| Literature DB >> 23010262 |
Fabrizio Giordanetto1, Andreas Wållberg, Saswati Ghosal, Tommy Iliefski, Johan Cassel, Zhong-Qing Yuan, Henrik von Wachenfeldt, Søren M Andersen, Tord Inghardt, Anders Tunek, Sven Nylander.
Abstract
Structure-based evolution of the original fragment leads resulted in the identification of 4-[2-hydroxyethyl(1-naphthylmethyl)amino]-6-[(2S)-2-methylmorpholin-4-yl]-1H-pyrimidin-2-one, (S)-21, a potent, selective phosphoinositide 3-kinases (PI3K) p110β isoform inhibitor with favourable in vivo antiplatelet effect. Despite its antiplatelet action, (S)-21 did not significantly increase bleeding time in dogs. Additionally, due to its enhanced selectivity over p110α, (S)-21 did not induce any insulin resistance in rats.Entities:
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Year: 2012 PMID: 23010262 DOI: 10.1016/j.bmcl.2012.08.102
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823