Laboratory of Molecular Design and Drug Discovery, School of Science, China Pharmaceutical University , 639 Longmian Avenue, Nanjing 211198, China.
School of Science, China Pharmaceutical University , 639 Longmian Avenue, Nanjing 211198, China.
J Med Chem. 2018 Jan 11;61(1):140-157. doi: 10.1021/acs.jmedchem.7b01091. Epub 2017 Dec 19.
Computational and experimental studies were applied to the discovery of a series of novel vascular endothelial growth factor receptor 2 (VEGFR-2) inhibitors. Eight compounds exhibited nanomolar IC values against VEGFR-2, and compounds 6, 19, 22, and 23 showed potent antiproliferative effects against several cell lines. Particularly, compound 23 behaved better than FDA approved drugs, sorafenib and sunitinib, in antiproliferative activity against cell lines related to all nine tumor types tested (GI values), and it was better or comparable in safety (LC values). Compound 23 even demonstrated a high potency on one of the drug-resistant cell lines (NCI/ADR-RES) responsible for ovarian cancer and cell lines contributing to prostate cancer, regarded as one of the VEGF/VEGFR pathway drug-resistant tumors. This compound is likely a promising candidate for the treatment of leukemia, non-small cell lung cancer (NSCLC), colon cancer, ovarian cancer, and breast cancer with a suitable balance of both efficacy and safety.
计算和实验研究被应用于一系列新型血管内皮生长因子受体 2(VEGFR-2)抑制剂的发现。八种化合物对 VEGFR-2 表现出纳摩尔 IC 值,化合物 6、19、22 和 23 对几种细胞系表现出强大的抗增殖作用。特别是化合物 23 在抗增殖活性方面优于 FDA 批准的药物索拉非尼和舒尼替尼,对测试的所有九种肿瘤类型相关的细胞系(GI 值),并且在安全性(LC 值)方面更好或相当。化合物 23 甚至对一种耐药细胞系(NCI/ADR-RES)表现出高活性,该细胞系负责卵巢癌和前列腺癌细胞系,被认为是 VEGF/VEGFR 通路耐药肿瘤之一。该化合物可能是治疗白血病、非小细胞肺癌(NSCLC)、结肠癌、卵巢癌和乳腺癌的有前途的候选药物,具有疗效和安全性的适当平衡。