Medicinal Chemistry, AstraZeneca R&D, CVGI iMed, Pepparedsleden 1, SE-431 83 Mölndal, Sweden.
Bioorg Med Chem Lett. 2012 Nov 1;22(21):6671-6. doi: 10.1016/j.bmcl.2012.08.102. Epub 2012 Sep 6.
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.
基于结构的原始片段进化导致发现了 4-[2-羟乙基(1-萘基甲基)氨基]-6-[(2S)-2-甲基吗啉-4-基]-1H-嘧啶-2-酮,(S)-21,一种强效、选择性的磷酸肌醇 3-激酶 (PI3K) p110β 同工型抑制剂,具有良好的体内抗血小板作用。尽管具有抗血小板作用,但 (S)-21 并未显著延长犬的出血时间。此外,由于其对 p110α 的选择性增强,(S)-21 不会在大鼠中引起任何胰岛素抵抗。