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List of articles in "Drug" category - Page 155

Tandamine

Tandamine is a selective norepinephrine reuptake inhibitor with a tricyclic structure. It was developed in the 1970s as an antidepressant but was never commercialized. Tandamine is analogous to pirandamine which […]


Litoxetine

Litoxetine (SL 81-0385) is an antidepressant which was under clinical development for the treatment of depression in the early 1990s. It acts as a serotonin reuptake inhibitor and 5-HT3 receptor […]


CAR-302196

CAR-302196 (also known as PCMG or just by its code number 302196) is a moderately potent and relatively short lasting anticholinergic deliriant drug related to the chemical warfare agent 3-Quinuclidinyl […]


EA-3443

EA-3443 is a potent and long lasting anticholinergic deliriant drug related to the chemical warfare agent 3-Quinuclidinyl benzilate (QNB). It was developed under contract to Edgewood Arsenal during the 1960s […]


Spiramide

Spiramide (AMI-193) is a selective 5-HT2A 5-HT1A and D2 receptor antagonist. It has negligible affinity for the 5-HT2C receptor.


Volinanserin

Volinanserin (MDL-100907) is a highly selective 5-HT2A receptor antagonist. It is widely used in scientific research to investigate the function of the 5-HT2A receptor. Volinanserin is also being trialed as […]


KML-010

KML-010 is a drug derived from spiperone. It functions as a highly selective 5-HT2A receptor antagonist with negligible affinity for the 5-HT1A or 5-HT2C receptors and over 400-fold lower affinity […]


Adapalene/benzoyl peroxide

Adapalene/benzoyl peroxide is a prescription drug combination for the treatment of acne marketed by Galderma under the trade name Epiduo. (Its trade name is Tactuo in Canada.) It consists of […]


Racemoramide

Racemoramide (INN BAN) or simply moramide is an opioid analgesic and a racemic mixture of the substances dextromoramide (the active component) and levomoramide (which is inactive) two enantiomers of a […]


PNU-22394

PNU-22394 is a drug which acts as an agonist at serotonin 5-HT2 receptors with strongest binding affinity for 5-HT2A and 5-HT2C and slightly weaker at 5-HT2B although it is only […]


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