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PD318088

    99%

PD318088

源葉(MedMol)
S80694
391210-00-7
C16H13BrF3IN2O4
561.1
5-bromo-N-(2,3-dihydroxypropoxy)-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)benzamide
品牌 貨號 產(chǎn)品規(guī)格 價格(RMB) 庫存(上海) 北京 武漢 南京 購買數(shù)量
源葉(MedMol) S80694-5mg 99% ¥290.00元 6 - - -
源葉(MedMol) S80694-10mg 99% ¥440.00元 7 - - -
源葉(MedMol) S80694-25mg 99% ¥670.00元 6 - - -
源葉(MedMol) S80694-50mg 99% ¥1130.00元 5 - - -
產(chǎn)品介紹 參考文獻 質(zhì)檢證書(COA) 摩爾濃度計算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

PD318088 is a potent, allosteric and non-ATP competitive MEK1/2 inhibitor, an analog of PD184352 (HY-50295). PD318088 binds simultaneously with ATP in a region of the MEK1 active site that is adjacent to the ATP-binding site. PD318088 can be used for cancer research
產(chǎn)品描述: PD318088 is a potent, allosteric and non-ATP competitive MEK1/2 inhibitor, an analog of PD184352 (HY-50295). PD318088 binds simultaneously with ATP in a region of the MEK1 active site that is adjacent to the ATP-binding site. PD318088 can be used for cancer research
靶點: MEK1;MEK2;MEK
參考文獻: 1. Ohren JF, et al. Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition. Nat Struct Mol Biol. 2004 Dec;11(12):1192-7. 2. Han S, et al. Identification of coumarin derivatives as a novel class of allosteric MEK1 inhibitors. Bioorg Med Chem Lett. 2005 Dec 15;15(24):5467-73.
溶解性: DMSO  :  ≥  100  mg/mL  (178.22  mM)
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 1.782 ml 8.911 ml 17.822 ml
5 mM 0.356 ml 1.782 ml 3.564 ml
10 mM 0.178 ml 0.891 ml 1.782 ml
50 mM 0.036 ml 0.178 ml 0.356 ml
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參考文獻

質(zhì)檢證書(COA)

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摩爾濃度計算器

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