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VX-702

    
≥99%

VX-702

源葉(MedMol)
S80931 一鍵復制產品信息
745833-23-2
C19H12F4N4O2
404.32
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S80931-5mg
≥99% ¥204.00 貨期:2-3天 - - -
S80931-10mg
99.5% ¥272.00 8 - - -
S80931-25mg
≥99% ¥489.60 貨期:2-3天 - - -
S80931-50mg
≥99% ¥680.00 貨期:2-3天 - - -
S80931-100mg
99.5% ¥1224.00 3 - - -
S80931-200mg
≥99% ¥2380.00 貨期:2-3天 - - -
S80931-250mg
≥99% ¥2720.00 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

VX-702 is a highly selective inhibitor of p38α MAPK, 14-fold higher potency against the p38α versus p38β

產品描述: VX-702 is a highly selective inhibitor of p38α MAPK, 14-fold higher potency against the p38α versus p38β
靶點: p38α MAPK;p38MAPK;Autophagy
體內研究: The half-life of VX-702 is 16 to 20 hours, with a median clearance of 3.75 L/h and a volume of distribution of 73 L/kg. Both AUC and Cmax values are dose proportional for VX-702, which is predominantly cleared renally. VX-702 (at a dose of 0.1 mg/kg twice daily) has an equivalent effect as that of methotrexate (0.1 mg/kg). In addition, VX-702 (5 mg/kg twice daily) also has an equivalent effect as prednisolone (10 mg/kg once daily), as measured by percentage inhibition of wrist joint erosion and inflammation score.
參考文獻: 1. Kuliopulos A, et al. Effect of selective inhibition of the p38 MAP kinase pathway on platelet aggregation. Thromb Haemost, 2004, 92(6), 1387-1393. 2. Braddock M, IDDB Meeting Report, 2005, March 14-15. 3. Gill A, IDDB Meeing Report, 2002, March 06-08. 4. Naka K, et al. Dipeptide species regulate p38MAPK-Smad3 signalling to maintain chronic myelogenous leukaemia stem cells. Nat Commun. 2015 Aug 20;6:8039.
溶解性: DMSO  :  ≥  42  mg/mL  (103.88  mM)
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.473 ml 12.366 ml 24.733 ml
5 mM 0.495 ml 2.473 ml 4.947 ml
10 mM 0.247 ml 1.237 ml 2.473 ml
50 mM 0.049 ml 0.247 ml 0.495 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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