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Discovery Antibodies/A-794278/5 mg/A-435-5 mg

价格
¥2740.00
货号:A-435-5mg
浏览量:127
品牌:Discovery
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商品描述
Cat #: A-435
  • Lyophilized Powder
  • Bioassay Tested
  • Source Synthetic
    MW: 342.46
    Purity: >98%
    Effective concentration 1-100 nM.
      • A-794278
    Chemical name 3-cycloheptyl-9-(dimethylamino)pyrido[1,2]thieno[3,4-d]pyrimidin-4-one.
    Molecular formula C18H22N4OS.
    CAS No.: 869802-57-3.
    PubChem CID 11537456
    Activity A-794278 is a potent and selective noncompetitive mGluR1 antagonist, acting on mGluR1 and mGluR5 with IC50 values of 4.1 nM and 147 nM, respectively1In vivo it shows analgesic properties, significantly attenuating spontaneous post-operative pain behavior in rats (ED50 = 50 μmol/kg)2.
      • Zheng, G.Z. et al. (2005) J. Med. Chem. 48, 7374.
      • Zhu, C.Z. et al. (2008) Eur. J. Pharmacol. 580, 314.
    Shipping and storage Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C. Protect from light and moisture.
    Solubility Soluble in DMSO. Centrifuge all product preparations before use (10000 x g 5 min).
    Storage of solutions -20°C.
      • A-794278
        Alomone Labs A-794278 inhibits mGluR1-mediated Ca2+ mobilization in U2OS cells.
        Dose-response of A-794278 (#A-435) normalized inhibition of human mGluR1-mediated, L-glutamate-evoked Ca2+ mobilization. Cells were loaded with calcium-sensitive dye, incubated with a range of A-794278 concentrations, and stimulated with 5 µM L-glutamate (EC80). Changes in intracellular Ca2+ following stimulation were detected as changes in maximum relative fluorescence (RLU) using FLIPRTETRA™. IC50 was determined at 4.16 nM.
    References - Scientific background
    • 1. Zheng, G.Z. et al. (2005) J. Med. Chem. 48, 7374.
    • 2. Zhu, C.Z. et al. (2008) Eur. J. Pharmacol. 580, 314.
      • A-794278 is a potent, non-competitive antagonist of mGluR1. It is a triazafluorenone derivative that also antagonizes mGluR5 receptors. It demonstrates IC50 values of 4.1 nM and 147 nM for mGluR1 and mGluR5, respectively1. A-794278 binds to a putative allosteric recognition site located within the seven-transmembrane domain of the receptor1,2.

        Glutamate is the most abundant excitatory neurotransmitter in the central nervous system. It modulates the activity of many types of synapses by activating in part metabotropic glutamate receptors (mGluRs). mGluRs consist of three groups: I, II, and III with a total of eight subtypes, mGluR1 to mGluR8. mGluR1 plays an important role in the central sensitization of pain and in a variety of functions with potential implications in neurological and psychiatric disorders1,2.

    Target mGluR1, mGluR5
    receive a 5 mg free trial sample!
    Last update: 25/09/2019

    A-794278 (#A-435) is a highly pure, synthetic, and biologically active compound.

    For research purposes only, not for human use
    Discovery Antibodies的Cyclin dependant kinase 2 (CDK2) is a serine/threonine protein kinase which controls both G1/S and G2/M transitions. CDKs along with cyclins and CDK inhibitors regulate cell cycle progression. Specific cyclins activate different CDKs; in early G1, CDK2 pairs with cyclin E to promote entry into the S phase before switching to partner with cyclin A to drive the cell through S phase. Once activated CDKs phosphorylate downstream proteins to initiate signalling cascades. CDK2 phosphorylates and inactivates the RB1 (pRb) tumour suppressor family of proteins.CDK的活动受到严格控制。CDK2活性可以被包括P21在内的一系列抑制剂抑制。细胞周期失调和增殖控制的丧失与细胞转化和癌症密切相关。CDK2在DNA损伤反应(DDR)中的细胞周期停滞中也似乎起着积极作用,它的抑制作用会阻碍DDR,并使细胞对电离辐射敏感,从而诱导细胞死亡。该抗体与AlexaFluor®488偶联。AlexaFluor®488是一种流行的鲜绿色荧光染料,具有高pH稳定性。
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