Discovery of potent, isoform-selective inhibitors of histone deacetylase containing chiral heterocyclic capping groups and a N-(2-aminophenyl)benzamide binding unit. (2013)
Attributed to:
TET protein function in conversion of 5mC to 5hmC during cell cycle entry
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1021/jm400634n
PubMed Identifier: 23829483
Publication URI: http://europepmc.org/abstract/MED/23829483
Type: Journal Article/Review
Volume: 56
Parent Publication: Journal of medicinal chemistry
Issue: 15
ISSN: 0022-2623