Summary
IMPPAT Phytochemical identifier: IMPHY000841
Phytochemical name: Cycloartane-3,24-dione
Synonymous chemical names:cycloartane-324-dione
External chemical identifiers:CID:44423576, ChEMBL:CHEMBL226135, ZINC:ZINC000028646895, SureChEMBL:SCHEMBL5824245
Chemical structure information
SMILES:
O=C(C(C)C)CC[C@H]([C@H]1CC[C@@]2([C@]1(C)CC[C@@]13[C@H]2CC[C@@H]2[C@]3(C1)CCC(=O)C2(C)C)C)CInChI:
InChI=1S/C30H48O2/c1-19(2)22(31)9-8-20(3)21-12-14-28(7)24-11-10-23-26(4,5)25(32)13-15-29(23)18-30(24,29)17-16-27(21,28)6/h19-21,23-24H,8-18H2,1-7H3/t20-,21-,23+,24+,27-,28+,29-,30+/m1/s1InChIKey:
UMXQMWZSVMNHGK-HDMIJCIJSA-NDeepSMILES:
O=CCC)C))CC[C@H][C@H]CC[C@@][C@]5C)CC[C@][C@H]6CC[C@@H][C@]6C7)CCC=O)C6C)C))))))))))))))C)))))CFunctional groups:
CC(C)=O
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C1CCC23CC24CCC2CCCC2C4CCC3C1Scaffold Graph/Node level:
OC1CCC23CC24CCC2CCCC2C4CCC3C1Scaffold Graph level:
CC1CCC23CC24CCC2CCCC2C4CCC3C1
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Steroids and steroid derivatives
ClassyFire Subclass: Cycloartanols and derivatives
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Triterpenoids
NP Classifier Class: Cycloartane triterpenoids
NP-Likeness score: 2.932
Chemical structure download