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merck millipore,默克密理博,124018,Akt Inhibitor VIII, Isozyme-Selective, Akti-1/2 - CAS 612847-09-3 - Calbiochem
产品名称:Akt Inhibitor VIII, Isozyme-Selective, Akti-1/2 - CAS 612847-09-3 - Calbiochem
产品型号:124018
The Akt Inhibitor VIII, Isozyme-Selective, Akti-1/2, also referenced under CAS 612847-09-3, controls the biological activity of Akt. This small molecule/inhibitor is primarily used for Phosphorylation More>>
merck millipore,默克密理博,124018,Akt Inhibitor VIII, Isozyme-Selective, Akti-1/2 - CAS 612847-09-3 - Calbiochem
- 产品介绍
- merck millipore,默克密理博,124018,Akt Inhibitor VIII, Isozyme-Selective, Akti-1/2 - CAS 612847-09-3 - Calbiochem
重要规格表
经验配方 CAS号 C₃₄H₂₉N₇O 612847-09-3 描述 概述 A cell-permeable and reversible quinoxaline compound that potently and selectively inhibits Akt1/Akt2 activity (IC50 = 58 nM, 210 nM, and 2.12 µM for Akt1, Akt2, and Akt3, respectively, in in vitro kinase assays). The inhibition appears to be pleckstrin homology (PH) domain-dependent. It does not exhibit any inhibitory effect against PH domain-lacking Akts, or other closely related AGC family kinases, PKA, PKC, and SGK, even at concentrations as high as 50 µM. Overcomes Akt1/Akt2-mediated resistance to chemotherapeutics in tumor cells and is shown to block basal and stimulated phosphorylation/activation of Akt1/Akt2 both in cultured cells in vitro and in mice in vivo. A 10 mM (1 mg/181 µl) solution of Akt Inhibitor VIII, Isozyme-Selective, Akti-1/2 (Cat. No. 124017) in DMSO is also available. 产品目录编号 124018 品牌系列 Calbiochem®
同义词 1,3-Dihydro-1-(1-((4-(6-phenyl-1H-imidazo[4,5-g]quinoxalin-7-yl)phenyl)methyl)-4-piperidinyl)-2H-benzimidazol-2-one, Akti-1/2 参考 参考 Calleja, V., et al. 2009. PLoS Biol. 7, e17.
Logie, L., et al. 2007. Diabetes 56, 228.
Barnett, S.F., et al. 2005. Biochem. J. 385, 399.
DeFeo-Jones, D., et al. 2005. Mol. Cancer Ther. 4, 271.
Zhao, Z., et al. 2005. Bioorg. Med. Chem. Lett. 15, 905.
Lindsley, C.W., et al. 2005. Bioorg. Med. Chem. Lett. 15, 761.产品信息 CAS号 612847-09-3 具有ATP竞争性 N 形式 Yellow solid Hill配方 C₃₄H₂₉N₇O 化学配方 C₃₄H₂₉N₇O Molar Mass 551.6 可逆 Y 结构配方图像 生物信息 主靶 Akt1, Akt2, Akt3 主靶IC50 58 nM, 210 nM, 2.12 µM against Akt1, Akt2, and Akt3, respectively, in in vitro kinase assays 纯度 ≥95% by HPLC 理化信息 细胞可渗透 Y 溶解度 DMSO 储存和货运信息 货运代码 Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
毒性 Standard Handling
储存 +2°C to +8°C
避光 Protect from light
无需冷冻 No
特殊指南 Following reconstitution, aliquot and freeze (-70°C). Stock solutions are stable for up to 6 months at -70°C. 包装信息 惰性气体下包装 Packaged under inert gas
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