Powder: -20°C for 3 years | In solvent: -80°C for 1 year
A-317567 is a potent acid-sensing ion channel 3 (ASIC-3) inhibitor with an IC50 of 1.025 μM, and it has antidepressant and antinociception effects[1][2].
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
25 mg | 10-14 weeks | $ 1,620.00 | |
50 mg | 10-14 weeks | $ 2,110.00 | |
100 mg | 10-14 weeks | $ 3,150.00 |
Description | A-317567 is a potent acid-sensing ion channel 3 (ASIC-3) inhibitor with an IC50 of 1.025 μM, and it has antidepressant and antinociception effects[1][2]. |
Targets&IC50 | ASIC3:1.025 μM |
In vitro | The effects of A-317567 on three distinct types of native ASIC currents evoked in acutely dissociated adult rat dorsal root ganglion (DRG) neurons are studied. A-317567 equipotently blocks the sustained phase of ASIC3-like current, a biphasic current akin to cloned ASIC3, which is predominant in DRG[2]. A-317567 produces concentration-dependent inhibition of all pH 4.5-evoked ASIC currents with an IC50 ranging between 2 and 30 μM, depending upon the type of ASIC current activated. |
In vivo | A-317567 is fully analgesic effects in the CFA model (ED50 of 17 μmol/kg, i.p., adult male Sprague-Dawley rats) and it has no significant effect on the withdrawal latency of the contralateral paw under these conditions[2]. |
Molecular Weight | 397.56 |
Formula | C27H31N3 |
CAS No. | 371217-32-2 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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A-317567 371217-32-2 Others A 317567 A317567 inhibitor inhibit