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(2R,8S,9R,10R,13R,14S,16R,17R)-17-[(E,2S)-2,6-dihydroxy-6-methylhept-4-en-2-yl]-2,16-dihydroxy-4,4,9,13,14-pentamethyl-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione

PubChem CID: 101280199

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Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 115.0
Hydrogen Bond Donor Count 4.0
Pfizer 3 75 Rule False
Scaffold Graph Level CC1CCC2C(CCC3C4CCCC4CC(C)C23)C1
Np Classifier Class Cucurbitane triterpenoids
Deep Smiles O[C@@H]C[C@@H]C=CC[C@@H][C@@]6C)C=O)C[C@][C@@]6C)C[C@H][C@@H]5[C@]C/C=C/CO)C)C)))))O)C)))O))))C))))))))CC6=O))C)C
Heavy Atom Count 36.0
Classyfire Class Steroids and steroid derivatives
Scaffold Graph Node Level OC1CCC2C(CCC3C4CCCC4CC(O)C23)C1
Classyfire Subclass Cucurbitacins
Isotope Atom Count 0.0
Molecular Complexity 1020.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 9.0
Iupac Name (2R,8S,9R,10R,13R,14S,16R,17R)-17-[(E,2S)-2,6-dihydroxy-6-methylhept-4-en-2-yl]-2,16-dihydroxy-4,4,9,13,14-pentamethyl-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 2.9
Gsk 4 400 Rule False
Molecular Formula C30H46O6
Scaffold Graph Node Bond Level O=C1CCC2C(=CCC3C4CCCC4CC(=O)C23)C1
Inchi Key IJFYQSUPMMVTOA-KUEPKPSOSA-N
Silicos It Class Moderately soluble
Rotatable Bond Count 4.0
Synonyms 22-deoxocucurbitacin d, 22-deoxocucurbitacin-d, 22-doxocucurbitacin d, cucurbitacin d,22-deoxo
Esol Class Moderately soluble
Functional Groups C/C=C/C, CC(C)=O, CC=C(C)C, CO
Compound Name (2R,8S,9R,10R,13R,14S,16R,17R)-17-[(E,2S)-2,6-dihydroxy-6-methylhept-4-en-2-yl]-2,16-dihydroxy-4,4,9,13,14-pentamethyl-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione
Exact Mass 502.329
Formal Charge 0.0
Monoisotopic Mass 502.329
Hydrogen Bond Acceptor Count 6.0
Molecular Weight 502.7
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 9.0
Total Bond Stereocenter Count 1.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C30H46O6/c1-25(2,35)12-9-13-29(7,36)23-20(32)15-27(5)21-11-10-17-18(14-19(31)24(34)26(17,3)4)30(21,8)22(33)16-28(23,27)6/h9-10,12,18-21,23,31-32,35-36H,11,13-16H2,1-8H3/b12-9+/t18-,19-,20-,21+,23+,27+,28-,29+,30+/m1/s1
Smiles C[C@@]12C[C@H]([C@@H]([C@]1(CC(=O)[C@@]3([C@H]2CC=C4[C@H]3C[C@H](C(=O)C4(C)C)O)C)C)[C@](C)(C/C=C/C(C)(C)O)O)O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 1.0
Egan Rule True
Np Classifier Superclass Triterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Lagenaria Siceraria (Plant) Rel Props:Reference:https://doi.org/10.15482/usda.adc/1239279