Synthesis and structure based optimization of 2-(4-phenoxybenzoyl)-5-hydroxyindole as a novel CaMKII inhibitor.
Masafumi Komiya, Shigehiro Asano, Nobuyuki Koike, Erina Koga, Junetsu Igarashi, Shogo Nakatani, Yoshiaki Isobe
Index: Bioorg. Med. Chem. 20(23) , 6840-7, (2012)
Full Text: HTML
Abstract
Based on 2-(4-phenoxybenzoyl)-5-hydroxyindole (2), a novel structural class of CaMKII inhibitors were synthesized and further optimized. The strong acidity of the hydroxyl group and the lipophilic group at the 4 and 6-positions were found to be necessary for strong CaMKII inhibition. Compound 25 was identified as a promising compound with 50-fold more potent inhibitory activity for CaMKII than 2. Compound 25 also showed high selectivity for CaMKII over off-target kinases.Copyright © 2012 Elsevier Ltd. All rights reserved.
Related Compounds
Related Articles:
2014-10-01
[Forensic Sci. Int. 243 , 117-25, (2014)]
2016-03-23
[Talanta 129 , 155-64, (2014)]
2016-04-01
[Talanta 150 , 568-76, (2016)]
2010-02-01
[Chirality 22(2) , 258-61, (2010)]
2011-01-01
[Yakugaku Zasshi 131(8) , 1207-11, (2011)]