PSB-12062 (N-(p-Methylphenylsulfonyl)phenoxazine)

PSB-12062 (N-(p-Methylphenylsulfonyl)phenoxazine) 是一种有效的选择性 P2X4 拮抗剂，对人 P2X4 的 IC50 为 1.38 μM。

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库存: 现货

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数量
5mg

￥637.00

510.00

- +
10mg

￥975.00

780.00

- +
25mg

￥2100.00

1680.00

- +
50mg

￥3737.00

2990.00

- +
100mg

￥6737.00

5390.00

- +

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货号: ajce45852
CAS: 55476-47-6
别名: N-(p-Methylphenylsulfonyl)phenoxazine
分子式: C19H15NO3S
分子量: 337.39
纯度: >98%
溶解度: DMSO : 25 mg/mL (74.10 mM)
储存: Store at -20°C
库存: 现货

Background

PSB-12062 is a potent and selective P2X4 antagonist with an IC50 of 1.38 μM for human P2X4.

PSB-12062 shows similar potency in human, rat, and mouse species. PSB-12062 shows to be allosteric in nature with a 35-fold selectivity toward P2X4 versus P2X1, P2X2, P2X3, and P2X7. However, PSB-12062 is unable to completely block ATP-induced P2X4-mediated calcium influx even when used at high concentrations (>30 μM)[1].

[1]. Hernandez-Olmos V, et al. N-substituted phenoxazine and acridone derivatives: structure-activity relationships of potent P2X4 receptor antagonists. J Med Chem. 2012 Nov 26;55(22):9576-88. [2]. Stokes L, et al. P2X4 Receptor Function in the Nervous System and Current Breakthroughs in Pharmacology.Front Pharmacol. 2017 May 23;8:291.

Protocol

Kinase experiment:

The competition binding studies are performed in assay buffer (50 mM Tris-HCl, pH 7.4) containing 1 mM EDTA and 0.2 nM [35S]ATPγS. The incubations are started by the addition of membranes (10-15 μg) and are performed in a 250 μL final assay volume. The reactions are terminated by vacuum filtration over GF/ B glass-fiber filters using a Brandell 48-well harvester. The filters are rinsed three times with ice-cold Tris-HCl buffer (50 mM, pH 7.4). The filters are punched out and transferred to 4 mL scintillation vials. Then 2.5 mL of Ultima Gold scintillation cocktail is added, and samples are counted after 6 h for 1 min each, using a liquid scintillation counter (LSC). Nonspecific binding of [35S]ATPγS is determined using 100 μM ATP[1].

参考文献:

[1]. Hernandez-Olmos V, et al. N-substituted phenoxazine and acridone derivatives: structure-activity relationships of potent P2X4 receptor antagonists. J Med Chem. 2012 Nov 26;55(22):9576-88.
[2]. Stokes L, et al. P2X4 Receptor Function in the Nervous System and Current Breakthroughs in Pharmacology.Front Pharmacol. 2017 May 23;8:291.