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Title: 4,5-seco-guaiane and a nine-membered sesquiterpene lactone from Holostylis reniformis. Author: Pereira MD, da Silva T, Lopes LM, Krettli AU, Madureira LS, Zukerman-Schpector J. Journal: Molecules; 2012 Nov 27; 17(12):14046-57. PubMed ID: 23187288. 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.[Abstract] [Full Text] [Related] [New Search]