PeptideDB

BzATP triethylammonium

CAS: 112898-15-4 F: C30H39N6O15P3 W: 816.58

BzATP triethylammonium acts as a P2X receptor agonist with pEC50s of 8.74, 5.26, 7.10, 7.50, 6.19, 6.31, 5.33 for P2X1,
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Bioactivity BzATP triethylammonium acts as a P2X receptor agonist with pEC50s of 8.74, 5.26, 7.10, 7.50, 6.19, 6.31, 5.33 for P2X1, P2X2, P2X3, P2X2/3, P2X4 and P2X7, respectively[1]. BzATP triethylammonium is potent at P2X7 receptors with EC50s of 3.6 μM and 285 μM for rat P2X7 and mouse P2X7, respectively[2].
Target pEC50: 8.74 (P2X1), 5.26 (P2X2), 7.10 (P2X3), 6.19 (P2X2/3), 6.31 (P2X4), 5.33 (P2X7)EC50 3.6 μM (rat P2X7); 285 μM (mouse P2X7)
Invitro BzATP (10-1000 μM;24 小时) triethylammonium 促进 U87 和 U251 胶质瘤细胞的增殖和迁移[3]。BzATP (100 μM;6-48 小时) triethylammonium 在人类胶质瘤细胞中诱导 P2X7R 蛋白表达。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> BzATP triethylammonium 相关抗体: Cell Proliferation Assay[3] Cell Line:
In Vivo 与假手术组和对照组相比,在盲肠结扎穿刺 (CLP) 诱导后,BzATP (5 mg/kg) triethylammonium 显著促进肠道中 P2X7R 的表达[4]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
CAS 112898-15-4
Formula C30H39N6O15P3
Molar Mass 816.58
Appearance 固体
Transport Room temperature in continental US; may vary elsewhere.
Storage

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Reference [1]. B R Bianchi, et al. Pharmacological characterization of recombinant human and rat P2X receptor subtypes. Eur J Pharmacol. 1999 Jul 2;376(1-2):127-38. [2]. Mark T Young, et al. Amino acid residues in the P2X7 receptor that mediate differential sensitivity to ATP and BzATP. Mol Pharmacol. 2007 Jan;71(1):92-100. [3]. Zhenhua Ji, et al. Involvement of P2X 7 Receptor in Proliferation and Migration of Human Glioma Cells. Biomed Res Int. 2018 Jan 9;2018:8591397. [4]. Xiuwen Wu, et al. Systemic blockade of P2X7 receptor protects against sepsis-induced intestinal barrier disruption. Sci Rep. 2017 Jun 29;7(1):4364.