AF-353 is a potent and orally bioavailable P2X3/P2X2/3 receptor antagonist, inhibits human and rat P2X3 (pIC50= 8.0).
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描述 | AF-353 (Ro-4) is a potent, selective, and orally bioavailable antagonist of P2X3 and P2X2/3 receptors, with a pIC50 of 8.0 for both human and rat P2X3, and a pIC50 of 7.3 for human P2X2/3[1][2]. |
Animal study | AF-353 (Ro-4) does not affect oxygen levels or cardiac function[2].AF-353 (Ro-4), administered intravenously at doses of 10 mg/kg and 20 mg/kg for 4-6 hours, suppresses the purinergic response in both normal and spinal cord-injured (SCI) rats[2].During the same treatment, AF-353 (Ro-4) reduces the inter-contractile interval in normal rats but not in SCI rats, while significantly lowering the frequency of non-voiding contractions in SCI rats[2]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.50mL 0.50mL 0.25mL |
12.49mL 2.50mL 1.25mL |
24.99mL 5.00mL 2.50mL |
CAS号 | 865305-30-2 |
分子式 | C14H17IN4O2 |
分子量 | 400.21 |
SMILES Code | NC1=NC=C(OC2=CC(I)=C(OC)C=C2C(C)C)C(N)=N1 |
MDL No. | MFCD18782750 |
别名 | Ro-4 |
运输 | 蓝冰 |
InChI Key | AATPYXMXFBBKFO-UHFFFAOYSA-N |
Pubchem ID | 15953802 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Keep in dark place, inert atmosphere, room temperature |
溶解方案 |
请根据您的动物给药指南选择适当的溶解方案。 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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