CAS NO: | 134234-12-1 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 |
Traxoprodil (CP101,606) is a potent and selectiveNMDAantagonist and protect hippocampal neurons with anIC50of 10 nM. |
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IC50& Target |
IC50: 10 nM (Neuroprotection)[1] |
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体内研究 (In Vivo) |
Traxoprodil is potent at blocking haloperidol-induced catalepsy and with an ED50less than 1 mg/kg. Traxoprodil is effective at 1 mg/kg to block NMDA (ip) stimulated cfos induction in mice[1]. Traxoprodil at a dose of 20 and 40 mg/kg exhibits antidepressant activity in the Forced swim test and it is not related to changes in animals’ locomotor activity[2]. Traxoprodil (20 nM i.c.v.) increases the latency to generalized tonic-clonic seizures induced by PTZ (70 mg/kg; i.p.). Traxoprodil (60 mg/kg, p.o.) increases the latency to clonic and generalized seizures, and decreases the total time spent in seizures[3].
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Clinical Trial |
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分子量 |
327.42 |
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性状 |
Solid |
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Formula |
C20H25NO3 |
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CAS 号 |
134234-12-1 |
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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 : 62.5 mg/mL(190.89 mM;Need ultrasonic) H2O : 0.1 mg/mL(0.31 mM;ultrasonic and warming and heat to 60℃)
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In Vivo:
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