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首页-小分子抑制剂&激动剂-PI3K/Akt/mTOR Pathway-Akt-MK-2206 dihydrochloride
MK-2206 dihydrochloride

Chemical Structure : MK-2206 dihydrochloride

CAS No.: 1032350-13-2

MK-2206 dihydrochloride (MK2206 dihydrochloride)

货号: PC-42551Not For Human Use, Lab Use Only.

MK-2206 dihydrochloride is a potent, orally active allosteric Akt inhibitor with IC50 of 5/12 nM for Akt1/Akt2 respectively.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

MK-2206 dihydrochloride is a potent, orally active allosteric Akt inhibitor with IC50 of 5/12 nM for Akt1/Akt2 respectively.
MK-2206 shows 5-fold less potent against human Akt3 (IC50=65 nM).
MK-2206 synergistically inhibits cell proliferation of human cancer cell lines in combination with erlotinib or lapatinib in vitro.
MK-2206 suppresses the Akt phosphorylation that is induced by carboplatin and gemcitabine.

物理化学性质&存储条件

分子量 480.389
分子式 C25H23Cl2N5O
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

DMSO

Chemical Name/SMILES

1,2,4-Triazolo[3,4-f][1,6]naphthyridin-3(2H)-one, 8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl-, hydrochloride (1:2)

参考文献

1. Hirai H, et al. Mol Cancer Ther. 2010 Jul;9(7):1956-67.

2. Cheng Y, et al. Mol Cancer Ther. 2012 Jan;11(1):154-64.

3. Whicker ME, et al. BMC Cancer. 2016 Jul 27;16:550.

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