| Literature DB >> 29608300 |
Haruka Sekiguchi1, Tomoko Kuroyanagi1, David Rhainds2,3, Kazuya Kobayashi4, Yuka Kobayashi1, Hiroaki Ohno1, Nikolaus Heveker2,3, Kenichi Akaji4, Nobutaka Fujii1, Shinya Oishi1.
Abstract
The atypical chemokine receptor 3 (ACKR3)/CXC chemokine receptor 7 (CXCR7) recognizes stromal cell-derived factor 1 (SDF-1)/CXCL12 and is involved in a number of physiological and pathological processes. Here, we investigated the SAR of the component amino acids in an ACKR3-selective ligand, FC313 [ cyclo(-d-Tyr-l-Arg-l-MeArg-l-Nal(2)-l-Pro-)], for the development of highly active ACKR3 ligands. Notably, modification at the l-Pro position with a bulky hydrophobic side chain led to improved bioactivity toward ACKR3.Entities:
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Year: 2018 PMID: 29608300 DOI: 10.1021/acs.jmedchem.8b00336
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446