| 貨號 | 規格 | 價格 | 上海 | 北京 | 武漢 | 南京 | 購買數量 |
|---|---|---|---|---|---|---|---|
S81863-1mg |
99.2% | ￥130.00 | 10 | - | - | - |
|
S81863-2mg |
99.2% | ￥190.00 | 10 | - | - | - |
|
S81863-5mg |
99.2% | ￥290.00 | 7 | - | - | - |
|
S81863-10mg |
99.2% | ￥440.00 | 6 | - | - | - |
|
S81863-25mg |
99.2% | ￥800.00 | 5 | - | - | - |
|
S81863-50mg |
≥98% | ￥1200.00 | 貨期：2-3天 | - | - | - |
|
S81863-100mg |
≥98% | ￥2100.00 | 貨期：2-3天 | - | - | - |
|
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： |
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| 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。 |
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危險品化學品經營許可證（不帶存儲）
營業執照(三證合一)
北京