Secondary metabolite: 12b-Acetoxy-3b,7b-dihydroxy-11,15,23-trioxolanost-8-en-26-oic acid butyl ester



12b-Acetoxy-3b,7b-dihydroxy-11,15,23-trioxolanost-8-en-26-oic acid butyl ester
Summary
Molecular formula: C36H54O9
SMILES: CCCCOC(=O)C(CC(=O)C[C@H]([C@H]1CC(=O)[C@@]2([C@]1(C)[C@H](OC(=O)C)C(=O)C1=C2[C@@H](O)C[C@@H]2[C@]1(C)CC[C@@H](C2(C)C)O)C)C)C
InChI: InChI=1S/C36H54O9/c1-10-11-14-44-32(43)20(3)16-22(38)15-19(2)23-17-27(41)36(9)28-24(39)18-25-33(5,6)26(40)12-13-34(25,7)29(28)30(42)31(35(23,36)8)45-21(4)37/h19-20,23-26,31,39-40H,10-18H2,1-9H3/t19-,20?,23-,24+,25+,26+,31-,34+,35+,36+/m1/s1
InChIKey: RTEHLCKIRCYCAH-AHVPDOLASA-N
Molecular scaffolds

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

Scaffold Graph/Node level:
OC1CCC2CC(O)C3C4CCCCC4CCC3C12

Scaffold Graph level:
CC1CCC2CC(C)C3C4CCCCC4CCC3C12
Chemical classification
Kingdom: Organic compounds
Super class: Lipids and lipid-like molecules
Class: Prenol lipids
Sub class: Triterpenoids
Synonymous chemical names:
12b-acetoxy-3b,7b-dihydroxy-11,15,23-trioxolanost-8-en-26-oic acid butyl ester
Chemical structure download

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