Synthesis and evaluation of antioxidant, antimicrobial activities of new 2,4-disubstituted thiazoles

dc.contributor.authorMalladi, S.
dc.contributor.authorIsloor, A.M.
dc.contributor.authorPeethambar, S.K.
dc.contributor.authorShivananda, K.N.
dc.date.accessioned2026-02-05T09:35:05Z
dc.date.issued2012
dc.description.abstractA new series of 2,4-disubstituted thiazole derivatives were synthesized by the reaction of various 3-aryl-1H-pyrazole-4- carbaldehyde thiosemicarbazones (2a-e) and phenacyl bromides. The compounds (3a-n) were characterized by IR, NMR, mass spectra and C, H, N analyses. All the synthesized compounds were screened for their antioxidant and antimicrobial activities. Antioxidant studies revealed that, compounds 3b, 3j and 3n showed significant scavenging activity whereas compounds 3e and 3n exhibited significant antimicrobial activity. The acute oral toxicity study for the compound 3e and 3n have revealed good safety profile till the uppermost dose (2000 mg/kg).
dc.identifier.citationInternational Journal of Pharmaceutical Research, 2012, 4, 3, pp. 81-88
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/26900
dc.subject2,4 disubstituted thiazole derivative
dc.subject3 (2,4 dichlorophenyl) 1h pyrazole 4 carbaldehyde(4 fluorophenyl 1,3 thiazol 2 yl)hydrazone
dc.subject3 (2,4 dichlorophenyl) 1h pyrazole 4 carbaldehyde(4 phenyl 1,3 thiazol 2 yl)hydrazone
dc.subject3 (4 chlorophenyl) 1h pyrazole 4 carbaldehyde(4 fluorophenyl 1,3 thiazol 2 yl)hydrazone
dc.subject3 (4 chlorophenyl) 1h pyrazole 4 carbaldehyde(4 methoxyphenyl 1,3 thiazol 2 yl)hydrazone
dc.subject3 (4 chlorophenyl) 1h pyrazole 4 carbaldehyde(4 phenyl 1,3 thiazol 2 yl)hydrazone
dc.subject3 (4 fluorophenyl) 1h pyrazole 4 carbaldehyde(4 fluorophenyl 1, 3 thiazol 2 yl)hydrazone
dc.subject3 (4 fluorophenyl) 1h pyrazole 4 carbaldehyde(4 methoxyphenyl 1,3 thiazol 2 yl)hydrazone
dc.subject3 (4 fluorophenyl) 1h pyrazole 4 carbaldehyde(4 phenyl 1,3 thiazol 2 yl)hydrazone
dc.subject3 (4 methoxyphenyl) 1h pyrazole 4 carbaldehyde(4 fluorophenyl 1,3 thiazol 2 yl)hydrazone
dc.subject3 (4 methoxyphenyl) 1h pyrazole 4 carbaldehyde(4 methoxyphenyl 1,3 thiazol 2 yl)hydrazone
dc.subject3 (4 methoxyphenyl) 1h pyrazole 4 carbaldehyde(4 phenyl 1,3 thiazol 2 yl)hydrazone
dc.subject3 (phenyl) 1h pyrazole 4 carbaldehyde(4 fluorophenyl 1,3 thiazol 2 yl)hydrazone
dc.subject3 (phenyl) 1h pyrazole 4 carbaldehyde(4 methoxyphenyl 1,3-thiazol 2 yl)hydrazone
dc.subject3 (phenyl) 1h pyrazole 4 carbaldehyde(4 phenyl 1,3 thiazol 2 yl)hydrazone
dc.subject3 aryl 1h pyrazole 4 carbaldehyde thiosemicarbazone derivative
dc.subjectbromine derivative
dc.subjectbutylcresol
dc.subjectcarbon
dc.subjectfluconazole
dc.subjecthydrogen
dc.subjectnitrogen
dc.subjectphenacyl bromide derivative
dc.subjectthiazole derivative
dc.subjectthiosemicarbazone derivative
dc.subjectunclassified drug
dc.subjectanimal experiment
dc.subjectantimicrobial activity
dc.subjectantioxidant activity
dc.subjectarticle
dc.subjectcontrolled study
dc.subjectdrug safety
dc.subjectdrug screening
dc.subjectdrug synthesis
dc.subjectfemale
dc.subjectinfrared spectroscopy
dc.subjectmale
dc.subjectmass spectrometry
dc.subjectmouse
dc.subjectnonhuman
dc.subjectnuclear magnetic resonance spectroscopy
dc.titleSynthesis and evaluation of antioxidant, antimicrobial activities of new 2,4-disubstituted thiazoles

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