GPR40/FFAR1 modulator 1

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

GPR40/FFAR1 modulator 1 是 Gq 偶联游离脂肪酸受体 1 (GPR40/FFAR1) 的激动剂和变构调节剂。

GPR40/FFAR1 modulator 1 is an agonist and an allosteric modulator for Gq-coupled free fatty acid receptor 1 (GPR40/FFAR1).(In Vitro):The long-chain fatty acid receptor FFAR1/GPR40 binds agonists in both an interhelical site between the extracellular segments of transmembrane helix (TM)-III and TM-IV and a lipid-exposed groove between the intracellular segments of these helices. Molecular dynamics simulations of FFAR1 with agonist removed demonstrated a major rearrangement of the polar and charged anchor point residues for the carboxylic acid moiety of the agonist in the interhelical site, which was associated with closure of a neighboring, solvent-exposed pocket between the extracellular poles of TM-I, TM-II, and TM-VII. A synthetic compound designed to bind in this pocket, and thereby prevent its closure, was identified through structure-based virtual screening and shown to function both as an agonist and as an allosteric modulator of receptor activation.

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Cell Cycle/DNA Damage

GPR

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874755-26-7

389.415

C21H19N5O3

>98% (HPLC)

In Vitro:?DMSO : 31.25 mg/mL (80.25 mM)

Cc1ccccc1Nc1nc(N)nc(COc2ccc3c(C)cc(=O)oc3c2)n1

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(-20℃)

With Ice Pack

≥ 2 years