Anodyne

Bexlosteride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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249.73 g/mol [1]
2.6 [1]
Structural Identifiers
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C14H16ClNO [1]
(4aR,10bR)-8-chloro-4-methyl-1,2,4a,5,6,10b-hexahydrobenzo[f]quinolin-3-one [1]
CN1[C@@H]2CCC3=C([C@H]2CCC1=O)C=CC(=C3)Cl [1]
InChI=1S/C14H16ClNO/c1-16-13-6-2-9-8-10(15)3-4-11(9)12(13)5-7-14(16)17/h3-4,8,12-13H,2,5-7H2,1H3/t12-,13-/m1/s1 [1]
InChIKeyWQBIOEFDDDEARX-CHWSQXEVSA-N [1]

Bexlosteride

Bexlosteride (also known as LY-191704, LY300502, LY-300502, (4aR,10bR)-8-Chloro-1,4,4a,5,6,10b-hexahydro-4-methylbenzo(f)quinolin-3(2H)-one, bexlosterid, Bexlosterida, (4aR,10bR)-8-Chloro-1,4,4a,5,6,10b-hexahydro-4-methylbenzo[f]quinolin-3(2H)-one, orb1685251, (4Ar,10br)-8-chloro-4-methyl-1h,2h,3h,4h,4ah,5h,6h,10bh-benzo[f]quinolin-3-one or 148905-79-7) is a substance of the amphetamine class.

Chemistry

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Bexlosteride is a absolute mixture

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 166562, Bexlosteride. Accessed July 19, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/166562

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Bexlosteride. UNII: 36X732P4P0. Global Substance Registration System. Accessed July 19, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/36X732P4P0