Antimycobacterial activity of bisbenzylisoquinoline alkaloids from Tiliacora triandra against multidrug-resistant isolates of Mycobacterium tuberculosis
Bisbenzylisoquinoline alkaloids, tiliacorinine (1), 2′-nortiliacorinine (2), and tiliacorine (3), isolated from the edible plant, Tiliacora triandra, as well as a synthetic derivative, 13′-bromo-tiliacorinine (4), were tested against 59 clinical isolates of multidrug-resistant Mycobacterium tubercul...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2012-04, Vol.22 (8), p.2902-2905 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Bisbenzylisoquinoline alkaloids, tiliacorinine (1), 2′-nortiliacorinine (2), and tiliacorine (3), isolated from the edible plant, Tiliacora triandra, as well as a synthetic derivative, 13′-bromo-tiliacorinine (4), were tested against 59 clinical isolates of multidrug-resistant Mycobacterium tuberculosis (MDR-MTB). The alkaloids 1–4 showed MIC values ranging from 0.7 to 6.2μg/ml, but they exhibited the MIC value at 3.1μg/ml against most MDR-MTB isolates. The present work suggests that bisbenzylisoquinoline alkaloids are potential new chemical scaffolds for antimycobacterial activity. |
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ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2012.02.053 |