Summary
SMILES: COC(=O)[C@@]1(C)CC[C@]2([C@@H](C1)C1=CC[C@H]3[C@@]([C@@]1(CC2)C)(C)CC[C@@H]1[C@]3(C)CC[C@@H](C1(C)C)OC(=O)C)C(=O)OInChI: InChI=1S/C33H50O6/c1-20(34)39-25-12-13-30(5)23(28(25,2)3)11-14-32(7)24(30)10-9-21-22-19-29(4,27(37)38-8)15-17-33(22,26(35)36)18-16-31(21,32)6/h9,22-25H,10-19H2,1-8H3,(H,35,36)/t22-,23-,24+,25-,29-,30-,31+,32+,33-/m0/s1InChIKey: UYHIXEUNWATGDQ-UBOYTANYSA-N
DeepSMILES: COC=O)[C@@]C)CC[C@][C@@H]C6)C=CC[C@H][C@@][C@@]6CC%10))C))C)CC[C@@H][C@]6C)CC[C@@H]C6C)C))OC=O)C))))))))))))))))C=O)O
Scaffold Graph/Node/Bond level: C1=C2C3CCCCC3CCC2C2CCC3CCCCC3C2C1
Scaffold Graph/Node level: C1CCC2C(C1)CCC1C2CCC2C3CCCCC3CCC21
Scaffold Graph level: C1CCC2C(C1)CCC1C2CCC2C3CCCCC3CCC21
Functional groups: CC(=O)O; CC(=O)OC; CC=C(C)C; COC(C)=O
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
Synonymous chemical names:spergulagenic acid a
Chemical structure download