Antimycobacterial Flavonoids from the Leaf Extract of Galenia africana

被引:30
作者
Mativandlela, Sannah P. N. [2 ]
Muthivhi, Tshilidzi
Kikuchi, Haruhisa [4 ]
Oshima, Yoshiteru [4 ]
Hamilton, Chris [3 ]
Hussein, Ahmed A. [5 ]
van der Walt, Martha L. [2 ]
Houghton, Peter J. [6 ]
Lall, Namrita [1 ]
机构
[1] Univ Pretoria, Dept Plant Sci, ZA-0002 Pretoria, South Africa
[2] S African MRC, S African Natl Blood Serv, TB Epidemiol & Intervent Res Unit, Pretoria, South Africa
[3] Univ E Anglia, Sch Chem Sci & Pharm, Norwich NR4 7TJ, Norfolk, England
[4] Tohuku Univ, Grad Sch Pharmaceut Sci, Sendai, Miyagi, Japan
[5] Natl Res Ctr, Div Pharmaceut Sci, Chem Med Plants Dept, Cairo, Egypt
[6] Kings Coll London, Dept Pharm, London SE1 9NN, England
来源
JOURNAL OF NATURAL PRODUCTS | 2009年 / 72卷 / 12期
基金
新加坡国家研究基金会; 英国医学研究理事会;
关键词
MYCOBACTERIUM-TUBERCULOSIS; REDUCTASE; CONSTITUENTS; DERIVATIVES; INHIBITORS;
D O I
10.1021/np800778b
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
The bioassay-guided fractionation of the EtOH extract of the leaves of Galenia africana led to the isolation of three known flavonoids, (2S)-5,7,2'-trihydroxyflavanone (1), (E)-3,2',4'-trihydroxychalcone (2), and (E)-2',4'-dihydroxychalcone (3), and the new (E)-3,2',4'-trihydroxy-3'-methoxychalcone (4). Compounds 1 and 3 exhibited moderate antituberculosis activity. During synergistic studies, a combination of compound 4 and an existing antituberculosis drug, isoniazid, reduced their original MICs 4-fold, resulting in a fractional inhibitory concentration of 0.50. The most pronounced effect was demonstrated by compound I and isoniazid reducing their MICs 16-fold and resulting in an FIC of 0.12. Both EtOH extract and isolated compounds failed to exhibit any NADPH oxidase activity at 800.0 mu M concentrations, indicating that mycothiol disulfide reductase is not the target for their antituberculosis activity.
引用
收藏
页码:2169 / 2171
页数:3
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