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1032350-13-2 分子结构
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8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl-2H,3H-[1,2,4]triazolo[3,4-f]1,6-naphthyridin-3-one dihydrochloride

ChemBase编号:72495
分子式:C25H23Cl2N5O
平均质量:480.38902
单一同位素质量:479.12796574
SMILES和InChIs

SMILES:
c1(ccccc1)c1c(nc2c(c1)c1n(cc2)c(=O)[nH]n1)c1ccc(cc1)C1(CCC1)N.Cl.Cl
Canonical SMILES:
O=c1[nH]nc2n1ccc1c2cc(c(n1)c1ccc(cc1)C1(N)CCC1)c1ccccc1.Cl.Cl
InChI:
InChI=1S/C25H21N5O.2ClH/c26-25(12-4-13-25)18-9-7-17(8-10-18)22-19(16-5-2-1-3-6-16)15-20-21(27-22)11-14-30-23(20)28-29-24(30)31;;/h1-3,5-11,14-15H,4,12-13,26H2,(H,29,31);2*1H
InChIKey:
HWUHTJIKQZZBRA-UHFFFAOYSA-N

引用这个纪录

CBID:72495 http://www.chembase.cn/molecule-72495.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl-2H,3H-[1,2,4]triazolo[3,4-f]1,6-naphthyridin-3-one dihydrochloride
IUPAC传统名
8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl-2H-[1,2,4]triazolo[3,4-f]1,6-naphthyridin-3-one dihydrochloride
别名
MK-2206 dihydrochloride
CAS号
1032350-13-2
PubChem SID
162037420
PubChem CID
46930998

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID 价格
Selleck Chemicals
S1078 external link 加入购物车 请登录
数据来源 数据ID
PubChem 46930998 external link

理论计算性质

理论计算性质

JChem
Acid pKa 9.419391  质子受体
质子供体 LogD (pH = 5.5) 1.4456975 
LogD (pH = 7.4) 2.2164652  Log P 3.8779166 
摩尔折射率 119.6071 cm3 极化性 48.37406 Å3
极化表面积 83.61 Å2 可自由旋转的化学键
里宾斯基五规则 true 

分子性质

分子性质

安全信息 药理学性质 产品相关信息 生物活性(PubChem)
保存条件
-20°C expand 查看数据来源
作用靶点
Akt expand 查看数据来源
成盐信息
dihydrochloride expand 查看数据来源

详细说明

详细说明

Selleck Chemicals Selleck Chemicals
Selleck Chemicals -  S1078 external link
Protocol
Kinase Assay [4]
Akt kinases assay Akt kinases are assayed by a GSK-derived biotinylated peptide substrate. The extent of peptide phosphorylation is determined by Homogeneous Time Resolved Fluorescence (HTRF) using a lanthanide chelate (Lance)-coupled monoclonal antibody specific for the phosphopeptide in combination with a streptavidin-linked allophycocyanin (SA-APC) fluorophore which will bind to the biotin moiety on the peptide. When the Lance and APC are in proximity, a non-radiative energy transfer takes place from the Lance to the APC, followed by emission of light from APC at 655 nm. Working Solution: 100X protease inhibitor cocktail (PIC): 1mg/mL benzamidine, 0.5 mg/mL pepstatin, 0.5 mg/mL leupeptin, 0.5 mg/mL aprotinin; 10X assay buffer: 500 mM HEPES, pH7.5, 1% PEG, 16.6 mM EDTA, 1 mM EGTA, 1% BSA, 20 mM 9-glycerol phosphate; Quench buffer 50 mM HEPES pH 7.3, 16.6 mM EDTA, 0.1% BSA, 0.1% Triton X-100, 0.17 nM labeled monoclonal antibody, 0.0067 mg/mL SA-APC; ATP/MgCl2 working solution: 1X Assay buffer, 1 mM DTT, 1X PIC, 5% glycerol, active Akt; Peptide working solution: 1X Assay buffer, 1 mM DTT, 1X PIC, 5% glycerol, 2 TM GSK biotinylated peptide. The reaction is assembled by adding 16 μL of ATP/MgCl2 working solution to the appropriate wells. MK-2206 or vehicle (1.0 μL) is added followed by 10 μL of peptide working solution. The reaction is started by adding 13 μL of the enzyme working solution and mixing. The reaction is allowed to proceed for 50 min and then stopped by the addition of 60 μL HTRF quench buffer. The stopped reactions are incubated at room temperature for at least 30 min and then read in the instrument.
Cell Assay [2]
Cell Lines A431, HCC827, NCI-H292, NCI-H358, NCI-H23, NCI-H1299, Calu-6 and NCI-H460 cells
Concentrations 0, 0.3, 1 and 3 μM
Incubation Time 72 or 96 hours
Methods MK-2206 is dissolved in DMSO as a stock solution and diluted by culture media before use. Cells are seeded at a density of 2-3 × 103 in 96-well plates and incubated for 24 hours. Then MK-2206 (0, 0.3, 1 and 3 μM) is added to the cells. Cell proliferation is determined after 72 or 96 hours.
Animal Study [2]
Animal Models SK-OV-3, NCI-H292, HCC70, PC-3, and NCI-H460 models in male CD1-nude mice
Formulation Formulated in 30% Captisol
Doses 120 mg/kg
Administration Orally administered
References
[1] Yan L, AACR Annual Meeting 2009: Abstract Number: DDT01-1.
[2] Hirai H, et al. Mol Cancer Therapy, 2010, 9(7), 1956-1967.
[3] Cheng Y, et al, Cancer Res, 2011, 71(7), 2654-2663.
[4] WO2008070016 (A2)

参考文献

参考文献

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专利

专利

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