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Biological Data Biological description Potent, selective, reversible T-type calcium channel blocker (IC50 = 100nM at DRG T currents) with no activity at high voltage calcium channels. Shows antinociceptive to reduces pain responses in mice. Also reverses thermal hyperalgesia in a streptozocin induced rat diabetes model.
Solubility & Handling Storage instructions +4°C
Solubility overview Soluble in DMSO (50 mM), and in ethanol (50 mM)
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use
Chemical Data Chemical name 3,5-Dichloro-N-((1-((2,2-dimethyltetrahydro-2H-pyran-4-yl) methyl)-4-fluoropiperidin-4-yl)methyl)benzamide
Chemical structure
Molecular Formula C21 H29 Cl2 FN2 O2
PubChem identifier 16005493
SMILES Clc1cc(cc(Cl)c1)C(=O)NCC1(F)CCN(CC1)CC1CC(C)(C)OCC1
InChi InChI=1S/C21H29Cl2FN2O2/c1-20(2)12-15(3-8-28-20)13-26-6-4-21(24,5-7-26)14-25-19(27)16-9-17(22)11-18(23)10-16/h9-11,15H,3-8,12-14H2,1-2H3,(H,25,27)
InChiKey DKNDOKIVCXTFHJ-UHFFFAOYSA-N
Appearance Pale brown solid
References for TTA-P2 References are publications that support the biological activity of the product
Inhibition of T-Type Calcium Channels With TTA-P2 Reduces Chronic Neuropathic Pain Following Spinal Cord Injury in Rats. Liu H et al (2023) The journal of pain 24 : 1681-1695 Enhanced T-type calcium channel 3.2 activity in sensory neurons contributes to neuropathic-like pain of monosodium iodoacetate-induced knee osteoarthritis. Shin SM et al (2020) Molecular pain 16 : 1744806920963807 TTA-P2 is a potent and selective blocker of T-type calcium channels in rat sensory neurons and a novel antinociceptive agent. Choe W et al (2011) Molecular pharmacology 80 : 900-10
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Potent, selective, reversible T-type calcium channel blocker
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