JPH07112962B2 - Plant filamentous fungus control agent - Google Patents
Plant filamentous fungus control agentInfo
- Publication number
- JPH07112962B2 JPH07112962B2 JP20419987A JP20419987A JPH07112962B2 JP H07112962 B2 JPH07112962 B2 JP H07112962B2 JP 20419987 A JP20419987 A JP 20419987A JP 20419987 A JP20419987 A JP 20419987A JP H07112962 B2 JPH07112962 B2 JP H07112962B2
- Authority
- JP
- Japan
- Prior art keywords
- control agent
- fusaric acid
- plant
- filamentous fungus
- parts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 241000233866 Fungi Species 0.000 title description 4
- DGMPVYSXXIOGJY-UHFFFAOYSA-N Fusaric acid Chemical compound CCCCC1=CC=C(C(O)=O)N=C1 DGMPVYSXXIOGJY-UHFFFAOYSA-N 0.000 claims description 39
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 208000031888 Mycoses Diseases 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 11
- -1 bilophyllite Substances 0.000 description 8
- 230000003902 lesion Effects 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 239000003814 drug Substances 0.000 description 5
- 229940079593 drug Drugs 0.000 description 5
- 241000208125 Nicotiana Species 0.000 description 4
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 230000001580 bacterial effect Effects 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 2
- 241000193830 Bacillus <bacterium> Species 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 230000003032 phytopathogenic effect Effects 0.000 description 2
- 244000000003 plant pathogen Species 0.000 description 2
- 230000003449 preventive effect Effects 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 241000235349 Ascomycota Species 0.000 description 1
- 241001530056 Athelia rolfsii Species 0.000 description 1
- 208000008035 Back Pain Diseases 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- 241000255789 Bombyx mori Species 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 229910021532 Calcite Inorganic materials 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 108010015720 Dopamine beta-Hydroxylase Proteins 0.000 description 1
- 102100033156 Dopamine beta-hydroxylase Human genes 0.000 description 1
- 241000223221 Fusarium oxysporum Species 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- 240000007049 Juglans regia Species 0.000 description 1
- 235000009496 Juglans regia Nutrition 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 208000008930 Low Back Pain Diseases 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 208000018737 Parkinson disease Diseases 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241000233622 Phytophthora infestans Species 0.000 description 1
- 206010035148 Plague Diseases 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 241000918585 Pythium aphanidermatum Species 0.000 description 1
- 241000813090 Rhizoctonia solani Species 0.000 description 1
- 206010039509 Scab Diseases 0.000 description 1
- 241000576755 Sclerotia Species 0.000 description 1
- 241000221696 Sclerotinia sclerotiorum Species 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 108091000117 Tyrosine 3-Monooxygenase Proteins 0.000 description 1
- 102000048218 Tyrosine 3-monooxygenases Human genes 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- 150000003943 catecholamines Chemical class 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 244000053095 fungal pathogen Species 0.000 description 1
- 244000000004 fungal plant pathogen Species 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- QPPQHRDVPBTVEV-UHFFFAOYSA-N isopropyl dihydrogen phosphate Chemical compound CC(C)OP(O)(O)=O QPPQHRDVPBTVEV-UHFFFAOYSA-N 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- FEMOMIGRRWSMCU-UHFFFAOYSA-N ninhydrin Chemical compound C1=CC=C2C(=O)C(O)(O)C(=O)C2=C1 FEMOMIGRRWSMCU-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 229940126585 therapeutic drug Drugs 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、フザリン酸を有効成分として含有する植物糸
状菌病防除剤に関する。TECHNICAL FIELD The present invention relates to a plant filamentous fungal disease control agent containing fusaric acid as an active ingredient.
フザリン酸は、フザリウム・オキシスポルム(Fusarium
oxysporum)など数種の糸状菌の培養ろ液中に産出され
る坑生物質であり、酢酸ブチルを用いて抽出精製された
ものより構造は5−ブチル・ピコリン酸と決定された
(Hidakaら、1971年)。その作用機作は、カテコールア
ミン生合成阻害、すなわちドーパミンβ−水酸化酵素お
よびチロシン水酸化酵素に対する阻害であり、高血圧症
およびパーキンソン病に対する治療薬として使用されて
いる。しかし、植物病原菌に対しての抗菌活性について
は知られていない。Fusaric acid is Fusarium oxysporum
oxysporum) is a mineral substance produced in the culture filtrate of several filamentous fungi, such as oxysporum), and the structure was determined to be 5-butylpicolinic acid from that extracted and purified using butyl acetate (Hidaka et al., 1971). Its mechanism of action is inhibition of catecholamine biosynthesis, that is, inhibition of dopamine β-hydroxylase and tyrosine hydroxylase, and it is used as a therapeutic drug for hypertension and Parkinson's disease. However, nothing is known about the antibacterial activity against plant pathogens.
本発明は、フザリン酸が有する植物病原菌に対する予防
的、治療的な抗菌活性を利用して、優れた防除剤を提供
することを目的とする。An object of the present invention is to provide an excellent control agent by utilizing the preventive and therapeutic antibacterial activity against phytopathogenic bacteria possessed by fusaric acid.
本発明者は、鋭意研究の結果、フザリン酸が数種の植物
病原菌に対して予防的、治療的な殺菌活性を有すること
を見出した。これらの植物病原菌には、種々の作用の舞
病菌(Pythium aphanidermatum(edson)Fitj,P.de b
aryanum Hessl)、疫病菌(Phytophthora infestan
s)、菌核病菌(Sclerotinia sclerotiorum)、白絹病
菌(Corticium rolfsii)、腰折病もしくは紋枯病菌
(Rhizoctonia solani)、半身萎凋病菌(Verticilliu
m albo−atrum)等があり、なかでも藻菌類の舞病菌お
よび疫病菌に対して顕著な殺菌効果を示し、また担子菌
類および子のう菌類菌核形成菌に対しては菌核形成を阻
止する作用を示す(第1表および第2表)。As a result of diligent research, the present inventor has found that fusaric acid has preventive and therapeutic bactericidal activity against several plant pathogenic fungi. These plant pathogens include Pythium aphanidermatum (edson) Fitj, P. de b
aryanum Hessl), Phytophthora infestan
s), Sclerotinia sclerotiorum, White silkworm (Corticium rolfsii), Lumbago or Bacterial wilt disease (Rhizoctonia solani), Wilt's wilt disease (Verticilliu)
, which shows a remarkable bactericidal effect against the fungal and pathogenic fungi of algae, and also inhibits the sclerotia formation against basidiomycetes and ascomycetes The action is shown (Table 1 and Table 2).
フザリン酸の添加により、菌体からニンヒドリン陽性物
質およびフェノール・硫酸陽性物質が漏出し、菌体重は
減少したことから、この薬剤は細胞膜の透過性を変化さ
せているものと推察される(第3表)。The addition of fusaric acid leaked ninhydrin-positive substances and phenol / sulfuric acid-positive substances from the cells, and the bacterial weight was reduced. Therefore, it is speculated that this drug alters the permeability of cell membranes (No. 3). table).
フザリン酸を防除剤の有効成分として用いる場合は、他
の何らの成分も加えずそのまま用いてもよいが、通常、
固体担体、液体担体、界面活性剤、その他の製剤用補助
剤と混合して水和剤、粉剤、液剤等に製剤化する。これ
らの製剤はフザリン酸を0.1〜99.9%含む。 When using fusaric acid as an active ingredient of the control agent, it may be used as it is without adding any other ingredient, but usually,
It is mixed with a solid carrier, a liquid carrier, a surfactant, and other auxiliaries for formulation to prepare wettable powders, powders, liquids and the like. These formulations contain 0.1-99.9% fusaric acid.
固体担体としては、カオリンクレー、アッタパルジャイ
ントクレー、ベントナイト、酸性白土、バイロフィライ
ト、タルク、珪藻土、方解石、トウモロコシ穂軸粉、ク
ルミ殻粉、合成含水酸化珪素等の微粉末あるいは粒状物
を用いることができる。As the solid carrier, kaolin clay, atta-puljain clay, bentonite, acid clay, bilophyllite, talc, diatomaceous earth, calcite, corn cob powder, walnut shell powder, fine powder or particles of synthetic hydrous silicon oxide, etc. Can be used.
液体担体としては、水等を用いることができる。Water or the like can be used as the liquid carrier.
乳化、分散、湿展等のために用いられる界面活性剤に
は、アルキル硫酸エステル塩、アルキル(アリール)ス
ルホン酸塩、ジアルキルスルホこはく酸塩、ポリオキシ
エチレンアルキルアリールエーテルりん酸エステル塩、
ナフタレンスルホン酸ホルマリン縮合物等の陰イオン界
面活性剤、ポリオキシエチレンアルキルエーテル、ポリ
オキシエチレンポリオキシプロピレンブロック共重合
体、ソルビタン脂肪酸エステル、ポリオキシエチレンソ
ルビタン脂肪酸エステル等の非イオン界面活性剤等があ
る。Surfactants used for emulsification, dispersion, wet spreading, etc. include alkyl sulfate ester salts, alkyl (aryl) sulfonates, dialkyl sulfosuccinates, polyoxyethylene alkyl aryl ether phosphate ester salts,
Anionic surfactants such as naphthalene sulfonic acid formalin condensates, polyoxyethylene alkyl ethers, polyoxyethylene polyoxypropylene block copolymers, nonionic surfactants such as sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters, etc. is there.
製剤用補助剤としては、リグニンスルホン酸塩、アルギ
ン酸塩、ポリビニルアルコール、アラビアゴム、CMC
(カルボキシメチルセルロース)、PAP(酸性りん酸イ
ソプロピル)が用いられる。Pharmaceutical aids include lignin sulfonate, alginate, polyvinyl alcohol, gum arabic, CMC
(Carboxymethyl cellulose) and PAP (isopropyl acid phosphate) are used.
以下、本発明の防除剤の実施例について説明する。な
お、ここで用いる部は重量部である。Hereinafter, examples of the control agent of the present invention will be described. The parts used here are parts by weight.
実施例1(水和剤) フザリン酸50部、珪藻土35部、ホワイトカーボン10部、
ラウリル硫酸ナトリウム3部、リグニンスルホン酸カル
シウム2部を混合粉砕することにより、フザリン酸含有
率50%の水和剤を得た。Example 1 (wettable powder) 50 parts of fusaric acid, 35 parts of diatomaceous earth, 10 parts of white carbon,
A wettable powder having a fusaric acid content of 50% was obtained by mixing and pulverizing 3 parts of sodium lauryl sulfate and 2 parts of calcium ligninsulfonate.
実施例2(粉剤) フザリン酸1部、カオリンクレー89部、タルク10部を充
分に混合粉砕することにより、フザリン酸含有率1%の
粉剤を得た。Example 2 (Dust) 1 part of fusaric acid, 89 parts of kaolin clay, and 10 parts of talc were thoroughly mixed and pulverized to obtain a powder having a fusaric acid content of 1%.
実施例3(液剤) フザリン酸50部、ラウリル硫酸ナトリウム2部、水48部
を混合することにより、フザリン酸含有率50%の溶剤を
得た。Example 3 (solution) By mixing 50 parts of fusaric acid, 2 parts of sodium lauryl sulfate and 48 parts of water, a solvent having a fusaric acid content of 50% was obtained.
これらの製剤は、そのままであるいは水等で希釈し、茎
葉処理あるいは土壌処理に用いる。土壌処理に用いる場
合には、製剤を土壌表面に散布する(必要に応じ、散布
土壌と混和する)か、または土壌に潅注する。These preparations are used as they are or diluted with water etc. for foliage treatment or soil treatment. When used for soil treatment, the formulation is applied to the surface of the soil (mixed with the applied soil, if necessary) or irrigated.
次に、本発明の防除剤の試験例について説明するが、各
例において比較対照に用いた化合物は、第4表に示した
化合物記号を用いて表わす。Next, test examples of the control agent of the present invention will be described. The compounds used as comparative controls in each example are represented by the compound symbols shown in Table 4.
供試化合物の殺菌活性は、供試植物の病斑長を測定し、
以下の如く求めた防除価を指標として比較した。 The bactericidal activity of the test compound measures the lesion length of the test plant,
The control values obtained as described below were used as an index for comparison.
薬剤処理n日後の病斑長−薬剤処理時の病斑長=A 試験例1(タバコ舞病菌殺菌活性試験) 18〜20葉期のタバコ(品種:バーレー21)の10〜12枚目
の葉に枚病菌を針接種して30℃湿室に置き、1〜2日後
に病斑が形成された後、フザリン酸および対照化合物の
溶液を葉面に充分に薬液が付着するようにそれぞれ散布
した。散布後は30℃湿室に戻し、3日後に病斑長を測定
して防除価を求めた。その結果を第5表に示す。Lesion length n days after drug treatment-lesion length at drug treatment = A Test Example 1 (bacterial bactericidal bactericidal activity test) 10 to 12 leaves of 18 to 20 leaf stage tobacco (variety: Burley 21) were inoculated with the fungus in a needle and placed in a humid chamber at 30 ° C. for 1 to 2 After the lesion was formed after a day, the solutions of fusaric acid and the control compound were sprayed so that the drug solution was sufficiently attached to the leaves. After spraying, it was returned to the humid chamber at 30 ° C., and after 3 days, the lesion length was measured to determine the control value. The results are shown in Table 5.
試験例2(タバコ疫病殺菌活性試験) 18〜20葉期のタバコ(品種:バーレー21)の10〜12枚目
の葉に疫病菌を針接種して20℃湿室に置き、1〜2日後
に病斑が形成された後、フザリン酸および対照化合物の
溶液を葉面に充分に薬液が付着するようにそれぞれ散布
した。散布後は20℃湿室に戻し、3〜5日後に病斑長を
測定して防除価を求めた。その結果を第6表に示す。 Test Example 2 (bacterial bactericidal bactericidal activity test) 10 to 12 leaves of 18 to 20 leaf stage tobacco (variety: Burley 21) are inoculated with the plague bacillus by needles and placed in a humid chamber at 20 ° C for 1 to 2 days After the lesions were formed later, the solutions of fusaric acid and the control compound were sprayed so that the drug solution adhered sufficiently to the leaf surface. After spraying, it was returned to a humid chamber at 20 ° C., and after 3 to 5 days, the lesion length was measured to determine the control value. The results are shown in Table 6.
これらの結果より明らかなように、フザリン酸はタバコ
疫病菌に対して顕著な殺菌活性を示し、タバコ舞病に対
しても優れた防除効果を示す。 As is clear from these results, fusaric acid has a remarkable bactericidal activity against tobacco bacillus and an excellent controlling effect against tobacco scab.
以上述べたように、フザリン酸は植物病原性糸状菌に対
する殺菌活性を有し、フザリン酸を含有する本発明の防
除剤は、植物糸状菌病に対する優れた防除効果を示す。As described above, fusaric acid has a bactericidal activity against phytopathogenic filamentous fungi, and the control agent of the present invention containing fusaric acid exhibits an excellent control effect against plant filamentous fungal diseases.
Claims (1)
を特徴とする植物糸状菌病防除剤。1. A plant filamentous fungal disease controlling agent, which comprises fusaric acid as an active ingredient.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20419987A JPH07112962B2 (en) | 1987-08-19 | 1987-08-19 | Plant filamentous fungus control agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20419987A JPH07112962B2 (en) | 1987-08-19 | 1987-08-19 | Plant filamentous fungus control agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6447703A JPS6447703A (en) | 1989-02-22 |
| JPH07112962B2 true JPH07112962B2 (en) | 1995-12-06 |
Family
ID=16486472
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP20419987A Expired - Lifetime JPH07112962B2 (en) | 1987-08-19 | 1987-08-19 | Plant filamentous fungus control agent |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07112962B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105638669A (en) * | 2016-03-23 | 2016-06-08 | 福建省农业科学院植物保护研究所 | Application of fusaric acid to inhibition of magaporthe grisea |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100743255B1 (en) * | 2006-05-04 | 2007-07-27 | 한국과학기술연구원 | Novel 1,3-dioxoisoindole derivatives active on T-type calcium channels |
-
1987
- 1987-08-19 JP JP20419987A patent/JPH07112962B2/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105638669A (en) * | 2016-03-23 | 2016-06-08 | 福建省农业科学院植物保护研究所 | Application of fusaric acid to inhibition of magaporthe grisea |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6447703A (en) | 1989-02-22 |
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