Inhibitors selective for HDAC6 in enzymes and cells
作者:Praveer K. Gupta、Robert C. Reid、Ligong Liu、Andrew J. Lucke、Steve A. Broomfield、Melanie R. Andrews、Matthew J. Sweet、David P. Fairlie
DOI:10.1016/j.bmcl.2010.09.100
日期:2010.12
Histone deacetylase inhibitors with anticancer or anti-inflammatory activity bind to Class I or Class I and II HDAC enzymes. Here we compare selectivity of inhibitors of a Class II HDAC enzyme (HDAC6) and find one that retains high selectivity in macrophages. (C) 2010 Elsevier Ltd. All rights reserved.
An efficient access to both enantiomers of pipecolic acid
作者:Louis A. Watanabe、Saori Haranaka、Binoy Jose、Minoru Yoshida、Tamaki Kato、Mitsuaki Moriguchi、Kenji Soda、Norikazu Nishino
DOI:10.1016/j.tetasy.2005.01.017
日期:2005.2
An efficient and convenient synthesis of bothenantiomers of pipecolicacid has been developed using the intramolecular cyclization of 2-amino-6-bromohexanoic acid under mild conditions.