1.0 2016-09-30 22:29:27 UTC 2020-04-22 15:03:12 UTC BMDB0000369 BMDB00369 3b,17b-Dihydroxyetiocholane 5b-Androstan-3b,17b-diol 5b-Androstane-3b,17b-diol C19H32O2 292.4562 292.240230268 (2S,5S,14S,15S)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol (2S,5S,14S,15S)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecane-5,14-diol 6038-31-9 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-/m0/s1 CBMYJHIOYJEBSB-WTVXNACZSA-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-beta-hydroxysteroids Cyclic alcohols and derivatives Hydrocarbon derivatives Secondary alcohols 17-hydroxysteroid 3-beta-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,5S,14S,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-/m0/s1 ChemAxon inchikey CBMYJHIOYJEBSB-WTVXNACZSA-N ChemAxon polar_surface_area 40.46 ChemAxon refractivity 84.63 ChemAxon polarizability 35.53 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::MsMs 314509 Specdb::MsMs 314510 Specdb::MsMs 314511 Specdb::MsMs 360277 Specdb::MsMs 360278 Specdb::MsMs 360279 Specdb::MsMs 2836341 Specdb::MsMs 2836342 Specdb::MsMs 2836343 Specdb::MsMs 2872352 Specdb::MsMs 2872353 Specdb::MsMs 2872354 Specdb::CMs 21836 Specdb::CMs 37472 Specdb::CMs 168656 Specdb::CMs 1059776 Specdb::CMs 1059778 Specdb::CMs 1059780 Specdb::CMs 1059782 Specdb::CMs 1059784 53477687 FDB021988 5358 36715 Hanson, James R.; Liman, Mansur D.; Uyanik, Cavit. The Stereochemistry of an Elimination Reaction accompanying the Hydroboration of a Steroidal Allylic Alcohol. Journal of Chemical Research, Synopses (1998), (3), 126-127.