Related Experiment Video
Updated: May 16, 2026

High-resolution Tandem Mass Spectrometry for Studying Chemical Constituents of Gynura bicolor DC
Published on: February 2, 2024
4,5-seco-guaiane and a nine-membered sesquiterpene lactone from Holostylis reniformis
Marcos D P Pereira1, Tito da Silva, Lucia M X Lopes
1Institute of Chemistry, São Paulo State University, UNESP, C.P. 355, 14801-970 Araraquara, SP, Brazil.
Abstract:
Root extracts of Holostylis reniformis (Aristolochiaceae) yielded three new natural sesquiterpenes, a sesquiterpene with an unusual carbon skeleton, 4,5-seco-guaiane (7-epi-11-hydroxychabrolidione A, 1), a nine-membered lactone with new carbon skeleton (holostylactone, 2), and a new megastigmane [(6S,7E)-6,9-dihydroxy-10-(2'-hydroxy-ethoxy)-4,7-megastigmadien-3-one, 3], together with bulnesol and sitosterol-3-O-β-D-glucopyranoside. The structures of these compounds were determined by spectroscopic analyses and B3LYP/STO-3G** theoretical studies.
