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Antitubercular sterols fromThalia multiflora Horkel ex Koernicke

Authors :
Scott G. Franzblau
Barbara N. Timmermann
Maria-Teresa Gutierrez-Lugo
Yuehong Wang
Enrique Suarez
Source :
Phytotherapy Research. 19:876-880
Publication Year :
2005
Publisher :
Wiley, 2005.

Abstract

Bioassay guided isolation of an antitubercular extract of the aerial parts of Thalia multiflora led to the isolation of nine stigmast-5-ene and stigmasta-5,22-dien steroids, four isorhamnetin and quercetin flavonoid glycosides, two ceramides, an indole alkaloid and two simple phenolic compounds. Stigmast-5-en-3beta-ol-7-one (2), stigmast-4-ene-6beta-ol-3-one (3), stigmast-5,22-dien-3beta-ol-7-one (7) and stigmast-4,22-dien-6beta-ol-3-one (8) were found to be the most active compounds with MIC values of 1.98 +/- 0.02, 4.2 +/- 0.17, 1.0 +/- 0.06 and 2.2 +/- 0.3 microg/mL, respectively. Compounds 2, 3, 7 and 8 were not cytotoxic to Vero cells at 102 microg/mL. This investigation constitutes the first report of a chemical study of a species of the genus Thalia.

Details

ISSN :
10991573 and 0951418X
Volume :
19
Database :
OpenAIRE
Journal :
Phytotherapy Research
Accession number :
edsair.doi.dedup.....5ef589a4ca30279545afb26741d56d18
Full Text :
https://doi.org/10.1002/ptr.1731