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Xylocarpin

PubChem CID: 21596319

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Compound Synonyms xylocarpin, methyl 2-((1R,2R,4S,5R,9R,10R,13R,14S,15S,17R)-17-acetyloxy-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo(12.3.1.02,4.04,13.05,10)octadecan-15-yl)acetate, methyl 2-[(1R,2R,4S,5R,9R,10R,13R,14S,15S,17R)-17-acetyloxy-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.02,4.04,13.05,10]octadecan-15-yl]acetate, CHEMBL501922, SCHEMBL2005012, 26808-27-5
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 122.0
Hydrogen Bond Donor Count 0.0
Pfizer 3 75 Rule False
Scaffold Graph Level CC1CC(C2CCCC2)C2CCC3C4CCCC(C4C)C4CC34C2C1
Np Classifier Class Limonoids
Deep Smiles COC=O)C[C@H]CC)C)[C@H]OC=O)C)))[C@H]C=O)[C@]6C)[C@H]CC[C@@][C@H][C@@]6[C@@H]%10O3)))CC=O)O[C@H]6cccoc5))))))))))C
Heavy Atom Count 38.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level OC1CC2C(CCC3C4CCCC(C4O)C4OC324)C(C2CCOC2)O1
Classyfire Subclass Triterpenoids
Isotope Atom Count 0.0
Molecular Complexity 1080.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 10.0
Iupac Name methyl 2-[(1R,2R,4S,5R,9R,10R,13R,14S,15S,17R)-17-acetyloxy-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.02,4.04,13.05,10]octadecan-15-yl]acetate
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 2.5
Gsk 4 400 Rule False
Molecular Formula C29H36O9
Scaffold Graph Node Bond Level O=C1CC2C(CCC3C4CCCC(C4=O)C4OC324)C(c2ccoc2)O1
Inchi Key OEAILFQKPDJEPG-KQOVNBMPSA-N
Silicos It Class Moderately soluble
Rotatable Bond Count 6.0
Synonyms xylocarpin
Esol Class Moderately soluble
Functional Groups CC(=O)OC, CC(C)=O, COC(C)=O, C[C@H]1O[C@]1(C)C, coc
Compound Name Xylocarpin
Exact Mass 528.236
Formal Charge 0.0
Monoisotopic Mass 528.236
Hydrogen Bond Acceptor Count 9.0
Molecular Weight 528.6
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/C29H36O9/c1-14(30)36-24-21-22(33)28(5,17(26(24,2)3)11-19(31)34-6)16-7-9-27(4)18(29(16)25(21)38-29)12-20(32)37-23(27)15-8-10-35-13-15/h8,10,13,16-18,21,23-25H,7,9,11-12H2,1-6H3/t16-,17+,18-,21-,23+,24-,25-,27-,28-,29-/m1/s1
Smiles CC(=O)O[C@@H]1[C@@H]2[C@@H]3[C@@]4(O3)[C@H](CC[C@@]5([C@H]4CC(=O)O[C@H]5C6=COC=C6)C)[C@@](C2=O)([C@H](C1(C)C)CC(=O)OC)C
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Triterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Xylocarpus Granatum (Plant) Rel Props:Reference:ISBN:9788172360481; ISBN:9788172363093