Planta Med 2014; 80 - PD19
DOI: 10.1055/s-0034-1382440

Isolation and structural clarification of triterpenes from Cyclocarya paliurus: Cyclocaric acid A and B

M Wright 1, J Byrd 1, Y Gao 2, J Stubblefield 2, H Park 2, N Dunlap 1
  • 1Department of Chemistry, The Tennessee Center for Botanical Medicine Research, Middle Tennessee State University, Murfreesboro, TN 37132
  • 2Department of Biology, The Tennessee Center for Botanical Medicine Research, Middle Tennessee State University, Murfreesboro, TN 37132

Two triterpenes were isolated using bioassay guided fractionation from the ethanol extract of Cyclocarya paliurus. Comparison to NMR spectra from a prior isolation reported in literature showed these two compounds to be previously reported Cyclocaric Acids A and B. However, after additional research into the oleanolic class of compounds, an independent synthesis of the reported Cyclocaric Acid A from hederagenin was completed. The conclusion is that the previously reported structures were incorrect. Updated structure and NMR spectral data will be presented.

Fig. 1