| Bioactivity | (Rac)-TTA-P2 is the inactive isomer of TTA-P2 (HY-10035), and can be used as an experimental control. TTA-P2 (T-Type calcium channel inhibitor) is a potent inhibitor of T-Type calcium channel. TTA-P2 penetrates well the CNS and blocks the native T-type currents in deep cerebellar nuclear neurons, the window current is completely abolished both for wild-type and mutant Cav3.1 channels. TTA-P2 has the potential for the research of neurology disease[1]. | ||||||||||||
| Name | (Rac)-TTA-P2 | ||||||||||||
| CAS | 918430-49-6 | ||||||||||||
| Formula | C21H29Cl2FN2O2 | ||||||||||||
| Molar Mass | 431.37 | ||||||||||||
| Appearance | Solid | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
| Storage |
|
||||||||||||
| Reference | [1]. M R Hellberg, et al. Preclinical efficacy of travoprost, a potent and selective FP prostaglandin receptor agonist. J Ocul Pharmacol Ther. 2001 Oct;17(5):421-32. |
(Rac)-TTA-P2
CAS: 918430-49-6 F: C21H29Cl2FN2O2 W: 431.37
(Rac)-TTA-P2 is the inactive isomer of TTA-P2 (HY-10035), and can be used as an experimental control. TTA-P2 (T-Type cal
Sales Email：peptidedb@qq.com
This product is for research use only, not for human use. We do not sell to patients.