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Stenandiol
PubChem Notes:
Androstenediol An intermediate in TESTOSTERONE biosynthesis, found in the TESTIS or the ADRENAL. Androstenediol, derived from DEHYDROEPIANDROSTERONE by the reduction of the 17-keto group (17-HYDROXYSTEROID DEHYDROGENASES), is converted to TESTOSTERONE by the oxidation of the 3-beta hydroxyl group to a 3-keto group (3-HYDROXYSTEROID DEHYDROGENASE).
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pre_formula( "InChI=1/C25H38O4/c1-5-22(26)28-17-11-13-24(3)16(15-17)7-8-18-19-9-10-21(29-23(27)6-2)25(19,4)14-12-20(18)24/h7,17-21H,5-6,8-15H2,1-4H3/t17-,18-,19-,20-,21-,24-,25-/m0/s1", "jqp073/16805.html" ); ?>
Molecular Formula:
C25H38O4
InChI: InChI=1/C25H38O4/c1-5-22(26)28-17-11-13-24(3)16(15-17)7-8-18-19-9-10-21(29-23(27)6-2)25(19,4)14-12-20(18)24/h7,17-21H,5-6,8-15H2,1-4H3/t17-,18-,19-,20-,21-,24-,25-/m0/s1
InChIKey: InChIKey=ZDDFOEZPFDWEQS-YMKPZFJOBS
SMILES: CCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4OC(=O)CC)C)C
Names:
Androstenediol dipropionate
Androst-5-ene-(3beta,17beta)-diol dipropionate
Androst-5-ene-3,17-diol, dipropanoate, (3-beta,17-beta)- (9CI)
ANDROST-5-ENE-3-beta,17-beta-DIOL, DIPROPIONATE
Bisexovis
Bisexovister
BRN 2547313
EINECS 218-943-3
Ginandrin
Stenandiol
[(3S,8S,9S,10R,13S,14S,17S)-10,13-dimethyl-17-propanoyloxy-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] propanoate
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Registries:
pre_registry_key( "InChI=1/C25H38O4/c1-5-22(26)28-17-11-13-24(3)16(15-17)7-8-18-19-9-10-21(29-23(27)6-2)25(19,4)14-12-20(18)24/h7,17-21H,5-6,8-15H2,1-4H3/t17-,18-,19-,20-,21-,24-,25-/m0/s1", "InChIKey=ZDDFOEZPFDWEQS-YMKPZFJOBS", "jqp073/16805.html" ); ?>
PubChem CID 16805
PubChem ID 160022
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