1. Academic Validation
  2. Design, synthesis, and biological evaluation of N-(pyridin-3-yl)pyrimidin-4-amine analogues as novel cyclin-dependent kinase 2 inhibitors for cancer therapy

Design, synthesis, and biological evaluation of N-(pyridin-3-yl)pyrimidin-4-amine analogues as novel cyclin-dependent kinase 2 inhibitors for cancer therapy

  • Bioorg Chem. 2024 Feb:143:107019. doi: 10.1016/j.bioorg.2023.107019.
Wen-Bin Zeng 1 Tang-Yang Ji 1 Yan-Ting Zhang 1 Yu-Feng Ma 1 Rou Li 1 Wen-Wei You 1 Pei-Liang Zhao 2
Affiliations

Affiliations

  • 1 Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Science, Southern Medical University, Guangzhou 510515, PR China.
  • 2 Guangdong Provincial Key Laboratory of New Drug Screening, School of Pharmaceutical Science, Southern Medical University, Guangzhou 510515, PR China. Electronic address: plzhao@smu.edu.cn.
Abstract

The discovery and development of CDK2 inhibitors has currently been validated as a hot topic in Cancer therapy. Herein, a series of novel N-(pyridin-3-yl)pyrimidin-4-amine derivatives were designed and synthesized as potent CDK2 inhibitors. Among them, the most promising compound 7l presented a broad antiproliferative efficacy toward diverse Cancer cells MV4-11, HT-29, MCF-7, and HeLa with IC50 values of 0.83, 2.12, 3.12, and 8.61 μM, respectively, which were comparable to that of Palbociclib and AZD5438. Interestingly, these compounds were less toxic on normal embryonic kidney cells HEK293 with high selectivity index. Further mechanistic studies indicated 7l caused cell cycle arrest and Apoptosis on HeLa cells in a concentration-dependent manner. Moreover, 7l manifested potent and similar CDK2/cyclin A2 nhibitory activity to AZD5438 with an IC50 of 64.42 nM. These findings revealed that 7l could serve as ahighly promisingscaffoldfor CDK2 inhibitors as potential Anticancer agents and functional probes.

Keywords

Antiproliferative activity; CDK2 inhibitor; N-(pyridin-3-yl)pyrimidin-4-amine.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-157516
    98.64%, CDK2 Inhibitor
    CDK