This is a demo store. No orders will be fulfilled.

MK-2206 2HCl, AKT 丝氨酸/苏氨酸激酶 1 的变构调节剂;AKT 丝氨酸/苏氨酸激酶 2 的变构调节剂;AKT 丝氨酸/苏氨酸激酶 3 的变构调节剂

  • CAS编号: 1032350-13-2
  • 分子式: C25H21N5O·2HCl
  • 分子量: 480.39
有货

库存信息

关闭
货号 (SKU) 包装规格 是否现货 价格 数量
M408752-1ml
1ml 现货 Stock Image
查看相关系列
Compound libraries (12333)

基本描述

规格或纯度 Moligand™, 10mM in DMSO
英文名称 MK-2206 2HCl
生化机理 MK-2206 2HCl 是一种高选择性的 Akt1/2/3 抑制剂,在无细胞实验中的 IC50 分别为 8 nM/12 nM/65 nM;未观察到对其他 250 种蛋白激酶的抑制活性。MK-2206 2HCl 可诱导癌细胞自噬和凋亡。第 2 阶段。
储存温度 -80℃储存
运输条件 超低温冰袋运输
作用类型 变构调节剂
作用机制 AKT 丝氨酸/苏氨酸激酶 1 的变构调节剂;AKT 丝氨酸/苏氨酸激酶 2 的变构调节剂;AKT 丝氨酸/苏氨酸激酶 3 的变构调节剂
产品介绍

MK-2206 2HCl是一种高度选择性的Akt1/2/3抑制剂,IC50分别为8 nM/12 nM/65 nM;对250种其他蛋白激酶没有抑制活性。A highly selective pan-Akt inhibitor activated by the pleckstrin homology domain

Information


In vitro

MK-2206 is an allosteric inhibitor and is activated by the pleckstrin homology domain. MK-2206 inhibits auto-phosphorylation of both Akt T308 and S473. MK-2206 also prevents Akt-mediated phosphorylation of downstream signaling molecules, including TSC2, PRAS40 and ribosomal S6 proteins. MK-2206 inhibits Ras wild-type (WT) cell lines (A431, HCC827, and NCI-H292) more potently when compared to Ras-mutant cell lines (NCI-H358, NCI-H23, NCI-H1299, and Calu-6). MK-2206 also shows synergistic responses in combination with cytotoxic agents such as erlotinib or lapatinib in lung NCI-H460 or ovarian A2780 tumor cells. MK-2206 or siRNA-mediated Akt inhibition strongly activates autophagy in human glioma cells. However, eukaryotic elongation factor-2 (eEF-2) silencing suppresses MK-2206-induced-autophagy, with a promotion of apoptotic cell death.

In vivo

MK-2206 shows 60% TGI and inhibits more than 70 % of phospho-Akt1/2 (T308 and S473) in A2780 ovarian cancer xenografts at a dose of 240 mg/kg. MK-2206 exhibits significant antitumor activity in NCI-H292 xenograft in combination with erlotinib or lapatinib.
Cell Data

cell lines:tumor (HT1080, RCC45, MiaPaca) and normal cells (Wi38, NKE-hTERT)

Concentrations:0, 0.3, 1 and 3 μM

Incubation Time:72 or 96 hours

Powder Purity:≥99%

关联靶点(人)

AKT3 Tchem RAC-γ 丝氨酸/苏氨酸蛋白激酶(RAC-gamma serine/threonine-protein kinase) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
AKT2 Tchem RAC-β丝氨酸/苏氨酸蛋白激酶(RAC-beta serine/threonine-protein kinase) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)
AKT1 Tchem RAC-alpha 丝氨酸/苏氨酸蛋白激酶(RAC-alpha serine/threonine-protein kinase) (1 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)

名称和识别符

Isomeric SMILES C1CC(C1)(C2=CC=C(C=C2)C3=C(C=C4C(=N3)C=CN5C4=NNC5=O)C6=CC=CC=C6)N.Cl.Cl
PubChem CID 46930998
分子量 480.39

化学和物理性质

溶解性 Solubility (25°C) In vitro Water: 3 mg/mL (10.74 mM); DMSO: Insoluble; Ethanol: Insoluble;
熔点 >225°C

质检证书(CoA,COO,BSE/TSE 和分析图谱)

C of A & Other Certificates(BSE/TSE, COO):
输入批号以搜索分析图谱:

溶液计算器