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Activity of 7-methyljuglone derivatives against Mycobacterium tuberculosis and as subversive substrates for mycothiol disulfide reductase.
- 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).
- Subjects :
- Anti-Bacterial Agents chemistry
Anti-Bacterial Agents pharmacology
Dose-Response Relationship, Drug
Microbial Sensitivity Tests
Molecular Structure
Mycobacterium tuberculosis enzymology
NADH, NADPH Oxidoreductases metabolism
Naphthoquinones pharmacology
Anti-Bacterial Agents chemical synthesis
Ebenaceae chemistry
Mycobacterium tuberculosis drug effects
NADH, NADPH Oxidoreductases chemistry
Naphthoquinones chemistry
Plant Roots chemistry
Subjects
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