Document Detail

Antimicrobial phenolic compounds from Anabasis aphylla L.
MedLine Citation:
PMID:  19413118     Owner:  NLM     Status:  MEDLINE    
Bioassay-guided fractionation of an ethyl acetate extract from the aerial parts of Anabasis aphylla, a Chenopodiaceous species widely distributed in the northwest of China, led to the isolation of six phenolic compounds, which were identified by means of spectrometric analysis as 1-(2-hydroxy-4,6-dimethoxyphenyl)-ethanone (1), 3,4-dihydroxy cinnamic acid tetracosyl ester (2), 4-hydroxy-3-methoxy benzoic acid (3), 2-hydroxy benzoic acid (4), 3,4-dihydroxy cinnamic acid methyl ester (5) and 4-hydroxy benzoic acid pentadecane ester (6). These compounds were further screened for their minimum inhibitory concentration (MIC) and median inhibitory concentration (IC50) by use of the micro-dilution-MTT assay for antimicrobial activity against one Gram-positive bacterium (Bacillus subtilis), three Gram-negative bacteria (Agrobacterium tumefaciens, Pseudomonas lachrymans, and Xanthomonas vesicatoria), and one yeast (Candida albicans). Apart from compound 6, which had no activity against any of the tested microorganisms, the other compounds showed selective inhibitory activity. This is the first report on the antimicrobial activity of the phenolic compounds isolated from A. aphylla. The obtained results provide promising baseline information for the potential use of the extract and some isolated compounds from this plant as antimicrobial agents to control plant and animal diseases.
Hua Du; Ye Wang; Xiaojiang Hao; Chun Li; Youliang Peng; Jihua Wang; Hao Liu; Ligang Zhou
Related Documents :
17873838 - Lupane triterpenoids from acacia mellifera with cytotoxic activity.
17979098 - The anti-invasive effect of lucidenic acids isolated from a new ganoderma lucidum strain.
8350088 - A novel amino acid glycoside and three amino acids from allium sativum.
10462448 - Incorporation of 1-[1-(13)c]deoxy-d-xylulose in chamomile sesquiterpenes.
25415658 - Acidity enhancement of unsaturated bases of group 15 by association with borane and ber...
2551068 - Inhibition by tranexamic acid of the conversion of single-chain tissue plasminogen acti...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Natural product communications     Volume:  4     ISSN:  1934-578X     ISO Abbreviation:  Nat Prod Commun     Publication Date:  2009 Mar 
Date Detail:
Created Date:  2009-05-05     Completed Date:  2009-06-01     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101477873     Medline TA:  Nat Prod Commun     Country:  United States    
Other Details:
Languages:  eng     Pagination:  385-8     Citation Subset:  IM    
College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Amaranthaceae / chemistry*
Anti-Infective Agents / analysis,  isolation & purification*
Drug Resistance, Bacterial
Magnetic Resonance Spectroscopy
Phenols / analysis*,  isolation & purification*
Reg. No./Substance:
0/Acetates; 0/Anti-Infective Agents; 0/Phenols; 141-78-6/ethyl acetate

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Phenolic glucosides from Flacourtia indica.
Next Document:  Aureobasidin, new antifouling metabolite from marine-derived fungus Aureobasidium sp.