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Ubiquitin Isopeptidase Inhibitor I, G5

    
≥98%

Ubiquitin Isopeptidase Inhibitor I, G5

源叶(MedMol)
S81919 一键复制产品信息
108477-18-5
C19H14N2O7S
414.3887
3,5-双(4-硝基苄叉)四氢噻喃-4-酮-1,1-二氧化物;4H-THIOPYRAN-4-ONE,TETRAHYDRO-3,5-BIS[(4-NITROPHENYL)METHYLENE]-1,1-DIOXIDE; UBIQUITIN ISOPEPTIDASE INHIBITOR I, G5; 3,5-bis-((Ξ)-4-nitro-benzylidene)-1,1-dioxo-tetrahyd
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S81919-5mg
≥98%

¥630.00

货期:3-5天 - - - -
S81919-10mg
≥98%

¥1090.00

货期:3-5天 - - - -
S81919-25mg
≥98%

¥2190.00

货期:3-5天 - - - -
S81919-50mg
≥98%

¥3510.00

货期:3-5天 - - - -
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: Ubiquitin Isopeptidase Inhibitor I, G5 (NSC 144303) is an apoptosome-independent caspase and apoptosis activator with IC50 values of 1.76 and 1.6 μM in E1A and E1A/C9DN cells, respectively.
靶点: IC50: 1.76 μM (E1A cells), 1.6 μM (E1A/C9DN cells);Apoptosis
体外研究: G5 is capable of activating an apoptosome-independent apoptotic pathway. It targets the ubiquitinproteasome system by inhibiting the ubiquitin isopeptidases. G5 induces a rather unique apoptotic pathway, which includes a Bcl-2-dependent but apoptosome-independent mitochondrial pathway with upregulation of the BH3-only protein Noxa, stabilization of the inhibitor of apoptosis antagonist Smac, but also the involvement of the death receptor pathway. G5 is a potent apoptotic inducer showing IC50s of 1.76 and 1.6 μM in E1A and E1A/C9DN cells, respectively
参考文献: 1. Aleo E, et al. Identification of new compounds that trigger apoptosome-independent caspase activation and apoptosis. Cancer Res. 2006 Sep 15;66(18):9235-44.
溶解性: soluble  in  DMSO、THF、Acetone
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.413 ml 12.066 ml 24.132 ml
5 mM 0.483 ml 2.413 ml 4.826 ml
10 mM 0.241 ml 1.207 ml 2.413 ml
50 mM 0.048 ml 0.241 ml 0.483 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

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