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.