Hantzsch reaction: Synthesis and characterization of some new 1,4-dihydropyridine derivatives as potent antimicrobial and antioxidant agents

dc.contributor.authorVijesh, A.M.
dc.contributor.authorIsloor, A.M.
dc.contributor.authorPeethambar, S.K.
dc.contributor.authorShivananda, K.N.
dc.contributor.authorArulmoli, T.
dc.contributor.authorIsloor, N.
dc.date.accessioned2026-02-05T09:35:37Z
dc.date.issued2011
dc.description.abstractIn the present study two new series of Hantzsch 1,4-dihydropyridine derivatives (1,4-DHPs) containing substituted pyrazole moiety (4a-f and 5a-f) were synthesized by the reaction of 3-aryl-1H-pyrazole-4-carbaldehydes with 1,3-dicarbonylcompounds (ethylacetoacetate and methylacetoacetate) and ammonium acetate. The newly synthesized compounds were characterized by IR, NMR, mass spectral study and also by C, H, N analyses. New compounds were screened for their antimicrobial activity by well plate method (zone of inhibition). Antioxidant studies of the synthesized compounds were also performed by measuring the DPPH radical scavenging assay. Compounds 4c, 4e and 4f were found to be potent antibacterial and antioxidant agents. The acute oral toxicity study for the compounds 4c, 4e and 4f were carried out and the experimental studies revealed that compounds 4c and 4e is safe up to 3000 mg/kg and no death of animals were recorded. However in compound 4f, we found mortality above 2000 mg and also significant behavioral changes in experimental animals. © 2011 Elsevier Masson SAS. All rights reserved.
dc.identifier.citationEuropean Journal of Medicinal Chemistry, 2011, 46, 11, pp. 5591-5597
dc.identifier.issn2235234
dc.identifier.urihttps://doi.org/10.1016/j.ejmech.2011.09.026
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/27159
dc.subject1,1 diphenyl 2 picrylhydrazyl
dc.subject1,4 dihydropyridine derivative
dc.subject3 (2,4 dichlorophenyl) 1h pyrazole 4 carbaldehyde
dc.subject3 (2,5 dichlorothiophen 3 yl) 1h pyrazole 4 carbaldehyde
dc.subject3 [4 (methylsulfanyl)phenyl] 1h pyrazole 4 carbaldehyde
dc.subjectantibiotic agent
dc.subjectantifungal agent
dc.subjectantioxidant
dc.subjectdiethyl 4 [3 (2,4 dichlorophenyl) 1h pyrazol 4 y] 2,6 dimethyl 1,4 dihydropyridine 3,5 dicarboxylate
dc.subjectdiethyl 4 [3 (2,5 dichlorothiophen 3 yl) 1h pyrazol 4 y] 2,6 dimethyl 1,4 dihydropyridine 3,5 dicarboxylate
dc.subjectdiethyl 4 [3 (4 chlorophenyl) 1h pyrazol 4 yl] 2,6 dimethyl 1,4 dihydropyridine 3,5 dicarboxylate
dc.subjectdiethyl 4 [3 (4 methoxyphenyl) 1h pyrazol 4 y] 2,6 dimethyl 1,4 dihydropyridine 3,5 dicarboxylate
dc.subjectdiethyl 4 [3 (biphenyl 4 yl) 1h pyrazol 4 yl] 2,6 dimethyl 1,4 dihydropyridine 3,5 dicarboxylate
dc.subjectdiethyl 4 [3 [4 (methylsulfanyl)phenyl] 1h pyrazol 4 yl] 2,6 dimethyl 1,4 dihydropyridine 3,5 dicarboxylate
dc.subjectdimethyl 4 [3 (2,4 dichlorophenyl) 1h pyrazol 4 yl] 2,6 dimethyl 1,4 dihydropyridine 3,5 dicarboxylate
dc.subjectdimethyl 4 [3 (2,5 dichlorothiophen 3 yl) 1h pyrazol 4 yl] 2,6 dimethyl 1,4 dihydropyridine 3,5 dicarboxylate
dc.subjectdimethyl 4 [3 (4 chlorophenyl) 1h pyrazol 4 yl] 2,6 dimethyl 1,4 dihydropyridine 3,5 dicarboxylate
dc.subjectdimethyl 4 [3 (4 methoxyphenyl) 1h pyrazol 4 y] 2,6 dimethyl 1,4 dihydropyridine 3,5 dicarboxylate
dc.subjectdimethyl 4 [3 (biphenyl 4 yl) 1h pyrazol 4 yl] 2,6 dimethyl 1,4 dihydropyridine 3,5 dicarboxylate
dc.subjectdimiethyl 4 [3 [4 (methylsulfanyl)phenyl] 1h pyrazol 4 yl] 2,6 dimethyl 1,4 dihydropyridine 3,5 dicarboxylate
dc.subjectunclassified drug
dc.subjectanimal experiment
dc.subjectantifungal activity
dc.subjectantimicrobial activity
dc.subjectantioxidant activity
dc.subjectarticle
dc.subjectchemical reaction
dc.subjectcontrolled study
dc.subjectdrug determination
dc.subjectdrug safety
dc.subjectdrug screening
dc.subjectdrug synthesis
dc.subjectHantzsch reaction
dc.subjectinfrared spectroscopy
dc.subjectLD 50
dc.subjectmass spectrometry
dc.subjectnonhuman
dc.subjectnuclear magnetic resonance spectroscopy
dc.subjecttoxicity testing
dc.subjectAnimals
dc.subjectAnti-Infective Agents
dc.subjectBacteria
dc.subjectBehavior, Animal
dc.subjectBiphenyl Compounds
dc.subjectChemistry Techniques, Synthetic
dc.subjectDihydropyridines
dc.subjectFemale
dc.subjectFree Radical Scavengers
dc.subjectFungi
dc.subjectMice
dc.subjectPicrates
dc.titleHantzsch reaction: Synthesis and characterization of some new 1,4-dihydropyridine derivatives as potent antimicrobial and antioxidant agents

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