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TAE226 (NVP-TAE226)

    
98.5%

TAE226 (NVP-TAE226)

源葉(MedMol)
S80943 一鍵復制產品信息
761437-28-9
C23H25ClN6O3
468.94
Benzamide, 2-[[5-chloro-2-[[2-methoxy-4-(4-morpholinyl)phenyl]amino]-4-pyrimidinyl]amino]-N-methyl-
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S80943-1mg
98.5% ¥255.00 5 - - -
S80943-2mg
98.5% ¥459.00 5 - - -
S80943-5mg
98.5% ¥680.00 5 - - -
S80943-10mg
98.5% ¥1190.00 6 - - -
S80943-25mg
98.5% ¥2380.00 6 - - -
S80943-50mg
98.5% ¥4590.00 5 - - -
S80943-100mg
≥98% ¥7300.00 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

NVP-TAE 226 (TAE226) is a potent and ATP-competitive dual FAK and IGF-1R inhibitor with IC50s of 5.5 nM and 140 nM, respectively. NVP-TAE 226 (TAE226) also effectively inhibits Pyk2 and insulin receptor (InsR) with IC50s of 3.5 nM and 44 nM, respectively

產品描述: NVP-TAE 226 (TAE226) is a potent and ATP-competitive dual FAK and IGF-1R inhibitor with IC50s of 5.5 nM and 140 nM, respectively. NVP-TAE 226 (TAE226) also effectively inhibits Pyk2 and insulin receptor (InsR) with IC50s of 3.5 nM and 44 nM, respectively
靶點: IC50: 5.5 nM (FAK), 3.5 nM (Pyk2), 140 nM (IGF-IR), 40 nM (InsR), 0.16 μM (c-Met), 0.36 μM (KDR), 0.48 μM (Flt3);Apoptosis;FAK;c-Met/HGFR;PYK2;IGF-1R
體內研究: Treatment with NVP-TAE 226 (TAE226) at 50 or 75 mg/kg extends the median survival of U87 xenograft animals by 6 and 7 days, respectively (P=0.084 and P=0.042, respectively, compared with vehicle-treated animals). However, NVP-TAE 226 treatment of LN229-engrafted animals significantly prolongs their median survival by 19 days (P<0.004 for both dosages, compared with vehicle-treated animals)
參考文獻: 1. Liu TJ, et al. Inhibition of both focal adhesion kinase and insulin-like growth factor-I receptor kinase suppresses glioma proliferation in vitro and in vivo. Mol Cancer Ther, 2007, 6(4), 1357-1367. 2. Delimont D, et al. Laminin α2-mediated focal adhesion kinase activation triggers Alport glomerular pathogenesis. PLoS One. 2014 Jun 10;9(6):e99083. 3. Lietha D, et al. Crystal structures of the FAK kinase in complex with TAE226 and related bis-anilino pyrimidine inhibitors reveal a helical DFG conformation. PLoS One. 2008;3(11):e3800.
溶解性: DMSO  :  11.11  mg/mL  (23.69  mM;  ultrasonic  and  warming  and  heat  to  60°C)
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.132 ml 10.662 ml 21.325 ml
5 mM 0.426 ml 2.132 ml 4.265 ml
10 mM 0.213 ml 1.066 ml 2.132 ml
50 mM 0.043 ml 0.213 ml 0.426 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)

如何獲取質檢證書(COA)?
請輸入貨號和一個與之匹配的批號。
例如:
批號:JS298415 貨號:S20001-25g
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摩爾濃度計算器

質量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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