Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6201
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dc.contributor.authorMONDAL, ABHISHEKen_US
dc.contributor.authorMALLA, JAVID AHMADen_US
dc.contributor.authorPAITHANKAR, HARSHADen_US
dc.contributor.authorSharma, Shilpyen_US
dc.contributor.authorCHUGH, JEETENDERen_US
dc.contributor.authorTALUKDAR, PINAKIen_US
dc.date.accessioned2021-08-27T11:21:36Z
dc.date.available2021-08-27T11:21:36Z
dc.date.issued2021-08en_US
dc.identifier.citationOrganic Letters, 23(15), 6131-6136.en_US
dc.identifier.issn1523-7060en_US
dc.identifier.issn1523-7052en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6201-
dc.identifier.urihttps://doi.org/10.1021/acs.orglett.1c02235en_US
dc.description.abstractWe report two pyridyl-linked benzimidazolyl hydrazones as HCl cotransporters that are 5 and 2 times superior to prodigiosin, a natural product whose transport efficiency has never been routed by synthetic molecules. These hydrazones provide a suitable HCl binding site through a cooperative protonation and chloride ion recognition. HCl transport by the most active compound induces lysosome deacidification. Viability assays confirmed that the compounds induce cytotoxicity toward human breast cancer MCF-7 cells but are relatively nontoxic toward noncancerous HEK293T cells.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectApoptosis-Inducing Activityen_US
dc.subjectAnion Transporten_US
dc.subjectPK(A) Shiftsen_US
dc.subjectChannelsen_US
dc.subjectPHen_US
dc.subject2021-AUG-WEEK3en_US
dc.subjectTOC-AUG-2021en_US
dc.subject2021en_US
dc.titleA Pyridyl-Linked Benzimidazolyl Tautomer Facilitates Prodigious H+/Cl– Symport through a Cooperative Protonation and Chloride Ion Recognitionen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic Lettersen_US
dc.publication.originofpublisherForeignen_US
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