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[(1S,2R,5S,6S,10S,12S,13R,14R,15R,17S)-13-acetyloxy-6-(furan-3-yl)-17-(2-methoxy-2-oxoethyl)-1,5,16,16-tetramethyl-8,18-dioxo-7,11-dioxapentacyclo[12.3.1.02,12.05,10.010,12]octadecan-15-yl] 2-methylpropanoate

PubChem CID: 102274582

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Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 148.0
Hydrogen Bond Donor Count 0.0
Pfizer 3 75 Rule False
Scaffold Graph Level CC1CC(C2CCCC2)C2CCC3C4CCCC(CC35CC25C1)C4C
Np Classifier Class Limonoids
Deep Smiles COC=O)C[C@H]CC)C)[C@H]OC=O)CC)C))))[C@H]C=O)[C@]6C)[C@H]CC[C@@][C@][C@]6[C@@H]%10OC=O)C))))O3))CC=O)O[C@H]6cccoc5))))))))))C
Heavy Atom Count 44.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level OC1CC23OC24CC2CCCC(C2O)C4CCC3C(C2CCOC2)O1
Classyfire Subclass Triterpenoids
Isotope Atom Count 0.0
Molecular Complexity 1290.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 10.0
Iupac Name [(1S,2R,5S,6S,10S,12S,13R,14R,15R,17S)-13-acetyloxy-6-(furan-3-yl)-17-(2-methoxy-2-oxoethyl)-1,5,16,16-tetramethyl-8,18-dioxo-7,11-dioxapentacyclo[12.3.1.02,12.05,10.010,12]octadecan-15-yl] 2-methylpropanoate
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 3.1
Gsk 4 400 Rule False
Molecular Formula C33H42O11
Scaffold Graph Node Bond Level O=C1CC23OC24CC2CCCC(C2=O)C4CCC3C(c2ccoc2)O1
Inchi Key QLZCMLMAZOYMSC-ZXYZIBDASA-N
Silicos It Class Poorly soluble
Rotatable Bond Count 9.0
Synonyms xyloccensin g
Esol Class Moderately soluble
Functional Groups CC(=O)OC, CC(C)=O, COC(C)=O, C[C@@]1(C)O[C@@]1(C)C, coc
Compound Name [(1S,2R,5S,6S,10S,12S,13R,14R,15R,17S)-13-acetyloxy-6-(furan-3-yl)-17-(2-methoxy-2-oxoethyl)-1,5,16,16-tetramethyl-8,18-dioxo-7,11-dioxapentacyclo[12.3.1.02,12.05,10.010,12]octadecan-15-yl] 2-methylpropanoate
Exact Mass 614.273
Formal Charge 0.0
Monoisotopic Mass 614.273
Hydrogen Bond Acceptor Count 11.0
Molecular Weight 614.7
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 10.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 False
Inchi InChI=1S/C33H42O11/c1-16(2)28(38)43-26-23-24(37)31(7,20(29(26,4)5)13-21(35)39-8)19-9-11-30(6)25(18-10-12-40-15-18)42-22(36)14-32(30)33(19,44-32)27(23)41-17(3)34/h10,12,15-16,19-20,23,25-27H,9,11,13-14H2,1-8H3/t19-,20+,23-,25+,26-,27-,30+,31-,32+,33+/m1/s1
Smiles CC(C)C(=O)O[C@@H]1[C@@H]2[C@H]([C@@]34[C@H](CC[C@@]5([C@@]3(O4)CC(=O)O[C@H]5C6=COC=C6)C)[C@@](C2=O)([C@H](C1(C)C)CC(=O)OC)C)OC(=O)C
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Triterpenoids