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U0126-EtOH

    
98%

U0126-EtOH

源葉(MedMol)
S81225 一鍵復(fù)制產(chǎn)品信息
1173097-76-1
C18H16N6S2.C2H6O
426.56
UO126 EtOH;(2Z,3Z)-2,3-bis(amino(2-aminophenylthio)methylene)succinonitrile,ethanol
貨號 規(guī)格 價格 上海 北京 武漢 南京 購買數(shù)量
S81225-5mg 98% ¥120.00 >10 - - -
S81225-10mg 98% ¥200.00 7 - - -
S81225-50mg 98% ¥650.00 >10 - - -
S81225-100mg 98% ¥1250.00 5 - - -
S81225-400mg 98% ¥3200.00 1 - - -
產(chǎn)品介紹 參考文獻(xiàn)(1篇) 質(zhì)檢證書(COA) 摩爾濃度計算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

U0126 (U0126-EtOH) is a potent, non-ATP competitive and selective MEK1 and MEK2 inhibitor, with IC50s of 72 nM and 58 nM, respectively. U0126 is an autophagy and mitophagy inhibitor

產(chǎn)品描述: U0126 (U0126-EtOH) is a potent, non-ATP competitive and selective MEK1 and MEK2 inhibitor, with IC50s of 72 nM and 58 nM, respectively. U0126 is an autophagy and mitophagy inhibitor
靶點: MEK2:60 nM (IC50);MEK1:70 nM (IC50);Mitophagy;?InfluenzaVirus;?MEK;?Autophagy
體內(nèi)研究: Mice are treated daily with U0126-EtOH (U0126; i.p., 10.5 mg/kg). In control experiment, tumor sizes are constant or slightly increase all over the kinetic. At the opposite, in all U0126-EtOH experiments, engraftment and early tumor growth are significantly decreased. Furthermore, a 60-70% reduction in the volume of tumors treated with U0126-EtOH is obtained 9 days after injection and thereafter. Rats are subjected to 120 minutes transient middle cerebral artery occlusion (tMCAO) and thereafter treated with the U0126-EtOH (U0126; i.p., 30 mg/kg) at 0 and 24 hours of reperfusion. After treatment with U0126-EtOH, the vasoconstriction to S6c is markedly reduced
參考文獻(xiàn): 1. Favata MF, et al. Identification of a novel inhibitor of mitogen-activated protein kinase kinase. J Biol Chem. 1998 Jul 17;273(29):18623-32. 2. Droebner K, et al. Antiviral activity of the MEK-inhibitor U0126 against pandemic H1N1v and highly pathogenic avian influenza virus in vitro and in vivo. Antiviral Res. 2011, 92(2), 195-203. 3. Bessard A, et al. RNAi-mediated ERK2 knockdown inhibits growth of tumor cells in vitro and in vivo. Oncogene. 2008 Sep 11;27(40):5315-25. 4. Ahnstedt H, et al. U0126 attenuates cerebral vasoconstriction and improves long-term neurologic outcome after stroke in female rats. J Cereb Blood Flow Metab. 2015 Mar;35(3):454-60.
溶解性: DMSO  :  50  mg/mL  (117.22  mM;  Need  ultrasonic)
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.344 ml 11.722 ml 23.443 ml
5 mM 0.469 ml 2.344 ml 4.689 ml
10 mM 0.234 ml 1.172 ml 2.344 ml
50 mM 0.047 ml 0.234 ml 0.469 ml
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摩爾濃度計算器

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