「analgesic」の共起表現一覧(1語右で並び替え)
該当件数 : 282件
| n-proprietary name used to denote a compound | analgesic, a combination of codeine phosphate with asp |
| However its | analgesic action against other kinds of pain is limite |
| ht that this family of drugs has a degree of | analgesic action, though this is, in comparison to the |
| hannels, possibly accounting in part for its | analgesic action. |
| Like epibatidine, tebanicline showed potent | analgesic activity against neuropathic pain in both an |
| At high doses, it exhibits | analgesic activity which is not fully reversed by opio |
| It is not known to have any | analgesic activity in its own right, however other der |
| nyl-γ-Dialkyamino-Butyramides, which show no | analgesic activity, but are extremely active physiolog |
| N-aminophenethyl group, which increases its | analgesic activity. |
| ecause of its morphine- (or endorphin-) like | analgesic activity. |
| phine and 75 mg of pethidine (meperidine) in | analgesic activity. |
| e; the other isomer is devoid of significant | analgesic activity." |
| It was developed as a potential | analgesic after the discovery that the selective Cav2. |
| General anesthetics, | analgesic agents and psycholeptics potentiate the seda |
| btype, and has been researched for use as an | analgesic, although it has not passed clinical trials. |
| nificantly more effective than aspirin as an | analgesic, although with a greater incidence of side e |
| eptors and has been researched for use as an | analgesic, although it has not passed clinical trials. |
| BmK AGAP has both | analgesic and antitumor properties and recombinant pro |
| alf as potent as chlorpromazine) with strong | analgesic and antiemetic properties. |
| l) is a quinazolinone derivative with potent | analgesic and antipyretic effects and also anti-inflam |
| Dihydrocodeinone enol acetate's | analgesic and antitussive potency is slightly higher t |
| It also has | analgesic and antiinflammatory properties, reduces fev |
| Ethenzamide is a common | analgesic and anti-inflammatory drug that is used for |
| It has | analgesic and neuroprotective effects and is used in s |
| is around half the potency of morphine as an | analgesic, and has been widely used for the treatment |
| or hypnotic effects, but instead acts as an | analgesic and antiinflammatory. |
| s generally considered to be a strong opioid | analgesic and is regulated in much the same way as mor |
| oot of the plant is traditionally used as an | analgesic and sedative, used for headache, period pain |
| been a regular user of opium as a relaxant, | analgesic and antidepressant and to treat numerous hea |
| lernia ilicifolia are used medicinally as an | analgesic and antiulcerogenic by the peoples of the Br |
| Xylopropamine was also reported as having | analgesic and anti-inflammatory effects but its side e |
| l is a metabolite of phenacetin with similar | analgesic and antipyretic effects, but the new formula |
| he was successful in rendering the convict | analgesic, and at once began to experiment with mesmer |
| dilatation, hypertension, anti-inflammation, | analgesic, and sedative and immunostimulation The LD50 |
| While it has | analgesic and antipyretic properties comparable to tho |
| lite 11-nor-9-carboxy-THC which shows useful | analgesic and anti-inflammatory effects without causin |
| It has | analgesic and respiratory depressant effects. |
| Benzoylecgonine is a topical | analgesic and metabolite. |
| Miroprofen (INN) is an | analgesic and NSAID. |
| hydrocodone as an | analgesic and codeine as a cough suppressant) Benzylmo |
| It also has | analgesic and anticonvulsant effects in animal models. |
| ces similar neuroprotective, antidepressant, | analgesic, and anxiolytic effects but with either simi |
| It has been shown to have | analgesic and sedative properties. |
| Ketoprofen is used for its antipyretic, | analgesic, and anti-inflammatory properties by inhibit |
| It is used in medicine as an | analgesic and antipyretic. |
| howed it to have anticonvulsant, anxiolytic, | analgesic and neuroprotective effects, and it was orig |
| It has potency and long-lasting | analgesic and diuretic effects. |
| file of combined antidepressant, anxiolytic, | analgesic and anti-addictive effects potentially usefu |
| qualified after traces of phenylbutazone, an | analgesic and anti-inflammatory drug, were found in th |
| The tree has medicinal value as an | analgesic and sedative. |
| s own right, it may still have a role in the | analgesic and antiinflammatory effects of cannabis, an |
| Salicylamide is a non-prescription drug with | analgesic and antipyretic properties. |
| n intermediate for the synthesis of specific | analgesic and antipsychotic agents. |
| azon, antipyrine (USAN), or analgesine is an | analgesic and antipyretic. |
| Properidine is an opioid | analgesic and the isopropyl analog of pethidine. |
| It has neuroprotective, | analgesic, and anti-Parkinsonian effects in animal stu |
| O-Desmethyltramadol is an opioid | analgesic and the main active metabolite of tramadol. |
| ne is a derivative of phenazone with similar | analgesic and antipyretic effects. |
| Its | analgesic and antipyretic effects begin to occur 1-2 h |
| B1 receptor, but while it exhibits selective | analgesic, anti-inflammatory and anti-hyperalgesic eff |
| nown to possess antibacterial, antidiabetic, | analgesic, anti-inflammatory, anti-diarrheal, anticanc |
| , antihepatotoxic, choleretic, hypoglycemic, | analgesic, anti-inflammatory, antimutagenic, antispasm |
| It has | analgesic, anti-inflammatory, and antipyretic effects. |
| Ampyrone is a metabolite of aminopyrine with | analgesic, anti-inflammatory, and antipyretic properti |
| Aminophenazone - a pyrazolone with | analgesic, anti-inflammatory, and antipyretic properti |
| i-fungal, anti-histamine, anti-inflammatory, | analgesic, anti-viral, decongestant and expectorant pr |
| It has been shown to produce useful | analgesic, antidepressant and anxiolytic effects in an |
| is metabolized to salicylamide which exerts | analgesic, antipyretic and antiinflammatory effects. |
| It also has | analgesic, antipyretic, and platelet-inhibitory action |
| Fenclozic acid is an | analgesic, antipyretic, and anti-inflammatory drug. |
| .C." or aspirin-phenacetin-caffeine compound | analgesic, as a remedy for fever and pain. |
| It has around the same efficacy as an | analgesic as codeine, and was evaluated for the treatm |
| ion when pethidine is used in medicine as an | analgesic, as when pethidine is used in high doses or |
| It is not marketed as an | analgesic because of side effects related to its impac |
| ch is some 200x stronger than morphine as an | analgesic but produces extremely dangerous toxic side |
| round 200 times stronger than morphine as an | analgesic but produces extremely dangerous toxic side |
| Codeinone is 1/3 as active as codeine as an | analgesic but it is an important intermediate in the p |
| d agonist suitable for intravenous use as an | analgesic, but did not proceed to human trials, with t |
| The plant is used as an | analgesic by the indigenous peoples of Australia. |
| O-2545 is an | analgesic cannabinoid derivative created by Organix In |
| O-1057 is an | analgesic cannabinoid derivative created by Organix In |
| JWH-398 is an | analgesic chemical from the naphthoylindole family, wh |
| JWH-019 is an | analgesic chemical from the naphthoylindole family, wh |
| JWH-073 is an | analgesic chemical from the naphthoylindole family, wh |
| JWH-007 is an | analgesic chemical from the naphthoylindole family, wh |
| pentyl-3-(2-chlorophenylacetyl)indole) is an | analgesic chemical from the phenylacetylindole family, |
| JWH-210 is an | analgesic chemical from the naphthoylindole family, wh |
| Hydrocodone, a narcotic | analgesic closely related to codeine, is first synthes |
| n or codeine alone and to be as effective as | analgesic combinations containing codeine or other opi |
| he potency and slightly less effective as an | analgesic compared to morphine, or oxycodone, but tend |
| perties of sedation and this makes it a good | analgesic component of anaesthetic regimen during an o |
| skin of the African clawed frog and a potent | analgesic compound called epibatidine was obtained fro |
| It is used as an ingredient in sunscreens, | analgesic creams, and cosmetics. |
| ed under the brandname Dividol) is an opioid | analgesic developed by the drugs company Zambon in the |
| oramide is the inactive isomer of the opioid | analgesic dextromoramide, invented by the chemist Paul |
| Because of its κ-agonist activity, at | analgesic doses butorphanol increases pulmonary arteri |
| N-Phenethylnormorphine is an opiate | analgesic drug derived from morphine by replacing the |
| AH-7921 is an opioid | analgesic drug selective for the mu opioid receptor, a |
| dylthiambutene (Piperidinohton) is an opioid | analgesic drug from the thiambutene family, which has |
| Acupan) is a centrally-acting but non-opioid | analgesic drug of the benzoxazocine chemical class whi |
| al mixed agonist-antagonist narcotic (opioid | analgesic) drug of the benzomorphan class of opioids u |
| A-40174 (SP-1) is an | analgesic drug which acts as a potent cannabinoid rece |
| JWH-147 is an | analgesic drug used in scientific research, which acts |
| J-113,397 is an opioid | analgesic drug which was the first compound found to b |
| 4-1539 (Furethylnorlevorphanol) is an opioid | analgesic drug from the morphinan series, which was de |
| cetaminophen), arguably the most widely used | analgesic drug in the world (Chandrasekharan et al., 2 |
| Picenadol, an opioid | analgesic drug |
| AM-855 is an | analgesic drug which is a cannabinoid agonist. |
| AM-087 is an | analgesic drug which is a cannabinoid agonist. |
| AMG-36 is an | analgesic drug which is a cannabinoid agonist. |
| JTC-801 is an opioid | analgesic drug used in scientific research. |
| AMG-3 is an | analgesic drug which is a cannabinoid agonist. |
| AMG-41 is an | analgesic drug which is a cannabinoid agonist. |
| Methopholine is an opioid | analgesic drug invented in the 1960s. |
| clidine (LY-297,802, NNC 11-1053) is a novel | analgesic drug which acts as a mixed agonist-antagonis |
| SNC-80 is an opioid | analgesic drug used in scientific research. |
| hyl-3,3-di-2-thienylallylamine) is an opioid | analgesic drug developed in the 1950s which was mainly |
| ridine (trade name: Leritine) is a synthetic | analgesic drug and is a member of the piperidine class |
| ine derivative that is related to the opioid | analgesic drug pethidine (meperidine). |
| AD-1211 is an opioid | analgesic drug invented in the 1970s by Dainippon Phar |
| ine derivative that is related to the opioid | analgesic drug pethidine (meperidine). |
| 512) is a prodrug for the anticonvulsant and | analgesic drug gabapentin. |
| Dihydroetorphine is a potent | analgesic drug (painkiller), which is used mainly in C |
| ine derivative that is related to the opioid | analgesic drug pethidine (meperidine). |
| AM-905 is an | analgesic drug which is a cannabinoid agonist with a c |
| ine derivative that is related to the opioid | analgesic drug pethidine (meperidine). |
| ine derivative that is related to the opioid | analgesic drug pethidine (meperidine). |
| AM-4030 is an | analgesic drug which is a cannabinoid receptor agonist |
| JWH-171 is an | analgesic drug which acts as a cannabinoid receptor ag |
| ine derivative that is related to the opioid | analgesic drug pethidine (meperidine). |
| ine derivative that is related to the opioid | analgesic drug pethidine (meperidine). |
| Pyrrolidinylthiambutene is an opioid | analgesic drug from the thiambutene family with around |
| derivative that is a precursor to the opioid | analgesic drug pethidine (meperidine). |
| oxy-3-methylfentanyl) is an extremely potent | analgesic drug which selectively binds to the µ-opioid |
| line (WIN 48,098) is an antiinflammatory and | analgesic drug, related in structure to non-steroidal |
| s a potent but short-acting synthetic opioid | analgesic drug, used for anaesthesia in surgery. |
| name Sufenta) is a powerful synthetic opioid | analgesic drug, approximately 5 to 10 times more poten |
| e (Doxpicodin, Doxpizodine) is a mild opioid | analgesic drug, acting as a mu-opioid receptor agonist |
| Codorphone (Conorphone) is an opioid | analgesic drug. |
| hydroxy-N-phenethylnormorphine) is an opiate | analgesic drug. |
| xypiperidine, Desmethylprodine) is an opioid | analgesic drug. |
| henylpiperidine derivative that is an opioid | analgesic drug. |
| nd "unnatural" enantiomers of various opioid | analgesic drugs including morphine, meperidine, fentan |
| uded as an adjutant to boost the activity of | analgesic drugs, and use in the treatment of insomnia |
| ors, they do not block the effects of opioid | analgesic drugs, and so can be used to counteract the |
| lved in various adverse properties of opioid | analgesic drugs, such as loss of efficacy with extende |
| e to severe pain as an alternative to opioid | analgesic drugs. |
| re less common with nefopam than with opioid | analgesic drugs. |
| The Thiambutenes are a family of opioid | analgesic drugs. |
| It has been suggested that the | analgesic effect of some antidepressants is due to sod |
| with long-term use, neither tolerance to its | analgesic effect nor psychological or physical depende |
| Its | analgesic effect is strong (equivalent to 15 mg of sub |
| By comparison, methadone has an | analgesic effect lasting from 3 to 6 hours although fo |
| s, morphine-3-glucuronide (M3G) which has no | analgesic effect and morphine-6-glucuronide (M6G),, wh |
| ng dose is 10-20 mg and it has a duration of | analgesic effect of 1 to 4 hours. |
| s a bitter substance that has a sedative and | analgesic effect, acting on the central nervous system |
| Kyotorphin has an | analgesic effect, but it does not interact with the op |
| on effect (by absorbing UVB rays) and to the | analgesic effect. |
| It has | analgesic effects in animal studies, but without canna |
| The | analgesic effects of N2O are linked to the interaction |
| unnatural" enantiomer (+)-thebaine does show | analgesic effects apparently mediated through opioid r |
| cannabis, and may contribute to the overall | analgesic effects of medical cannabis. |
| and is slightly more potent than codeine in | analgesic effects but associated with somewhat greater |
| The | analgesic effects have also been proven, by acting as |
| It has potent | analgesic effects in animal studies comparable to thos |
| dicated for the reversal of the sedative and | analgesic effects of dexmedetomidine and medetomidine |
| ssive effects, and reduces the rewarding and | analgesic effects of morphine, although it did not pre |
| In animal studies of TROX-1, | analgesic effects were observed with similar efficacy |
| It does not have | analgesic effects in its own right, but prevents the d |
| potent than THC, and exhibits antiemetic and | analgesic effects via activation of CB1 and CB2 cannab |
| It has also been shown to produce | analgesic effects in animals, thought to be because it |
| his also renders the animals tolerant to the | analgesic effects of N2O. |
| ance, as well as having antihyperalgesic and | analgesic effects in its own right. |
| use, due to its useful anti-inflammatory and | analgesic effects in addition to the sedative and anxi |
| ly reversible, and it produces fairly potent | analgesic effects mediated through the μ-opioid recept |
| At lower doses, it antagonizes the | analgesic effects of alfentanil and substitutes for na |
| -100,635 has also been found to increase the | analgesic effects of opioid drugs in a dose-dependent |
| blocks the nociceptin receptor and produces | analgesic effects in a variety of animal studies, and |
| It has | analgesic effects and is used in scientific research. |
| red to other potent opioid agonists, but its | analgesic effects were somewhat disappointing in human |
| Tolerance to the | analgesic effects of morphine is fairly rapid. |
| Difenoxin also has some sedative and | analgesic effects as with other opioids, but diphenoxy |
| poor metabolisers") will tend to get reduced | analgesic effects from tramadol. |
| It has | analgesic effects in animal studies, particularly agai |
| Analgesic effects last about 2 hours, it does not crea | |
| It has potent | analgesic effects and is around 10x more potent than m |
| ay be partially or fully responsible for the | analgesic effects of paracetamol. |
| It has anticonvulsant, antidepressant and | analgesic effects in animal studies, but also inhibits |
| It also has | analgesic effects several times stronger than codeine, |
| Studies in primates showed it to have | analgesic effects but without producing respiratory de |
| It has | analgesic effects, promotes proliferation of neural st |
| The parent compound thiambutene has no | analgesic effects, but several compounds from this gro |
| ike its analogue orphenadrine which also has | analgesic effects, nefopam has been found to act as a |
| ins an alkaloid called horsfiline, which has | analgesic effects, as well as several other compounds |
| ine was found to exhibit unexpectedly strong | analgesic effects, which appeared at doses ten times s |
| While metazocine has significant | analgesic effects, mediated through a mixed agonist-an |
| ne reuptake is thought to be involved in its | analgesic effects, and there may be other modes of act |
| It has sedative and | analgesic effects, with analgesia lasting for up to 24 |
| tent and selective κ-opioid agonist, and has | analgesic effects. |
| tent and selective κ-opioid agonist, and has | analgesic effects. |
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