Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1438
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dc.contributor.authorMONDAL, DEBASHISen_US
dc.contributor.authorSATHYAN, ANJANAen_US
dc.contributor.authorShinde, Sopan Valibaen_US
dc.contributor.authorMISHRA, KAMAL K.en_US
dc.contributor.authorTALUKDAR, PINAKIen_US
dc.date.accessioned2018-12-28T06:44:31Z
dc.date.available2018-12-28T06:44:31Z
dc.date.issued2018-10en_US
dc.identifier.citationOrganic & Biomolecular Chemistry, Vol.16(45) pp8690-8694.en_US
dc.identifier.issn1477-0520en_US
dc.identifier.issn1477-0539en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1438-
dc.identifier.urihttps://doi.org/10.1039/C8OB01345Den_US
dc.description.abstractTris-carboxyamide and tris-sulfonamide-based anion transporters with a cyanuric acid core are reported. Interestingly, Cl- ion binding and transmembrane transport properties of carboxyamides are better compared to those of their tris-sulfonamide analogs. The carboxyamide derivatives act as mobile carriers of Cl- and exchange anions via antiport mechanism.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectAnion-Pi Slidesen_US
dc.subjectChloride Transporten_US
dc.subjectIon Channelsen_US
dc.subjectApoptosisen_US
dc.subjectRolesen_US
dc.subjectTOC-DEC-2018en_US
dc.subject2018en_US
dc.titleTripodal cyanurates as selective transmembrane Cl- transportersen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic & Biomolecular Chemistryen_US
dc.publication.originofpublisherForeignen_US
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