Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1178
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dc.contributor.authorKULKARNI, AMOGHen_US
dc.contributor.authorSHARMA, AJAY KUMARen_US
dc.contributor.authorCHAKRAPANI, HARINATHen_US
dc.date.accessioned2018-10-04T03:31:09Z
dc.date.available2018-10-04T03:31:09Z
dc.date.issued2018-09en_US
dc.identifier.citationIUBMB Life. Vol. 70 (9).en_US
dc.identifier.issn1521-6551en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1178
dc.identifier.urihttps://doi.org/10.1002/iub.1867en_US
dc.description.abstractThe emergence of drug resistance has posed a major challenge to treatment of tuberculosis worldwide. The new drug candidates in the pipeline are few and therefore there is an urgent need to develop antimycobacterials with novel mechanisms of action. Maintenance of redox homeostasis is integral to mycobacterial survival and growth. Therefore, perturbation of this equilibrium can result in irreversible stress induction and inhibition of growth. Herein, we review a number of small molecules that have either been designed to induce redox stress or were found to do so after their discovery. A number of these small molecules are quite effective against drug-resistant mycobacterial strains and thus offer scope for exploration of potentially new mechanism of action. The progress in redox-guided antimycobacterial compounds and the challenges towards clinical applications are reviewed. (c) 2018 IUBMB Life, 70(9):826-835, 2018en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectOxidative stressen_US
dc.subjectThiolsen_US
dc.subjectRedox homeostasisen_US
dc.subjectAntioxidantsen_US
dc.subjectTOC-SEP-2018en_US
dc.subject2018en_US
dc.titleRedox-guided small molecule antimycobacterialsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleIUBMB Lifeen_US
dc.publication.originofpublisherForeignen_US
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