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(1R,3aS,5aS,5bR,7S,7aR,11aR,11bR,13aR,13bR)-7-hydroxy-5b,8,8,11a-tetramethyl-9-oxo-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysene-3a,5a-dicarboxylic acid

PubChem CID: 12040950

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Compound Synonyms CHEMBL508080
Topological Polar Surface Area 112.0
Hydrogen Bond Donor Count 3.0
Heavy Atom Count 36.0
Isotope Atom Count 0.0
Molecular Complexity 1030.0
Database Name cmaup_ingredients;npass_chem_all;pubchem
Defined Atom Stereocenter Count 10.0
Iupac Name (1R,3aS,5aS,5bR,7S,7aR,11aR,11bR,13aR,13bR)-7-hydroxy-5b,8,8,11a-tetramethyl-9-oxo-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysene-3a,5a-dicarboxylic acid
Prediction Hob 0.0
Xlogp 5.1
Molecular Formula C30H44O6
Prediction Swissadme 0.0
Inchi Key BLMDUACVPBWIGN-CNOSFRAYSA-N
Fcsp3 0.8333333333333334
Logs -3.457
Rotatable Bond Count 3.0
Logd 3.686
Compound Name (1R,3aS,5aS,5bR,7S,7aR,11aR,11bR,13aR,13bR)-7-hydroxy-5b,8,8,11a-tetramethyl-9-oxo-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysene-3a,5a-dicarboxylic acid
Prediction Hob Swissadme 0.0
Exact Mass 500.314
Formal Charge 0.0
Monoisotopic Mass 500.314
Hydrogen Bond Acceptor Count 6.0
Molecular Weight 500.7
Covalent Unit Count 1.0
Total Atom Stereocenter Count 10.0
Total Bond Stereocenter Count 0.0
Esol -5.933991200000001
Inchi InChI=1S/C30H44O6/c1-16(2)17-9-12-29(24(33)34)13-14-30(25(35)36)18(22(17)29)7-8-20-27(5)11-10-21(32)26(3,4)23(27)19(31)15-28(20,30)6/h17-20,22-23,31H,1,7-15H2,2-6H3,(H,33,34)(H,35,36)/t17-,18+,19-,20+,22+,23-,27+,28+,29-,30+/m0/s1
Smiles CC(=C)[C@@H]1CC[C@]2([C@H]1[C@H]3CC[C@@H]4[C@]5(CCC(=O)C([C@@H]5[C@H](C[C@]4([C@@]3(CC2)C(=O)O)C)O)(C)C)C)C(=O)O
Nring 5.0
Defined Bond Stereocenter Count 0.0

  • 1. Outgoing r'ship FOUND_IN to/from Viburnum Odoratissimum (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all