Anti-staphylococcal and cytotoxic compounds from Hyptis pectinata

Fragoso-Serrano, Mabel, Gibbons, Simon and Pereda-Miranda, Rogelio (2005) Anti-staphylococcal and cytotoxic compounds from Hyptis pectinata. Planta Medica, 71 (3). pp. 278-280. ISSN 0032-0943

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Bioassay-guided fractionation of a CHCl3 extract prepared from the Mexican medicinal plant Hyptis pectinata led to the isolation of four pyrones, pectinolides A - C (1 - 3) and H (4). Activity was tracked using cultured KB cells. Multidrug-resistant strains of Staphylococcus aureus were sensitive to pectinolide H (4; KB > 20 μg/mL) in the concentration range of 32 - 64 μg/mL. The absolute stereochemistry of this new compound was established as 5S-[(4S-acetyloxy)-(1S-hydroxy)-2Z-octenyl]-2(5H)-furanone on the basis of spectral, chiroptical data and chemical correlation with pectinolide A (1). Mosher ester derivatives were used with pectinolide B (2) for confirmation of the 3′-(S) absolute stereochemistry on the side chain chiral center of pectinolides A - C.

Item Type: Article
Faculty \ School: Faculty of Science > School of Pharmacy
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Depositing User: LivePure Connector
Date Deposited: 27 Jun 2020 00:03
Last Modified: 04 Mar 2024 17:56
DOI: 10.1055/s-2005-837831

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