Hermaphrodiol

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: C₁₉H₃₀O₂

InChI: InChI=1/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h3,13-17,20-21H,4-11H2,1-2H3/t13-,14-,15-,16-,17-,18-,19-/m0/s1

InChIKey: InChIKey=QADHLRWLCPCEKT-LOVVWNRFBV
SMILES: [H][C@@]12CC=C3C[C@@H](O)CC[C@]3(C)[C@@]1([H])CC[C@]4(C)[C@@H](O)CC[C@@]24[H]

Names:
    Androstenediol
    Androst-5-enediol
    Androst-5-ene-3beta,17beta-diol
    androst-5-ene-3beta,17beta-diol
    Hermaphrodiol
    ZINC03814414
    (3S,8S,9S,10R,13S,14S,17S)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,17-diol
    3beta,17beta-Dihydroxyandrost-5-ene
    3beta,17beta-Dihydroxy-5-androstene
    521-17-5

Registries:
    PubChem CID 10634
    ChEBI 2710
    Kegg C04295
    PubChem ID 12146100
    PubChem ID 6955