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BRD3731
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
BRD3731图片
规格:98%
分子量:377.52
包装与价格:
包装价格(元)
5mg电议
10mg电议
50mg电议
100mg电议

产品介绍
BRD3731 是一种选择性的 GSK3β 抑制剂,抑制 GSK3β 和 GSK3α 的 IC50 值分别为 15 nM 和 215 nM。BRD3731 有潜力用于创伤后应激障碍 (PTSD) 精神障碍、糖尿病和神经退行性障碍的研究。
货号:ajcx34584
CAS:2056262-07-6
分子式:C24H31N3O
分子量:377.52
溶解度:DMSO : 50 mg/mL (132.44 mM; Need ultrasonic)
纯度:98%
存储:Store at -20°C
库存:现货

Background:

BRD3731 is a selective GSK3β inhibitor, with IC50s of 15 nM and 215 nM for GSK3β and GSK3α, respectively. BRD3731 is potentail for the research of post-traumatic stress disorder (PTSD), psychiatric disorder, diabetes, and neurodegenerative disorders[1].

BRD3731 is a GSK3β- selective inhibitor extracted from patent US20160375006A1, compound example 272[1].BRD3731 (1-10 μM; 24 hours) inhibits the phosphorylation of CRMP2 in SH-SY5Y cells[1].BRD3731 (20 μM; 24 hours) decreases β-catenin S33/37/T41 phosphorylation and induces β-catenin S675 phosphorylation in HL-60 cells[2].BRD3731 (10-20 μM; 7-10 days) impairs colony formation in TF-1 and increases colony forming ability in the MV4-11 cell line[2]

[1]. Edward Scolnick, et al. Uses of paralog-selective inhibitors of gsk3 kinases. US20160375006A1.
[2]. Wagner FF, et, al. Exploiting an Asp-Glu "switch" in glycogen synthase kinase 3 to design paralog-selective inhibitors for use in acute myeloid leukemia. Sci Transl Med. 2018 Mar 7;10(431):eaam8460.