Wu Kaiyue, Peng Xiaoyu, Li Yang, Chen Miaojia, Liu Yunfan, Liu Dan, Jiang Lizhi, He Yan, Peng Junmei, Cao Xuan
Institute of Pharmacy and Pharmacology, Hunan Province, Cooperative Innovation Center for Molecular Target New Drug Study, College of Pharmacy, Hengyang Medical School, University of South China, Hengyang, China.
Department of Chemistry, Tsinghua University, Beijing, China.
Chem Biol Drug Des. 2023 Jun;101(6):1335-1347. doi: 10.1111/cbdd.14216. Epub 2023 Mar 5.
Poly (ADP-ribose) polymerase-1 (PARP-1) inhibitors have been successfully applied in the clinical treatment of various cancer. Side effects and drug resistant cases were reported, and more effective PARP-1 inhibitors were required. However, studies on the AD site of PARP-1 inhibitors are currently incomplete. Therefore, to synthesize more potential candidate PARP-1 inhibitors and disclose some AD site SAR of the PARP-1 inhibitors, herein, a series of 2-phenyl-benzimidazole-4-carboxamide derivatives using different saturated nitrogen-contained heterocycles as linker group (6a-6t) have been designed, synthesized, and evaluated PARP-1 inhibitory activity and proliferation inhibitory against BRCA-1 mutant MDA-MB-436 cell line in vitro. The results showed 6b (IC50 = 8.65 nM) exhibited the most PARP-1 enzyme inhibitory activity comparable with Veliparib (IC50 = 15.54 nM) and Olaparib (IC50 = 2.77 nM); 6m exhibited the strongest MDA-MB-436 cell anti-proliferation activity (IC50 = 25.36 ± 6.06 μM) comparable with Olaparib (IC50 = 23.89 ± 3.81 μM). The compounds 6b, 6r, and 6m could be potential candidates for effective PARP-1 inhibitors and valuable for further optimization. The analysis of activity data also showed that the holistically anti-proliferation activity of the 1,4-diazepane group was about~twofold than that of the piperazine group. Meanwhile, the terminal 3-methyl-furanyl group exhibited the most robust PARP-1 inhibitory and anti-proliferation activity. It is hoped that the results could benefitable for further optimization of PARP-1 inhibitors. Furthermore, we note that some compounds (6d,6g,6n,6p,6s) showed poor PARP-1 inhibitory (>500 nM) but relatively good anti-proliferation activity, which indicates the proliferation inhibitory mechanism against MDA-MB-436 cell line was worth investigating in-depth.
聚(ADP - 核糖)聚合酶 -1(PARP -1)抑制剂已成功应用于多种癌症的临床治疗。有副作用和耐药病例的报道,因此需要更有效的PARP -1抑制剂。然而,目前关于PARP -1抑制剂作用位点的研究并不完整。因此,为了合成更多潜在的PARP -1抑制剂候选物并揭示PARP -1抑制剂的一些作用位点构效关系,本文设计、合成了一系列以不同饱和含氮杂环为连接基团的2 - 苯基 - 苯并咪唑 -4 - 甲酰胺衍生物(6a - 6t),并在体外评估了它们对PARP -1的抑制活性以及对BRCA -1突变的MDA - MB -436细胞系的增殖抑制作用。结果表明,6b(IC50 = 8.65 nM)表现出最强的PARP -1酶抑制活性,与维利帕尼(IC50 = 15.54 nM)和奥拉帕尼(IC50 = 2.77 nM)相当;6m表现出最强的MDA - MB -436细胞抗增殖活性(IC50 = 25.36 ± 6.06 μM),与奥拉帕尼(IC50 = 23.89 ± 3.81 μM)相当。化合物6b、6r和6m可能是有效的PARP -1抑制剂的潜在候选物,对进一步优化具有重要价值。活性数据分析还表明,1,4 - 二氮杂环庚烷基团的整体抗增殖活性约为哌嗪基团的两倍。同时,末端的3 - 甲基 - 呋喃基表现出最强的PARP -1抑制和抗增殖活性。希望这些结果有助于PARP -1抑制剂的进一步优化。此外,我们注意到一些化合物(6d、6g、6n、6p、6s)显示出较差的PARP -1抑制作用(>500 nM)但相对较好的抗增殖活性,这表明针对MDA - MB -436细胞系的增殖抑制机制值得深入研究。