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. |
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IC50& Target |
Adenosine receptor[1]. |
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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].
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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].
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Clinical Trial |
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分子量 |
386.41 |
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性状 |
Solid |
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Formula |
C18H22N6O4 |
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CAS 号 |
89705-21-5 |
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中文名称 |
N6-[2-(4-氨基苯基)乙基]腺嘌呤 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 250 mg/mL(646.98 mM;Need ultrasonic)
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In Vivo:
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