细胞周期蛋白依赖激酶
化学
激酶
选择性
小分子
体外
IC50型
结构-活动关系
药理学
细胞周期
生物化学
细胞
生物
催化作用
作者
Peter L. Toogood,Patricia J. Harvey,Joseph T. Repine,D. Sheehan,Scott N. Vanderwel,Hairong Zhou,Paul R. Keller,Dennis J. McNamara,Debra Sherry,Tong Zhu,Joanne Brodfuehrer,Chung Sik Choi,Mark R. Barvian,David W. Fry
摘要
A pharmacological approach to inhibition of cyclin-dependent kinases 4 and 6 (Cdk4/6) using highly selective small molecule inhibitors has the potential to provide novel cancer therapies for clinical use. Achieving high levels of selectivity for Cdk4/6, versus other ATP-dependent kinases, presents a significant challenge. The pyrido[2,3-d]pyrimidin-7-one template provides an effective platform for the inhibition of a broad cross-section of kinases, including Cdks. It is now demonstrated that the modification of pyrido[2,3-d]pyrimidin-7-ones to include a 2-aminopyridine side chain at the C2-position provides inhibitors with exquisite selectivity for Cdk4/6 in vitro. This selectivity profile is recapitulated in cells where the most selective inhibitors create a G1 block at concentrations up to 100-fold the IC50 for cell proliferation. On the basis of its selectivity profile and pharmacokinetic profile, compound 43 (PD 0332991) was identified as a drug candidate for the treatment of cancer.
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