4.3 Article

Sesquiterpene derivatives from Ocotea minarum leaves

Journal

PHYTOCHEMISTRY LETTERS
Volume 42, Issue -, Pages 8-14

Publisher

ELSEVIER
DOI: 10.1016/j.phytol.2021.01.004

Keywords

Bisabolane sesquiterpenes; Bergamotene; Norbisabolane; Farnesene; Lauraceae; Antifungal

Funding

  1. Fundacao de Apoio ao Desenvolvimento do Ensino, Ciencia e Tecnologia do Estado de Mato Grosso do Sul (FUNDECT-MS) [020793, 7438]
  2. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) [001]
  3. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)
  4. Dean's Office for Research and Graduate Studies (CPQ-PROPP) of the Universidade Federal de Mato Grosso do Sul

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New bisabolane derivatives and related compounds were obtained from the leaves of Ocotea minarum, showing antifungal activity against Candida species and Cryptococcus neoformans in vitro.
(+)-?-Sesquiphellandrene-12-oic acid (1) and 4-oxo-lanceolic acid (3), two new bisabolane derivatives; (+)-2methyl-6[4-oxo-2-cyclohexen-1-yl]-2-(E)-heptenoic acid (4), a new nor-bisabolane derivative; (+)-(E)-exo?-bergamoten-12-oic acid (5), a new bergamotene-type sesquiterpene; (2E,6E)-2,6-dimethyl-10-methylenedodecatrienoic acid (6), a farnesene-type sesquiterpene reported for the first time as a natural product; and (?)-curcumen-12-oic acid (7), an aromatic bisabolene derivative that is new in Lauraceae, were obtained, together with lanceolic acid (2) and the terpenic lactone loliolide (8), from the leaves of Ocotea minarum. The chemical structures of these compounds were determined by 1D- and 2D-NMR and HRESIMS. Evaluated in vitro against standard strains of Candida species and Cryptococcus neoformans, compounds 1, 2, and 4-8 exhibited MIC values in the 50?100 ?g mL?1 range.

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