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Cucurbitacin P

PubChem CID: 441822

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Compound Synonyms CUCURBITACIN P, 25383-26-0, (2R,3S,8S,9R,10R,13R,14S,16R,17R)-17-[(2R)-2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl]-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one, DTXSID30331637, (2R,3S,8S,9R,10R,13R,14S,16R,17R)-17-((2R)-2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta(a)phenanthren-11-one, CHEBI:3951, SCHEMBL10307359, DTXCID30282731, (10alpha)-2alpha,3alpha,16alpha,20,25-Pentahydroxy-9beta-methyl-19-norlanost-5-ene-11,22-dione, LMST01010114, NSC-135074, C08804, Q27106269, 19-Norlanost-5-ene-11, 2,3,16,20,25-pentahydroxy-9-methyl-, (2.alpha.,3.alpha.,9.beta.,10.alpha.,16.alpha.)-
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 135.0
Hydrogen Bond Donor Count 5.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CC2CCCC2C2CCC3CCCCC3C12
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=O)CCCO)C)C)))))O)C)))O))))C))))))))C[C@@H]6O))C)C
Heavy Atom Count 37.0
Classyfire Class Steroids and steroid derivatives
Scaffold Graph Node Level OC1CC2CCCC2C2CCC3CCCCC3C12
Classyfire Subclass Cucurbitacins
Isotope Atom Count 0.0
Molecular Complexity 1020.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 10.0
Iupac Name (2R,3S,8S,9R,10R,13R,14S,16R,17R)-17-[(2R)-2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl]-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 2.0
Gsk 4 400 Rule False
Molecular Formula C30H48O7
Scaffold Graph Node Bond Level O=C1CC2CCCC2C2CC=C3CCCCC3C12
Inchi Key VVBWBGOEAVGFTN-SYJGCRHZSA-N
Silicos It Class Soluble
Rotatable Bond Count 5.0
Synonyms cucurbitacin p
Esol Class Soluble
Functional Groups CC(C)=O, CC=C(C)C, CO
Compound Name Cucurbitacin P
Exact Mass 520.34
Formal Charge 0.0
Monoisotopic Mass 520.34
Hydrogen Bond Acceptor Count 7.0
Molecular Weight 520.7
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
Inchi InChI=1S/C30H48O7/c1-25(2,36)12-11-21(33)30(8,37)23-19(32)14-27(5)20-10-9-16-17(13-18(31)24(35)26(16,3)4)29(20,7)22(34)15-28(23,27)6/h9,17-20,23-24,31-32,35-37H,10-15H2,1-8H3/t17-,18-,19-,20+,23+,24-,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@H](C4(C)C)O)O)C)C)[C@](C)(C(=O)CCC(C)(C)O)O)O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Triterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Picrorhiza Kurroa (Plant) Rel Props:Reference:https://doi.org/10.1093/database/bav075