2008
DOI: 10.1016/j.ejmech.2007.07.001
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Synthesis and antituberculosis activity of new thiazolylhydrazone derivatives

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Cited by 58 publications
(26 citation statements)
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“…[1][2][3][4][5][6][7][8][9][10][11] Thiazolidinones in particular have been investigated in great detail because of its biological importance. 12 Thiazolidinone nucleus containing compounds shows anti-inflammatory, 13-20 anticonvulsant, [21][22][23][24] hypnotic, 25-27 antitubercular, [25][26][27] antibacterial, antifungal and anticancer [28][29][30][31][32][33][34][35] activities.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4][5][6][7][8][9][10][11] Thiazolidinones in particular have been investigated in great detail because of its biological importance. 12 Thiazolidinone nucleus containing compounds shows anti-inflammatory, 13-20 anticonvulsant, [21][22][23][24] hypnotic, 25-27 antitubercular, [25][26][27] antibacterial, antifungal and anticancer [28][29][30][31][32][33][34][35] activities.…”
Section: Introductionmentioning
confidence: 99%
“…An example is diflunisal, a hydrazide/hydrazone derivative, which has dual effect acting with antimicrobial/anti-inflammatory properties. Furthermore, in thiazolylhydrazone derivatives, SAR studies have found that substitutions on the phenyl ring affect anti-TB activity (45, figure 14) (Turan-Zitouni et al, 2008). Another example of a thiazolylhydrazine is compound 46 (figure 14), which has high anti-TB activity with a IC50 of 6.22 µg/mL and low toxicity (CC50> 40 µg/mL).…”
Section: Hydrazides/hydrazones Derivativesmentioning
confidence: 99%
“…Thiazolylhydrazone derivatives (Figure 4b): All the synthesized compounds of the series was highly potent with the ability of more than 90% hindrance to the growth of the bacilli along with least or none cytotoxicity has been reported within the range of MIC (MIC > 6.25µg/ml) [59].…”
Section: Newly Synthesized Compounds For Lead Determination N 1 -Nicomentioning
confidence: 99%