| Literature DB >> 29314840 |
Chien-Huang Wu1, Jen-Shin Song1, Hsuan-Hao Kuan1, Szu-Huei Wu1, Ming-Chen Chou1, Jiing-Jyh Jan1, Lun K Tsou1, Yi-Yu Ke1, Chiung-Tong Chen1, Kai-Chia Yeh1, Sing-Yi Wang1, Teng-Kuang Yeh1, Chen-Tso Tseng1, Chen-Lung Huang1, Mine-Hsine Wu1, Po-Chu Kuo1, Chia-Jui Lee1, Kak-Shan Shia1.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2018 PMID: 29314840 DOI: 10.1021/acs.jmedchem.7b01322
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446