Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5035
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dc.contributor.authorMALLA, JAVID AHMADen_US
dc.contributor.authorSHARMA, VIRENDER KUMARen_US
dc.contributor.authorLAHIRI, MAYURIKAen_US
dc.contributor.authorTALUKDAR, PINAKIen_US
dc.date.accessioned2020-09-16T03:45:56Z
dc.date.available2020-09-16T03:45:56Z
dc.date.issued2020-09en_US
dc.identifier.citationChemistry—A European Journal, 26(52), 11946-11949.en_US
dc.identifier.issn0947-6539en_US
dc.identifier.issn1521-3765en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/5035
dc.identifier.urihttps://doi.org/10.1002/chem.202002964en_US
dc.description.abstractThe formation of a supramolecular synthetic M+/Cl− channel in the membrane phospholipid bilayer has been reported upon activation of a methyl pivalate‐linked N1,N3‐dialkyl‐2‐hydroxyisophthalamide by esterases. The channel formation induces apoptosis in cancer cells via the intrinsic pathway. Interestingly, the supramolecular channel was also shown to disrupt autophagy in cancer cells by causing alkalization of lysosomes – a feature that has been confirmed at the cellular and protein level.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectApoptosisen_US
dc.subjectAutophagyen_US
dc.subjectEnzyme responsiveen_US
dc.subjectIon channelsen_US
dc.subjectSupramolecular chemistryen_US
dc.subject2020en_US
dc.subject2020-SEP-WEEK2en_US
dc.subjectTOC-SEP-2020en_US
dc.titleEsterase‐Activatable Synthetic M+/Cl− Channel Induces Apoptosis and Disrupts Autophagy in Cancer Cellsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemistry—A European Journalen_US
dc.publication.originofpublisherForeignen_US
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