Journal of Medicinal Chemistry · 2015 · 23 citations · 43 references
MedicineMedicinal ChemistryPharmacologyCell SignalingDrug DiscoveryRegenerative MedicineCancer Stem CellsChemokine NetworksChemokine SignalingRenal IschemiaRenal Ischemic InjuryStem Cell MobilizationAdult Hematopoietic Stem CellsChemokine Receptor Cxcr4 AntagonismCirculating Hematopoietic Stem CellsEndothelial Progenitor CellsIschemic Acute Kidney InjuryProgenitor CellsRenoprotective EffectsRenoprotective Therapies
We have discovered a novel series of quinazoline-based CXCR4 antagonists. Of these, compound 19 mobilized CXCR4(+) cell types, including hematopoietic stem cells and endothelial progenitor cells, more efficiently than the marketed 1 (AMD3100) with subcutaneous administration at the same dose (6 mg/kg) in mice. This series of compounds thus provides a set of valuable tools to study diseases mediated by the CXCR4/SDF-1 axis, including myocardial infarction, ischemic stroke, and cancer metastasis. More importantly, treatment with compound 19 significantly lowered levels of blood urea nitrogen and serum creatinine in rats with renal ischemia-reperfusion injury, providing evidence for its therapeutic potential in preventing ischemic acute kidney injury. CXCR4 antagonists such as 19 might also be useful to increase circulating levels of adult stem cells, thereby exerting beneficial effects on damaged and/or inflamed tissues in diseases that currently are not treated by standard approaches.
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Structures of the CXCR4 Chemokine GPCR with Small-Molecule and Cyclic Peptide Antagonists
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Medicine, Hematology, Pharmacology +15