S81689 |
GW791343 (dihydrochloride) |
源葉(MedMol) | 94% |
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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
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