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S81689

GW791343 (dihydrochloride)

源葉(MedMol) 94%
  • 英文名:
  • GW791343 (dihydrochloride)
  • 別名:
  • 2-[(3,4-二氟苯基)氨基]-N-[2-甲基-5-(1-哌嗪基甲基)苯基]乙酰胺鹽酸鹽
  • CAS號:
  • 1019779-04-4
  • 分子式:
  • C20H26Cl2F2N4O
  • 分子量:
  • 447.3495
品牌貨號產(chǎn)品規(guī)格價格(RMB) 庫存(上海) 北京 武漢 南京 數(shù)量計量單位 加入購物車...
源葉(MedMol) S81689-5mg 94% ¥990.00元 預(yù)計交期:2-3天 - - - EA 加入購物車
源葉(MedMol) S81689-10mg 94% ¥1400.00元 預(yù)計交期:2-3天 - - - EA 加入購物車
源葉(MedMol) S81689-50mg 94% ¥5500.00元 預(yù)計交期:2-3天 - - - EA 加入購物車
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參考文獻(xiàn)

質(zhì)檢證書(COA)

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  • 產(chǎn)品描述: GW791343 dihydrochloride is a potent human P2X7 receptor negative allosteric modulator (exhibits species-specific activity), produces a non-competitive antagonist effect on human P2X7 receptor, with a pIC50 of 6.9-7.2. GW791343 dihydrochloride can enhance ATP rhythm. GW791343 dihydrochloride can be used in study of neurological disease
  • 靶點: P2X7 Receptor:6.9-7.2 (pIC50);P2XReceptor
  • 體外研究:
    GW791343 dihydrochloride (0.01, 0.03, 0.1, 0.3, 1, 3, 10 μM; 40 min) shows a non-competitive antagonistic activity to the human P2X7 receptor. GW791343 dihydrochloride (3, 10, 30 μM; 40 min) shows an anegative allosteric modulate activity to the human P2X7 receptor. GW791343 dihydrochloride (5 μM; 24-48 h; ATP measured every 4 h) enhances ATP rhythm in SCN cells. Cell Viability Assay Cell Line: HEK293 cells (expressing human recombinant P2X7 receptors) Concentration: 0.01, 0.03, 0.1, 0.3, 1, 3, 10 μM Incubation Time: 40 min (pre-incubate for 10 min and incubate with other P2X7 receptor antagonists for another 30 min) Result: Inhibited agonist-stimulated ethidium accumulation in both sucrose and NaCl buffer.Reduced maximal responses toATP and BzATP in sucrose buffer. Cell Viability Assay Cell Line: HEK293 cells (expressing human recombinant P2X7 receptors) Concentration: 3, 10, 30 μM Incubation Time: 40 min (pre-incubate for 10 min and incubate with other P2X7 receptor antagonists for another 30 min) Result: Showed slow reversal effects at the human P2X7 receptor (after 45 min had reversed sufficiently), and had a rapid dissociation rate. Cell Viability Assay Cell Line: SCN cells (from 16-to 21- day-old Wistar rats, which are kept under a controlled 12-12 h light-dark cycle from birth) Concentration: 5 μM (replace the medium with fresh drug-containing culture medium every 4 h). Incubation Time: 24-48 h (ATP measured every 4 h) Result: Enhanced the amplitude of ATP release rhythm and
  • 參考文獻(xiàn):
    1. Michel AD, et al. Negative and positive allosteric modulators of the P2X(7) receptor. Br J Pharmacol. 2008 Feb;153(4):737-50. 2. Svobodova I, et al. Circadian ATP Release in Organotypic Cultures of the Rat Suprachiasmatic Nucleus Is Dependent on P2X7 and P2Y Receptors. Front Pharmacol. 2018 Mar 6;9:192.
  • 溶解性: Soluble  in  DMSO、H2O
  • 保存條件: -20℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.235 ml 11.177 ml 22.354 ml
    5 mM 0.447 ml 2.235 ml 4.471 ml
    10 mM 0.224 ml 1.118 ml 2.235 ml
    50 mM 0.045 ml 0.224 ml 0.447 ml
  • 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。
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