BRD3731
目录号: PL02683 纯度: ≥98%
CAS No. :2056262-07-6
商品编号 规格 价格 会员价 是否有货 数量
PL02683-5mg 5mg ¥5192.73 请登录
PL02683-10mg 10mg ¥8654.55 请登录
PL02683-50mg 50mg ¥24109.09 请登录
PL02683-100mg 100mg ¥36472.73 请登录
PL02683-200mg 200mg 询价 询价
PL02683-500mg 500mg 询价 询价
PL02683-10mM*1mLinDMSO 10mM*1mLinDMSO ¥5712.00 请登录
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
中文名称
BRD3731
中文别名
5H-PYRAZOLO[3,4-B]QUINOLIN-5-ONE, 3-(2,2-DIMETHYLPROPYL)-1,2,4,6,7,8-HEXAHYDRO-4,7,7-TRIMETHYL-4-PHE;化合物 BRD3731
英文名称
BRD3731
英文别名
BRD3731;(4S)-3-(2,2-Dimethylpropyl)-4,7,7-trimethyl-4-phenyl-2,6,8,9-tetrahydropyrazolo[3,4-b]quinolin-5-one;CID 135567205
Cas No.
2056262-07-6
分子式
C24H31N3O
分子量
377.52
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
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。
生物活性
BRD3731 is a selective GSK3β inhibitor, with IC 50 s 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.
性状
Solid
IC50 & Target[1][2]
GSK-3β 15 nM (IC50) GSK-3α 215 nM (IC
体外研究(In Vitro)
BRD3731 is a GSK3β- selective inhibitor extracted from patent US20160375006A1, compound example 272.
BRD3731 (1-10 μM; 24 hours) inhibits the phosphorylation of CRMP2 in SH-SY5Y cells.
BRD3731 (20 μM; 24 hours) decreases β-catenin S33/37/T41 phosphorylation and induces β-catenin S675 phosphorylation in HL-60 cells.
BRD3731 (10-20 μM; 7-10 days) impairs colony formation in TF-1 and increases colony forming ability in the MV4-11 cell line has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[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.
溶解度数据
In Vitro: DMSO : 50 mg/mL (132.44 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2