「opioid」の共起表現一覧(1語右で並び替え)
該当件数 : 290件
| ng anti-diarrheal effects despite only limited | opioid action. |
| f N-substituted derivatives, but it has little | opioid activity in its own right. |
| nt between different patients, with consistent | opioid activity only being seen at a dose several tim |
| Normorphine has relatively little | opioid activity in its own right, but is a useful int |
| They lack | opioid activity but are potent stimulators of GH rele |
| Norcodeine has relatively little | opioid activity in its own right, but is formed as a |
| Adrenorphin exhibits potent | opioid activity, acting as a balanced μ- and κ-opioid |
| in China as a substitute maintenance drug for | opioid addicts, in a similar way to how the related d |
| It is a strong | opioid agonist analgesic two to three times as potent |
| c effects at high doses, suggesting some kappa | opioid agonist action. |
| Methadone is a full | opioid agonist and so is the preferred treatment in h |
| tine is a drug with antimuscarinic and weak mu | opioid agonist effects. |
| metabolite is considerably more potent as a μ | opioid agonist than the parent compound. |
| Opioid Agonist Treatment, or OAT, refers to the treat | |
| Buprenorphine is a partial | opioid agonist and has virtually no withdrawal effect |
| nt of incarcerated men and women maintained on | opioid agonist medications. |
| a high potential for abuse as with any potent | opioid agonist, and is sometimes found along with des |
| Eseroline is a drug which acts as an | opioid agonist. |
| phan is a morphinan derivative that acts as an | opioid agonist. |
| nol) is a morphinan derivative that acts as an | opioid agonist. |
| omer of ohmefentanyl is one of the most potent | opioid agonists yet discovered, possessing an analges |
| inorin B. Most derivatives are selective kappa | opioid agonists as with Salvinorin A, although some a |
| oduce effects similar to those of other potent | opioid agonists, including strong analgesia, sedation |
| oduce effects similar to those of other potent | opioid agonists, including strong analgesia, sedation |
| oduce effects similar to those of other potent | opioid agonists, including strong analgesia, sedation |
| espiratory depression compared to other potent | opioid agonists, but its analgesic effects were somew |
| oduce effects similar to those of other potent | opioid agonists, including strong analgesia, sedation |
| Unlike conventional | opioid agonists, RB-101 also failed to produce respir |
| enantiomers in this series are more active as | opioid agonists, but the less active (R) enantiomer o |
| , since a significant fraction (up to 60 %) of | opioid analgesia can be mediated by opioid receptors |
| (WIN 1161-3, Methiodone) is an analogue of the | opioid analgesic methadone, where the carbonyl group |
| Developed in 1984, it is a potent | opioid analgesic several times stronger than fentanyl |
| Ciramadol (WY-15,705) is an | opioid analgesic that was developed in the late 1970s |
| f moderate to severe pain as an alternative to | opioid analgesic drugs. |
| events are less common with nefopam than with | opioid analgesic drugs. |
| oxone (Heptalgin, Morphidone, Heptazone) is an | opioid analgesic of the open chain class (methadone a |
| adoxone is generally considered to be a strong | opioid analgesic and is regulated in much the same wa |
| J-113,397 is an | opioid analgesic drug which was the first compound fo |
| tralia) is a potent but short-acting synthetic | opioid analgesic drug, used for anaesthesia in surger |
| 0, brand name Sufenta) is a powerful synthetic | opioid analgesic drug, approximately 5 to 10 times mo |
| R-4066 is a drug which is an analogue of the | opioid analgesic methadone, where the metabolically l |
| Ro4-1539 (Furethylnorlevorphanol) is an | opioid analgesic drug from the morphinan series, whic |
| Meptazinol (trade name Meptid) is an | opioid analgesic for use with moderate to severe pain |
| o be involved in various adverse properties of | opioid analgesic drugs, such as loss of efficacy with |
| Herkinorin is an | opioid analgesic that is an analogue of the natural p |
| Metazocine, an | opioid analgesic |
| Picenadol, an | opioid analgesic drug |
| Codorphone (Conorphone) is an | opioid analgesic drug. |
| oxpicomine (Doxpicodin, Doxpizodine) is a mild | opioid analgesic drug, acting as a mu-opioid receptor |
| Bromadoline is an | opioid analgesic selective for the mu-opioid receptor |
| hyl-1-methyl-3,3-di-2-thienylallylamine) is an | opioid analgesic drug developed in the 1950s which wa |
| Metazocine is an | opioid analgesic related to pentazocine. |
| Norlevorphanol is an | opioid analgesic of the morphinan class. |
| normal" and "unnatural" enantiomers of various | opioid analgesic drugs including morphine, meperidine |
| JTC-801 is an | opioid analgesic drug used in scientific research. |
| Levomethorphan - A potent | opioid analgesic that was never clinically developed. |
| -propionoxypiperidine, Desmethylprodine) is an | opioid analgesic drug. |
| Methopholine is an | opioid analgesic drug invented in the 1960s. |
| Proheptazine is an | opioid analgesic from the phenazepine family. |
| SNC-80 is an | opioid analgesic drug used in scientific research. |
| Metethoheptazine (WY-535) is an | opioid analgesic from the phenazepine family. |
| The Thiambutenes are a family of | opioid analgesic drugs. |
| AH-7921 is an | opioid analgesic drug selective for the mu opioid rec |
| Hydroxypethidine (Bemidone) is an | opioid analgesic that is an analogue of pethidine (me |
| ylpiperidine derivative that is related to the | opioid analgesic drug pethidine (meperidine). |
| Meprodine is an | opioid analgesic that is an analogue of pethidine (me |
| AD-1211 is an | opioid analgesic drug invented in the 1970s by Dainip |
| Propylketobemidone is an | opioid analgesic that is an analogue of ketobemidone. |
| Trimeperidine is an | opioid analgesic that is an analogue of prodine. |
| Thiofentanyl is an | opioid analgesic that is an analogue of fentanyl. |
| ylpiperidine derivative that is related to the | opioid analgesic drug pethidine (meperidine). |
| Para-fluorofentanyl is an | opioid analgesic that is an analogue of fentanyl. |
| β-Methylfentanyl is an | opioid analgesic that is an analogue of fentanyl. |
| β-hydroxythiofentanyl is an | opioid analgesic that is an analogue of fentanyl. |
| codone (OxyContin and other brand names) is an | opioid analgesic medication synthesized from opium-de |
| Ethoheptazine (trade name Zactane) is an | opioid analgesic from the phenazepine family. |
| Properidine is an | opioid analgesic and the isopropyl analog of pethidin |
| is a 4-phenylpiperidine derivative that is an | opioid analgesic drug. |
| Benzylmorphine is an active metabolite of the | opioid analgesic myrophine, formed in the liver. |
| etoxyketobemidone (O-Acetylketobemidone) is an | opioid analgesic that is an acetylated derivative of |
| α-methylacetylfentanyl is an | opioid analgesic that is an analogue of fentanyl. |
| β-hydroxyfentanyl is an | opioid analgesic that is an analogue of fentanyl. |
| ylpiperidine derivative that is related to the | opioid analgesic drug pethidine (meperidine). |
| ylpiperidine derivative that is related to the | opioid analgesic drug pethidine (meperidine). |
| O-Desmethyltramadol is an | opioid analgesic and the main active metabolite of tr |
| α-methyl-thiofentanyl is an | opioid analgesic that is an analogue of fentanyl. |
| ylpiperidine derivative that is related to the | opioid analgesic drug pethidine (meperidine). |
| ylpiperidine derivative that is related to the | opioid analgesic drug pethidine (meperidine). |
| dine (trade names Prisilidine, Nisentil) is an | opioid analgesic that is an analogue of pethidine (me |
| 33799) is an analogue of the popular synthetic | opioid analgesic fentanyl, and is one of the most pot |
| (INN; trade names Amidalgon, Spasmoxal) is an | opioid analgesic which is a diphenylacetic acid deriv |
| ylpiperidine derivative that is related to the | opioid analgesic drug pethidine (meperidine). |
| Pyrrolidinylthiambutene is an | opioid analgesic drug from the thiambutene family wit |
| Diampromide is an | opioid analgesic from the ampromide family of drugs, |
| peridine derivative that is a precursor to the | opioid analgesic drug pethidine (meperidine). |
| l (marketed under the brandname Dividol) is an | opioid analgesic developed by the drugs company Zambo |
| Levomoramide is the inactive isomer of the | opioid analgesic dextromoramide, invented by the chem |
| Phenampromide is an | opioid analgesic from the ampromide family of drugs, |
| Piperidylthiambutene (Piperidinohton) is an | opioid analgesic drug from the thiambutene family, wh |
| rototypical mixed agonist-antagonist narcotic ( | opioid analgesic) drug of the benzomorphan class of o |
| antagonist properties in addition to being an | opioid analgesic). |
| Methyldesorphine is an | opioid analgesic. |
| Phenomorphan is an | opioid analgesic. |
| Levorphanol - A potent | opioid analgesic. |
| Hydrocodone is a semi-synthetic | opioid analgesic. |
| uch higher doses, whereas levomethorphan is an | opioid analgesic. |
| ptors and platelet aggregation, and acts as an | opioid analgesic. |
| cations of nitrates, beta-blockers, lidocaine, | opioid analgesics and/or benzodiazepines should be em |
| rse the respiratory depression produced by the | opioid analgesics and barbiturates which are used for |
| ly, mixed kappa receptor agonist mu antagonist | opioid analgesics can cause dose-related psychotomime |
| as analgesic-sparing (potentiating) effects on | opioid analgesics, commonly reducing codeine, dihydro |
| cal class of psychoactive drugs, consisting of | opioid analgesics, cough suppressants, and dissociati |
| distinguish it from other, more commonly used | opioid analgesics, although it does have a slightly l |
| venous formulation of CX-717 for use alongside | opioid analgesics, along with an oral formulation of |
| ntly at a level of pain with an indication for | opioid analgesics. |
| Other | opioid analogues even more potent still than 3-MF are |
| s on the body include cholinergic, adrenergic, | opioid and nitric oxide donating actions, all of whic |
| y broadening the antinociceptive action of the | opioid and possibly other mechanisms, generally lower |
| onfirm what is wrong, the team treat Alex with | opioid antagonist drugs and induce a coma in order to |
| from the seeds, akuammine, was found to be an | opioid antagonist when tested in vitro and canceled o |
| Cyprodime is a selective | opioid antagonist which blocks the μ-opioid receptor, |
| Cyprodime is an | opioid antagonist from the morphinan family of drugs. |
| Oxilorphan is an | opioid antagonist from the morphinan family of drugs. |
| Several | opioid antagonist drugs were found to act as antagoni |
| Propiram exhibits weak | opioid antagonist activity on the mu receptor -- quit |
| rug which is the "unnatural" enantiomer of the | opioid antagonist drug (-)-naloxone. |
| Naloxonazine is an irreversible mu | opioid antagonist. |
| Not to mention the fact that | opioid antagonists can block the effects of THC.--Met |
| e mechanical ventilation and/or treatment with | opioid antagonists would have been life-saving for ma |
| atory stimulants such as doxapram and specific | opioid antagonists such as naloxone. |
| These effects were not blocked by | opioid antagonists such as naloxone, and it was event |
| tudied separately, in contrast to better known | opioid antagonists such as naloxone which block all t |
| g adequate supplies of naloxone or naltrexone ( | opioid antagonists) to prevent complications in many |
| lgesic activity which is not fully reversed by | opioid antagonists, suggesting that the drug has both |
| use of the agent, but were instructed to bring | opioid antagonists. |
| ug of the morphinan family which is used as an | opioid antidote or antagonist. |
| Whereas increasing the dose of | opioid can be an effective way to overcome tolerance, |
| Butamirate (or brospamin) is an nonaddictive | opioid central cough suppressant. |
| Pentazocine and Butorphanol fall under this | opioid class. |
| ne rings form the core structure of a group of | opioid compounds sometimes known as azocines. |
| the American Association for the Treatment of | Opioid Dependence AATOD, CODAC is funded by Federal, |
| treatment for the treatment and management of | opioid dependence if patients fail to respond to drug |
| Methadone maintenance has been used to treat | opioid dependence for more than 45 years. |
| d to be more likely to adhere to treatment for | opioid dependence. |
| -antagonist naloxone, will cause withdrawal in | opioid dependent persons), Talwin, Talwin PX (without |
| vivo and is made to block the activity of the | opioid depressants already in the bloodstream that it |
| However conventional | opioid derivatives are not strong enough to rapidly t |
| s an antidote for treating overdose of certain | opioid derivatives which are used in humans, such as |
| Presumably it has similar effects to other | opioid derivatives, such as analgesia, sedation, naus |
| Presumably it has similar effects to other | opioid derivatives, such as analgesia, sedation, naus |
| Unlike most | opioid derivatives, oxpheneridine is not specifically |
| It has similar effects to other | opioid derivatives, such as analgesia, sedation, naus |
| Presumably it has similar effects to other | opioid derivatives, such as analgesia, sedation, naus |
| tional Drug and Alcohol Research Centre, rapid | opioid detoxification was determined to be the most e |
| Russian: Колокол, English bell) is a synthetic | opioid, developed for use as an aerosolizable incapac |
| ine (Dihydroheterocodeine) is a semi-synthetic | opioid drug developed in Germany in 1936, controlled |
| Moreover, some weak or atypical | opioid drugs such as tramadol and the newer agent tap |
| trated that it can be used in humans alongside | opioid drugs to reduce this side effect without affec |
| tive analgesic with similar efficacy to strong | opioid drugs but comparatively milder side effects. |
| hat act to reverse some of the side effects of | opioid drugs such as constipation without affecting a |
| n, which should have less abuse potential than | opioid drugs and less propensity to cause gastric ulc |
| Several commonly used | opioid drugs including etorphine and buprenorphine ha |
| een found to increase the analgesic effects of | opioid drugs in a dose-dependent manner, in contrast |
| and it not only enhances analgesia produced by | opioid drugs, but also reduces the development of tol |
| Like codeine, dihydrocodeine and similar weak | opioid drugs, ethylmorphine is listed under the inter |
| n, drug addiction, development of tolerance to | opioid drugs, and psychological disorders such as anx |
| awal symptoms in patients who are dependent on | opioid drugs, or more rarely when used post-operative |
| cular clinical advantages over other available | opioid drugs, and was never commercially marketed. |
| Like other | opioid drugs, pethidine has the potential to cause ph |
| rphanol a lower potential for abuse than other | opioid drugs. |
| osely related to other established families of | opioid drugs. |
| which is structurally unrelated to most other | opioid drugs. |
| tching and constipation, but without affecting | opioid effects in the brain such as analgesia. |
| e, so pethidine intermediate A might also show | opioid effects. |
| It is a derivative of the more well-known | opioid etorphine, which is used as a very potent vete |
| it is thought to be a derivative of the potent | opioid fentanyl, most probably 3-methylfentanyl disso |
| mall dose of levallorphan is used alongside an | opioid full agonist this can in fact produce greater |
| Met-enkephalin, sometimes referred to as | opioid growth factor (OGF) is an endogenous opioid pe |
| ok up the half-life of oxymorphone and find an | opioid in the list that has a similar half-life. |
| eloped in subcutaneous and oral forms to treat | opioid induced constipation (OIC). |
| lasting from 3 to 6 hours although for use in | opioid maintenance the dose is different from that us |
| mplete abstinence from opioids while receiving | opioid maintenance therapy, and 70% to 95% are able t |
| ivity of pravadoline cannot be explained by an | opioid mechanism, because pravadoline-induced antinoc |
| gardless, Fentanyl is considered the most safe | opioid medication on the market, as well as the least |
| (1) Do you desire to continue taking your | opioid medication? |
| tivity that tends to cause problems with other | opioid mixed agonist-antagonists such as pentazocine. |
| Cyclorphan is a hallucinogenic | opioid mixed agonist-antagonist related to levorphano |
| e-MIF-1 (Tyr-Pro-Leu-Gly-NH2) is an endogenous | opioid modulator. |
| f its effect by being a prodrug for a stronger | opioid, namely hydromorphone, which is formed in the |
| Although an | opioid of low to moderate strength and use in medicin |
| An | opioid overdose is due to excessive use of narcotics. |
| he cause, rather than just the symptoms, of an | opioid overdose. |
| Opioid overdoses associated with a conjunction of ben | |
| α-neo-endorphin is an endogenous | opioid peptide whose amino acid sequence is: Tyr-Gly- |
| Alpha-endorphin is an endogenous | opioid peptide whose amino acid sequence is: Tyr-Gly- |
| β-neo-endorphin is an endogenous | opioid peptide whose amino acid sequence is: Tyr-Gly- |
| rphin is an endogenous, C-terminally amidated, | opioid peptide generated as a cleavage product of pro |
| A is a form of dynorphin, it is an endogenous | opioid peptide whose sequence is: Tyr - Gly - Gly - P |
| B is a form of dynorphin, it is an endogenous | opioid peptide whose sequence is: Tyr - Gly - Gly - P |
| Leu-enkephalin is an endogenous | opioid peptide neurotransmitter found naturally in th |
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