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Activity of 7-methyljuglone derivatives against Mycobacterium tuberculosis and as subversive substrates for mycothiol disulfide reductase.

Authors :
Mahapatra A
Mativandlela SP
Binneman B
Fourie PB
Hamilton CJ
Meyer JJ
van der Kooy F
Houghton P
Lall N
Source :
Bioorganic & medicinal chemistry [Bioorg Med Chem] 2007 Dec 15; Vol. 15 (24), pp. 7638-46. Date of Electronic Publication: 2007 Sep 06.
Publication Year :
2007

Abstract

The naphthoquinone 7-methyljuglone (5-hydroxy-7-methyl-1,4-naphthoquinone) has previously been isolated and identified as an active component of root extracts of Euclea natalensis which displays antitubercular activity. Herein, a series of synthetic and plant-derived naphthoquinone derivates of the 7-methyljuglone scaffold have been prepared and evaluated for antibacterial activity against Mycobacterium tuberculosis. Several of these compounds have been shown to operate as subversive substrates with mycothiol disulfide reductase. The absence of a direct correlation between antitubercular activity and subversive substrate efficiency with mycothiol disulfide reductase, might be a consequence of their non-specific reactivity with multiple biological targets (e.g. other disulfide reductases).

Details

Language :
English
ISSN :
1464-3391
Volume :
15
Issue :
24
Database :
MEDLINE
Journal :
Bioorganic & medicinal chemistry
Publication Type :
Academic Journal
Accession number :
17888665
Full Text :
https://doi.org/10.1016/j.bmc.2007.08.064