Discovery of small molecule human FPR1 receptor antagonists-Reference-Cited by-同舟云学术

Discovery of small molecule human FPR1 receptor antagonists

Published:2011-05 Issue:10 Volume:21 Page:2991-2997
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Unitt John,Fagura Malbinder,Phillips Tim,King Sarah,Perry Matthew,Morley Andrew,MacDonald Cathy,Weaver Richard,Christie Jadeen,Barber Simon,Mohammed Rukhsana,Paul Melanie,Cook Andrew,Baxter Andrew

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference26 articles.

1. N-formylpeptide and complement C5a receptors are expressed in liver cells and mediate hepatic acute phase gene regulation.

2. Human platelets exhibit chemotaxis using functional N-formyl peptide receptors

3. International Union of Basic and Clinical Pharmacology. LXXIII. Nomenclature for the Formyl Peptide Receptor (FPR) Family

4. N-formylmethionyl peptides as chemoattractants for leucocytes.

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis and characterization of bis-amide SSE1917 as a microtubule-stabilizing anticancer agent;Bioorganic Chemistry;2024-02

2. Development of potent isoflavone-based formyl peptide receptor 1 (FPR1) antagonists and their effects in gastric cancer cell models;European Journal of Medicinal Chemistry;2023-12

3. A Half‐Century of the Ugi Reaction: Classic Variant;Organic Reactions;2023-05-05

4. Annexin‐A1: The culprit or the solution?;Immunology;2022-03

5. Direct C3-H carbamoylation of quinoxalin-2(1H)-ones with isocyanides enabled by selectfluor II under mild conditions;Tetrahedron Letters;2022-01