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CAS: 347323-96-0
分子式: C22H17N3OS
分子量: 371.45
英文名称: 
itx3
2-[(2,5-dimethyl-1-phenyl-1h-pyrrol-3-yl)methylene]-thiazolo[3,2-a]benzimidazol-3(2h)-one
用途: ITX3是无毒性的TrioN(N-terminal GEF domain of the multidomain Trio protein)抑制剂,IC50为76 uM,能体外抑制TrioN刺激的RhoG交换。
推荐供应商
货号品牌产品名称规格包装、参考价格详情
I879442MACKLINITX3 98%485元/5mg;   891元/10mg;   展开
储存:2-8℃
状态:粉末
I1411Sigma-AldrichITX3≥98% (HPLC)1044.37元/5 MG;   3816.61元/25 MG;   展开

产品说明

包装

5, 25 mg in glass bottle

生化/生理作用

ITX3 is a specific inhibitor of endogenous TrioN activity acting on the GEF domain and selective cell active inhibitor of the Trio/RhoG/Rac1 pathway. The compound is active in whole cell assay where it inhibits the formation of TrioN-dependent cell structures. ITX3 appears to be specific for TrioN inhibition rather than other RhoGEFs.

特点和优势

This compound is a featured product for Cyclic Nucleotide research. Click here to discover more featured Cyclic Nucleotide products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the GTP Binding Proteins (Low Molecular Weight) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

基本信息

经验(实验)分子式C22H17N3OS
分子量371.45
MDL编号MFCD02629172
PubChem化学物质编号329815351
NACRESNA.77

产品性质

质量水平100
测定≥98% (HPLC)
形式powder
溶解性DMSO: ≥4 mg/mL
储存温度room temp
SMILES stringCc1cc(\C=C2\Sc3nc4ccccc4n3C2=O)c(C)n1-c5ccccc5
InChI1S/C22H17N3OS/c1-14-12-16(15(2)24(14)17-8-4-3-5-9-17)13-20-21(26)25-19-11-7-6-10-18(19)23-22(25)27-20/h3-13H,1-2H3/b20-13+
InChI keySJMYMKPBODEZSH-DEDYPNTBSA-N

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
645890Sigma-AldrichTrio N-Terminal RhoGEF Domain Inhibitor, ITX3-CAS 347323-96-0-CalbiochemThe Trio N-Terminal RhoGEF Domain Inhibitor, ITX3, also referenced under CAS 347323-96-0, controls the biological activity of Trio N-Terminal RhoGEF Domain. This small molecule/inhibitor is primarily 1954.93元/10 MG;   展开

产品说明

一般描述

A cell-permeable thiazolo-benzimidazolone compound that inhibits Trio N-terminal RhoGEF domain- (TrioN) mediated RhoG activation (IC50 = 76 µM) and effectively reduces cellular Rac activation (by 80% with 50 µM ITX3) caused by TrioN, but not GEF337 (RhoA GEF), Tiam1 (Rac GEF), or Vav2 (Rac1/RhoA/Cdc42 GEF), overexpression in HEK293T cells. Culture treatment of ITX at 100 µM is shown to reduce NGF-induced neurite outgrowth of rat PC12 pheochromocytoma cells by 50% and block the formation of multinucleated myotubes by 78% in C2C12 mouse myoblasts cultures induced for differentiation, while the differentiation-associated Myogenin and Troponin T expressions in Trio knock-down C2C12 cells are not affected by ITX at the same concentration.

包装

Packaged under inert gas

警告

Toxicity: Standard Handling (A)

重悬

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

其他说明

Bouquier, N., et al. 2009. Chem. Biol.16, 657.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

基本信息

经验(实验)分子式C22H17N3OS
分子量371.45
MDL编号MFCD02629172

产品性质

质量水平100
测定≥95% (HPLC)
形式solid
manufacturer/tradenameCalbiochem®
储存条件OK to freeze
protect from light
颜色 yellow
溶解性DMSO: 2 mg/mL
运输ambient
储存温度2-8℃

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
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