孤儿受体
ROR1型
癌症研究
癌症
受体
乳腺癌
癌细胞
医学
药理学
细胞凋亡
受体酪氨酸激酶
肺癌
癌症治疗
酪氨酸
作用机理
酪氨酸激酶
化学
铅化合物
细胞
虚拟筛选
细胞培养
肺癌的治疗
联合疗法
生物
靶向治疗
癌症治疗
细胞毒性
作者
Dongdong Luo (4966684),Xingyang Qiu (11439610),Qingquan Zheng (18874165),Yue Ming (438455),Wencheng Pu (18874168),Ming Ai (6087665),Jianhua He (341366),Yong Peng (255569)
出处
期刊:
[Figshare (United Kingdom)]
日期:2024-06-24
标识
DOI:10.1021/acs.jmedchem.4c00175.s004
摘要
Receptor tyrosine kinase-like orphan receptor 1 (ROR1) is an oncogenic membrane protein in several malignancies and has been considered an attractive target for the treatment of human cancers. In this study, structure-based virtual screening and structure optimization were conducted to identify novel ROR1 inhibitors. Based on hit compound 2, 45 novel ROR1 inhibitors were designed and synthesized, and the detailed structure–activity relationship was investigated. Representative compound 19h potently binds ROR1 with a KD value of 0.10 μM, exhibiting antitumor activity in lung cancer and breast cancer cell lines (IC50: 0.36–1.37 μM). Additionally, a mechanism investigation demonstrated that compound 19h induces the apoptosis of tumor cells. Importantly, compound 19h significantly suppressed tumor growth in a mouse model without obvious toxicity. Overall, this work identified compound 19h as a new ROR1 inhibitor, providing a novel lead compound for the treatment of lung cancer and breast cancer.
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