothiocyanato, sulfinyl, sulfonyl, sulfo, , sulfonate, and oxo (=0). Wherever a group is described as “optionally substituted” that group can be substituted with the above substituents.

As understood by one of ordinary skill in the art, if a compound contains positively or negatively charged substituent groups, for example, 803—, it may also contains a negatively or positively charged counterion such that the compound as a whole is neutral.

It is to be understood that certain radical naming conventions can include either a mono-radical or a di-radical, ing on the context. For example, where a substituent requires two points of attachment to the rest ofthe le, it is understood that the substituent is a di-radical. For example, a substituent identified as alkyl that requires two points of attachment includes di-radicals such as —CH2—, —CH2CH2—, —CH2CH(CH3)CH2—, and the like. Other radical naming conventions clearly indicate that the radical is a di-radical such as “alkylene” or “alkenylene.” When two “adjacent” R groups are said to form a ring “together with the atom to which they are attached,” it is meant that the collective unit of the atoms, intervening bonds, and the two R groups are the recited ring. For example, when the following substructure is present: and R1 and R2 are defined as selected from the group ting ofhydrogen and alkyl, or R1 and R2 er with the atoms to which they are attached form an aryl or carbocyclyl, it is meant that R1 and R2 can be selected from hydrogen or alkyl, or atively, the substructure has structure: where A is an aryl ring or a carbocyclyl containing the depicted double bond.

Labeled Nucleotides The dye compounds described herein are suitable for ment to substrate moieties. Substrate moieties can be Virtually any molecule or substance to which the fluorescent dyes described herein can be conjugated and, by way of non-limiting example, may include nucleosides, tides, polynucleotides, carbohydrates, ligands, particles, solid surfaces, organic and inorganic polymers and combinations or lages thereof, such as chromosomes, nuclei, living cells and the like. The dyes can be conjugated by an optional linker by a variety ofmeans including hydrophobic attraction, ionic attraction and covalent attachment. ularly the dyes are conjugated to the substrate by covalent attachment. More particularly the covalent attachment is by means of a linker group. In some instances, such labeled nucleotides are also referred to as “modified nucleotides.” A particular useful ation of the new fluorescent dyes with long Stokes shift as bed herein is for labeling ofbiomolecules, for example, nucleotides or oligonucleotides. Some embodiments of the present application are directed to a tide or oligonucleotide labeled with the new cent nds as described herein.

The attachment to the biomolecules may be via -C(=O)R moiety of the compound of Formula (I) or (V). In some embodiments, R is -OR7 and R7 is a substituted alkyl, which may be used for attachment to the amino group of the biomolecules. In one embodiment, -C(O)R moiety may be an activated ester residue most suitable for further amide/peptide bond formation. The term “activated ester” as used herein, refers to a carboxy group tive which is capable of reacting in mild conditions, for example, with a compound containing an amino group. Non-limiting examples of activated esters include but not limited to ophenyl, pentafluorophenyl and succinimido esters. In some other embodiments, R is -NR8R9 and at least one of R8 or R9 contains at least one functional group which may be used for attachment to the biomolecules, for example, one of R8 or R9 is a substituted alkyl comprising at least one carboxyl.

In some embodiments, the dye compounds may be covalently attached to oligonucleotides or nucleotides via the nucleotide base. For e, the labeled nucleotide or oligonucleotide may have the label ed to the C5 position of a pyrimidine base or the C7 position of a 7-deaza purine base through a linker moiety. The labeled nucleotide or ucleotide may also have a 3'-OH blocking group covalently attached to the ribose or deoxyribose sugar of the nucleotide.

Linkers The dye compounds as disclosed herein may include a reactive linker group at one of the substituent positions for covalent attachment of the compound to another molecule. Reactive linking groups are es capable of g a covalent bond. In a ular ment the linker may be a cleavable linker. Use of the term “cleavable linker” is not meant to imply that the whole linker is required to be removed. The cleavage site can be located at a position on the linker that ensures that part of the linker remains attached to the dye and/or substrate moiety after cleavage.

Cleavable linkers may be, by way of non-limiting example, electrophilically cleavable linkers, nucleophilically cleavable linkers, photocleavable linkers, ble under reductive conditions (for example disulfide or azide containing linkers), oxidative conditions, cleavable via use of safety-catch linkers and cleavable by elimination mechanisms. The use of a cleavable linker to attach the dye compound to a substrate moiety ensures that the label can, if required, be removed after detection, avoiding any interfering signal in downstream steps.

Non-limiting es oflinker groups include those disclosed in PCT Publication No. /018493 n incorporated by nce), which connect the bases of nucleotides to labels such as, for example, the new fluorescent compounds described herein. These s may be d using water-soluble phosphines or water-soluble transition metal catalysts formed from a transition metal and at least partially water-soluble ligands. In aqueous solution the latter form at least partially soluble transition metal complexes. Additional suitable linkers that may be used include those disclosed in PCT Publication No. W02004/018493 and (both of which are herein incorporated by nces. It was discovered that by altering, and in particular increasing, the length of the linker between a fluorescent dye (fluorophore) and the guanine base, by introducing a polyethylene glycol spacer group, it is possible to increase the fluorescence intensity compared to the same fluorophore attached to the guanine base through other linkages known in the art. The design of the linkers, and especially their increased length, also allows improvements in the brightness of fluorophores attached to the guanine bases of guanosine nucleotides when incorporated into polynucleotides such as DNA. Thus, when the dye is for use in any method of is which requires detection of a fluorescent dye label attached to a guanine-containing nucleotide, it is advantageous if the linker comprises a spacer group of formula —((CH2)2O)n—, wherein n is an integer between 2 and 50, as described in . sides and nucleotides may be labeled at sites on the sugar or nucleobase. As understood by one of ry skill in the art, a "nucleotide" consists of a enous base, a sugar, and one or more phosphate groups. In RNA the sugar is ribose and in DNA is a deoxyribose, i.e. a sugar lacking a hydroxyl group that is present in ribose. The nitrogenous base is a derivative of purine or pyrimidine. The purines are adenine (A) and guanine (G), and the pyrimidines are cytosine (C) and thymine (T) or in the context of RNA, uracil (U). The C—l atom of deoxyribose is bonded to N-l of a 2017/074880 dine or N—9 ofa purine. A nucleotide is also a phosphate ester of a nucleoside, with esterification occurring on the hydroxyl group attached to the C—3 or C—5 ofthe sugar. Nucleotides are usually mono, di- or triphosphates.

A "nucleoside" is structurally similar to a nucleotide but is missing the phosphate moieties. An example of a nucleoside analog would be one in which the label is linked to the base and there is no phosphate group attached to the sugar molecule.

Although the base is usually referred to as a purine or pyrimidine, the skilled person will appreciate that derivatives and analogues are available which do not alter the capability of the nucleotide or nucleoside to undergo Watson-Crick base pairing. "Derivative" or "analogue" means a compound or le whose core ure is the same as, or closely resembles that of a parent nd but which has a chemical or al ation, such as, for example, a different or additional side group, which allows the derivative nucleotide or side to be linked to another molecule. For example, the base may be a deazapurine. The derivatives should be capable of undergoing Watson-Crick pairing. "Derivative" and "analogue" also mean a synthetic nucleotide or nucleoside derivative having modified base es and/or modified sugar moieties. Such derivatives and analogues are discussed in, for example, Scheit, Nucleotide analogs (John Wiley & Son, 1980) and Uhlman et al., Chemical Reviews 90:543-584, 1990. Nucleotide analogues can also comprise modified odiester linkages including orothioate, phosphorodithioate, alkylphosphonate , phosphoranilidate, phosphoramidate linkages and the like.

The dye may be attached to any position on the nucleotide base, through a linker, provided that Watson-Crick base pairing can still be carried out. Particular nucleobase labeling sites include the C5 position of a pyrimidine base or the C7 position of a 7-deaza purine base. As described above a linker group may be used to covalently attach a dye to the side or nucleotide.

In particular embodiments the labeled nucleoside or nucleotide may be enzymatically incorporable and enzymatically extendable. Accordingly a linker moiety may be of sufficient length to connect the nucleotide to the nd such that the compound does not significantly interfere with the overall binding and recognition of the nucleotide by a nucleic acid replication enzyme. Thus, the linker can also comprise a spacer unit. The spacer distances, for example, the nucleotide base from a cleavage site or label.

Nucleosides or nucleotides labeled with the new fluorescent dyes bed herein may have the formula: B-L-Dye R’O R’” where Dye is a dye compound, B is a nucleobase, such as, for e uracil, thymine, ne, adenine, guanine and the like and L is an optional linker group which may or may not be present. R' can be H, monophosphate, diphosphate, triphosphate, thiophosphate, a phosphate ester analog, —0— attached to a reactive phosphorous ning group or —O— protected by a blocking group. R" can be H, OH, a phosphoramidite or a 3'-OH blocking group and R'" is H or OH; where R" is phosphoramidite, R' is an leavable hydroxyl protecting group which allows subsequent monomer coupling under automated synthesis conditions.

In some instances, the blocking group is separate and independent of the dye compound, i.e. not attached to it. Alternatively, the dye may comprise all or part ofthe 3'—OH blocking group. Thus R" can be a 3'—OH blocking group which may or may not comprise the dye compound. In additional ative embodiments, there is no blocking group on the 3' carbon of the pentose sugar and the dye (or dye and linker construct) attached to the base, for e, can be of a size or structure sufficient to act as a block to the incorporation of a further nucleotide from a point other than the 3' site. Thus the block can be due to steric hindrance or can be due to a combination of size, charge and ure.

The use of a blocking group allows polymerization to be controlled, such as by stopping ion when a modified nucleotide is incorporated. If the blocking effect is reversible, for example by way of non-limiting example by changing chemical conditions or by removal of a chemical block, extension can be stopped at n points and then allowed to continue.

Non-limiting examples of 3'-OH blocking groups include those disclosed in and WO2014/139596, which are hereby incorporated by references. For example the ng group may be azidomethyl (-CH2N3) or substituted azidomethyl (e.g., -CH(CHF2)N3 or F)N3), or allyl.

In a particular embodiment the linker and ng group are both present and are separate moieties which are both cleavable under substantially similar conditions. Thus deprotection and deblocking processes may be more efficient since only a single treatment will be required to remove both the dye compound and the blocking group.

The present disclosure also directs to encompassing polynucleotides incorporating dye compounds described herein. Such cleotides may be DNA or RNA comprised respectively of deoxyribonucleotides or ribonucleotides joined in phosphodiester linkage. Polynucleotides may comprise naturally occurring nucleotides, non-naturally occurring (or modified) nucleotides other than the labeled nucleotides described herein or any ation thereof, provided that at least one nucleotide labeled with a dye nd, according to the present application is present.

Polynucleotides may also include non-natural ne linkages and/or non-nucleotide chemical modifications. Chimeric structures comprised of es of ribonucleotides and deoxyribonucleotides comprising at least one labeled nucleotide are also contemplated.

Non-limiting exemplary d nucleotides as described herein include: ffC-I-1 ffC-l-6 0H ffC-I-9 WO 60482 O O —N N~Jf‘”»\1<:;>H OfN \ \ \RO N3 H N /~\/ HO\’ é?\q o Ho—F]=O O\‘ /O ffC-l-11 OH Some embodiments disclosed herein are kits including nucleosides and/or nucleotides labeled with the new fluorescent dyes described herein. Such kits will generally include at least one nucleotide or nucleoside labeled with a dye together with at least one further component.

The r component(s) may be fithher modified or unmodified nucleotides or nucleosides. For example, nucleotides labeled with dyes may be supplied in ation with unlabeled or native nucleotides, and/or with fluorescently labeled nucleotides or any ation thereof. Combinations of nucleotides may be provided as separate individual components or as nucleotide es. In some embodiments, the kits comprise one or more nucleotides wherein at least one nucleotide is a nucleotide labeled with a new fluorescent compound described herein. The kits may se two or more labeled nucleotides. The nucleotides may be labeled with two or more fluorescent labels. Two or more of the labels may be excited using a single excitation source, which may be a laser.

The kits may contain four labeled nucleotides, where the first of four nucleotides is labeled with a compound as disclosed herein, and the , third, and fourth nucleotides are each labeled with a different compound, wherein each compound has a distinct fluorescence maximum and each of the compounds is distinguishable from the other three compounds. The kits may be such that two or more of the compounds have a similar absorbance maximum but different Stokes shift.

The fluorescent dye compounds, d nucleotides or kits described herein may be used in sequencing, expression analysis, hybridization analysis, genetic analysis, RNA analysis or protein binding . The use may be on an automated cing instrument. The sequencing ment may contain two lasers operating at ent wavelengths.

Where kits se a plurality, particularly two, more particularly four, nucleotides labeled with a dye compound, the different nucleotides may be labeled with different dye compounds, or one may be dark, with no dye compounds. Where the different nucleotides are labeled with different dye compounds it is a feature of the kits that said dye compounds are spectrally distinguishable fluorescent dyes. As used herein, the term "spectrally distinguishable fluorescent dyes" refers to fluorescent dyes that emit cent energy at wavelengths that can be distinguished by fluorescent detection equipment (for example, a commercial capillary based DNA sequencing platform) when two or more such dyes are present in one sample. When two nucleotides labeled with fluorescent dye compounds are supplied in kit form, the spectrally distinguishable fluorescent dyes can be excited at the same wavelength, such as, for example by the same laser in some embodiments.

When four nucleotides labeled with fluorescent dye compounds are supplied in kit form, two of the spectrally distinguishable fluorescent dyes can both be excited at one wavelength and the other two spectrally guishable dyes can both be excited at another wavelength in some embodiments. ular excitation wavelengths are about 460 nm.

In one embodiment a kit comprises a nucleotide d with a nd described herein and a second nucleotide labeled with a second dye wherein the dyes have a difference in absorbance maximum of at least 10 nm, particularly 20 nm to 50 nm. More particularly the two dye nds have Stokes shifts ofbetween 15-40 nm or between 20-40 nm. As used herein, the term "Stokes shift" is the difference between ons of the band maxima of the absorption and emission spectra of the same electronic transition.

In a further embodiment said kit fithher comprises two other nucleotides labeled with fluorescent dyes wherein said dyes are excited by the same laser at about 460 nm to about 540 In an alternative embodiment, the kits may contain nucleotides where the same base is labeled with two different compounds. A first nucleotide may be labeled with a compound described herein. A second tide may be labeled with a spectrally distinct compound, for example a ‘red’ dye absorbing at greater than 600 nm. A third nucleotide may be labeled as a mixture ofthe fluorescent dye compound bed herein and the spectrally distinct compound, and the fourth nucleotide may be ‘dark’ and contain no label. In simple terms therefore the tides l-4 may be labeled ‘green’, ‘red’, ‘red/green’, and dark. To simplify the instrumentation further, four nucleotides can be labeled with a two dyes excited with a single laser, and thus the labeling ofnucleotides l-4 may be ‘green 1’, ‘green 2’ ‘green 1/green 2’, and dark.

In other embodiments the kits may include a polymerase enzyme capable of catalyzing incorporation of the nucleotides into a polynucleotide. Other components to be included in such kits may include buffers and the like. The tides labeled with the new fluorescent dyes described , and other any nucleotide components ing mixtures of different nucleotides, may be provided in the kit in a concentrated form to be diluted prior to use. In such embodiments a suitable dilution buffer may also be included. 2017/074880 Methods of Sequencing Nucleotides (or nucleosides) comprising a new fluorescent dye bed herein may be used in any method of analysis which requires detection of a fluorescent label attached to a nucleotide or nucleoside, r on its own or incorporated into or associated with a larger molecular structure or ate. Some embodiments of the present application are directed to methods of sequencing including: (a) incorporating at least one labeled nucleotide as described herein into a polynucleotide; and (b) detecting the labeled nucleotide(s) orated into the cleotide by detecting the fluorescent signal from the new fluorescent dye attached to said modified nucleotide(s).

In some embodiments, at least one d nucleotide is incorporated into a polynucleotide in the synthetic step by the action of a polymerase enzyme. However, other methods of orating labeled nucleotides to polynucleotides, such as chemical ucleotide synthesis or ligation of labeled oligonucleotides to unlabeled oligonucleotides, are not excluded. Therefore, the term "incorporating" a nucleotide into a polynucleotide encompasses polynucleotide synthesis by chemical methods as well as enzymatic methods.

In all embodiments ofthe methods, the detection step may be carried out whilst the polynucleotide strand into which the labeled nucleotides are incorporated is annealed to a template strand, or after a denaturation step in which the two strands are separated. Further steps, for example chemical or tic reaction steps or ation steps, may be included between the synthetic step and the detection step. In particular, the target strand incorporating the labeled nucleotide(s) may be isolated or purified and then processed further or used in a subsequent analysis. By way of example, target polynucleotides labeled with modified nucleotide(s) as bed herein in a synthetic step may be subsequently used as labeled probes or primers. In other ments the product ofthe synthetic step (a) may be subject to further reaction steps and, if desired, the product ofthese uent steps purified or ed.

Suitable conditions for the synthetic step will be well known to those familiar with standard molecular biology techniques. In one embodiment the synthetic step may be analogous to a standard primer extension reaction using nucleotide precursors, including modified nucleotides according to the present disclosure, to form an extended target strand complementary to the template strand in the presence of a suitable polymerase enzyme. In other embodiments the synthetic step may itself form part of an amplification on producing a labeled double stranded amplification product comprised of annealed complementary strands derived from copying of the target and template polynucleotide strands. Other exemplary "synthetic" steps include nick translation, strand WO 60482 displacement polymerization, random primed DNA labeling etc. The polymerase enzyme used in the synthetic step must be capable of catalyzing the incorporation of modified nucleotides ing to the present disclosure. Otherwise, the precise nature of the rase is not particularly limited but may depend upon the conditions ofthe synthetic reaction. By way ofexample, ifthe synthetic on is carried out using thermocycling then a thermostable polymerase is required, whereas this may not be essential for rd primer extension reactions. Suitable thermostable polymerases which are capable of incorporating the modified nucleotides according to the present disclosure include those described in or WC 2006/120433. In synthetic reactions which are carried out at lower temperatures such as 37°C, polymerase enzymes need not necessarily be thermostable polymerases, therefore the choice of rase will depend on a number of factors such as reaction temperature, pH, strand-displacing activity and the like.

In specific non-limiting embodiments, the modified nucleotides or nucleosides labeled with the new fluorescent dyes with longer Stokes shifi according to the present application may be used in a method ofnucleic acid sequencing, re-sequencing, whole genome sequencing, single nucleotide polymorphism scoring, any other application involving the detection of the modified nucleotide or nucleoside when orated into a polynucleotide, or any other ation requiring the use of polynucleotides labeled with the modified nucleotides comprising fluorescent dyes according to the present application.

In a particular embodiment the t application provides use of modified nucleotides comprising dye compounds described herein in a polynucleotide "sequencing-by- synthesis" reaction. cing-by—synthesis generally es sequential addition of one or more nucleotides or oligonucleotides to a growing cleotide chain in the 5' to 3' direction using a polymerase or ligase in order to form an extended polynucleotide chain complementary to the template nucleic acid to be sequenced. The identity ofthe base present in one or more ofthe added nucleotide(s) is determined in a detection or "imaging" step. The ty ofthe added base may be determined afier each nucleotide incorporation step. The sequence of the template may then be inferred using conventional Watson-Crick base-pairing rules. The use ofthe modified nucleotides labeled with dyes according to the present sure for determination of the identity of a single base may be useful, for example, in the scoring of single nucleotide polymorphisms, and such single base extension reactions are within the scope of this application.

In an embodiment, the sequence of a template polynucleotide is determined by detecting the oration of one or more nucleotides into a t strand complementary to the te polynucleotide to be sequenced through the detection of fluorescent label(s) attached to the incorporated nucleotide(s). Sequencing ofthe te polynucleotide is primed with a suitable primer (or prepared as a hairpin construct which will contain the primer as part ofthe hairpin), and the nascent chain is ed in a stepwise manner by addition of nucleotides to the 3' end of the primer in a polymerase-catalyzed reaction.

In particular embodiments each of the different nucleotide triphosphates (A, T, G and C) may be labeled with a unique fluorophore and also comprises ablocking group at the 3' position to prevent uncontrolled polymerization. Alternatively one of the four nucleotides may be unlabeled (dark). The polymerase enzyme incorporates a nucleotide into the t chain complementary to the template cleotide, and the blocking group prevents further incorporation of nucleotides. Any unincorporated nucleotides are removed and the cent signal from each incorporated nucleotide is "read" optically by suitable means, such as a charge-coupled device using laser excitation and suitable emission filters. The 3'-blocking group and fluorescent dye compounds are then removed (deprotected), particularly by the same chemical or enzymatic method, to expose the nascent chain for further nucleotide incorporation. Typically the identity of the incorporated nucleotide will be determined after each incorporation step but this is not strictly essential. Similarly, US. Pat. No. ,302,509 discloses a method to sequence polynucleotides lized on a solid support. The method relies on the incorporation of fluorescently labeled, cked nucleotides A, G, C and T into a growing strand complementary to the immobilized polynucleotide, in the presence of DNA rase. The polymerase incorporates a base complementary to the target polynucleotide, but is prevented from fithher addition by the 3'-blocking group. The label of the incorporated nucleotide can then be determined and the blocking group removed by chemical cleavage to allow further polymerization to occur. The nucleic acid template to be sequenced in a sequencing-by—synthesis reaction may be any polynucleotide that it is desired to sequence. The nucleic acid template for a sequencing reaction will typically comprise a double stranded region having a free 3' yl group which serves as a primer or initiation point for the addition of further nucleotides in the cing reaction. The region of the template to be sequenced will overhang this fiee 3' hydroxyl group on the complementary strand. The overhanging region ofthe template to be sequenced may be single stranded but can be —stranded, provided that a "nick is present" on the strand complementary to the template strand to be sequenced to e a free 3' OH group for initiation ofthe sequencing reaction.

In such ments sequencing may proceed by strand displacement. In certain ments a primer g the free 3' hydroxyl group may be added as a separate component (e.g. a short oligonucleotide) which hybridizes to a -stranded region of the template to be sequenced.

Alternatively, the primer and the template strand to be ced may each form part of a partially self-complementary nucleic acid strand capable of forming an intra-molecular duplex, such as for example a hairpin loop structure. Hairpin polynucleotides and methods by which they may be attached to solid supports are disclosed in PCT Publication Nos. and . tides are added successively to the free 3'-hydroxyl group, resulting in synthesis of a polynucleotide chain in the 5' to 3' direction. The nature of the base which has been added may be determined, particularly but not necessarily after each nucleotide addition, thus ing sequence information for the nucleic acid template. The term "incorporation" of a nucleotide into a nucleic acid strand (or polynucleotide) in this context refers to joining of the nucleotide to the free 3' hydroxyl group of the nucleic acid strand via formation ofa phosphodiester linkage with the 5' phosphate group of the tide.

The nucleic acid template to be sequenced may be DNA or RNA, or even a hybrid molecule comprised of ucleotides and ribonucleotides. The nucleic acid template may comprise naturally occurring and/or non-naturally occurring nucleotides and natural or non-natural backbone linkages, provided that these do not t copying of the template in the sequencing reaction.

In certain ments the nucleic acid template to be sequenced may be attached to a solid support via any suitable linkage method known in the art, for example via covalent attachment. In certain embodiments template polynucleotides may be attached directly to a solid support (e.g. a silica-based support). However, in other embodiments the surface of the solid support may be modified in some way so as to allow either direct nt ment of template cleotides, or to immobilize the template polynucleotides through a hydrogel or polyelectrolyte multilayer, which may itself be non-covalently attached to the solid support.

Arrays in which polynucleotides have been directly attached to silica—based supports are those for example disclosed in PCT ation No. WO 06770, wherein polynucleotides are immobilized on a glass support by reaction between a pendant epoxide group on the glass with an internal amino group on the cleotide. In addition, PCT Publication No.

W02005/047301 ses arrays of polynucleotides attached to a solid support, e.g. for use in the preparation of SMAs, by reaction of a sulfur-based nucleophile with the solid support. A still further example of supported template polynucleotides is where the template cleotides are attached to hydrogel supported upon -based or other solid supports. Silica-based supports are typically used to support hydrogels and hydrogel arrays as described in PCT Publication Nos. WO 00/31148, WO 43, WOO2/12566, WO 03/014392, WO 00/53812 and US. Pat. No. 6,465,178.

A particular surface to which template polynucleotides may be lized is a polyacrylamide hydrogel. Polyacrylamide hydrogels are described in the prior art, some of which is discussed above. Specific hydrogels that may be used in the present application include those described in and US. Pub. No. 2014/0079923. In one embodiment, the hydrogel is PAZAM (poly(N-(5-azidoacetamidylpentyl) acrylamide-co-acrylamide)).

DNA template molecules can be attached to beads or microparticles for the purposes of sequencing; for example as described in US. Pat. No. 6,172,218. Further examples of the preparation of bead libraries where each bead contains different DNA sequences can be found in Margulies et al., Nature 437, 376-380 (2005); Shendure et al., Science. 309(5741): 1728-1732 (2005).

Sequencing of arrays of such beads using nucleotides as described is within the scope of the t application.

The template(s) to be ced may form part of an "array" on a solid t, in which case the array may take any convenient form. Thus, the method of the present disclosure is applicable to all types of "high density" arrays, including single-molecule arrays, clustered arrays and bead arrays. Modified nucleotides labeled with dye compounds ofthe present ation may be used for sequencing templates on essentially any type of array formed by immobilization of nucleic acid molecules on a solid support, and more particularly any type of high-density array. However, the modified nucleotides labeled with the new fluorescent dyes described herein are particularly advantageous in the context of sequencing of clustered arrays.

In multi-polynucleotide or clustered arrays, ct s on the array se le polynucleotide template molecules. The term "clustered array" refers to an array wherein distinct regions or sites on the array comprise multiple polynucleotide molecules that are not individually able by optical means. Depending on how the array is formed each site on the array may comprise multiple copies of one individual polynucleotide molecule or even multiple copies of a small number of ent polynucleotide molecules (e.g. multiple copies of two mentary nucleic acid strands). Multi-polynucleotide or clustered arrays of nucleic acid molecules may be produced using techniques generally known in the art. By way of e, WO 98/44151 and WO 00/18957 both describe methods of amplification of nucleic acids wherein both the template and amplification products remain lized on a solid support in order to form arrays comprised of rs or "colonies" of immobilized nucleic acid molecules. The c acid molecules present on the clustered arrays prepared according to these methods are suitable templates for cing using the modified nucleotides labeled with the new fluorescent dyes described herein.

The modified nucleotides labeled with dye compounds of the present application are also useful in sequencing of templates on single molecule arrays. The term "single molecule array" or "SMA" as used herein refers to a population of polynucleotide molecules, distributed (or d) over a solid support, wherein the spacing of any dual polynucleotide from all others of the population is such that it is possible to effect dual resolution of the polynucleotides. The target nucleic acid les immobilized onto the surface of the solid support should thus be capable of being resolved by optical means. This means that, within the able area ofthe particular imaging device used, there must be one or more distinct signals, each representing one cleotide.

This may be achieved wherein the g n adjacent polynucleotide molecules on the array is at least 100 nm, more particularly at least 250 nm, still more particularly at least 300 nm, even more particularly at least 350 nm. Thus, each le is individually resolvable and detectable as a single molecule fluorescent point, and fluorescence from said single molecule fluorescent point also exhibits single step photo-bleaching.

The terms "individually resolved" and "individual resolution" are used herein to specify that, when ized, it is possible to distinguish one molecule on the array from its neighboring les. Separation between individual molecules on the array will be determined, in part, by the particular technique used to resolve the individual molecules. The general features of single molecule arrays will be understood by reference to PCT Publication Nos. and WO 57248. Although one application of the ed nucleotides ofthe present disclosure is in sequencing-by-synthesis reactions, the utility of such labeled nucleotides is not limited to such methods. In fact, the nucleotides may be used advantageously in any sequencing methodology which requires detection of fluorescent labels attached to nucleotides incorporated into a polynucleotide.

In particular, the modified nucleotides labeled with dye nds of the present ation may be used in automated fluorescent sequencing protocols, particularly fluorescent dye- terminator cycle sequencing based on the chain termination sequencing method of Sanger and co- workers. Such methods generally use enzymes and cycle sequencing to incorporate fluorescently labeled dideoxynucleotides in a primer extension sequencing reaction. So called Sanger sequencing methods, and related protocols (Sanger-type), rely upon randomized chain termination with labeled dideoxynucleotides.

Thus, the present disclosure also encompasses modified nucleotides labeled with dye compounds as described herein which are ynucleotides lacking hydroxyl groups at both of the 3' and 2' positions, such modified dideoxynucleotides being suitable for use in Sanger type sequencing methods and the like.

Methods of ation Some additional embodiments described herein are related to a method ofpreparing a compound of Formula (la), the methods include reacting a compound of Formula (Ha) N CHZCOZR" N CHZCN (Ila) or a (IIb) (”b) with a compound of Formula (111) (”D to form where the variables R1, R1,, R2, R3, R4, R5, R6, X, m and n are defined above in the disclosure of compounds ofFormula (I), and R” is selected from the group consisting of H, optionally substituted alkyl, alkenyl, alkynyl, aminoalkyl, haloalkyl, hetero alkyl, alkoxyalkyl, sulfo, optionally substituted aryl; optionally tuted heteroaryl, optionally substituted yclyl, and optionally substituted heterocyclyl.

Some additional embodiments described herein are d to a method ofpreparing a compound of Formula (Ia’), the methods include reacting a compound of Formula (Ila) N CH2002R" N CHZCN (Ila) or a (IIb) (”b) with a compound of Formula (Illa) (Illa) to form where the variables R1,R1’, R2, R3, R4, R5, R6, R7, R”, X, m and n are defined above. 2017/074880 Some additional embodiments described herein are related to a method ofpreparing a compound of Formula (Ia’), the method includes converting a compound of Formula (Ia) to a compound of Formula (Ia’) through carboxylic acid tion: R6( n) 0 X . OH \ \ X R1 activation 5% —> m) / R4 R2 R4 (I a) (Ia') Where the variables R1, R1,, R2, R3, R4, R5, R6, R7, R8, R9, X, m and n are defined above in the disclosure of compounds ula (I).

Some additional embodiments described herein are related to a method ofpreparing a compound of Formula (1b), the method includes converting a compound of Formula (Ia) to a compound of Formula (Ia’) through carboxylic acid activation: R6(\:1) . OH \ X R1 activation 5% —> m) / R4 R2 R4 (I a) (Ia') R4 (IV) (Ia') (I b) Where the variables R1, R1,, R2, R3, R4, R5, R6, R7, R8, R9, X, m and n are defined above in the disclosure of nds ofFormula (I).

Some additional embodiments described herein are related to a method ofpreparing a compound of Formula (Ib), the s include reacting a compound of Formula (Ila) N CH2002R" N CHZCN (Ila) or Formula (IIb) (”b) with a compound ofFormula (IIIb) (IIIb) to form where the variables R1, R1,, R2, R3, R4, R5, R6, R7, R”, X, m and n are defined above.

The preparation of compounds of Formula (Ia) can be accomplished by reacting starting materials of Formula (Ila) or (IIb) with the intermediate compound ofFormula (III) preferably in one to one molar ratio in organic solvent with or without a catalyst. Both organic catalysts (for example, trifluoroacetic acid or methanesulfonic acid) and inorganic catalysts (for example, phosphoric or sulfuric acid) may be used. In some embodiments the preparation may be fulfilled without a solvent or using a catalyst as solvent.

The preparation ofcompounds ofFormula (Ia’) or (Ib) can be accomplished by first acid activation of starting materials of Formula (Ia) in organic solvent at room temperature using, for example, carbodiimide, O-(benzotriazol-l-yl)-N,N,N’,N’-tetramethyluronium salts, BOP or PyBOP as an activation reagent, ed by reaction with appropriate hydroxy derivatives HOR7 or amine of formula (IV) for the coupling step.

Compounds of a (V), (Va) or (Vb) may be prepared following similar tic schemes as described above in the preparation of compounds of Formula (Ia), (Ia’) or (Ib). nds ofFormula (I) may be used in some organic reactions, for e in electrophilic aromatic substitution reactions as starting materials for new dyes sis. For example, it was demonstrated previously by Alan S. Waggoner njugate Chemistry, 1993, 05-111; see also US. Pat. Pub. No. 2015/0274976) that some cyanine dyes molecules modifications by sulfonation reaction may improve fluorescent properties such tives.

Sulfonation of compounds (I) can be fulfilled by reaction with sulfiir de, with sulfur trioxide derivatives or solutions, for e in sulfuric acid WO 60482 (I) (I-Sulfo) Sulfochlorination of compounds (I) can be fulfilled by reaction with chlorosulfonic acid.

(I) (l—SulfoCl) Compounds of Formula (1) containing sulfonic- or chlorosulfonic groups can be further d, for example, by reacting with ammonia, primary- or secondary amines formula (IV): (I-SulfoCI) (I-SulfoAmino) where the variables R1, R1,, R2, R3, R4, R5, R6, R7, R8, R9, X, n are defined above in the disclosure of compounds ofFormula (I).

EXAMPLES onal embodiments are disclosed in filrther detail in the following examples, which are not in any way intended to limit the scope of the claims. 2017/074880 General Procedure for the Synthesis of compounds of a (Ia) Q8 I COZH “11 + / R1 ° 0 r O O HO N R2 f?“ Mixture of ethyl benzothiazolyl-2 acetic acid (2.2 g, 0.01 mol) and an appropriate derivative ofhydroxy benzoyl benzoic acid (0.01 1 mol) was dissolved in trated sulfilric acid (5 mL). This reaction mixture was stirred at room temperature for 1 hour and then heated, for e, at 80-120°C for 1-2 hours till the reaction was completed. The reaction mixture was poured into ice (about 50 g) and the product was d, washed with water. In many cases, the final products do not need any fithher purification.

General Procedure for the S nthesis of com ounds of Formula Ia’ A compound of Formula (Ia) (0.001 mol) was dissolved in anhydrous DMF (1.5 mL). To this solution carbodiimide (0.0012 mol) or another activation reagent was added. This reaction mixture was stirred at room temperature for 3 hour and then appropriate hydroxy derivatives R7OH was added. The on mixture was stirred overnight then filtered and poured into ice (about 50 g). The product was filtered off, washed with water. Yield: 55-75%. In many cases, the final products do not need any further purification.

General Procedure for the Synthesis of compounds of Formula (1b) A nd of Formula (Ia) (0.001 mol) was dissolved in suitable anhydrous organic solvent (DMF, 1.5 mL). To this solution TSTU, BOP or PyBOP as activation reagent was added. This reaction e was stirred at room temperature for about 20 min and then appropriate amine NHR°R9 was added. The reaction mixture was stirred overnight, filtered and excess of the activation reagent was quenched with 0.1M TEAB solution in water. Solvents were evaporated in vacuum and the residue was purified by HPLC. Yield: .

EXAMPLE 1 acid (Compound I-3) ( ,8 ZCZH5 + o HO N Sulfuric acid (2 mL) was placed into a round—bottomed flask then cooled down to about 0-5°C and 0.325 g (1.0 mmol, 1 eq) of 2-(1-ethylhydroxy-l,2,3,4-tetrahydroquinoline carbonyl)benzoic acid was added with stirring following by addition of 0.3 g (1.4 mmol, 1.4 eq) ethyl 2-(benzothiazolyl)acetate. This reaction mixture was stirred at room temperature (about 20°C) for min then heated for 1.5 hours while stirring at 100°C. Reaction progress was monitored by TLC (DCM-MeOH, 10 %) and by LCMS.

Reaction mixture was left at room temperature (about 20°C) for 0.5 hour and then was poured into e of crushed ice (about100 g) and sodium acetate (about5 g). After 1 hour the product was filtered off and washed with water until neutral, then the e was air dried. Yield: 0.35 g (0.73 mmol, 73%). The final product was used without r purification. MS (DUIS): MW Calculated 482.13. Found: (-) 481 (M-l), (+) 483 (M+1). 1H NMR (400 MHz, DMSO-dg) 5 12.71 (s, 1H), 8.11 — 8.02 (m, 1H), 7.96 (dd, J= 7.4,1.6 Hz, 1H), 7.56 (tt, J= 7.5, 5.8 Hz, 2H), 7.40 (d, J= 7.2 Hz, 1H), 7.39 — 7.25 (m, 2H), 7.16 (dd, J: 6.6, 2.1 Hz, 1H), 6.67 (s, 1H), 6.35 (s, 1H), 3.48 (q, J: 7.0 Hz, 2H), 3.36 (t, J: 5.7 Hz, 2H), 2.65 — 2.55 (m, 2H), 1.79 (q, J: 6.3 Hz, 2H), 1.15 (t, J: 7.0 Hz, 3H). 2-[10-(Benzothiazolyl)—l.1,7,7-tetramethyl-1 l—oxo-2,3 .6,7-tetrahydro- 1 H,5H.1 1H-pyrano[2,3- flpyrido [3 .2.1-ij]quinolinyl]benzoic acid (Compound I-5) H020 NTK/COZCZH5 + Mixture of 0.75 g (1.90 mmol, 1 eq) of 2-(8-hydroxy—1,1,7,7-tetramethyl-2,3,6,7- tetrahydro-lH,5H-pyrido[3,2,l-ij]quinolinecarbonyl)benzoic acid and 0.44 g (1.99 mmol, 1.04 eq) ethyl 2-(benzothiazol-2 -yl)acetate was added with stirring to concentrated sulfuric acid (7 mL) at room temperature(about 20 °C). This reaction mixture was stirred at room temperature for 30 min then heated 2.5 hours while stirring at 120°C. Reaction progress was monitored by TLC (DCM-MeOH, %) and by LCMS. Reaction mixture was left at room temperature (about 20°C) for 0.5 hour and then was poured into mixture of crushed ice (about 50 g) and sodium acetate (about 5 g). After 1 hour the product was filtered off and washed with water until neutral and air dried. Yield: 0.58 g (1.05 mmol, 55%). The final product was used without fithher purification. MS (DUIS): MW Calculated 550.19. Found: (-) 549 (M-l).

EXAMPLE 3 2- 3- Benzothiazol I eth lamino meth loxo-2H-chromen—4- lbenzoic acid Com ound Sulfuric acid (5 mL) was placed into a round—bottomed flask then cooled doom to about 0-5°C and 0.7 g (2.34 mmol, 1 eq) of 2-(4-(ethylamino)—2-hydroxy—5-methylbenzoyl)benzoic acid was added with ng following by addition of0.7 g (3.16 mmol, 1 .35 eq) ethyl zothiazol- 2-yl)acetate. This reaction e was stirred for 30 min at room ature (about 20 °C) then heated for 1 hour while stirring at 95°C. Reaction progress was monitored by TLC (DCM-MeOH, %) and by LCMS.

The reaction mixture was left at room temperature (about 20 °C) for 0.5 hour and then was poured into mixture ofcrushed ice (about 100 g) and sodium acetate (about 5 g). After 1 hour the product was filtered off and washed with water until neutral and air dried. Yield: 1.01 g (2.22 mmol, 95%). The final product was used t fithher purification. MS : MW Calculated 456.11. Found: (-) 455 (M-1), (+) 457 (M+1). 1H NMR (400 MHz, Methanol-d4) 5 8.19 — 8.12 (m, 1H), 7.92 — 7.78 (m, 1H), 7.64 (dd, J: 8.3,1.1 Hz, 1H), 7.61 — 7.48 (m, 2H), 7.43 — 7.36 (m, 1H), 7.36 — 7.26 (m, 1H), 7.21 — 7.14 (m, 1H), 6.60 (s, 1H), 6.56 (d, J=1.1Hz,1H), 3.41 — 3.34 (m, 2H), 2.03 (s, 3H), 1.38 — 1.27 (m, 3H).

EXAMPLE 4-1 2-[10-(Benzothiazolyl)—1 1-imino-2 ,3 ,6 ,7 -tetrahydro- l H.5H,l 1H-pyrano[2,3-f]pyrido[3,2,1- ijjquinolinyl]benzoic acid und I-4A) SulfiJric acid (10 mL) was placed into a round-bottomed flask then 1 g (2.96 mmol, 1 eq) of 2-(8-hydroxy-2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij]quinolinecarbonyl)benzoic acid was added with stirring following by addition of 0.57 g (3.26 mmol, 1.1 eq) 2-(benzothiazol yl)acetonitrile. This reaction mixture was stirred at room temperature (about 20 °C) for 30 min then heated for 1.5 hours while stirring at 80°C and 1h at 90°C. Reaction progress was monitored by TLC eOH, 10 %) and by LCMS.

Reaction mixture was left at room temperature (about 20°C) for 0.5 hour and then was poured into mixture of crushed ice (about 100 g). After 0.5 hour the t was filtered off and washed with water until neutral and air dried. Yield: 0.8 g (1.62 mmol, 55 %). The final product was used without further ation. MS (DUIS): MW Calculated 493.15. Found: (-) 492 (M-l), (+) 494 (M+1).

EXAMPLE 4-2 2-[10-(Benzothiazolyl)-l 1 -oxo-2,3,6,7-tetrahydro-1H,5H, 1 1H-pyrano[2,3-f]pyrido[3 ,2,1- ij |guinolinyl |benzoic acid (Compound I-4 ). sion ofthe imine (I-4A) from previous step (example 4- 1) and water (25 ml) was stirred 5h at 80 °C. At the end of this time red color of starting material almost gone and very strong cence developed. Reaction progress was monitored by TLC (DCM-MeOH, 10 %) and by LCMS. The reaction e was left at room temperature (about 20 CC) for 0.5 hour and then the product was filtered off and washed with water and air dried. Yield: 0.77 g (1.56 mmol, 96 %). The final product was used without further purification. MS (DUIS): MW ated 494.13. Found: (-) 493 (M-l), (+) 495 (M+1).

EXAMPLE 5 2-[10-(Benzothiazolyl)—1 1-oxo-2,3,6,7-tetrahydro-1H.5H,1 1H-pyrano[2,3-f]pyrido[3,2,1- ijjquinolinyl]benzoic acid (Compound I-4) N=i\,,CN + Sulfilric acid (10 mL) was placed into a round-bottomed flask then 1 g (2.96 mmol, 1 eq) of 2-(8-hydroxy-2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij]quinolinecarbonyl)benzoic acid was added with stirring following by addition of 0.57 g (3.26 mmol, 1.1 eq) 2- cyanomethylbenzothiazole. This reaction mixture was d at room temperature (about 20 CC) for min then heated for 2 hours while stirring at 95°C. Reaction mixture was left to cool down to room temperature (about 20°C) and then was poured into mixture ofwater and crushed ice (about75 g). This mixture was stirred overnight at room temperature and the product was filtered off and washed with water until neutral and air dried. The final product was used without further purification. Yield: 1.09 g (2.21 mmol, 75%). MS (DUIS): MW Calculated 494.13. Found: (-) 493 (M-l), (+) 495 (M+1).

EXAMPLE 6 2-[3-(benzothiazol—2-yl)(dimethylamino)oxo-2H-chromen—4-yl]benzoic acid (Compound I-2) H020 + o » NaCOZCZH5 HO N Mixture of 0.285 g (1.0 mmol, 1 eq) of 2-[4-(dimethylamino) hydroxybenzoyl]benzoic acid and 0.243 g (1.1 mmol, 1.1 eq) ethyl zothiazolyl)acetate was added with stirring to sulfuric acid (5 mL) at room temperature(about 20°C). This reaction mixture was stirred at room temperature for 3 hours then heated for 4 hours while stirring at 100°C. Reaction progress was monitored by TLC (DCM-MeOH, 10%) and by LCMS. Reaction mixture was left at room temperature (about 20°C) overnight and then was poured into mixture of water-crushed ice (about 100 g) and sodium acetate (about 5 g). After 1 hour the product was filtered off and washed with water until neutral and air dried. Yield: 0.429 g (0.96 mmol, 97 %). The final product was used t filrther purification. MS (DUIS): MW Calculated 442.10. Found: (-) 441 (M-l). 1H NMR (400 MHZ, DMSO-ds) 8 12.70 (s, 1H), 8.14 — 8.04 (m, 1H), 8.04 — 7.94 (m, 1H), 7.58 (h, J= 6.5 Hz, 2H), 7.43 (d, J: 7.8 Hz,1H), 7.40 — 7.29 (m, 2H), 7.19 (dd, J: 7.2,1.7 Hz, 1H), 6.78 — 6.63 (m, 3H), 3.07 (s, 6H).

EXAMPLE 7-1 2-[3—(Benzothiazolyl)(diethylamino)—2-oxo-2H-chromenyl]benzoic acid (Compound I-l).

Sulfuric acid (8 mL) was placed into a round—bottomed flask then 0.25 g (0.8 mmol, 1 eq) 2-[4-(diethylamino)hydroxybenzoyl]benzoic acid was added with stirring following by addition of 0.14 g (0.8 mmol, 1 eq) 2-cyanomethylbenzothiazole. The reaction mixture was stirred at room temperature (about 20°C) for 30 min then heated for 2 hours while stirring at 95°C. This reaction mixture was poured into ice-cold water (about 75 g). At this stage, the corresponding imine intermediate (I-lA) was formed and it may be isolated by ion. In water or in organic solvents with presence of water and ularly in acid condition the fithher hydrolysis of the imine ediate may be achieved. |-1A ) This mixture was stirred overnight at room temperature and the product was filtered offand washed with water until neutral and air dried. Yield: 0.33 g (0.7 mmol, 88 %). The final product was used without further purification. MS (DUIS): MW Calculated . Found: (-) 469 (M-1), (+) 471 (M+1).1H NMR (400 MHz, DMSO-d6) 5 12.71 (s, 1H), 8.08 (dt, J: 7.6, 1.7 Hz, 1H), 8.03 — 7.92 (m, 1H), 7.64 — 7.52 (m, 2H), 7.45 — 7.39 (m, 1H), 7.39 — 7.27 (m, 2H), 7.19 (dd, J: 6.9, 2.3 Hz, 1H), 6.70 (d, J: 1.9 Hz, 1H), 6.69 — 6.61 (m, 2H), 3.47 (q, J: 7.2 Hz, 4H), 1.23 — 1.05 (m, 6H).

EXAMPLE 7—2 2-(7-(Diethylamino)—2-oxo(6-sulfobenzothiazolyl)-2H-chromenyl)benzoic acid (Compound I-13 ).

SO3H Benzothiazolyl)(diethylamino)—2-oxo-2H-chromeny1]benzoic acid (Compound H) (1.3 g, 2.76 mmol) was placed into a round-bottomed flask, dried in high vacuum, then cooled down in acetone-dry ice bath. Fuming sulfuric acid (20%, 5.8 mL, 27 mmol) was added dropwise while stirring. This on mixture was stirred at room temperature for 1 hour then heated for 1 hour at 50°C and starting material was dissolved. The reaction mixture was chilled down and anhydrous ether was added with precaution. Off-white hydro scopic itate was filtered off and the filtrate was triturated with ether again and then with EtOH. Pink precipitate was collected. Yield 1.21 g (80%). The final t was used without further purification. MS (DUIS): MW ated 550.09.

Found: (-) 549 (M-1), (+) 551 (M+1). 1H NMR (400 MHz, TFA) 8 8.85 — 8.78 (m, 1H), 8.69 (s, 1H), 8.57 — 8.45 (m, 2H), 8.26 — 8.15 (m, 2H), 7.94 (s, 1H), 7.67 (d, J: 9.4 Hz, 1H), 7.63 — 7.56 (m, 1H), 7.45 (dd, J= 8.8, 4.5 Hz, 1H), 3.94 (q, J= 7.2 Hz, 4H), 1.38 (t, J= 7.1 Hz, 6H). In according with HPLC and NMR spectra analysis this product consists mainly from one isomer.

EXAMPLE 7-3 2-(7-(Diethylamino)—2-oxo chlorosulfonylbenzothiazol-2 -yl)-2H-chromen—4-yl)benzoic acid 1 Compound I-14 ).

SOZCI Chlorosulfonic acid (5 ml, 75 mmol) was cooled in an ice bath and dye I-l (1.2 g, 2.55 mmol) was carefiJlly added with stirring portion-wise over a period of 5 minutes. The combined mixture was stirred at room temperature (~20°C) for 1.5 hours and then heated at 95-100°C for 6 hours. After cooling to room temperature, the mixture was added very slowly to ca. 20 ml ice/water mixture. A red colored solid separated which was quickly filtered off and was washed with cold water (2 x 30 ml) and dried in vacuum. Yield 1.2 g (83%, 2.11 mmol). This compound was used in next step without additional purification.

EXAMPLE 7-4 2-(7-(Diethylamino)—2-oxo(6-aminosulfonylbenzothiazolyl)-2H-chromenyl)benzoic acid 1Comp_ound I-15 ). sozm SOZNHZ 2-(7-(Diethylamino)oxo(6-chlorosulfonylbenzothiazolyl)-2H-chromen yl) benzoic acid (I-14) (1.2 g, 2.11 mmol) was carefully added portion-wise with stirring to ammonia solution (5 ml, 25 %) cooled in an ice bath over a period of5 s. The reaction mixture was stirred at room ature (~20°C) for 1 hour and solvent was led off at room temperature in vacuum.

Compound was purified by flash column (silica gel, DCM—MeOH as eluent). Yield 0.34 g (30 %, 0.62 mmol). This compound contain small amount of other isomers and was used in next step without additional purification. MS (DUIS): MW Calculated 549.10. Found: (—) 548 (M-l), (+) 550 (M+l). 1H NMR (400 MHZ, TFA) 5 8.83—8.73 (m, 1H), 8.62 (d, J: 1.6 HZ, 1H), 8.57 (d, J: 8.9 Hz, 1H), 8.42 (dd, J: 8.9, 1.8 Hz, 1H), 8.24—8.13 (m, 2H), 7.82 (d, J: 2.1 HZ, 1H), 7.64—7.52 (m, 2H), 7.38 (d, J = 8.8 Hz, 1H), 3.90 (q, J: 7.2 Hz, 4H), 1.37 (t, J: 7.2 Hz, 6H).

EXAMPLE 8 4-Nitrophenyl 2-[3 -(benzothiazolyl)(diethylamino)oxo-2H-chromenyl]benzoate 1Compound I-lB 1 |-1B In anhydrous DMF (1.5 mL) 94 mg (0.2 mmol, 1 eq) of 2-[3-(benzothiazolyl)- 7-(diethylamino)oxo-2H-chromenyl]benzoic acid (I-1, NR440) was dissolved. To this solution dicyclohexylcarbodiimide (62 mg, 0.3 mmol, 1.5 eq) was added. This reaction mixture was stirred at room temperature for 3 hour and then p-nitrophenol (33 mg, 0.24 mmol, 1.2 eq) was added. The reaction mixture was stirred overnight then dicyclohexyl urea was d off. Solvent was distilled off in vacuum at room temperature and the oily residue was poured into ice (about 5 g). The solid yellow product was filtered off, washed with water. Yield: 79 mg (67 %, 0.134 mmol). MS (DUIS): MW Calculated 591.15. Found: (—) 590 (M-l), (+) 592 (M+1).

EXAMPLE 9 Triethylammonio 1 0-(benzothiazoly1)-1 1-oxo-2.3.6.7-tetrahydro-1H,5H.1 1H-pyrano[2.3- flpyrido [3 ,2 .1 -ijj quinolinyl)-N-(4-(tert-butoxy)oxobutyl)benzamido)_propane-1 -sulfonate 1 Compound 1-9A’! NH+(02H5)3 I-9A' Compound L4 (150 mg, 0.3 mmol, 1 eq) was dissolved in ous DMA (1.5 ml). To this solution excess of triethylamine (1 mL) and [(lH-benzotriazol-l- yl)oxy]tris(dimethylamino)phosphonium uoroborate (140 mg, 0.36 mmol, 1.2 eq) as an activation reagent was added. This reaction mixture was d at room temperature for about 20 min and then 3-((3-(tert-butoxy)carbony1)amino)propanesulfonic acid (140 mg, 0.5 mmol, 1.6 eq) was added. on progress was monitored by TLC (Acetonitrile-Water, 10%) and by LCMS.

The reaction e was stirred overnight, filtered and excess of activation reagent was quenched with 0.1M TEAB solution in water. Solvents were evaporated in vacuum and the residue was purified by HPLC. Yield: 180 mg (0.21 mmol, 69 %).MS (DUIS): MW Calculated 757.25. Found: (-) 756 (M-l), (+) 758 (M+1) for the corresponding protonated anion Compound I-9A: I-9A E 10 ylammonio 4-(2-(10-(benzothiazolyl)-1 1 -oxo-2.3.6,7-tetrahydro-1H.5H. 1 1H-pyrano[2.3- flpyrido [3 ,2.1 -ij] quinolinyl)-N-(3-su1fonatopropy1)benzamido)butanoate (Compound I-9 ’) H020 -OSS\/\/N NH+(02H5)3 l-9A' W Compound I-9A’ from the previous step after evaporation of solvents (180 mg, 0.21 mmol) was dissolved in DCM (150 mL) and trifluoroacetic acid (5 mL) was added. The reaction mixture was left at room temperature overnight. Progress of the ection reaction was monitored by TLC (Acetonitrile-Water, 10 % as an eluent) and by LCMS. DCM was distilled off. The e was dissolved in acetonitrile and triethylamine (1 mL) was added. The yellow precipitate was filtered off. MS (DUIS): MW Calculated 701.19. Found: (-) 700 (M-l) for the corresponding protonated anion Compound L9: EXAMPLE 1 1 Triethylammonio 3-(2 -(3-(benzothiazolyl)(diethylamino)—2 -oxo-2H-chromenyl)—N—(4-(tert- butoxv)oxobutyl)benzamido)propane-1 -sulfonate. (Compound I-6A’) NH (Csz)3+ I-6A' 2-(3-(Benzothiazolyl)(diethylamino)—2-oxo-2H-chromenyl)benzoic acid (Compound H) (94 mg, 0.2 mmol, 1 eq) was ved in anhydrous DMA (2 mL). To this solution excess of N—ethyl—N,N-diisopropylamine (1 mL) was added. To this solution was added [(1H- benzotriazol-l-yl)oxy]tris(dimethylamino)phosphonium tetrafluoroborate (80 mg, 0.21 mmol, 1.04 eq) as an activation reagent. The reaction mixture was stirred at room temperature.

The on progress was monitored by TLC (Acetonitrile-Water, 10 % as an eluent). Then 3-((3-(tert-butoxy)carbony1)amino)propanesulfonic acid (70 mg, 0.25 mmol, 1.25 eq) was added. The reaction mixture was d ght at room temperature, filtered and excess of the activation reagent was quenched with 0.1M TEAB solution in water (3 mL). Solvents were evaporated in vacuum and the residue was purified by HPLC. Yield: 113 mg (0.136 mmol, 68%). MS (DUIS): MW Calculated . Found: (-) 732 (M-l) for the corresponding protonated anion Compound 1- EXAMPLE 12 Triethylammonio 4-(2-(3 -(benzothiazol-2 -yl)-7 hylamino)—2—oxo -2H-chromenyl)-N-(3- sulfonatopropyl)benzamido)butanoate, (Compound 1-6’) Compound I-6A’ (180 mg, 0.21 mmol) from the previous step after evaporation of solvents was dissolved in DCM (50 mL) and trifluoroacetic acid (2.5 mL) was added. The reaction mixture was left with stirring at room temperature ght. The reaction progress was monitored by TLC (Acetonitrile-Water, 10 % as an eluent). Solvent was led off and the e was dissolved in acetonitrile and triethylamine (1.8 mL) added. itrile and excess oftriethylamine was distilled off. To the residue in the flask anhydrous diethyl ether was added and the product was formed as a yellow crystalline precipitate and filtered off. MS (DUIS): MW Calculated 677.19. Found: (-) 676 (M- 1) for the acid 1-6: (CH2)3303H C(O)lll(CH2)3C(O)OH O O N(C2H5)2 EXAMPLE l3 tert—Butyl 4-(2-(10-(benzothiazolyl)-l l-oxo-2,3,6,7-tetrahydro- l H,5H,l 1H-pyrano[2,3- rido 3 2 l-i' uinolin lbenzamido butanoate I-10A Compound L4 (97 mg, 0.196 mmol, 1 eq) was dissolved in freshly distilled anhydrous DMF (2.5 mL). To this solution excess ofN—ethyl-N,N—diisopropylamine (0.253 mg, 1.961 mmol, 10 eq) and [(1H-benzotriazol-l-yl)oxy]tris(dimethylamino)phosphonium tetrafluoroborate (113 mg, 0.294 mmol, 1.5 eq) as an activation reagent was added. The reaction mixture was stirred at room temperature for about 20 min and then tert-butyl 4-aminobutanoate hydrochloride (58 mg, 0.294 mmol, 1.5 eq) was added. Reaction progress was monitored by TLC (Acetonitrile-Water, 10 %) and by LCMS.

The reaction e was stirred overnight, filtered and excess of activation reagent was quenched with 0.1M TEAB solution in water. Solvents were evaporated in vacuum and the residue was purified by HPLC. Yield: 105 mg (0.165 mmol, 84%). MS (DUIS): MW Calculated 635.25.

Found: (-) 634 (M-l), (+) 636 (M+1).

EXAMPLE l4 4-(2-( l 0-(Benzothiazol-2 -yl)-l 1-oxo-2,3,6,7-tetrahydro- l H,5H,l ano[2,3-f]pyrido [3 ,2,1 - i' uinolin—9- lbenzamido ic acid Com ound I—10 HOZC |-10A |-10 Compound I-10A (64 mg, 0.1 mmol) from the previous step after evaporation of ts was dissolved in DCM (25 mL) and roacetic acid (3.5 mL) was added. The reaction e was left at room temperature overnight. The reaction progress was monitored by TLC (Acetonitrile-Water, 10 % as an eluent) and by LCMS. Solvents were distilled off. The residue was dissolved in itrile and triethylamine (1 ml) added. Acetonitrile and excess oftriethylamine were 2017/074880 distilled off. Residue in the flask was dried overnight in vacuum then was sonicated with petroleum ester (25 ml) for 1 hour. Yellow precipitate filtered off. MS (DUIS): MW Calculated 579.18. Found: (-) 578 (M-1), (+) 580 (M+l).

EXAMPLE 15 |-1 B l'7 Compound 1-1B (180 mg, 0.3 mmol, 1 eq) was dissolved in anhydrous DMF (5 mL) and dimethylaminopyridine (56 mg, 0.45 mmol, 1.5 eq) was added. To this reaction mixture 4- aminobutanoic acid (47 mg, 0.45 mmol, 1.5 eq) was added and this reaction mixture was left at room temperature overnight. The reaction progress was red by TLC (Acetonitrile-Water, 10 % as an eluent) and by LCMS. Solvents were distilled off in vacuum at room temperature. The residue was diluted with water (25 m1) and the product was formed as a yellow precipitate and filtered off. MS (DUIS): MW Calculated 555.18. Found: (-) 554 (M-l), (+) 556 (M+l).

EXAMPLE 16 2-(3 -(5-Chlorobenzoxazolyl)(diethylamino)oxo-2H-chromenyl)benzoic acid und [-161 I-16 Mixture of 0.313 g (1.0 mmol, 1 eq) of diethylamino) hydroxybenzoyl]benzoic acid and 0.263 g (1.1 mmol, 1.1 eq) ethyl 2-(5-chlorobenzoxazol yl)acetate was added with stirring to sulfiiric acid (5 mL) at room temperature (about 20°C). This on mixture was stirred at room temperature for 3 hours then heated for 4 hours while ng at 100°C. Reaction progress was monitored by TLC (DCM-MeOH, 10% as ) and by LCMS.

Reaction e was left at room temperature (about 20°C) overnight and then was poured into mixture ofwater-crushed ice (about 100 g) and sodium acetate (about 5 g). After 1 hour, the product was filtered off and washed with water until neutral reaction (pH about 7) and air dried. Yield: 0.453 g (0.93 mmol, 93 %). The final product was used without further purification. MS (DUIS): MW Calculated 488.11. Found: (-) 487 (M-1).

E 17 General Procedure for the Synthesis of Fully Functional Nucleotide Conjugates New dyes-nucleotide conjugates were synthesized from compounds (I) or compounds (V-O) by coupling with appropriate nucleotides derivatives.

N\ BF4_ o —> O\ Dye-COOH + 0 Y O\ L / Dye +1 N O | | TSTU 0 —N o \ o HszM>KQ ‘3‘ \ N ‘Ro YQN \ N3 N0 H N O 0 Dye O Q _.

HO 4N3 O P‘Q O Qo-R‘O 0.-.O HO'P‘OH pppC-LN3 0 0 \ —N Hfmw \ N \ \2O N3 NO}H N ___,>- Dye~j( O 0 O Ho.Q IV 0 J3 BO 0 I904?0 ffC-l Q'P'O Anhydrous DMA (2.5 mL), N,N,N',N'-Tetramethyl-O-(N-succinimidyl)uronium tetrafluoroborate (20 mg, 60 umol) and Hunig’s Base (0.05 mL) were added to the dried sample of the appropriate dye (50 umol). The reaction mixture was stirred at room temperature. ing to TLC (Acetonitrile-Water, 10%) the activation usually was completed in 20-30 min. After activation was completed, the solution -LN3 as a triethylammonium salt (55 umol) in mixture ofDMA (0.75 mL) and water (0.30 mL) was added to the reaction mixture. The reaction mixture was d at room temperature under nitrogen atmosphere overnight. The on mixture was cooled down to about 4°C with an ice-bath, then a solution of 0.1 M TEAB (5 mL) in water was added and the mixture was stirred at room temperature for 10 min. The reaction mixture was applied to column with about 25g of DEAE ex resin suspension in 0.05 M TEAB solution in water and washed with TEAB (concentration gradient from 0.1 M up to 1 M). Colored fractions were collected and evaporated then co-evaporated again with water to remove more TEAB and vacuum down to dryness. The residue was then re-dissolved in TEAB 0.1 M. This solution was filtered h a syringe filter 0.2 nm pore size.

The product was purified by HPLC using C18 reverse phase column with acetonitrile-0.1 M TEAB.

Yield: 60-75%.

Using the general procedure described above, the ing nucleotides conjugates were prepared: ffC-I-6 HO’ \OH O fiN mew ‘5)L7N -‘ H \ >:=O N3 0 H N Ofo/\/ N3 HO\’O/MO? ,J ,?‘o O So-R=O O o :‘P’ HO \OH ffC-I-11 HO OH EXAMPLE 18 In this example, the spectral ties ofvarious fluorescent dyes described herein and the corresponding nucleotide ates were tested and compared to commercially ble dyes.

Table 1A illustrates the spectral properties of the new fluorescent dyes described herein as compared to some exemplary cial dyes with absorption in the same spectral region in ethanol solution. It can be observed that each ofthe new fluorescent dyes ofthe present application have longer Stokes shift compared to Star440sx.

Table 1A. Comparison of Spectral Properties Varies Dyes in EtOH solution Dyes Absorption Emission Stokes Max (nm) Max (nm) Shift (nm) Star4403x * 433 502 69 1-9 460 540 80 1-10 457 543 86 1-6 450 525 75 1-1 445 520 75 1-8 424 510 86 1-3 427 511 84 1-5 465 538 73 *Star4405x — commercial Long Stokes Shift Dye In addition, the spectral ties of dye 1-1 was compared to the sulfonated dyes I-13 and I-15 in methanol solution and the results were summarized in Table 1B. These data demonstrate that sulfonated derivatives I-13 and I-15 have 2 to 5 times stronger fluorescence in on when compared with the corresponding unsubstituted analog I-l. These results demonstrates the potential use of the sulfonated dyes as biomarkers.

Table 1B. Comparison of al Properties of Sulfonated Dyes in methanol solution Absorption Fluorescence Fhilfififgigce Stokes Dye Max (nm) Max (nm) Shift (nm) (normalized)% 14 | 410 506 | 100 95 1—13 | 418 511 | 235 93 1-15 | 425 511 | 496 86 illustrates the fluorescent spectra ofthe new fluorescent dyes ofthe present application as compared to a commercial dye Star4403x which has absorption in the same al region (solution in Universal Scanning Mixture; dyes were excited at 460 nm). Due to the larger Stokes shift, these newly ped dyes can provide more signal in detection region with better separation from excitation light at 460 nm.

Table 2 illustrates the relative fluorescent intensities of C-nucleotide labeled with new dyes as ed with appropriate nucleotide labeled with commercial dye which has absorption in the same spectral region. It shows that the new fluorescent dyes described herein can provide 60— 400% more signal at 570 nm tion region) when excited with light at 460 nm due to their stronger fluorescence and larger Stokes shift.

Table 2. Relative Fluorescence Intensities of the Exemplary Labeled Fully Functional C- Nucleotide ffC Intensity @570 nm ffC-star4405x * 1.0 ffC-I-9 3.5 ffC-I-10 4.0 ffC-I-6 1.6 l 2.3 Assuming E for dyes I-l, I-6, I-9 and I-10 30,000 *8 for Star440sx 22,700 Table 3 illustrates the spectral properties of the C-nucleotides labeled with the new fluorescent dyes described herein in solution, which is consistent with the observation in Table 1 that most of nucleotides labeled with the fluorescent dyes of the present application have longer Stokes shift ing with commercial dye for the same al region.

Table 3. Spectral Properties of Exemplary Labeled Fully Functionalized C-Nucleotide in Solution Absorption Emission Stokes Max (nm) Max (nm) Shift (nm) ar4405x 44 7 5I 6 69 ffC-I-9 475 542 67 ffC-I-l 0 467 545 78 ffC-I—6 453 527 74 ffC-I-l 449 530 81 illustrates the usability ofthe eotides labeled with the new fluorescent dyes described herein (shown in black) for sequencing analysis. In this sequencing example, the two- channel detection method was used. With respect to the two -channel s described herein, nucleic acids can be sequenced utilizing methods and systems described in US. Patent Application Publication No. 2013/0079232, the disclosure of which is incorporated herein by reference in its entirety. In the two-channel detection, a nucleic acid can be sequenced by providing a first nucleotide type that is detected in a first channel, a second nucleotide type that is detected in a second channel, a third nucleotide type that is detected in both the first and the second channel and a fourth nucleotide type that lacks a label that is not, or minimally, detected in either channel.

In each of FIGS. 2A and 2B, “G” nucleotide is unlabeled and shown as the lower left cloud. There is a mix oftwo labeled “A” nucleotides, one labeled with a coumarine derivative dye at 0.5 uM and one with the benzopyran derivative I-6 at 1.5 uM, shown as the upper right cloud. The signal from the NR550S0 dye labeled “T” nucleotide is ted by the upper left cloud, and the labeled “C” nucleotide signal is indicated by the lower right cloud. The X-axis shows the signal intensity for one l and the Y-axis shows the signal intensity for the other channel. In FIGS. 2A and 2B, the ffC is labeled with I-6 and I-l respectively. Experiment settings: Instrument: M15 Cycle #: C-I-6 at C5, C-I-l at C9, Sequencing lib.: standard PhiX. It shows that the fully onal C- nucleotide conjugates labeled with dyes I-6 and LI provided sufficient signal ities and better clouds separation. illustrates the relative fluorescent ities of the C-nucleotides labeled with s fluorescent dyes when they been excited with Blue (460 nm) or Green (530 nm) light.

This bar chart shows the raw intensity of clusters that have incorporated the dye indicated. Each measurement was taken manually at Ex460nm and exposing for lsec at 60°C. MTS [MiSeq R&D (Test) Software] was used on M15 to take the images and image analysis tool Firecrest was used to extract the intensity data.

The results show that the fsz labeled with the new cent dyes described herein provided up to 300% brighter signal when compared with commercial long Stokes dye for the same al region. rates the relative brightness of the conjugated C-nucleotides labeled with commercial and new cent dye I-6 when they been excited with Blue (460 nm) light at two different temperatures (room temperature at 22°C and elevated ature at 60°C). The ffC labeled with the new fluorescent dye 1-6 provided er signal when compared with ffC labeled with commercial long Stokes dye Star4401s for the some spectral region at both atures.

The headings and subheadings used herein are only for reading convenience and are not intended to define or limit the scope ofthe present disclosure. The present application described above relates to compounds and methods that are susceptible to modifications in the methods and materials, as well as alterations in the fabrication methods and equipment. Such modifications will become apparent to those skilled in the art from a consideration of this disclosure or practice of the application disclosed herein. Consequently, it is not intended that the present disclosure be limited to the specific embodiments disclosed herein, but that it cover all modifications and alternatives coming within the true scope and spirit of the disclosure.

Claims (46)

WHAT IS CLAIMED IS:

1. A compound of Formula (I) or mesomeric forms thereof: wherein each R1, R2, and R1’ is ndently selected from the group consisting of H, alkyl, substituted alkyl, alkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, alkoxyalkyl, amino, aminoalkyl, aminosulfonyl, halo, cyano, hydroxy, hydroxyalkyl, heteroalkyl, C-carboxy, O-carboxy, C-amido, N- amido, nitro, sulfonyl, sulfo, sulfino, sulfonate, yl halide, S- sulfonamido, onamido, optionally substituted carbocyclyl, optionally substituted aryl, optionally substituted heteroaryl and optionally substituted heterocyclyl; alternatively, R1 and R1’ together and with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally substituted carbocyclyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally tuted heterocyclyl; each R3 and R4 is independently selected from the group ting of H, alkyl, substituted alkyl, alkenyl, alkynyl, lkyl, haloalkyl, heteroalkyl, alkoxyalkyl, sulfonyl hydroxide, optionally substituted aryl, optionally substituted heteroaryl, ally substituted carbocyclyl, and optionally substituted heterocyclyl; atively, R1 and R3 together with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally substituted 5-10 membered heteroaryl or optionally substituted 5-10 membered heterocyclyl; alternatively, R2 and R4 er with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally tuted 5-10 membered heteroaryl and optionally substituted 5- 10 membered heterocyclyl; R5 and R6 is independently selected from the group consisting of alkyl, substituted alkyl, alkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, alkoxyalkyl, amino, aminoalkyl, aminosulfonyl, halo, cyano, hydroxy, hydroxyalkyl, alkyl, C-carboxy, O-carboxy, C-amido, N-amido, nitro, sulfonyl, sulfo, sulfino, sulfonate, sulfonyl halide, S-sulfonamido, N-sulfonamido, optionally substituted carbocyclyl, optionally substituted aryl, optionally substituted heteroaryl and optionally substituted heterocyclyl; R is selected from -OR7 or -NR8R9; R7 is selected from the group consisting of H, alkyl, substituted alkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted carbocyclyl, and optionally substituted cyclyl; each R8 and R9 is independently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, alkynyl, lkyl, carboxyalkyl, sulfonatoalkyl, kyl, heteroalkyl, alkoxyalkyl, sulfo, optionally substituted aryl, optionally substituted aryl, optionally substituted yclyl, and optionally substituted heterocyclyl; X is selected from the group ting of O, S, NR10, and Se; R10 is selected from the group consisting of H, alkyl, substituted alkyl, optionally substituted aryl, optionally substituted aryl, optionally substituted carbocyclyl, and optionally tuted heterocyclyl; m is an integer selected from 0 to 4; and n is an integer selected from 0 to 4; provided that when each R1, R1’ and R2 is H; each R3 and R4 is ethyl; each m and n is 0; R is CH3)CH2OH; then X is selected from O, S or Se; when each R1, R1’ and R2 is H; each R3 and R4 is ethyl; each m and n is 0; R is-OH; then X is selected from S or Se; when each R1, R1’ and R2 is H; each R3 and R4 is ethyl; m is 1 and R5 is methyl; n is 0; R is -OH or -OEt; then X is selected from S, NR10 or Se; and when each R1, R1’ and R2 is H; each R3 and R4 is ethyl; m is 1 and R5 is -S(O2)Et; n is 0; R is -OH or -OEt; then X is selected from S, NR10 or Se.

2. The compound of claim 1, wherein X is S or O.

3. The compound of claim 1 or 2, wherein R is -OR7.

4. The compound of any one of claims 1 to 3, wherein R7 is H or alkyl.

5. The nd of claim 1 or 2, wherein R is -NR8R9.

6. The compound of claim 5, wherein each R8 and R9 is H.

7. The compound of claim 5, wherein R8 is H and R9 is alkyl or substituted alkyl.

8. The compound of claim 5, wherein both R8 and R9 are alkyl or substituted alkyl.

9. The compound of claim 7 or 8, wherein substituted alkyl is selected from alkyl substituted with carboxyl or yl hydroxide.

10. The compound of any one of claims 1 to 9, wherein each R1, R1’ and R2 is

11. The compound of any one of claims 1 to 9, wherein at least one of R1, R1’ and R2 is an alkyl.

12. The compound of any one of claims 1 to 11, n each R3 and R4 is an alkyl.

13. The compound of Claim 12, wherein each R3 and R4 is ed from methyl or ethyl.

14. The compound of any one of claims 1 to 11, wherein R3 is H and R4 is an alkyl.

15. The compound of any one of claims 1 to 9, wherein R1 and R3 together with the atoms to which they are attached form an optionally tuted 3 to 7 membered heterocyclyl.

16. The compound of claim 15, wherein R1 and R3 together with the atoms to which they are attached form an optionally tuted 6 membered heterocyclyl.

17. The compound of claim 15 or 16, wherein R4 is selected from H or alkyl.

18. The compound of any one of claims 15 to 17, wherein at least one of R1’ and R2 is H.

19. The compound of any one of claims 1 to 9, n R2 and R4 together with the atoms to which they are attached form an optionally substituted 3 to 7 membered heterocyclyl.

20. The compound of claim 19, wherein R2 and R4 together with the atoms to which they are attached form an optionally substituted 6 membered heterocyclyl.

21. The compound of claim 19 or 20, wherein R3 is selected from H or alkyl.

22. The compound of any one of claims 19 to 21, wherein at least one of R1’ and R1 is H.

23. The compound of any one of claims 1 to 9, wherein R1 and R3 together with the atoms to which they are attached form an optionally substituted 3 to 7 membered heterocyclyl, and n R2 and R4 together with the atoms to which they are attached form an optionally substituted 3 to 7 membered cyclyl.

24. The compound of claim 23, wherein R1 and R3 together with the atoms to which they are attached form an optionally substituted 3 to 7 membered heterocyclyl, and wherein R2 and R4 together with the atoms to which they are attached form an optionally substituted 6 membered heterocyclyl.

25. The compound of any one of claims 15 to 24, wherein the cyclyl contains one atom.

26. The nd of claim 24, wherein the heterocyclyl is substituted with one or more alkyl.

27. The compound of any one of claims 1 to 26, wherein m is 0.

28. The compound of any one of claims 1 to 26, wherein m is 1 and R5 is selected from halo, sulfo, aminosulfonyl, or sulfonyl halide.

29. The compound of any one of claims 1 to 28, wherein n is 0.

30. The compound of claim 1 or 2, selected from the group consisting of: , , , , , , , , , , , , , , , and , or mesomeric isomers thereof.

31. The compound of claim 1 or 2, wherein the compound is covalently attached to a nucleotide or oligonucleotide via , wherein R is -OR7, and wherein R7 is a substituted alkyl.

32. The compound of claim 1 or 2, wherein the compound is covalently attached to a nucleotide or oligonucleotide via C(=O)R, wherein R is -NR8R9, and wherein at least one of R8 or R9 is a substituted alkyl.

33. A nucleotide or oligonucleotide labeled with a compound according to any one of claims 1 to 32.

34. The labeled nucleotide or oligonucleotide of claim 33, wherein the compound is covalently attached to the nucleotide or oligonucleotide via -C(=O)R, wherein R is -OR7, and R7 is a substituted alkyl.

35. The labeled nucleotide or oligonucleotide of claim 33, wherein the compound is ntly attached to the nucleotide or ucleotide via -C(=O)R, wherein R is -NR8R9, and wherein at least one of R8 or R9 is a substituted alkyl.

36. The labeled nucleotide or oligonucleotide of any one of claims 33 to 35, n the compound is attached to the C5 position of a pyrimidine base or the C7 on of a 7-deaza purine base of the nucleotide or oligonucleotide through a linker moiety.

37. The labeled nucleotide or oligonucleotide of any one of claims 33 to 36, further comprising a 3’-OH blocking group covalently attached to the ribose or deoxyribose sugar of the nucleotide or oligonucleotide.

38. A kit comprising one or more nucleotides wherein at least one nucleotide is a labeled nucleotide ing to claims 33 to 37.

39. The kit of claim 38, comprising two or more labeled tides.

40. The kit of claim 39, wherein the two labeled nucleotides are excited using a single laser.

41. The kit of any one of claims 38 to 40, further comprising a third and a fourth tide, wherein each of the second, third and fourth nucleotide is labeled with a different compound, wherein each nd has a distinct absorbance maximum and each of the compound is distinguishable from the other compounds.

42. A method of sequencing sing incorporating a labeled nucleotide according to any one of claims 33 to 37 in a sequencing assay.

43. The method of claim 42, further comprising detecting the nucleotide.

44. The method of claim 42 or 43, n the sequencing assay is performed on an automated sequencing ment, and wherein the automated sequencing instrument comprises two light sources operating at different wavelengths.

45. A method of preparing a compound of Formula (Ia), comprising: reacting a compound of Formula (IIa) or (IIb) with a compound of Formula (III) to form wherein each R1, R2, and R1’ is independently selected from the group ting of H, alkyl, substituted alkyl, alkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, alkoxyalkyl, amino, aminoalkyl, aminosulfonyl, halo, cyano, hydroxy, hydroxyalkyl, alkyl, C-carboxy, O-carboxy, C-amido, N-amido, nitro, sulfonyl, sulfo, sulfino, sulfonate, sulfonyl halide, S-sulfonamido, N-sulfonamido, optionally substituted carbocyclyl, optionally substituted aryl, optionally tuted heteroaryl and optionally tuted cyclyl; alternatively, R1 and R1’ together and with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally tuted carbocyclyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted heterocyclyl; each R3 and R4 is ndently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, l, aminoalkyl, haloalkyl, heteroalkyl, alkoxyalkyl, sulfonyl hydroxide, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted carbocyclyl, and optionally substituted heterocyclyl; alternatively, R1 and R3 together with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally substituted 5-10 membered heteroaryl or optionally substituted 5-10 ed heterocyclyl; alternatively, R2 and R4 together with the atoms to which they are attached form a ring or ring system selected from the group consisting of optionally substituted 5-10 membered heteroaryl and optionally substituted 5-10 membered heterocyclyl; R5 and R6 is independently selected from the group consisting of alkyl, substituted alkyl, alkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, alkoxyalkyl, amino, aminoalkyl, aminosulfonyl, halo, cyano, hydroxy, yalkyl, heteroalkyl, C-carboxy, O-carboxy, C-amido, N-amido, nitro, sulfonyl, sulfo, sulfino, sulfonate, sulfonyl halide, S-sulfonamido, N-sulfonamido, optionally substituted carbocyclyl, optionally substituted aryl, optionally tuted heteroaryl and optionally substituted heterocyclyl; X is selected from the group consisting of O, S, NR10, and Se; R10 is selected from the group consisting of H, alkyl, substituted alkyl, optionally substituted aryl, ally substituted aryl, optionally substituted carbocyclyl, and ally substituted heterocyclyl; R” is selected from the group consisting of H, ally substituted alkyl, alkenyl, alkynyl, aminoalkyl, kyl, heteroalkyl, alkoxyalkyl, sulfo, ally substituted aryl; optionally substituted heteroaryl, optionally substituted carbocyclyl, and optionally substituted cyclyl; m is an integer selected from 0 to 4; and n is an integer selected from 0 to 4.

46. A method for preparation a compound of Formula (Ib), comprising: converting a compound of Formula (Ia) to a compound of Formula (Ia’) through carboxylic acid activation; reacting the compound of Formula (Ia’) with a primary or secondary amine of Formula (IV), n the compound of Formula (Ia) is prepared according to Claim 45; R7 is selected from the group consisting of H, alkyl, substituted alkyl, optionally substituted aryl, optionally substituted aryl, optionally substituted carbocyclyl, and optionally substituted heterocyclyl; and each R8 and R9 is ndently selected from the group consisting of H, alkyl, substituted alkyl, alkenyl, alkynyl, aminoalkyl, carboxyalkyl, sulfonatoalkyl, haloalkyl, heteroalkyl, alkoxyalkyl, sulfo, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted carbocyclyl, and ally substituted heterocyclyl.