Literature DB >> 29608300

Structure-Activity Relationship Study of Cyclic Pentapeptide Ligands for Atypical Chemokine Receptor 3 (ACKR3).

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.

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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


  3 in total

Review 1.  CXCR7 Targeting and Its Major Disease Relevance.

Authors:  Chuan Wang; Weilin Chen; Jianzhong Shen
Journal:  Front Pharmacol       Date:  2018-06-21       Impact factor: 5.810

2.  GPCR Pharmacological Profiling of Aaptamine from the Philippine Sponge Stylissa sp. Extends Its Therapeutic Potential for Noncommunicable Diseases.

Authors:  Harmie Luyao; Hendrik Luesch; Mylene Uy
Journal:  Molecules       Date:  2021-09-16       Impact factor: 4.411

Review 3.  Advances in CXCR7 Modulators.

Authors:  Nicole Lounsbury
Journal:  Pharmaceuticals (Basel)       Date:  2020-02-21
  3 in total

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