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[(E,6R)-6-[(2S,9R,13R,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate

PubChem CID: 122130491

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Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 138.0
Hydrogen Bond Donor Count 3.0
Pfizer 3 75 Rule False
Scaffold Graph Level CC1CCC2C(CCC3C4CCCC4CC(C)C23)C1
Np Classifier Class Cucurbitane triterpenoids, Lanostane, Tirucallane and Euphane triterpenoids
Deep Smiles CC=O)OC/C=C/C=O)[C@@][C@H][C@H]O)CC[C@]5C)CC=O)[C@@]C6CC=CC6C[C@H]O)C=O)C6C)C))))))))))C)))))C)))))O)C)))))C)C
Heavy Atom Count 40.0
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 1210.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 6.0
Iupac Name [(E,6R)-6-[(2S,9R,13R,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 2.6
Gsk 4 400 Rule False
Molecular Formula C32H46O8
Scaffold Graph Node Bond Level O=C1CCC2C(=CCC3C4CCCC4CC(=O)C23)C1
Inchi Key IXQKXEUSCPEQRD-LTWLCXHNSA-N
Silicos It Class Moderately soluble
Rotatable Bond Count 6.0
Synonyms cucurbitacin
Esol Class Moderately soluble
Functional Groups C/C=C/C(C)=O, CC(C)=O, CC=C(C)C, CO, COC(C)=O
Compound Name [(E,6R)-6-[(2S,9R,13R,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate
Exact Mass 558.319
Formal Charge 0.0
Monoisotopic Mass 558.319
Hydrogen Bond Acceptor Count 8.0
Molecular Weight 558.7
Gi Absorption False
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/C32H46O8/c1-17(33)40-27(2,3)13-12-23(36)32(9,39)25-21(35)15-29(6)22-11-10-18-19(14-20(34)26(38)28(18,4)5)31(22,8)24(37)16-30(25,29)7/h10,12-13,19-22,25,34-35,39H,11,14-16H2,1-9H3/b13-12+/t19?,20-,21+,22?,25-,29?,30+,31-,32-/m0/s1
Smiles CC(=O)OC(C)(C)/C=C/C(=O)[C@@](C)([C@H]1[C@@H](CC2([C@@]1(CC(=O)[C@@]3(C2CC=C4C3C[C@@H](C(=O)C4(C)C)O)C)C)C)O)O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 1.0
Egan Rule False
Np Classifier Superclass Triterpenoids

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