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ST271

    
98%

2-Propenamide, 2-cyano-3-(4-hydroxy-3,5-bis(1-methylethyl)phenyl)-

源葉(MedMol)
S81863 一鍵復制產品信息
106392-48-7
C16H20N2O2
272.342
ST 271
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S81863-1mg 98% ¥130.00 10 - - -
S81863-2mg 98% ¥190.00 10 - - -
S81863-5mg 98% ¥290.00 7 - - -
S81863-10mg 98% ¥440.00 6 - - -
S81863-25mg 98% ¥800.00 5 - - -
S81863-50mg 98% ¥1200.00 貨期:2-3天 - - -
S81863-100mg 98% ¥2100.00 貨期:2-3天 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

ST271 is a potent inhibitor of protein tyrosine kinase (PTK), inhibits phospholipase D activation stimulated by fMet-Leu-Phe and PAF, with IC50s of 6.7 and 9 μM, respectively.

產品描述: ST271 is a potent inhibitor of protein tyrosine kinase (PTK), inhibits phospholipase D activation stimulated by fMet-Leu-Phe and PAF, with IC50s of 6.7 and 9 μM, respectively.
靶點: IC50: 6.7 μM (phospholipase D, stimulated by fMet-Leu-Phe), 9 μM (phospholipase D, stimulated by PAF);Phospholipase;?TyrosineKinases
參考文獻: 1. Martinson EA, et al. Inhibition of phospholipase D of human platelets by protein tyrosine kinase inhibitors. Cell Mol Biol (Noisy-le-grand). 1994 Jul;40(5):627-34. 2. Blake RA, et al. Fc gamma receptor II stimulated formation of inositol phosphates in human platelets is blocked by tyrosine kinase inhibitors and associated with tyrosine phosphorylation of the receptor. 3. Uings IJ, et al. Tyrosine phosphorylation is involved in receptor coupling to phospholipase D but not phospholipase C in the human neutrophil. Biochem J. 1992 Feb 1;281 (Pt 3):597-600.
溶解性: DMSO  :  ≥  110  mg/mL  (403.91  mM)
保存條件: 2-8℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 3.672 ml 18.359 ml 36.719 ml
5 mM 0.734 ml 3.672 ml 7.344 ml
10 mM 0.367 ml 1.836 ml 3.672 ml
50 mM 0.073 ml 0.367 ml 0.734 ml
注意: 部分產品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。

參考文獻

質檢證書(COA)

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摩爾濃度計算器

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