20立方厘米
C-C趋化因子受体6型
趋化性
结直肠癌
癌症研究
苯并呋喃
外周血单个核细胞
细胞毒性T细胞
药理学
癌症
化学
免疫学
医学
趋化因子
免疫系统
体外
生物化学
立体化学
内科学
受体
趋化因子受体
作者
F. Barbieri,Maria Grazia Martina,Carmine Giorgio,María Chiara,Marika Allodi,Joseph Durante,Simona Bertoni,Marco Radi
标识
DOI:10.1002/cmdc.202400389
摘要
The correlation between the CCL20/CCR6 axis and autoimmune and non-autoimmune disorders is widely recognized. Inhibition of the CCL20-dependent cell migration represents therefore a promising approach for the treatment of many diseases, such as inflammatory bowel diseases and colorectal cancer. We report herein our efforts to explore the biologically relevant chemical space around the benzofuran scaffold of MR120, a modulator of the CCL20/CCR6 axis previously discovered by our group. A functional screening allowed us to identify C4 and C5-substituted derivatives as the most effective inhibitors of the CCL20-induced chemotaxis of human peripheral blood mononuclear cells (PBMC). Moreover, selected compounds (16 e and 24 b) also proved to potently inhibit the growth of different colon cancer cell lines, with cytotoxic/cytostatic and antiproliferative activity.
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