Structure-Based Design of 3-(4-Aryl-1H-1,2,3-triazol-1-yl)-Biphenyl Derivatives as P2Y14 Receptor Antagonists

详细信息    查看全文

• 作者：Anna Junker ; Ramachandran Balasubramanian ; Antonella Ciancetta ; Elisa Uliassi ; Evgeny Kiselev ; Chiara Martiriggiano ; Kevin Trujillo ; Giorgi Mtchedlidze ; Leah Birdwell ; Kyle A. Brown ; T. Kendall Harden ; Kenneth A. Jacobson
• 刊名：Journal of Medicinal Chemistry
• 出版年：2016
• 出版时间：July 14, 2016
• 年：2016
• 卷：59
• 期：13
• 页码：6149-6168
• 全文大小：853K
• 年卷期：0
• ISSN：1520-4804

文摘

UDP and UDP-glucose activate the P2Y₁₄ receptor (P2Y₁₄R) to modulate processes related to inflammation, diabetes, and asthma. A computational pipeline suggested alternatives to naphthalene of a previously reported P2Y₁₄R antagonist (3, PPTN) using docking and molecular dynamics simulations on a hP2Y₁₄R homology model based on P2Y₁₂R structures. By reevaluating the binding of 3 to P2Y₁₄R computationally, two alternatives, i.e., alkynyl and triazolyl derivatives, were identified. Improved synthesis of fluorescent antagonist 4 enabled affinity quantification (IC₅₀s, nM) using flow cytometry of P2Y₁₄R-expressing CHO cells. p-F₃C-phenyl-triazole 65 (32) was more potent than a corresponding alkyne 11. Thus, additional triazolyl derivatives were prepared, as guided by docking simulations, with nonpolar aryl substituents favored. Although triazoles were less potent than 3 (6), simpler synthesis facilitated further structural optimization. Additionally, relative P2Y₁₄R affinities agreed with predicted binding of alkynyl and triazole analogues. These triazoles, designed through a structure-based approach, can be assessed in disease models.