نتایج جستجو برای: antitubercular
تعداد نتایج: 2540 فیلتر نتایج به سال:
reaction of 2-hydrazinocarbonyl-3-chloro-5-phenoxy-benzo[b] thiophene with different substituted phenyl isothiocyanate gave n-substituted arylthiosemi-carbazide derivatives (1a-h). 1,3,4-thiadiazole derivatives (2a-h) were prepared by the cyclization of arylthiosemicarbazides (1a-h) with concentrated sulphuric acid. all the compounds were screened for their antitubercular activity against mycob...
Pseudomembranous colitis is known to develop with long-term antibiotic administration, but antitubercular agents are rarely reported as a cause of this disease. We experienced a case of pseudomembranous colitis associated with rifampin. The patient was twice admitted to our hospital for the management of frequent bloody, mucoid, jelly-like diarrhea and lower abdominal pain that developed after ...
Tuberculosis is a contagious disease caused by Mycobacterium tuberculosis. After a long period during which this disease seemed to be declining, the last two decades have seen an unexpected return recorded (Raviglione et al., 1995). Isoniazid, pyraziniamide, ethambutol, rifampicin and streptomycin, generally used in combination, are still the current drugs of choice in the therapy of tuberculos...
Isolation and Evaluation of the Enantiospecific Antitubercular Activity of a Novel Triazole Compound
Cyclohex-3-enyl(5-phenyl-4H-1,2,4-triazol-3-yl)methanol (MSDRT 12) is a novel triazole-based antitubercular compound with two chiral centers. To evaluate the enantiospecific antitubercular activity, the four stereoisomers were isolated using preparative chiral chromatography and the individual stereoisomers were evaluated using the resazurin microtiter assay method (REMA) and a microbroth dilut...
Microwave activation coupled with dry media technique as a green chemistry procedure has been applied to synthesis of a series of some new title compounds. They have been obtained by the reaction of in situ synthesized 1,3-dihydro-3-[2-(phenyl/4-fluorophenyl)-2-oxoethylidene)-indol-2(1H)-one (4a, b) with substituted aminobenzenethiols (5a-d). The key intermediates 4a, b were also prepared in on...
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