Displaying drugs 326 - 332 of 332 in total
Flupirtine
Flupirtine is a pyridine derivative that is in clinical use as a nonopioid analgesic. It was approved for the treatment of pain in 1984 in Europe. It is not approved for use in the U.S. or Canada, but is currently in phase II trials for the treatment of fibromyalgia.
Investigational
Matched Iupac: … ethyl N-(2-amino-6-{[(4-fluorophenyl)methyl]amino}pyridin-3-yl)carbamate …
Matched Salts cas: … 75507-68-5 ... 815586-85-7 …
Matched Categories: … Heterocyclic Compounds, 1-Ring …
Matched Salts cas: … 75507-68-5 ... 815586-85-7 …
Matched Categories: … Heterocyclic Compounds, 1-Ring …
Tridihexethyl
Tridihexethyl is a synthetic anticholinergic agent which has been shown in experimental and clinical studies to have a pronounced antispasmodic and antisecretory effect on the gastrointestinal tract. Tridihexethyl is an antimuscarinic, anticholinergic drug. Tridihexethyl is no longer available in the US market.
Withdrawn
Matched Iupac: … (3-cyclohexyl-3-hydroxy-3-phenylpropyl)triethylazanium …
Matched Salts cas: … 4310-35-4 …
Matched Salts cas: … 4310-35-4 …
Glisoxepide
Glisoxepide is one of the sulphonamide-derived oral antidiabetic drugs. It inhibits the uptake of bile acids into isolated rat hepatocytes. However it inhibits taurocholate uptake only in the absence of sodium ions. Glisoxepide uptake could be further inhibited by blockers of the hepatocellular monocarboxylate transporter, by the loop diuretic bumetanide,...
Investigational
Matched Iupac: … N-{2-[4-({[(azepan-1-yl)carbamoyl]amino}sulfonyl)phenyl]ethyl}-5-methyl-1,2-oxazole-3-carboxamide …
Matched Description: … are consistent with the transport of glisoxepide via the transport system for the unconjugated bile acid …
Matched Categories: … Cytochrome P-450 Substrates ... Cytochrome P-450 CYP2C9 Substrates …
Matched Description: … are consistent with the transport of glisoxepide via the transport system for the unconjugated bile acid …
Matched Categories: … Cytochrome P-450 Substrates ... Cytochrome P-450 CYP2C9 Substrates …
3-Methylfentanyl
3-Methylfentanyl is an opioid analgesic and is an analog of the potent opioid, fentanyl. 3-Methylfentanyl is one of the most powerful opioid drugs sold illegally and is estimated to be between 400-6000 times more potent than morphine in certain cases. 3-Methylfentanyl was initially discovered in 1974 and widespread illegal use...
Illicit
Matched Synonyms: … 3-MF …
Matched Name: … 3-Methylfentanyl …
Matched Iupac: … N-[3-methyl-1-(2-phenylethyl)piperidin-4-yl]-N-phenylpropanamide …
Matched Description: … 3-Methylfentanyl is an opioid analgesic and is an analog of the potent opioid, fentanyl. 3-Methylfentanyl ... illegally and is estimated to be between 400-6000 times more potent than morphine in certain cases. 3- …
Matched Categories: … Heterocyclic Compounds, 1-Ring …
Matched Name: … 3-Methylfentanyl …
Matched Iupac: … N-[3-methyl-1-(2-phenylethyl)piperidin-4-yl]-N-phenylpropanamide …
Matched Description: … 3-Methylfentanyl is an opioid analgesic and is an analog of the potent opioid, fentanyl. 3-Methylfentanyl ... illegally and is estimated to be between 400-6000 times more potent than morphine in certain cases. 3- …
Matched Categories: … Heterocyclic Compounds, 1-Ring …
Morniflumate
Morniflumate is a non-steroidal anti-inflammatory drug with antipyretic properties. It is the morpholinoethyl ester of niflumic acid . In one study, post morniflumate ingestion, physical examination and clinical symptoms of those with bronchitis showed improvement .
Experimental
Matched Iupac: … 2-(morpholin-4-yl)ethyl 2-{[3-(trifluoromethyl)phenyl]amino}pyridine-3-carboxylate …
Matched Description: … It is the morpholinoethyl ester of niflumic acid [L1496]. …
Matched Categories: … Carboxylic Acids ... Heterocyclic Compounds, 1-Ring …
Matched Description: … It is the morpholinoethyl ester of niflumic acid [L1496]. …
Matched Categories: … Carboxylic Acids ... Heterocyclic Compounds, 1-Ring …
Tea tree oil
Tea tree oil is an essential oil derived mainly from the Australian native plant Melaleuca alternifolia via steam distillation of the of the leaves and terminal branches . It may be referred to as Melaleuca alternifolia oil. It has been a popular ingredient in a variety of household and cosmetic...
Experimental
Nutraceutical
Carfentanil
Carfentanil or carfentanyl (Wildnil) is an analogue of the popular synthetic opioid analgesic fentanyl, and is one of the most potent opioids known (also the most potent opioid used commercially). Carfentanil was first synthesized in 1974 by a team of chemists at Janssen Pharmaceutica which included Paul Janssen. It has...
Illicit
Investigational
Vet approved
Matched Iupac: … methyl 1-(2-phenylethyl)-4-(N-phenylpropanamido)piperidine-4-carboxylate …
Matched Description: … 10,000 times that of morphine and 100 times that of fentanyl, with activity in humans starting at about 1 …
Matched Salts cas: … 61380-27-6 …
Matched Categories: … Heterocyclic Compounds, 1-Ring …
Matched Description: … 10,000 times that of morphine and 100 times that of fentanyl, with activity in humans starting at about 1 …
Matched Salts cas: … 61380-27-6 …
Matched Categories: … Heterocyclic Compounds, 1-Ring …
Displaying drugs 326 - 332 of 332 in total