期刊
PHYTOCHEMISTRY
卷 95, 期 -, 页码 291-297出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phytochem.2013.06.021
关键词
Clidemia hirta; Endophytes; Natural products; Cytotoxicity; Antimicrobial activity; Cryptosporiopsis
资金
- CSIR [IIIM-MLP 1008]
- Council of Scientific and Industrial Research (CSIR)
An endophytic Cryptosporiopsis sp. was isolated from Clidemia hirta and analyzed for its secondary metabolites that lead to the isolation of three bioactive molecules. The compounds were purified from the culture broth of the fungus and their structures were determined by spectroscopic methods as (R)-5-hydroxy-2-methylchroman-4-one (1), 1-(2,6-dihydroxyphenyl)pentan-1-one (2) and (Z)-1-(2-(2-butyryl-3-hydroxyphenoxy)-6-hydroxyphenyl)-3-hydroxybut-2-en-1-one (3). Compound 1 exhibited significant cytotoxic activity against the human leukemia cell line, HL-60 with an IC50 of 4 mu g/ml. This compound induced G2 arrest of the HL-60 cell cycle significantly. In addition, out of these compounds, 2 and 3 were active against several bacterial pathogens. Compound 2 was active against Bacillus cereus, Escherichia coli and Staphylococcus aureus with IC50 values varying from 18 to 30 mu g/ml, and compound 3 displayed activity against Pseudomonas fluorescens with an IC50 value of 6 mu g/ml. Compounds 2 and 3 are novel whereas compound 1 was reported earlier but the stereochemistry of its C-2 methyl is established for the first time. (C) 2013 Elsevier Ltd. All rights reserved.
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