IMPPAT Phytochemical information:
Oleanonic aldehyde
Summary
IMPPAT Phytochemical identifier: IMPHY009057
Phytochemical name: Oleanonic aldehyde
Synonymous chemical names:oleanonic aldehyde
External chemical identifiers:CID:89262164, ZINC:ZINC000013558224, SureChEMBL:SCHEMBL14151411
Chemical structure information
SMILES:
O=C[C@]12CC[C@@]3(C(=CC[C@H]4[C@@]3(C)CC[C@@H]3[C@]4(C)CCC(=O)C3(C)C)[C@@H]2CC(CC1)(C)C)CInChI:
InChI=1S/C30H46O2/c1-25(2)14-16-30(19-31)17-15-28(6)20(21(30)18-25)8-9-23-27(5)12-11-24(32)26(3,4)22(27)10-13-29(23,28)7/h8,19,21-23H,9-18H2,1-7H3/t21-,22-,23+,27-,28+,29+,30+/m0/s1InChIKey:
QGPIUZIWMRUUCS-CHMVMOPFSA-NDeepSMILES:
O=C[C@@]CC[C@@]C=CC[C@H][C@@]6C)CC[C@@H][C@]6C)CCC=O)C6C)C)))))))))))))[C@@H]6CCCC%10))C)C)))))CFunctional groups:
CC(C)=O, CC=C(C)C, CC=O
Molecular scaffolds
Scaffold Graph/Node/Bond level:
O=C1CCC2C(CCC3C4CCC5CCCCC5C4=CCC23)C1Scaffold Graph/Node level:
OC1CCC2C(CCC3C2CCC2C4CCCCC4CCC23)C1Scaffold Graph level:
CC1CCC2C(CCC3C2CCC2C4CCCCC4CCC23)C1
Chemical classification
ClassyFire Kingdom: Organic compoundsClassyFire Superclass: Lipids and lipid-like moleculesClassyFire Class: Prenol lipids
ClassyFire Subclass: Triterpenoids
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Triterpenoids
NP Classifier Class: Oleanane triterpenoids
NP-Likeness score: 3.335
Chemical structure download