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CZ415

    
10mM in DMSO

CZ415

源叶(MedMol)
T95934 一键复制产品信息
1429639-50-8
C22H29N5O4S
459.56
Urea,N-​[4-​[5,​7-​dihydro-​7,​7-​dimethyl-​4-​[(3S)​-​3-​methyl-​4-​morpholinyl]​-​6,​6-​dioxidothieno[3,​4-​d]​pyrimidin-​2-​yl]​phenyl]​-​N'-​ethyl-
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
T95934-1ml促销
10mM in DMSO

¥712.00 ¥640.00

5 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: mTOR抑制剂;mTOR Inhibitors;;InformationCZ415 CZ415, a potent ATP-competitive mTOR inhibitor with very good cell permeability.TargetsmTOR (Cell-free assay) 8.07(pIC50)In vitroCZ415 shows no genotoxic potential and has very good cell permeability. Treatment of CZ415 leads to inhibition of phosphorylation for downstream targets of mTORC1 and mTORC2(IC50=14.5 nM for pS6RP and IC50=14.8 nM for pAKT). The immunosuppressive effect of CZ415 is measured by detecting secreted IFNγ after 18 h in stimulated human whole blood, and the resulting IC50 was 226 nM. CZ415 shows no genotoxic potential. It is neither mutagenic in a bacterial mutation assay (Ames test) nor does it show genotoxicity in the mouse lymphoma assay (MLA), in either the presence or absence of rat-liver S9 mix.In vivoIn vivo studies show that CZ415 has moderate clearance and good oral bioavailability. In an anti-CD3 mouse model CZ415 efficiently inhibits mTOR downstream signaling and, in a CIA mouse model, shows significant antiinflammatory effects. With its extraordinary selectivity, drug-like properties and proven efficacy CZ415 represents an ideal molecule for the pharmacological investigation of mTOR pathophysiological role in vivo.Cell Research(from reference)Cell lines:HEK294T17 cells Concentrations:3 µM start, 8 points 1:3 dilution steps. Incubation Time:2 h 
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.176 ml 10.88 ml 21.76 ml
5 mM 0.435 ml 2.176 ml 4.352 ml
10 mM 0.218 ml 1.088 ml 2.176 ml
50 mM 0.044 ml 0.218 ml 0.435 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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