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).

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

Registries:
    PubChem CID 16805
    PubChem ID 160022