MK-2206

SKU: orb1306994

特色

描述

MK-2206 2HCl is a potent, selective, and orally bioavailable allosteric inhibitor of Akt isoforms (Akt1/2/3). It demonstrates antitumor efficacy in preclinical models and is utilized in cancer research for studying PI3K/Akt signaling in both cellular and animal studies.

研究领域

Cell Biology

图片与验证

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关键属性

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CAS 号	1032350-13-2
MW	480.39
纯度	>98%
分子式	C₂₅H₂₁N₅O·2HCl
SMILES	Cl.Cl.NC1(CCC1)c1ccc(cc1)-c1nc2ccn3c(n[nH]c3=O)c2cc1-c1ccccc1
靶点	Kinase
溶解性	Soluble in DMSO ( up to 10 mg/ml with warming)

生物活性

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靶点 IC50	Akt3:65 nM (cell free)\|Akt1:8 nM (cell free)\|Akt2:12 nM (cell free)
体内	METHODS: To detect anti-tumor activity in vivo, MK-2206 dihydrochloride (120 mg/kg three times per week or 360 mg/kg once per week, 30% Captisol) and erlotinib (50 mg/kg five times per week, 0.5% methylcellulose + 0.1% Tween 80) were orally administered to CD1 mice bearing human lung cancer tumor NCI-H292 for two weeks. RESULTS: Three-times-weekly MK-2206 monotherapy was ineffective, and the once-weekly regimen mediated only moderate antitumor efficacy. Although erlotinib alone mediated significant tumor growth inhibition, combination therapy with MK-2206 significantly enhanced its antitumor efficacy, including tumor regression. METHODS: To assay antitumor activity in vivo, MK-2206 dihydrochloride (120 mg/kg in 30% captisol) was administered by gavage to NSG mice bearing human endometrial cancer tumors twice a week for three weeks. RESULTS: MK-2206 dihydrochloride treatment resulted in significant inhibition of the growth of three different types and grades of PDX tumors.
体外	METHODS: Fourteen tumor cells were treated with MK-2206 dihydrochloride for 72 h. Cell viability was measured by CellTiter-Glo assay. RESULTS: MK-2206 dihydrochloride inhibited the growth of tumor cells with IC50 ranging from 0.1 to 28.6 μmol/L. METHODS: Human nasopharyngeal carcinoma cell lines CNE-2 and HONE-1 were treated with MK-2206 dihydrochloride (0.625-10 μM) for 24-48 h, and the cell cycle was detected by Flow Cytometry. RESULTS: MK-2206 dihydrochloride caused a dose-dependent increase in the percentage of cells in G0/G1 phase and a decrease in the number of cells in S phase.MK-2206 dihydrochloride induced cell cycle arrest in G1 phase. MK-2206 dihydrochloride induces cell cycle arrest in the G1 phase.
细胞研究	Cells were seeded at a density of 2 to 3 × 103 per well in 96-well plates. Twenty-four hours after plating, varying concentrations of the drug, either as a single agent or in combination, were added to the wells. Cell proliferation was determined by using the CellTiter-Glo assay at 72 or 96 hours after dosing. The nature of the drug interaction was evaluated by using the combination index (CI) according to the method of Chou and Talalay. A commercial software package was obtained from Calcusyn. In combination with docetaxel, we tested three treatment sequences: (a) MK-2206 followed by docetaxel—cells were exposed to MK-2206 for 24 hours, and then after washout of MK-2206, cells were treated with docetaxel for an additional 72 hours; (b) docetaxel followed by MK-2206—cells were exposed to docetaxel for 24 hours, and then after washout of docetaxel, cells were treated with MK-2206 for an additional 72 hours; and (c) concurrent treatment—cells were exposed to both MK-2206 and docetaxel for 72 hours .
动物研究	When the mean tumor size reached 0.13 cm3 for the SK-OV-3 or 0.2 cm3 for the NCI-H292, HCC70, PC-3, and NCI-H460 models, the mice were randomized into control and treatment groups with approximately equivalent ranges of tumor volume between groups (n = 5 animals per group). The following vehicles were used to dose the compounds: 30% Captisol (Cydex) for MK-2206; 0.5% methylcellulose + 0.1% Tween 80 for erlotinib; distilled water for lapatinib; 0.73% ethanol in saline for docetaxel; and saline for carboplatin and gemcitabine. The control group received vehicle only. Tumor volume was measured with calipers twice a week. Animal body weight and physical signs were monitored during the experiments. Tumor volume was calculated, taking length to be the longest diameter across the tumor and width to be the perpendicular diameter, by using the following formula: (length × width)2 × 0.5. Relative tumor volume was assessed by dividing the tumor volume on different observation days with the starting tumor volume. Statistical significance was evaluated by using the two-way repeated ANOVA test followed by Dunnett's test or an unpaired t-test .

储存与操作

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储存	-20°C
有效期	12 months from date of receipt.
免责声明	For research use only

别名

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breast, Akt, Autophagy, Akt2, Akt3, Akt1, Apoptosis, cancer, oral, MK 2206, MK 2206 Dihydrochloride, MK 2206 dihydrochloride, MK2206, MK-2206, MK-2206 (2HCl), MK-2206 2HCl, MK2206 dihydrochloride, MK2206 Dihydrochloride, MK-2206 Dihydrochloride, Inhibitor, inhibit, loss, mutant, PIK3CA, PKB, sensitive, selective, Protein kinase B, PTEN

相似产品

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MK-2206 [orb1687434]
CAS 号：
1032349-77-1
MW:
443.94
分子式：
C₂₅H₂₂ClN₅O
可选规格： 1 mg, 5 mg, 25 mg
MK-2206 free base [orb1942981]
CAS 号：
1032349-93-1
MW:
407.47
分子式：
C₂₅H₂₁N₅O
可选规格： 5 mg, 50 mg
MK 2206 dihydrochloride [orb1227109]
纯度：
>98% (HPLC)
CAS 号：
1032350-13-2
MW:
480.389
分子式：
C₂₅H₂₃Cl₂N₅O
可选规格： 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg, 500 mg, 1 g, 2 mg
4SC-202 free base [orb1223678]
纯度：
>98% (HPLC)
CAS 号：
910462-43-0
MW:
447.51
分子式：
C??H??N?O?S
可选规格： 2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg, 500 mg, 1 g

质量保证

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化合物标识

PubChem CID

46930998 ↗

关键属性

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暂无计算属性。

实验方案信息

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CAS 号：	1032349-77-1
MW:	443.94
分子式：	C₂₅H₂₂ClN₅O

CAS 号：	1032349-93-1
MW:	407.47
分子式：	C₂₅H₂₁N₅O

纯度：	>98% (HPLC)
CAS 号：	1032350-13-2
MW:	480.389
分子式：	C₂₅H₂₃Cl₂N₅O

MK-2206

描述

研究领域

图片与验证

关键属性

生物活性

储存与操作

别名

相似产品

MK-2206 [orb1687434]

MK-2206 free base [orb1942981]

MK 2206 dihydrochloride [orb1227109]

4SC-202 free base [orb1223678]

质量保证

化合物标识

关键属性

实验方案信息

可选规格