貨號	規(guī)格	價格	上海	北京	武漢	南京
S81863-1mg	99.2%	￥130.00 S81863-1mg ￥130.00 現(xiàn)貨	10 10	-	-	-
S81863-2mg	99.2%	￥190.00 S81863-2mg ￥190.00 現(xiàn)貨	10 10	-	-	-
S81863-5mg	99.2%	￥290.00 S81863-5mg ￥290.00 現(xiàn)貨	7 7	-	-	-
S81863-10mg	99.2%	￥440.00 S81863-10mg ￥440.00 現(xiàn)貨	6 6	-	-	-
S81863-25mg	99.2%	￥800.00 S81863-25mg ￥800.00 現(xiàn)貨	5 5	-	-	-
S81863-50mg	≥98%	￥1200.00 S81863-50mg ￥1200.00 2-3天	0 貨期：2-3天	-	-	-
S81863-100mg	≥98%	￥2100.00 S81863-100mg ￥2100.00 2-3天	0 貨期：2-3天	-	-	-

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產(chǎn)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(chǎn)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(diǎn)：

IC50: 6.7 μM (phospholipase D, stimulated by fMet-Leu-Phe), 9 μM (phospholipase D, stimulated by PAF);Phospholipase;?TyrosineKinases

參考文獻(xiàn)：

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(chǎn)品我司僅能提供部分信息，我司不保證所提供信息的權(quán)威性，僅供客戶參考交流研究之用。

參考文獻(xiàn)

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ST271

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