Synthesis, characterization and antimicrobial studies of some new quinoline incorporated benzimidazole derivatives

dc.contributor.authorGarudachari, B.
dc.contributor.authorSatyanarayana, M.N.
dc.contributor.authorThippeswamy, B.
dc.contributor.authorShivakumar, C.K.
dc.contributor.authorShivananda, K.N.
dc.contributor.authorHegde, G.
dc.contributor.authorIsloor, A.M.
dc.date.accessioned2026-02-05T09:35:12Z
dc.date.issued2012
dc.description.abstractTwo new series of quinoline incorporated benzimidazole derivatives (4a-i and 8a-f) were synthesized from substituted aniline and isatin through multi-step reaction. 6-substituted-4-carboxyquinolines (3a,b and 7) were synthesized by multi component one pot reactions (via Doebner reaction and Pfitzinger reaction respectively) and the targeted benzimidazole derivatives were obtained by the reaction of 6-substituted-4-carboxyquinolines (3a,b and 7) with substituted aromatic diamines in acidic media. All the newly synthesized compounds were characterized by IR, NMR mass spectral study and also by C, H, N analyses. The final compounds were screened for their in-vitro antibacterial and antifungal activity by well plate method (zone of inhibition). The results revealed that, compounds 4c, 4d, 8c and 8d showed significant antibacterial activity. The compound 8b was found to be potent antifungal agent. 4a, 8a and 8f showed moderate to good antimicrobial activity as compared to the standard drugs against all tested microbial strains. © 2012 Elsevier Masson SAS. All rights reserved.
dc.identifier.citationEuropean Journal of Medicinal Chemistry, 2012, 54, , pp. 900-906
dc.identifier.issn2235234
dc.identifier.urihttps://doi.org/10.1016/j.ejmech.2012.05.027
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/26982
dc.subject2 (4 fluorophenyl) 4 (1h imidazo[4,5]pyridin 2 yl)quinoline
dc.subject2 (4 fluorophenyl) 4 (6 methoxy 1h benzimidazol 2 yl)quinoline
dc.subject4 (1h benzimidazol 2 yl) 2 (4 fluorophenyl)quinoline
dc.subject4 (1h benzimidazol 2 yl) 6 fluoro 2 (4 fluorophenyl)quinoline
dc.subject4 (1h benzimidazole 2 yl) 6 chloro 2 (4 fluorophenyl) quinoline
dc.subject4 (5 chloro 1h benzimidazol 2 yl) 2 (4 fluorophenyl)quinoline
dc.subject4 (5 chloro 1h benzimidazol 2 yl) 6 fluoro 2 (4 fluorophenyl)quinoline
dc.subject4 (5 fluoro 1h benzimidazol 2 yl) 2 (4 fluorophenyl)quinoline
dc.subject4 (5,6 dichloro 1h benzimidazol 2 yl) 2 (4 fluorophenyl)quinoline
dc.subject4 (5,6 dichloro 1h benzimidazol 2 yl) 6 fluoro 2 (4 fluorophenyl)quinoline
dc.subject6 chloro 2 (4 fluorophenyl) 4 (1h imidazo[4,5]pyridin 2 yl)quinoline
dc.subject6 chloro 4 (5 chloro 1h benzimidazol 2 yl) 2 (4 fluorophenyl)quinoline
dc.subject6 chloro 4 (5,6 dichloro 1h benzimidazol 2 yl) 2 (4 fluorophenyl)quinoline
dc.subject6 fluoro 2 (4 fluorophenyl) 4 (1h imidazo[4,5]pyridin 2 yl)quinoline
dc.subject6 fluoro 4 (5 fluoro 1h benzimidazol 2 yl) 2 (4 fluorophenyl)quinoline
dc.subjectantibiotic agent
dc.subjectantifungal agent
dc.subjectbenzimidazole derivative
dc.subjectciprofloxacin
dc.subjectfluconazole
dc.subjectquinoline derivative
dc.subjectunclassified drug
dc.subjectantibacterial activity
dc.subjectantifungal activity
dc.subjectarticle
dc.subjectAspergillus flavus
dc.subjectAspergillus niger
dc.subjectAspergillus terreus
dc.subjectcarbon nuclear magnetic resonance
dc.subjectdrug structure
dc.subjectdrug synthesis
dc.subjectEscherichia coli
dc.subjectinfrared spectrometry
dc.subjectnonhuman
dc.subjectone pot synthesis
dc.subjectPenicillium
dc.subjectproton nuclear magnetic resonance
dc.subjectSalmonella
dc.subjectStaphylococcus aureus
dc.subjectsubstitution line
dc.subjectXanthomonas
dc.subjectAnti-Infective Agents
dc.subjectBacteria
dc.subjectBenzimidazoles
dc.subjectChemistry Techniques, Synthetic
dc.subjectFungi
dc.subjectQuinolines
dc.titleSynthesis, characterization and antimicrobial studies of some new quinoline incorporated benzimidazole derivatives

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