528111

PI 3-Kα Inhibitor IV

The PI 3-Kα Inhibitor IV, also referenced under CAS 1188890-32-5, controls the biological activity of PI 3-Kα. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

• 别名: PI 3-Kα Inhibitor IV, 3-(4-Morpholinothieno[3,2-d]pyrimidin-2-yl)phenol, 2HCl, PI 3-K Inhibitor IV
• 经验公式（希尔记法）: C₁₆H₁₅N₃O₂S · 2HCl
• CAS号: 1188890-32-5
• 分子量: 386.30
• MDL编号: MFCD24368998
• UNSPSC代码: 12352200
• NACRES: NA.77

属性

• 质量水平: 100
• 方案: ≥95% (HPLC)
• 表单: solid
• 制造商/商品名称: Calbiochem^®
• 储存条件: OK to freeze; desiccated (hygroscopic); protect from light
• 颜色: off-white
• 溶解性: DMSO: 10 mg/mL
• 运输: ambient
• 储存温度: 2-8°C
• SMILES字符串: [s]1c2c(nc(nc2N4CCOCC4)c3cc(ccc3)O)cc1.Cl.Cl
• InChI key: WPSXNMUJNQUDND-UHFFFAOYSA-N

说明

一般描述

A cell-permeable morpholino-thienopyrimidine compound that acts as a potent and isoform-selective inhibitor of PI 3-kinases (IC₅₀ = 2 nM, 16 nM, 660 nM, and 220 nM for p110α, p110β p110γ, and PI 3-K C2β, respectively) and inhibits non-PI 3-K kinases only at much higher concentrations (IC₅₀ ≥3.4 µM for Cdk2/E, KDR, PKA, and PKCα). Shown to inhibit cell proliferation (IC₅₀ = 580 nM) and serum-stimulated Akt phosphorylation (IC₅₀<3 µM) in A375 melanoma cells.

生化/生理作用

Cell permeable: yes

Primary Target
PI 3-Kα

Product does not compete with ATP.

Reversible: no

Target IC₅₀: 2 nM, 16 nM, 660 nM, and 220 nM for p110α, p110β p110γ, and PI 3-K C2β, respectively

包装

Packaged under inert gas

警告

Toxicity: Irritant (B)

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

Hayakawa, M., et al. 2006. Bioorg. Med. Chem.14, 6847.

法律信息

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

安全信息

• 储存分类代码: 11 - Combustible Solids
• WGK: WGK 1
• 闪点(°F): Not applicable
• 闪点(°C): Not applicable