ORG-37,684
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Systematic (IUPAC) name | |
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(3S)-3-[(2,3-dihydro-5-methoxy-1H-inden-4-yl)oxy]pyrrolidine | |
Legal status | |
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Identifiers | |
PubChem | CID 9794656 |
IUPHAR/BPS | 171 |
Chemical data | |
Formula | C14H19NO2 |
Molar mass | 233.305 g/mol[[Script error: No such module "String".]] |
Script error: No such module "collapsible list". | |
ORG-37,684 is a drug developed by Organon, which acts as a potent and selective agonist for the 5-HT2 receptor family, with highest affinity at 5-HT2C and lowest at 5-HT2B subtypes.[1][2] It has anorectic effects in animal studies and has been researched as a potential weight loss drug for use in humans.[3]
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45px | This drug article relating to the gastrointestinal system is a stub. You can help ssf by expanding it. |
- ↑ Adams, D.; Duncton, M. (2001). "EFFICIENT SYNTHESIS OF THE 5-HT2C RECEPTOR AGONIST, ORG 37684". Synthetic Communications. 31: 2029. doi:10.1081/SCC-100104420. edit
- ↑ Knight AR, Misra A, Quirk K, Benwell K, Revell D, Kennett G, Bickerdike M. Pharmacological characterisation of the agonist radioligand binding site of 5-HT(2A), 5-HT(2B) and 5-HT(2C) receptors. Naunyn Schmiedebergs Archives of Pharmacology. 2004;370:114-123. PMID 15322733
- ↑ Schreiber R, De Vry J. Role of 5-hT2C receptors in the hypophagic effect of m-CPP, ORG 37684 and CP-94,253 in the rat. Progress in Neuropsychopharmacology and Biological Psychiatry. 2002 Apr;26(3):441-9. PMID 11999893
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