1.0 2016-09-30 22:29:43 UTC 2020-04-22 15:03:17 UTC BMDB0000383 BMDB00383 3a,17a-Dihydroxy-5b-androstane 3 alpha,5 beta,7 alpha-3,7-Dihydroxyandrostan-17-one 3 alpha,7 alpha-5 beta-3,7-Dihydroxyandrostan-17-one 3,7-DHARN-17-one 3,7-Dihydroxyandrostan-17-one 3,7-Dihydroxyandrostan-17-one, (3beta,5alpha,7alpha)-isomer 3,7-Dihydroxyandrostan-17-one, (3beta,5alpha,7beta)-isomer 3,7-Dihydroxyandrostan-17-one, (3beta,5beta,7beta)-isomer 5b-Androstane-3a,17a-diol C19H32O2 292.4562 292.240230268 (2S,5R,14R,15S)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol (2S,5R,14R,15S)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol 5856-10-0 C[C@]12CCC3C(CCC4C[C@H](O)CC[C@]34C)C1CC[C@H]2O InChI=1S/C19H32O2/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/h12-17,20-21H,3-11H2,1-2H3/t12?,13-,14?,15?,16?,17-,18+,19+/m1/s1 CBMYJHIOYJEBSB-CRQQDORFSA-N belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. Organic compounds Lipids and lipid-like molecules Steroids and steroid derivatives Androstane steroids Androgens and derivatives 17-hydroxysteroids 3-alpha-hydroxysteroids Cyclic alcohols and derivatives Hydrocarbon derivatives Secondary alcohols 17-hydroxysteroid 3-alpha-hydroxysteroid 3-hydroxysteroid Alcohol Aliphatic homopolycyclic compound Androgen-skeleton Cyclic alcohol Hydrocarbon derivative Hydroxysteroid Organic oxygen compound Organooxygen compound Secondary alcohol Aliphatic homopolycyclic compounds Solid logp 3.56 ALOGPS logs -4.18 ALOGPS logp 3.2 ChemAxon pka_strongest_acidic 18.3 ChemAxon pka_strongest_basic -0.76 ChemAxon iupac (2S,5R,14R,15S)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol ChemAxon average_mass 292.4562 ChemAxon mono_mass 292.240230268 ChemAxon smiles C[C@]12CCC3C(CCC4C[C@H](O)CC[C@]34C)C1CC[C@H]2O ChemAxon formula C19H32O2 ChemAxon inchi InChI=1S/C19H32O2/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/h12-17,20-21H,3-11H2,1-2H3/t12?,13-,14?,15?,16?,17-,18+,19+/m1/s1 ChemAxon inchikey CBMYJHIOYJEBSB-CRQQDORFSA-N ChemAxon polar_surface_area 40.46 ChemAxon refractivity 84.63 ChemAxon polarizability 35.28 ChemAxon rotatable_bond_count 0 ChemAxon acceptor_count 2 ChemAxon donor_count 2 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon number_of_rings 4 ChemAxon bioavailability 1 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Specdb::CMs 10617 Specdb::CMs 37484 Specdb::CMs 156631 Specdb::CMs 1060130 Specdb::CMs 1060131 Specdb::CMs 1060133 Specdb::CMs 1060135 Specdb::CMs 1060137 Specdb::MsMs 289405 Specdb::MsMs 289406 Specdb::MsMs 289407 Specdb::MsMs 328813 Specdb::MsMs 328814 Specdb::MsMs 328815 Specdb::MsMs 2439109 Specdb::MsMs 2439110 Specdb::MsMs 2439111 Specdb::MsMs 2524092 Specdb::MsMs 2524093 Specdb::MsMs 2524094 C07632 53477690 FDB022001 5372 27727 Miller, A. M.; Dorfman, Ralph I. Metabolism of the steroid hormones: Isolation of etiocholane-3(a),17(a)-diol from human urine. Endocrinology (1948), 42 174-5.