| Literature DB >> 21334896 |
Weiping Tang1, Tuoping Luo, Edward F Greenberg, James E Bradner, Stuart L Schreiber.
Abstract
We have developed an efficient method for synthesizing candidate histone deacetylase (HDAC) inhibitors in 96-well plates, which are used directly in high-throughput screening. We selected building blocks having hydrazide, aldehyde and hydroxamic acid functionalities. The hydrazides were coupled with different aldehydes in DMSO. The resulting products have the previously identified 'cap/linker/biasing element' structure known to favor inhibition of HDACs. These compounds were assayed without further purification. HDAC8-selective inhibitors were discovered from this novel collection of compounds.Entities:
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Year: 2011 PMID: 21334896 PMCID: PMC3403710 DOI: 10.1016/j.bmcl.2011.01.134
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823