化学
脚手架
班级(哲学)
激酶
药理学
癌症研究
立体化学
生物化学
组合化学
计算机科学
医学
生物
生物医学工程
人工智能
作者
Zhicheng Xie,Bing Wu,Yingqiang Liu,Wenming Ren,Linjiang Tong,Caigui Xiang,Aihuan Wei,Yuanzhuo Gao,Limin Zeng,Hua Xie,Wei Tang,Youhong Hu
标识
DOI:10.1021/acs.jmedchem.9b01912
摘要
Colony-stimulating factor 1 receptor (CSF-1R) is involved in inflammatory disorders as well as in many types of cancer. Based on high-throughput screening and docking results, we performed a detailed structure–activity-relationship study, leading to the discovery of a new series of compounds with nanomolar IC50 values against CSF-1R without the inhibition of fibroblast growth factor receptors. One of the most promising hits, compound 29, potently inhibited CSF-1R kinase with an IC50 value of 0.7 nM, while it showed no inhibition to the same family member FMS-like tyrosine kinase 3. Compound 29 displayed excellent anti-inflammatory effects against RAW264.7 macrophages indicated by significant inhibition against the activation of the CSF-1R pathway with low cytotoxicity. In addition, compound 29 exhibited strong in vivo anti-inflammatory efficacy alongside favorable drug characteristics. This novel compound 29 may serve as a new drug candidate with promising applications in inflammatory disorders.
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