CAS NO: | 89705-21-5 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | APNEA (N6-[2-(4-Aminophenyl)ethyl]adenosine) is a potent, non-selective A3adenosine receptoragonist. | ||||||||||||||||
IC50& Target | Adenosine receptor[1]. | ||||||||||||||||
体外研究 (In Vitro) | APNEA (N6-[2-(4-Aminophenyl)ethyl]adenosine) is a non-selective agonist of the adenosine A3 receptors, at the subprotective dose of 1 mg/kg against electroconvulsions, significantly potentiates the anticonvulsive action of phenobarbital, diphenylhydantoin and valproate against maximal electroshock, being ineffective at lower doses. APNEA (0.0039-1 mg/kg) also enhances the protective activity of carbamazepine. APNEA at low doses potentiates the protective activity of Carbamazepine most likely through the A subtype of adenosine receptors. At higher doses, APNEA seems to enhance the anticonvulsive effect of other antiepileptics via adenosine A1 receptors[1]. | ||||||||||||||||
体内研究 (In Vivo) | APNEA (N6-[2-(4-Aminophenyl)ethyl]adenosine; 2-4 mg/kg) has no significant effect on seizure parameters (seizure severity, seizure duration and afterdischarge duration) in amygdala-kindled rats. N6-[2-(4-Aminophenyl)ethyl]adenosine is combined with antiepileptic drugs administered at doses ineffective in fully kindled rats[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 386.41 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C18H22N6O4 | ||||||||||||||||
CAS 号 | 89705-21-5 | ||||||||||||||||
中文名称 | N6-[2-(4-氨基苯基)乙基]腺嘌呤 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 250 mg/mL(646.98 mM;Need ultrasonic) 配制储备液
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