Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/4117
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dc.contributor.authorBasavanna, V-
dc.contributor.authorChandramouli, M-
dc.contributor.authorKempaiah, C-
dc.contributor.authorBhadraiah, U K-
dc.contributor.authorLingegowda, N S-
dc.contributor.authorDoddamani, S-
dc.contributor.authorNingaiah, S-
dc.date.accessioned2022-10-26T09:05:29Z-
dc.date.available2022-10-26T09:05:29Z-
dc.date.issued2021-11-
dc.identifier.citationRussian Journal of General Chemistry;91(11):2257-2266en_US
dc.identifier.urihttps://doi.org/10.1134/s1070363221110128-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/4117-
dc.description.abstractA series of 1,3,4-oxadiazole bridged pyrazole/isoxazole bearing quinoline derivatives has been designed and synthesized by a clean and convenient method. Structures of the newly synthesized compounds have been confirmed by FTIR, 1H and 13C NMR, and HRMS spectral data. The titled compounds have been evaluated for their molecular docking guided antimicrobial and anti-inflammatory activity. One of 1,3,4-oxadiazole bridged quinolinyl-pyrazole derivatives has interacted efficiently with E. Coli protein (PDB file: 1KZN), and has been characterized by good antimicrobial activity against the majority of the tested pathogens. Another product has exhibited excellent anti-inflammatory activity.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.subject1,3,4-oxadiazoleen_US
dc.subjectpyrazoleen_US
dc.subjectisoxazoleen_US
dc.subjectquinolineen_US
dc.subjectmolecular dockingen_US
dc.subjectantimicrobialen_US
dc.subjectanti-inflammatoryen_US
dc.titleA New Series of 1,3,4-Oxadiazole Linked Quinolinyl-Pyrazole/Isoxazole Derivatives: Synthesis and Biological Activity Evaluationen_US
dc.typeArticleen_US
Appears in Collections:2021

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