Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8565
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dc.contributor.authorMONDAL, ABHISHEKen_US
dc.contributor.authorSIWACH, MANISHAen_US
dc.contributor.authorAHMAD,MANZOORen_US
dc.contributor.authorRADHAKRISHNAN, SUNISH KUMARen_US
dc.contributor.authorTALUKDAR, PINAKIen_US
dc.date.accessioned2024-02-29T09:18:20Z-
dc.date.available2024-02-29T09:18:20Z-
dc.date.issued2024-02en_US
dc.identifier.citationACS Infectious Diseases, 10(02), 371–376.en_US
dc.identifier.issn2373-8227en_US
dc.identifier.urihttps://doi.org/10.1021/acsinfecdis.3c00455en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8565-
dc.description.abstractThe development of potent antibacterial agents has become increasingly difficult as bacteria continue to evolve and develop resistance to antibiotics. It is therefore imperative to find effective antimicrobial agents that can address the evolving challenges posed by infectious diseases and antimicrobial resistance. Using artificial transmembrane ion transporters is an emerging and promising avenue to address this issue. We report pyridyl-linked hetero hydrazones as highly efficient transmembrane HCl symporters. These compounds offer an appropriate HCl binding site through cooperative protonation, followed by recognition of chloride ions. HCl transport by these compounds inhibits the growth of different Gram-negative bacterial strains with high efficacy by affecting the cell envelope homeostasis. This specific class of compounds holds substantial promise in the ongoing pursuit of developing highly efficient antibacterial agents.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectAnionsen_US
dc.subjectAntibiotic resistanceen_US
dc.subjectAntimicrobial agentsen_US
dc.subjectBacteriaen_US
dc.subjectCharge transporten_US
dc.subject2024-FEB-WEEK3en_US
dc.subjectTOC-FEB-2024en_US
dc.subject2024en_US
dc.titlePyridyl-Linked Hetero Hydrazones: Transmembrane H+/Cl– Symporters with Efficient Antibacterial Activityen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleACS Infectious Diseasesen_US
dc.publication.originofpublisherForeignen_US
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