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4,5-seco-guaiane and a nine-membered sesquiterpene lactone from Holostylis reniformis.


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.

SUBMITTER: Pereira MD 

PROVIDER: S-EPMC6268306 | biostudies-literature | 2012 Nov

REPOSITORIES: biostudies-literature

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4,5-seco-guaiane and a nine-membered sesquiterpene lactone from Holostylis reniformis.

Pereira Marcos D P MD   da Silva Tito T   Lopes Lucia M X LM   Krettli Antoniana U AU   Madureira Lucas S LS   Zukerman-Schpector Julio J  

Molecules (Basel, Switzerland) 20121127 12


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 spectr  ...[more]

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