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5-(2-Benzothiazolyl)-3-ethyl-2-[2-(methylphenylamino)ethenyl]-1-phenyl-1H-benzimidazolium iodide_分子结构_CAS_681281-88-9)
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5-(2-Benzothiazolyl)-3-ethyl-2-[2-(methylphenylamino)ethenyl]-1-phenyl-1H-benzimidazolium iodide

产品号 B2311 公司名称 Sigma Aldrich
CAS号 681281-88-9 公司网站 http://www.sigmaaldrich.com
分子式 C31H27IN4S 电 话 1-800-521-8956
分子量 614.54235 传 真
纯 度 ≥98% (HPLC) 电子邮件
保 存 Chembase数据库ID: 153854

产品价格信息

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产品别名

标题
5-(2-Benzothiazolyl)-3-ethyl-2-[2-(methylphenylamino)ethenyl]-1-phenyl-1H-benzimidazolium iodide
IUPAC标准名
5-(1,3-benzothiazol-2-yl)-3-ethyl-2-{2-[methyl(phenyl)amino]ethenyl}-1-phenyl-1H-1,3-benzodiazol-3-ium iodide
IUPAC传统名
6-(1,3-benzothiazol-2-yl)-1-ethyl-2-{2-[methyl(phenyl)amino]ethenyl}-3-phenyl-1,3-benzodiazol-1-ium iodide

产品登记号

CAS号 681281-88-9
PubChem SID 24724416
MDL号 MFCD00570739

产品性质

Empirical Formula (Hill Notation) C31H27IN4S
纯度 ≥98% (HPLC)
外观 orange solid
溶解度 DMSO: ≥10 mg/mL
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H315-H319-H335
欧盟危险性物质标志 刺激性(Irritant) 刺激性(Irritant) (Xi)
MSDS下载 下载链接
个人保护装置 dust mask type N95 (US), Eyeshields, Gloves
GHS警示性声明 P261-P305 + P351 + P338
危险公开号 36/37/38
安全公开号 26-36
保存温度 2-8°C
德国WGK号 3

产品详细信息

详细说明 (English)
Biochem/physiol Actions
5-(2-Benzothiazolyl)-3-ethyl-2-[2-(methylphenylamino)-ethenyl]-1-phenyl-1H-benzimidazolium or Akt Inhibitor IV is a cell-permeable benzimidazole compound that inhibits Akt phosphorylation/activation by targeting the ATP binding site of a kinase upstream of Akt, but downstream of PI3K. Shown to block Akt-mediated FOXO1a nuclear export (IC50 = 0.625μM) and cell proliferation (IC50 < 1.25μM) in 786-O cells. Unlike phosphatidylinositol analog-based Akt inhibitors, this inhibitor does not affect PI3K.
详细说明 (简体中文)
Biochem/physiol Actions
5-(2-Benzothiazolyl)-3-ethyl-2-[2-(methylphenylamino)-ethenyl]-1-phenyl-1H-benzimidazolium or Akt Inhibitor IV is a cell-permeable benzimidazole compound that inhibits Akt phosphorylation/activation by targeting the ATP binding site of a kinase upstream of Akt, but downstream of PI3K. Shown to block Akt-mediated FOXO1a nuclear export (IC50 = 0.625μM) and cell proliferation (IC50 < 1.25μM) in 786-O cells. Unlike phosphatidylinositol analog-based Akt inhibitors, this inhibitor does not affect PI3K.

参考文献