4.6 Article

Antimycobacterial activity and cytotoxicity of flavonoids from the flowers of Chromolaena odorata

Journal

ARCHIVES OF PHARMACAL RESEARCH
Volume 27, Issue 5, Pages 507-511

Publisher

PHARMACEUTICAL SOC KOREA
DOI: 10.1007/BF02980123

Keywords

Chromolaena odorata; asteraceae; flavonoids; anti mycobacterial activity; cytotoxicity; struture-activity relationship

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From the flowers of Chromolaena odorata (Eupatorium odoratum) four flavanones, isosakuranetin (5,7-dihydroxy-4'-methoxyflavanone) (1), persicogenin (5,3'-dihydroxy-7,4'-dimethoxyflavanone) (2), 5,6,7,4'-tetramethoxyflavanone (3) and 4'-hydroxy-5,6,7-trimethoxyflavanone (4), two chalcones, 2'-hydroxy-4,4',5',6'-tetramethoxychalcone (5) and 4,2'-dihydroxy4',5',6'-trimethoxychalcone (6), and two flavones, acacetin (5,7-dihydroxy-4'-methoxyflavone) (7) and luteolin (5,7,3',4'-tetrahydroxyflavone) (8) were isolated and identified. Compound 1 exhibited moderate anti mycobacterial activity against Mycobacterium tuberculosis with the MIC value of 174.8 muM, whereas compounds 4, 7, and 8 exhibited weak activity with the MIC values of 606.0, 704.2 and 699.3 muM respectively. Compound 7 showed moderate cytotoxicity against human small cell lung cancer (NCl-H187) cells with the MIC value of 24.6 muM, whereas compound 8 exhibited moderate toxicity against NCl-H187 cells and week toxicity against human breast cancer (BC) cells with the MIC values of 19.2 and 38.4 muM respectively.

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