coprostanol
chemical compound
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coprostanol
Summary
coprostanol is a type of chemical entity[1].
Key Facts
- coprostanol's instance of is recorded as type of chemical entity[2].
- coprostanol's canonical SMILES is recorded as OC1CCC2(C)C(CCC3C4CCC(C(C)CCCC(C)C)C4(C)CCC32)C1[3].
- coprostanol's chemical formula is recorded as C₂₇H₄₈O[4].
- coprostanol is a type of cholestanol[5].
- coprostanol is a type of (3R,5S,8R,9S,10S,13R,14S)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol[6].
- coprostanol's Commons category is recorded as Coprostanol[7].
- coprostanol's found in taxon is recorded as Phallusia nigra[8].
- coprostanol's found in taxon is recorded as Petrosia ficiformis[9].
- coprostanol's found in taxon is recorded as Homo sapiens[10].
- coprostanol's isomeric SMILES is recorded as O[C@H]4CC[C@]3(C@HC4)CC@HC4)C">[11].
- coprostanol's mass is recorded as {'unit': 'Q483261', 'amount': '+388.370516156'}[12].
- coprostanol's stereoisomer of is recorded as Epicholestanol[13].
- coprostanol's stereoisomer of is recorded as dihydrocholesterol[14].
- coprostanol's stereoisomer of is recorded as (3S,5R)-10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol[15].
- coprostanol's stereoisomer of is recorded as Cholestan-3-ol, (3beta,5alpha)-[16].
- coprostanol's stereoisomer of is recorded as epicoprosterol[17].
- coprostanol's stereoisomer of is recorded as epidihydrocholesterin[18].
- coprostanol's stereoisomer of is recorded as cholestan-3-ol[19].
- coprostanol's stereoisomer of is recorded as Cholestan-3-ol, (3.beta.)-[20].
- coprostanol's stereoisomer of is recorded as (3S,5S,8S,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol[21].
- coprostanol's stereoisomer of is recorded as (3S,5S,8R,9R,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol[22].
- coprostanol's stereoisomer of is recorded as 5a-Cholestan-3beta-ol[23].