Secondary metabolite: 20-Hydroxy ganoderic acid AM 1



20-Hydroxy ganoderic acid AM 1
Summary
Molecular formula: C30H42O8
SMILES: O=C(C[C@](C1CC(=O)[C@@]2([C@]1(C)CC(=O)C1=C2C(=O)CC2[C@]1(C)CC[C@@H](C2(C)C)O)C)(O)C)CC(C(=O)O)C
InChI: InChI=1S/C30H42O8/c1-15(25(36)37)10-16(31)13-29(6,38)20-12-22(35)30(7)24-17(32)11-19-26(2,3)21(34)8-9-27(19,4)23(24)18(33)14-28(20,30)5/h15,19-21,34,38H,8-14H2,1-7H3,(H,36,37)/t15?,19?,20?,21-,27-,28+,29+,30-/m0/s1
InChIKey: IZUVOOWNBDYDKF-RGRRTADBSA-N
Molecular scaffolds

Scaffold Graph/Node/Bond level:
O=C1CC2CCC(=O)C2C2=C1C1CCCCC1CC2=O

Scaffold Graph/Node level:
OC1CCC2CC(O)C3C4CCCCC4CC(O)C3C12

Scaffold Graph level:
CC1CCC2CC(C)C3C4CCCCC4CC(C)C3C12
Chemical classification
Kingdom: Organic compounds
Super class: Lipids and lipid-like molecules
Class: Prenol lipids
Sub class: Triterpenoids
Synonymous chemical names:
20-hydroxy ganoderic acid am 1
Chemical structure download

Designed by R.P. Vivek-Ananth, M Karthikeyan and Ajaya Kumar Sahoo