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Q-VD-OPh

Cat. No.:YN250332

  • CAS No. :1135695-98-5

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    • 产品名称: Q-VD-OPh
      CAS No.: 1135695-98-5
      Chemical Name: (3S)-5-(2,6-difluorophenoxy)-3-[[(2S)-3-methyl-1-oxo-2-[(2-quinolinylcarbonyl)amino]butyl]amino]-4-oxo-pentanoic acid
      Synonyms:QVD-OPH; Quinoline-Val-Asp-Difluorophenoxymethylketone
      分子量:513.49
      分子式:C₂₆H₂₅F₂N₃O₆
      SMILES:O=C(O)C[C@H](NC([C@@H](NC(C1=NC2=CC=CC=C2C=C1)=O)C(C)C)=O)C(COC3=C(F)C=CC=C3F)=O
      存储:Please store the product under the recommended conditions in theCertificate of Analysis.
      运输:Room temperature in continental US; may vary elsewhere.
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      Purity: 98%
    • 产品描述: Q-VD-OPh 是一种不可逆的泛胱天蛋白酶 (caspase) 抑制剂,具有高效的抗凋亡能力。抑制胱天蛋白酶 7 的IC50值别为 48 nM,抑制胱天蛋白酶 1,3,8,9,10,12 的IC50值在 25-400 nM 之间。Q-VD-OPh 可抑制HIV感染。Q-VD-OPh 能透过血脑屏障。
      IC50和靶点: [{name:"Caspase-3:25-400 nM (IC50)"},{name: "Caspase-7:48 nM (IC50)"},{name: "Caspase-1:25-400 nM (IC50)"},{name: "Caspase-8:25-400 nM (IC50)"},{name: "Caspase-9:25-400 nM (IC50)"},{name: "Caspase-10:25-400 nM (IC50)"},{name: "Caspase-12:25-400 nM (IC50)"}]
      In Vitro:
      In Vivo:
      Clinical Trial:
      Solvent & Solubility:
    • Caserta, T.M., Smith, A.N., Gultice, A.D., et al.Q-VD-OPh, a broad spectrum caspase inhibitor with potent antiapoptotic propertiesApoptosis8(4),345-352(2003)

      Kuzelová, K., Grebenová, D., and Brodská, B.Dose-dependent effects of the caspase inhibitor Q-VD-OPh on different apoptosis-related processesJ. Cell. Biochem.112(11),3334-3342(2011)

      Renolleau, S., Fau, S., Goyenvalle, C., et al.Specific caspase inhibitor Q-VD-OPh prevents neonatal stroke in P7 rat: A role for genderJ. Neurochem.100(4),1062-1071(2007)

      Braun, J.S., Prass, K., Dirnagl, U., et al.Protection from brain damage and bacterial infection in murine stroke by the novel caspase-inhibitor Q-VD-OPHExp. Neurol.206(2),183-191(2007)

      Chen-Deutsch, X., Kutner, A., Harrison, J.S., et al.The pan-caspase inhibitor QVD has anti-leukemia effects and can interact with vitamin D analogs to increase HPK1 signaling in AML cellsLeuk. Res.36(7),884-888(2012)

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