Novel substituted fluoroquinolone derivatives, compounds 6-20 were designed, synthesized, and evaluated for antituberculosis and antibacterial activity. Antibacterial activities of the compounds were determined and compound 14 was found to be the most potent antimicrobial agent owing to minimal inhibitory concentration (MIC) value of <1.16 mu g/mu l for all tested bacteria. Further, compounds were tested in vitro for their antimycobacterial activity against Mycobacterium tuberculosis H37Rv. Most of the compounds showed antimycobacterial effects with 1.56-25.00 mu g/ml MIC values. Compounds 14 and 18 were found to be the most active derivatives due to their MIC at 1.56 mu g/ml. Selected compounds 11, 14, 17, and 18 were tested for M. tubercu...
Thirty-four newer 1-cyclopropyl-1,4-dihydro-6-fluoro-7-(substituted secondary amino)-8-methoxy-5-(su...
Fluoroquinolone (FQ) resistance in Mycobacterium tuberculosis (Mtb), caused by amino acid substituti...
<p>A classical protein sequence alignment and homology modeling strategy were used for building thre...
Fifty-one novel 1-(cyclopropyl/2,4-difluorophenyl/t-butyl)-1,4-dihydro-6-fluoro-7-(sub secondary ami...
The antimycobacterial activity (both in vitro and in vivo) and DNA gyrase inhibition of newly synthe...
Twenty-one novel alkyl/acyl/sulfonyl substituted fluoroquinolone derivatives were designed, synthesi...
Objective. Quinolone moiety is an important class of nitrogen containing heterocycles widely used as...
Thirty novel 9-fluoro-2,3-dihydro-8,10-(mono/di-sub)-3-methyl-8-nitro-7-oxo-7H-[1,4]oxazino[2,3,4-ij...
Thirty novel 9-fluoro-2,3-dihydro-8,10-(mono/di-sub)-3-methyl-8-nitro-7-oxo-7H-[1,4]oxazino[2,3,4-ij...
Currently we screened 9 newer synthesized fluoroquinolone derivatives 5(a–i) against two gram positi...
A series of 5-substituted-1,3,4-thiadiazole-based fluoroquinolone derivatives were designed as poten...
Tuberculosis continues to be a major cause of morbidity and mortality all over the world. Various 7-...
A set of 21 new fluoroquinolones bearing an aromatic or heteroaromatic moiety at C-7 and an alkyl gr...
Microbial infections remain a grave threat to global health security due to increasing antibiotic re...
DNA gyrase is a clinically validated target for developing drugs against Mycobacterium tuberculosis ...
Thirty-four newer 1-cyclopropyl-1,4-dihydro-6-fluoro-7-(substituted secondary amino)-8-methoxy-5-(su...
Fluoroquinolone (FQ) resistance in Mycobacterium tuberculosis (Mtb), caused by amino acid substituti...
<p>A classical protein sequence alignment and homology modeling strategy were used for building thre...
Fifty-one novel 1-(cyclopropyl/2,4-difluorophenyl/t-butyl)-1,4-dihydro-6-fluoro-7-(sub secondary ami...
The antimycobacterial activity (both in vitro and in vivo) and DNA gyrase inhibition of newly synthe...
Twenty-one novel alkyl/acyl/sulfonyl substituted fluoroquinolone derivatives were designed, synthesi...
Objective. Quinolone moiety is an important class of nitrogen containing heterocycles widely used as...
Thirty novel 9-fluoro-2,3-dihydro-8,10-(mono/di-sub)-3-methyl-8-nitro-7-oxo-7H-[1,4]oxazino[2,3,4-ij...
Thirty novel 9-fluoro-2,3-dihydro-8,10-(mono/di-sub)-3-methyl-8-nitro-7-oxo-7H-[1,4]oxazino[2,3,4-ij...
Currently we screened 9 newer synthesized fluoroquinolone derivatives 5(a–i) against two gram positi...
A series of 5-substituted-1,3,4-thiadiazole-based fluoroquinolone derivatives were designed as poten...
Tuberculosis continues to be a major cause of morbidity and mortality all over the world. Various 7-...
A set of 21 new fluoroquinolones bearing an aromatic or heteroaromatic moiety at C-7 and an alkyl gr...
Microbial infections remain a grave threat to global health security due to increasing antibiotic re...
DNA gyrase is a clinically validated target for developing drugs against Mycobacterium tuberculosis ...
Thirty-four newer 1-cyclopropyl-1,4-dihydro-6-fluoro-7-(substituted secondary amino)-8-methoxy-5-(su...
Fluoroquinolone (FQ) resistance in Mycobacterium tuberculosis (Mtb), caused by amino acid substituti...
<p>A classical protein sequence alignment and homology modeling strategy were used for building thre...