Jump to main content
Jump to site search


Isolation and identification of L/D-lactate-conjugated bufadienolides from toad eggs revealing lactate racemization in amphibians

Author affiliations

Abstract

Three pairs of bufadienolide L/D-lactate epimers (1–6) were isolated from the eggs of the toad Bufo bufo gargarizans. The structures were elucidated by using spectroscopic methods, X-ray diffraction analysis and a modified Mosher's method. Compounds 1–6 represent the first occurrence of lactate-conjugated bufadienolides in nature, and illustrate the existence of an enzyme-controlled epimerization from L- to D-lactate in amphibians. The biosynthetic pathways, in which two key enzymes might be involved (i.e., lactate racemase and acyltransferase), were proposed. In addition, the biological assays revealed that compounds 1–4 are potent cytotoxic agents against human gastric cancer cells BGC-823 and human lung cancer cells A549 with IC50 values in a range of 8.0 to 80.0 nM.

Graphical abstract: Isolation and identification of l/d-lactate-conjugated bufadienolides from toad eggs revealing lactate racemization in amphibians

Back to tab navigation

Supplementary files

Publication details

The article was received on 01 May 2017, accepted on 14 Jun 2017 and first published on 14 Jun 2017


Article type: Paper
DOI: 10.1039/C7OB01055A
Citation: Org. Biomol. Chem., 2017, Advance Article
  •   Request permissions

    Isolation and identification of L/D-lactate-conjugated bufadienolides from toad eggs revealing lactate racemization in amphibians

    S. Zhou, Q. Zheng, X. Huang, Y. Wang, S. Luo, R. Jiang, L. Wang, W. Ye and H. Tian, Org. Biomol. Chem., 2017, Advance Article , DOI: 10.1039/C7OB01055A

Search articles by author

Spotlight

Advertisements