(R)-CE3F4 是一种有效、选择性的 cAMP 活化交换蛋白 1 (Epac1) 抑制剂，IC50 值为 4.2 μM，对其选择性是对 Epac2 (IC50，44 μM) 的 10 倍。(R)-CE3F4 的活性高于 racemic CE3F4 和 (S)-CE3F4。
CAS：1593478-56-8
分子式：C11H10Br2FNO
分子量：351.01
纯度：98%
存储：Store at -20°C

Background:

(R)-CE3F4 is a potent and selective inhibitor of exchange protein directly activated by cAMP isoform 1 (Epac1), with an IC50 of 4.2 μM, with 10-fold selectivity for Epac1 over Epac2 (IC50, 44 μM). (R)-CE3F4 is more potent than racemic CE3F4 and (S)-CE3F4[1].

[1]. Courilleau D, et al. The (R)-enantiomer of CE3F4 is a preferential inhibitor of human exchange protein directly activated by cyclic AMP isoform 1 (Epac1). Biochem Biophys Res Commun. 2013 Oct 25;440(3):443-8.