(Rac)-TTA-P2
Product Specifications
UNSPSC Description
(Rac)-TTA-P2 is the 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].
Target Antigen
Others
Type
Reference compound
Related Pathways
Others
Applications
Neuroscience-Neuromodulation
Field of Research
Neurological Disease
Assay Protocol
https://www.medchemexpress.com/rac-tta-p2.html
Purity
98.69
Solubility
DMSO : ≥ 50 mg/mL
Smiles
O=C(NCC1(F)CCN(CC2CC(OCC2)(C)C)CC1)C3=CC(Cl)=CC(Cl)=C3
Molecular Weight
431.37
References & Citations
[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.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Product Datasheet
http://file.medchemexpress.com/batch_PDF/HY-50707/Rac-TTA-P2-DataSheet-MedChemExpress.pdf
Product MSDS
http://file.medchemexpress.com/batch_PDF/HY-50707/Rac-TTA-P2-SDS-MedChemExpress.pdf
Clinical Information
No Development Reported
CAS Number
918430-49-6
Available Sizes
Curated Selection
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