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[(5R,6R,8R,9S,10R,13R,14R,15S)-17-[(1S)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-5,6,14-trihydroxy-10,13-dimethyl-1-oxo-4,6,7,8,9,11,12,15-octahydrocyclopenta[a]phenanthren-15-yl] acetate

PubChem CID: 14216306

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Compound Synonyms CHEMBL3897718
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 130.0
Hydrogen Bond Donor Count 3.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CCCC(CC2CCC3C2CCC2C3CCC3CCCC(C)C32)C1
Np Classifier Class Ergostane steroids
Deep Smiles CC=O)O[C@H]C=C[C@@][C@]5O)[C@@H]C[C@@H]O)[C@@][C@][C@H]6CC%10)))C)C=O)C=CC6)))))O))))))C))[C@@H][C@H]CC=CC=O)O6))C))C))))C
Heavy Atom Count 38.0
Classyfire Class Steroids and steroid derivatives
Scaffold Graph Node Level OC1CCCC(CC2CCC3C2CCC2C3CCC3CCCC(O)C32)O1
Classyfire Subclass Steroid lactones
Isotope Atom Count 0.0
Molecular Complexity 1180.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 10.0
Uniprot Id n.a.
Iupac Name [(5R,6R,8R,9S,10R,13R,14R,15S)-17-[(1S)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-5,6,14-trihydroxy-10,13-dimethyl-1-oxo-4,6,7,8,9,11,12,15-octahydrocyclopenta[a]phenanthren-15-yl] acetate
Prediction Hob 0.0
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 1.9
Gsk 4 400 Rule False
Molecular Formula C30H40O8
Scaffold Graph Node Bond Level O=C1C=CCC(CC2=CCC3C2CCC2C3CCC3CC=CC(=O)C32)O1
Prediction Swissadme 0.0
Inchi Key REOWXEUUAXLCRM-DTRRUJLXSA-N
Silicos It Class Soluble
Fcsp3 0.7
Logs -4.523
Rotatable Bond Count 4.0
Logd 1.126
Synonyms withaminimin
Esol Class Moderately soluble
Functional Groups CC(=O)OC, CC1=C(C)C(=O)OCC1, CC=C(C)C, CC=CC(C)=O, CO
Compound Name [(5R,6R,8R,9S,10R,13R,14R,15S)-17-[(1S)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-5,6,14-trihydroxy-10,13-dimethyl-1-oxo-4,6,7,8,9,11,12,15-octahydrocyclopenta[a]phenanthren-15-yl] acetate
Prediction Hob Swissadme 0.0
Exact Mass 528.272
Formal Charge 0.0
Monoisotopic Mass 528.272
Hydrogen Bond Acceptor Count 8.0
Molecular Weight 528.6
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 10.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Esol -4.075780400000001
Inchi InChI=1S/C30H40O8/c1-15-12-22(38-26(34)16(15)2)17(3)20-14-25(37-18(4)31)30(36)21-13-24(33)29(35)10-7-8-23(32)28(29,6)19(21)9-11-27(20,30)5/h7-8,14,17,19,21-22,24-25,33,35-36H,9-13H2,1-6H3/t17-,19-,21+,22+,24+,25-,27+,28-,29-,30-/m0/s1
Smiles CC1=C(C(=O)O[C@H](C1)[C@@H](C)C2=C[C@@H]([C@@]3([C@@]2(CC[C@H]4[C@H]3C[C@H]([C@@]5([C@@]4(C(=O)C=CC5)C)O)O)C)O)OC(=O)C)C
Nring 5.0
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Steroids

  • 1. Outgoing r'ship FOUND_IN to/from Physalis Angulata (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all
  • 2. Outgoing r'ship FOUND_IN to/from Physalis Indica (Plant) Rel Props:Reference:ISBN:9788172362461
  • 3. Outgoing r'ship FOUND_IN to/from Physalis Minima (Plant) Rel Props:Reference:ISBN:9780387706375; ISBN:9788172362461