Structure–activity relationship of for-l-Met l-Leu-l-Phe-OMe analogues in human neutrophils
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry
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1. Structural Requirements for Molecular Recognition by fMLP Analogs Receptors: Comparative Conformational Analysis of (for-Met-Leu-Phe-OMe) and its Thioamide Analog (for-Met-Leuψ[CSNH]Phe-OMe);Acta Chimica Slovenica;2018-09-15
2. Development of Small Molecule Non-peptide Formyl Peptide Receptor (FPR) Ligands and Molecular Modeling of Their Recognition;Current Medicinal Chemistry;2014-03-31
3. Synthesis and biological evaluation of new active For-Met-Leu-Phe-OMe analogues containing para-substituted Phe residues;Journal of Peptide Science;2012-04-24
4. Discovery of small molecule human FPR1 receptor antagonists;Bioorganic & Medicinal Chemistry Letters;2011-05
5. Gastrin-Releasing Peptide/Neuromedin B Receptor Antagonists PD176252, PD168368, and Related Analogs Are Potent Agonists of Human Formyl-Peptide Receptors;Molecular Pharmacology;2010-10-13
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