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M22 NEDD8 inhibitor

    
98.20%

源叶(MedMol)
S89147 一键复制产品信息
864420-54-2
C20H24Cl2N2
363.326
M22 NEDD8 inhibitor; M22; M-22; M 22
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S89147-5mg买3赠1
98.20%

¥800.00

>10 - - - -
S89147-10mg买3赠1
98.20%

¥1400.00

>10 - - - -
S89147-25mg买3赠1
98.20%

¥2800.00

>10 - - - -
S89147-100mg
98.20%

¥8400.00

>10 - - - -
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: NAE-IN-M22 is a potent, selective and reversible inhibitor of NEDD8 activating enzyme (NAE), with potency in micromolar range. NAE-IN-M22 inhibits multiple cancer cell lines and induces apoptosis in A549 cells. NAE-IN-M22 also can inhibit tumor growth in vivo
靶点: NEDD8 activating enzyme (NAE);Apoptosis; E1/E2/E3Enzyme
体外研究: M22 (0.37-90 μM; 24 h) blocks neddylation pathway selectively and suppresses degradation of CRL substrates in A549 cells. M22 (0.1-100 μM; 48 h) inhibits A549 cell proliferation completely at 30 µM (GI50=5.5 µM, GI90=19.3 µM). M22 (15-30 μM; 36 h) promotes apoptosis in A549 cell line. Cell Viability Assay Cell Line: A549 cells Concentration: 0.37, 1.11, 3.33, 10, 30, 90 μM Incubation Time: 24 hours Result: Inhibited formations of Uba3-NEDD8 and Ubc12-NEDD8.Resulted in a corresponding decrease in the abundance of Cullins-NEDD8.Decreased the degradations of p27 and CDT1.Prevented p53 from degradation.
体内研究: M22 (60 mg/kg; i.p. once daily for 14 d) inhibits tumor growth in nude mice bearing AGS xenografts[1].M22 (0.36-90 μM) has low acute toxicity in zebrafish model
参考文献: 1. Lu P, et, al. Discovery of a novel NEDD8 Activating Enzyme Inhibitor with Piperidin-4-amine Scaffold by Structure-Based Virtual Screening. ACS Chem Biol. 2016 Jul 15;11(7):1901-7.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.752 ml 13.762 ml 27.523 ml
5 mM 0.55 ml 2.752 ml 5.505 ml
10 mM 0.275 ml 1.376 ml 2.752 ml
50 mM 0.055 ml 0.275 ml 0.55 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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