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Development of Stem-Cell-Mobilizing Agents Targeting CXCR4 Receptor for Peripheral Blood Stem Cell Transplantation and Beyond.

Chien-Huang WuJen-Shin SongHsuan-Hao KuanSzu-Huei WuMing-Chen ChouJiing-Jyh JanLun Kelvin TsouYi-Yu KeChiung-Tong ChenKai-Chia YehSing-Yi WangTeng-Kuang YehChen-Tso TsengChen-Lung HuangMine-Hsine WuPo-Chu KuoChia-Jui LeeKak-Shan Shia
Published in: Journal of medicinal chemistry (2018)
The function of the CXCR4/CXCL12 axis accounts for many disease indications, including tissue/nerve regeneration, cancer metastasis, and inflammation. Blocking CXCR4 signaling with its antagonists may lead to moving out CXCR4+ cell types from bone marrow to peripheral circulation. We have discovered a novel series of pyrimidine-based CXCR4 antagonists, a representative (i.e., 16) of which was tolerated at a higher dose and showed better HSC-mobilizing ability at the maximal response dose relative to the approved drug 1 (AMD3100), and thus considered a potential drug candidate for PBSCT indication. Docking compound 16 into the X-ray crystal structure of CXCR4 receptor revealed that it adopted a spider-like conformation striding over both major and minor subpockets. This putative binding mode provides a new insight into CXCR4 receptor-ligand interactions for further structural modifications.
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