TC-2559 difumarate

TC-2559 difumarate Suppliers list
Company Name: Guangzhou Younan Technology Co., Ltd  
Tel: 020-82000279 18988941452
Email: YN_research@163.com
Company Name: RD International Technology Co., Limited  
Tel: 18024082417
Email: market@ubiochem.com
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
TC-2559 difumarate Basic information
Product Name:TC-2559 difumarate
Synonyms:
CAS:2454492-41-0
MF:C16H22N2O5
MW:322.36
EINECS:
Product Categories:
Mol File:2454492-41-0.mol
TC-2559 difumarate Structure
TC-2559 difumarate Chemical Properties
form Solid
color White to off-white
Water Solubility Soluble to 100 mM in water
Safety Information
MSDS Information
TC-2559 difumarate Usage And Synthesis
UsesTC-2559 idifumarate is a CNS-selective, orally active α4β2 subtype of nicotinic acetylcholine receptor (nAChR) partial agonist (EC50=0.18 μM). TC-2559 difumarate shows selectivity for α4β2 over α2β4, α4β4 and α3β4 receptors, with EC50s in the range of 10-30 μM. Antinociceptive effect[1][2].
Biological ActivityTC 2559 difumarate is a subtype-selective partial agonist for α4β2 nicotinic acetylcholine receptors (EC50 values are 0.18, 12.5, 14.0, > 30, > 100 and > 100 μM for α4β2, α4β4, α2β4, α3β4, α3β2 and α7 receptor subtypes respectively). Displays selectivity for (α4)2(β2)3 receptor stoichiometry and enhanced CNS-PNS selectivity ratio. Attenuates scopolamine-induced cognitive deficits in a step-through passive avoidance task.
in vivo

TC-2559 difumarate (1-10 mg/kg; i.p.) dose dependently reduces acute formalin-induced biphasic nociceptive responses in mice[2].
TC-2559 difumarate (0.3-3 mg/kg; i.p.) dose dependently inhibits CCI-induced neuropathic pain in rats[2].

Animal Model:Adult male mice (body weight 15-30 g) (formalin test)[2]
Dosage:1, 3, 10 mg/kg
Administration:I.p.
Result:Dose dependently reduced both early and late phases of formalin induced nociceptive behavioral responses.
Animal Model:Adult male SD rats (body weight 200-220 g) (chronic constriction injury (CCI))[2]
Dosage:0.3, 1, 3 mg/kg
Administration:I.p.
Result:Significantly reversed CCI induced the paw withdrawal threshold decreases.
storageDesiccate at RT
References[1] Bencherif M, et al. TC-2559: a novel orally active ligand selective at neuronal acetylcholine receptors. Eur J Pharmacol. 2000;409(1):45-55. DOI:10.1016/s0014-2999(00)00807-4
[2] Cheng LZ, et al. Enhanced inhibitory synaptic transmission in the spinal dorsal horn mediates antinociceptive effects of TC-2559. Mol Pain. 2011;7:56. Published 2011 Aug 4. DOI:10.1016/s0028-3908(03)00189-8
TC-2559 difumarate Preparation Products And Raw materials
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