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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3344
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dc.contributor.authorSakhuja, Rajeev-
dc.date.accessioned2021-11-11T10:58:04Z-
dc.date.available2021-11-11T10:58:04Z-
dc.date.issued2021-
dc.identifier.urihttps://www.eurekaselect.com/174688/article-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3344-
dc.description.abstractBacterial infections are considered as one of the major global health threats, so it is very essential to design and develop new antibacterial agents to overcome the drawbacks of existing antibacterial agents. Methods: The aim of this work is to synthesize a series of new fluoroquinolone-3-carboxamide amino acid conjugates by molecular hybridization. We utilized benzotriazole chemistry to synthesize the desired hybrid conjugates.en_US
dc.language.isoenen_US
dc.publisherBentham Scienceen_US
dc.subjectChemistryen_US
dc.subjectAntibacterial agentsen_US
dc.subjectAntimicrobialen_US
dc.subjectFluoroquinoloneen_US
dc.subjectAmino aciden_US
dc.subjectConjugatesen_US
dc.titleFluoroquinolone-3-carboxamide Amino Acid Conjugates: Synthesis, Antibacterial Properties And Molecular Modeling Studiesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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