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2,3-Didehydrosomnifericin

PubChem CID: 70684083

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Compound Synonyms 2,3-Didehydrosomnifericin, 173614-88-5, (2R)-5-(hydroxymethyl)-4-methyl-2-[(1S)-1-[(4S,5S,6S,8S,9S,10R,13S,14S,17R)-4,5,6-trihydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-17-yl]ethyl]-2,3-dihydropyran-6-one, 2,3-Dehydrosomnifericin, CHEMBL2047416, HY-N5069, AKOS040760195, FS-7447, DA-49254, CS-0032278, E88830, (6R)-6-[(1S)-1-[(1R,3aS,3bS,5S,5aS,6S,9aR,9bS,11aS)-5,5a,6-trihydroxy-9a,11a-dimethyl-9-oxo-1H,2H,3H,3aH,3bH,4H,5H,6H,9bH,10H,11H-cyclopenta[a]phenanthren-1-yl]ethyl]-3-(hydroxymethyl)-4-methyl-5,6-dihydropyran-2-one
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 124.0
Hydrogen Bond Donor Count 4.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CCCC(CC2CCC3C2CCC2C3CCC3CCCC(C)C32)C1
Np Classifier Class Ergostane steroids
Deep Smiles OCC=CC)C[C@@H]OC6=O)))[C@H][C@H]CC[C@@H][C@]5C)CC[C@H][C@H]6C[C@@H][C@][C@]6C)C=O)C=C[C@@H]6O))))))O))O))))))))))))C
Heavy Atom Count 35.0
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 986.0
Database Name imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 11.0
Uniprot Id n.a., P17066
Iupac Name (2R)-5-(hydroxymethyl)-4-methyl-2-[(1S)-1-[(4S,5S,6S,8S,9S,10R,13S,14S,17R)-4,5,6-trihydroxy-10,13-dimethyl-1-oxo-6,7,8,9,11,12,14,15,16,17-decahydro-4H-cyclopenta[a]phenanthren-17-yl]ethyl]-2,3-dihydropyran-6-one
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 2.8
Gsk 4 400 Rule False
Molecular Formula C28H40O7
Scaffold Graph Node Bond Level O=C1C=CCC(CC2CCC3C2CCC2C3CCC3CC=CC(=O)C32)O1
Inchi Key MYGPMUHRIQQNSB-DAKZBPTQSA-N
Silicos It Class Soluble
Rotatable Bond Count 3.0
Synonyms 2,3-dehydrosomnifericin
Esol Class Moderately soluble
Functional Groups CC1=C(C)C(=O)OCC1, CC=CC(C)=O, CO
Compound Name 2,3-Didehydrosomnifericin
Exact Mass 488.277
Formal Charge 0.0
Monoisotopic Mass 488.277
Hydrogen Bond Acceptor Count 7.0
Molecular Weight 488.6
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 11.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C28H40O7/c1-14-11-21(35-25(33)17(14)13-29)15(2)18-5-6-19-16-12-24(32)28(34)23(31)8-7-22(30)27(28,4)20(16)9-10-26(18,19)3/h7-8,15-16,18-21,23-24,29,31-32,34H,5-6,9-13H2,1-4H3/t15-,16-,18+,19-,20-,21+,23-,24-,26+,27-,28+/m0/s1
Smiles CC1=C(C(=O)O[C@H](C1)[C@@H](C)[C@H]2CC[C@@H]3[C@@]2(CC[C@H]4[C@H]3C[C@@H]([C@]5([C@@]4(C(=O)C=C[C@@H]5O)C)O)O)C)CO
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 Withania Somnifera (Plant) Rel Props:Reference:https://doi.org/10.15482/usda.adc/1239279