10204 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 8 8 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 3 3 3 3 4 4 4 5 5 5 6 6 6 7 7 7 8 8 8 9 9 10 10 11 11 11 12 12 12 13 13 14 14 15 15 16 16 16 17 17 17 18 18 18 19 19 19 20 20 10 49 21 4 5 11 22 8 10 16 6 12 23 7 9 24 14 17 18 9 25 26 27 28 13 29 13 30 31 15 32 33 34 35 15 20 36 37 38 39 40 19 41 42 43 44 45 21 46 47 21 48 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 3 4 11 5 22 2 1 4 3 10 8 16 2 1 5 3 6 12 23 1 1 6 5 7 9 24 1 1 7 6 17 14 18 2 1 10 1 4 13 29 1 1 1 5 255 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 8.65 2 7.3931 7.3931 6.5271 5.661 4.751 6.5271 5.661 8.3393 8.3393 6.5431 8.9229 4.743 5.6451 7.3931 3.8242 4.7587 2.8763 3.8076 2.868 7.483 7.2664 6.3972 6.9256 6.1285 5.449 5.0504 7.9018 8.0883 8.8767 6.7612 7.1523 9.3838 9.3838 5.2478 6.046 8.0131 7.3931 6.7731 4.2324 3.4343 5.3787 4.7635 4.1388 2.6718 2.2647 3.81 9.2566 2.1128 -2.1948 -0.1425 0.8575 -0.6425 -0.1425 -0.6493 1.3575 0.8575 1.1623 -0.4472 -1.684 0.3575 -1.6909 -2.2117 1.8575 -0.0852 0.3507 -0.6132 -2.2406 -1.6981 -0.9877 -1.0618 0.2825 1.8325 1.8325 1.4401 0.7499 1.6016 -1.0141 -0.7564 -2.2644 -1.5685 -0.0572 0.7723 -2.6877 -2.6846 1.8575 2.4775 1.8575 0.3814 0.3968 0.3459 0.9706 0.3554 -0.0279 -0.7146 -2.8606 2.2406 6 5 5 6 5 6 3 4 5 6 7 10 22 16 23 24 18 1 0 Compound Canonicalized 5 2011.04.04 1 Compound Complexity 7 E_COMPLEXITY 3.396 Cactvs xemistry.com 2012.02.08 508 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.396 Cactvs xemistry.com 2012.02.08 2 Count Hydrogen Bond Donor 5 E_NHDONORS 3.396 Cactvs xemistry.com 2012.02.08 1 Count Rotatable Bond 5 E_NROTBONDS 3.396 Cactvs xemistry.com 2012.02.08 0 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.396 Cactvs xemistry.com 2012.02.08 00000371E0783000000000000000000000000000000180000000306080000000000060C00000001A00000800000F14A080020200000002008802A052000000000020000000080100004800101200010000400004800008010388C8F08F8000000000000000800004000020000080000C000000 IUPAC Name Allowed 1 2.1.0 LexiChem openeye.com 2012.02.08 (8R,9S,10R,13S,14S,17R)-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one IUPAC Name CAS-like Style 1 2.1.0 LexiChem openeye.com 2012.02.08 (8R,9S,10R,13S,14S,17R)-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one IUPAC Name Preferred 1 2.1.0 LexiChem openeye.com 2012.02.08 (8R,9S,10R,13S,14S,17R)-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one IUPAC Name Systematic 1 2.1.0 LexiChem openeye.com 2012.02.08 (8R,9S,10R,13S,14S,17R)-10,13-dimethyl-17-oxidanyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one IUPAC Name Traditional 1 2.1.0 LexiChem openeye.com 2012.02.08 (8R,9S,10R,13S,14S,17R)-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one InChI Standard 1 1.0.4 InChI nist.gov 2012.02.08 InChI=1S/C19H28O2/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/h11,14-17,21H,3-10H2,1-2H3/t14-,15-,16-,17+,18-,19-/m0/s1 InChIKey Standard 1 1.0.4 InChI nist.gov 2012.02.08 MUMGGOZAMZWBJJ-KZYORJDKSA-N Log P XLogP3 7 3.0 sioc-ccbg.ac.cn 2012.02.08 3.3 Mass Exact 7 2.1 PubChem ncbi.nlm.nih.gov 2012.02.08 288.20893 Molecular Formula 1 2.1 PubChem ncbi.nlm.nih.gov 2012.02.08 C19H28O2 Molecular Weight 7 2.1 PubChem ncbi.nlm.nih.gov 2012.02.08 288.42442 SMILES Canonical 1 1.7.6 OEChem openeye.com 2012.02.08 CC12CCC3C(C1CCC2O)CCC4=CC(=O)CCC34C SMILES Isomeric 1 1.7.6 OEChem openeye.com 2012.02.08 C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@H]2O)CCC4=CC(=O)CC[C@]34C Topological Polar Surface Area 7 E_TPSA 3.396 Cactvs xemistry.com 2012.02.08 37.3 Weight MonoIsotopic 7 2.1 PubChem ncbi.nlm.nih.gov 2012.02.08 288.20893 21 6 6 0 0 0 0 0 1 5