Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/11010
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dc.contributor.authorGediya, Piyush-
dc.contributor.authorParikh, Palak K.-
dc.contributor.authorVyas, Vivek K.-
dc.contributor.authorGhate, Manjunath D.-
dc.date.accessioned2022-03-15T09:55:01Z-
dc.date.available2022-03-15T09:55:01Z-
dc.date.issued2021-
dc.identifier.urihttp://10.1.7.192:80/jspui/handle/123456789/11010-
dc.descriptionEuropean Journal of Medicinal Chemistry 216 (2021) 113332en_US
dc.description.abstractHistone deacetylases (HDACs) have been implicated in a number of diseases including cancer, cardiovascular disorders, diabetes mellitus, neurodegenerative disorders and inflammation. For the treatment of epigenetically altered diseases such as cancer, HDAC inhibitors have made a significant progress in terms of development of isoform selective inhibitors. Isoform specific HDAC inhibitors have less adverse events and better safety profile. A HDAC isoform i.e., HDAC2 demonstrated significant role in the development of variety of diseases, mainly involved in the cancer and neurodegenerative disorders. Discovery and development of selective HDAC2 inhibitors have a great potential for the treatment of target diseases. In the present compilation, we have reviewed the role of HDAC2 in progression of cancer and neurodegenerative disorders, and information on the drug development opportunities for selective HDAC2 inhibition.en_US
dc.publisherElsevieren_US
dc.relation.ispartofseriesIPFP0470;-
dc.subjectHistone deacetylases (HDACs)en_US
dc.subjectCanceren_US
dc.subjectNeurodegenerative disordersen_US
dc.subjectHDAC2en_US
dc.subjectEpigenetic mutationen_US
dc.subjectHDAC inhibitorsen_US
dc.titleHistone Deacetylase 2: A Potential Therapeutic Target for Cancer and Neurodegenerative Disordersen_US
dc.typeFaculty Papersen_US
Appears in Collections:Faculty Papers

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