Powder: -20°C for 3 years
In solvent: -80°C for 2 years
Traxoprodil is a selective NMDA antagonist and protects hippocampal neurons (IC50: 10 nM).
Description | Traxoprodil is a selective NMDA antagonist and protects hippocampal neurons (IC50: 10 nM). |
Targets&IC50 | NMDA Receptor:10 nM |
In vivo | Traxoprodil is potent at blocking haloperidol-induced catalepsy and with an ED50 less than 1 mg/kg. Traxoprodil is effective at 1 mg/kg to block NMDA (i.p.) stimulated c-fos 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]. |
Animal Research | The effect of traxoprodil and SPD on PTZ-induced seizures is investigated by injecting the Adult (90-100 days-old) male Wistar rats (250-300 g) with traxoprodil (0.2, 2 or 20 nM/site), SPD (0.02, 0.2 or 2 nM/site), or with vehicle (0.9% NaCl, 1 μL) 15 min before the administration of PTZ (35 or 70 mg/kg, i.p.) [3]. The Forced swim test is done on male Albino Swiss mice (25-30 g). Traxoprodil (5, 10, 20, 40 mg/kg), imipramine and saline are administered i.p. 60 min before the test. The antidepressant activity is measured [2]. |
Synonyms | 曲索罗地, CP101606 |
Molecular Weight | 327.42 |
Formula | C20H25NO3 |
CAS No. | 134234-12-1 |
Powder: -20°C for 3 years
In solvent: -80°C for 2 years
H2O: < 0.1 mg/mL (insoluble)
DMSO: 62.5 mg/mL (190.89 mM), Need ultrasonic
( < 1 mg/ml refers to the product slightly soluble or insoluble )
You can also refer to dose conversion for different animals. More
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Traxoprodil 134234-12-1 离子通道 神经科学 iGluR NMDAR Ionotropic glutamate receptors inhibit CP101606 Inhibitor inhibitor