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List of articles in "Drug" category - Page 114

Cloforex

Cloforex (Oberex) is an anorectic of the amphetamine class. It is a prodrug to chlorphentermine.


A-836339

A-836339 is a drug developed by Abbott Laboratories that acts as a potent cannabinoid receptor full agonist. It is selective for CB2 with Ki values of 0.64nM at CB2 vs […]


JWH-007

JWH-007 is an analgesic chemical from the naphthoylindole family which acts as a cannabinoid agonist at both the CB1 and CB2 receptors. It was the most active of the first […]


4′-Fluorococaine

4′-Fluorococaine is a tropane derivative drug which is a synthetic analogue of cocaine. Unlike related compounds such as the corresponding 4′-fluorophenyltropane derivative CFT and the 2′-hydroxy analogue salicylmethylecgonine 4′-fluorococaine has […]


JWH-122

JWH-122 is a synthetic cannabimimetic that was discovered by John W. Huffman. It is a methylated analogue of JWH-018. It has a Ki of 0.69 nM at CB1 and 1.2 […]


JWH-210

JWH-210 is an analgesic chemical from the naphthoylindole family which acts as a potent cannabinoid agonist at both the CB1 and CB2 receptors with Ki values of 0.46nM at CB1 […]


Sarizotan

Sarizotan (EMD-128130) is a selective 5-HT1A receptor agonist and D2 receptor antagonist which has antipsychotic effects and has also shown efficacy in reducing dyskinesias resulting from long-term anti-Parkinsonian treatment with […]


JWH-203

JWH-203 (1-pentyl-3-(2-chlorophenylacetyl)indole) is an analgesic chemical from the phenylacetylindole family that acts as a cannabinoid agonist with approximately equal affinity at both the CB1 and CB2 receptors having a Ki […]


Osemozotan

Osemozotan (MKC-242) is a selective 5-HT1A receptor agonist with some functional selectivity acting as a full agonist at presynaptic and a partial agonist at postsynaptic 5-HT1A receptors. It has antidepressant […]


4-Methylmethylphenidate

threo-4-Methylmethylphenidate (4-MeTMP) is a stimulant drug related to methylphenidate. It is slightly less potent than methylphenidate and has relatively low efficacy at blocking dopamine reuptake despite its high binding affinity […]


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