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Quinonoid and phenazine compounds: synthesis and evaluation against H37Rv, rifampicin and isoniazid-resistance strains of Mycobacterium tuberculosis.
- Source :
-
European journal of medicinal chemistry [Eur J Med Chem] 2011 Sep; Vol. 46 (9), pp. 4521-9. Date of Electronic Publication: 2011 Jul 23. - Publication Year :
- 2011
-
Abstract
- Several quinonoid and phenazine compounds were synthesized in moderate to high yields and showed activity against H(37)Rv, rifampicin and isoniazid-resistance strains of Mycobacterium tuberculosis. The cytotoxity of the compounds were evaluated against human peripheral blood mononuclear cells (PBMC) and these substances emerge as promising antitubercular prototypes.<br /> (Copyright © 2011 Elsevier Masson SAS. All rights reserved.)
- Subjects :
- Antitubercular Agents chemistry
Cells, Cultured
Drug Resistance, Microbial
Isoniazid pharmacology
Magnetic Resonance Spectroscopy
Microbial Sensitivity Tests
Models, Molecular
Phenazines chemistry
Phenazines pharmacology
Quinones chemistry
Quinones pharmacology
Rifampin pharmacology
Spectrometry, Mass, Electrospray Ionization
Spectrophotometry, Infrared
X-Ray Diffraction
Antitubercular Agents chemical synthesis
Antitubercular Agents pharmacology
Mycobacterium tuberculosis drug effects
Phenazines chemical synthesis
Quinones chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1768-3254
- Volume :
- 46
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- European journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 21820768
- Full Text :
- https://doi.org/10.1016/j.ejmech.2011.07.026