Author
Keywords
Abstract

Bromodomain and plant homeodomain (PHD) finger containing protein 1 (BRPF1) is a member of subfamily İV of the human bromodomains. Experimental evidence suggests that BRPF1 is involved in leukemia. In a previous high-throughput docking campaign we identified several chemotypes targeting the BRPF1 bromodomain. Here, pharmacophore searches using the binding modes of two of these chemotypes resulted in two new series of ligands of the BRPF1 bromodomain. The 2,3-dioxo-quinoxaline 21 exhibits a 2-μM affinity for the BRPF1 bromodomain in two different competition binding assays, and more than 100-fold selectivity for BRPF1 against other members of subfamily İV and representatives of other subfamilies. Cellular activity is confirmed by a viability assay in a leukemia cell line. Isothermal titration calorimetry measurements reveal enthalpy-driven binding for compounds 21, 26 (KD = 3 μM), and the 2,4-dimethyl-oxazole derivative 42 (KD = 10μM). Multiple molecular dynamics simulations and a dozen co-crystal structures at high resolution provide useful information for further optimization of affinity for the BRPF1 bromodomain.

Year of Publication
2018
Journal
European Journal of Medicinal Chemistry
Start Page
337
Issue
155
Number of Pages
337-352
Date Published
May 23 2018
Type of Article
Research Article
ISSN Number
0223-5234
URL
https://www.sciencedirect.com/science/article/pii/S0223523418304501
DOI
10.1016/j.ejmech.2018.05.037
Alternate Journal
Eur. J. Med. Chem.
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