Summary
IMPPAT Phytochemical identifier: IMPHY010739
Phytochemical name: Pridentigenin D
Synonymous chemical names:pridentigenin d
Chemical structure information
SMILES:OC[C@@]1(C)CC[C@]23[C@@H](C1)[C@]1(CC[C@H]4[C@@](C1(CC3=O)C)(C)CC[C@@H]1[C@]4(C)CC[C@@H](C1(C)C)O)OC2InChI:InChI=1S/C30H48O4/c1-24(2)19-7-11-27(5)20(26(19,4)10-9-22(24)32)8-12-30-21-15-25(3,17-31)13-14-29(21,18-34-30)23(33)16-28(27,30)6/h19-22,31-32H,7-18H2,1-6H3/t19-,20+,21+,22-,25-,26-,27+,28?,29+,30-/m0/s1InChIKey:LMZWLCRAIXEHTG-MVYRLNSYSA-N
DeepSMILES:OC[C@@]C)CC[C@@][C@@H]C6)[C@]CC[C@H][C@@]C6CC%10=O)))C))C)CC[C@@H][C@]6C)CC[C@@H]C6C)C))O))))))))))))OC5
Functional groups:CC(C)=O, CO, COC
Molecular scaffolds
Scaffold Graph/Node/Bond level:O=C1CC2C3CCC4CCCCC4C3CCC23OCC12CCCCC23
Scaffold Graph/Node level:OC1CC2C3CCC4CCCCC4C3CCC23OCC12CCCCC23
Scaffold Graph level:CC1CC2C3CCC4CCCCC4C3CCC23CCC12CCCCC23
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire 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: 3.187
Chemical structure download