2015
DOI: 10.1016/j.bmcl.2015.10.057
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New INH–pyrazole analogs: Design, synthesis and evaluation of antitubercular and antibacterial activity

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Cited by 67 publications
(29 citation statements)
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“…) (zone of inhibition = 23 ± 0.2 mm against Staphylococcus aureus, 24 ± 0.2 mm against Escherichia coli and 19 ± 0.3 mm against Pseudomonas aeruginosa) at 75 µg/mL concentration was found to be most potent antibacterial agents as compared to reference drug Ciprofloxacin. Similar trend of antibacterial activity was observed when 50 µg/mL concentrations were used[50].…”
supporting
confidence: 81%
“…) (zone of inhibition = 23 ± 0.2 mm against Staphylococcus aureus, 24 ± 0.2 mm against Escherichia coli and 19 ± 0.3 mm against Pseudomonas aeruginosa) at 75 µg/mL concentration was found to be most potent antibacterial agents as compared to reference drug Ciprofloxacin. Similar trend of antibacterial activity was observed when 50 µg/mL concentrations were used[50].…”
supporting
confidence: 81%
“…Pyrazoles are considered as important therapeutic scaffolds, which is widely used in the pharmaceuticals and agrochemicals, such as fipronil and chlorantraniliprole How to design and synthesize novel pyrazole compounds have increasingly attracted interest because of their excellent synthetic utility.…”
Section: Introductionmentioning
confidence: 99%
“…Interesting biological activities are associated with pyrazole derivatives such as anti-tubercular, [2] antimicrobial, [3] anti-consultant, [4] anticancer, [5] anti-viral, [6] and so forth. Pyrimidinthione derivatives are very important in pharmaceutical and medicinal chemistry as they showed wide range of biological activities.…”
Section: Introductionmentioning
confidence: 99%