Issue 3, 2022

Euphorstranoids A and B, two highly rearranged ingenane diterpenoids from Euphorbia stracheyi: structural elucidation, chemical transformation, and lipid-lowering activity

Abstract

Euphorstranoids A (1) and B (2), two highly rearranged ingenane diterpenoids with an unusual 5/6/7/3 carbon ring system, were isolated from Euphorbia stracheyi. Their structures were determined by a combination of spectral, chemical, and X-ray diffraction methods. The plausible biosynthetic pathway of 1 and 2 was proposed and chemically mimicked. Compounds 1 and 2 significantly inhibited the triglyceride (TG) level in 3T3-L1 adipocytes via retarding cell adipogenesis at the early stage.

Graphical abstract: Euphorstranoids A and B, two highly rearranged ingenane diterpenoids from Euphorbia stracheyi: structural elucidation, chemical transformation, and lipid-lowering activity

Supplementary files

Article information

Article type
Research Article
Submitted
12 Nov 2021
Accepted
18 Dec 2021
First published
21 Dec 2021

Org. Chem. Front., 2022,9, 775-780

Euphorstranoids A and B, two highly rearranged ingenane diterpenoids from Euphorbia stracheyi: structural elucidation, chemical transformation, and lipid-lowering activity

F. Yuan, Y. Pan, A. Yin, W. Li, D. Huang, X. Yan, S. Wu, G. Tang, R. Pu and S. Yin, Org. Chem. Front., 2022, 9, 775 DOI: 10.1039/D1QO01705E

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