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AB120282

A 803467, NaV1.8 channel blocker

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(4 Publications)

MW 357.8 Da, Purity >98%. Selective blocker of NaV1.8 channels (IC50 = 8 nM for human NaV1.8 ). Shows greater than 100-fold selectivity over human NaV1.2, NaV1.3, NaV1.5, and NaV1.7 (IC50 values =1 μM). Shows no significant activity against TRPV1, P2X2/3, CaV2.2 and KCNQ2/3 channels. Antinociceptive.
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Chemical Structure - A 803467, NaV1.8 channel blocker (AB120282)
  • Chemical Structure

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Chemical Structure - A 803467, NaV1.8 channel blocker (AB120282)

2D chemical structure image of ab120282, A 803467, NaV1.8 channel blocker

Key facts

CAS number

944261-79-4

Purity

>98%

Form

Solid

form

Molecular weight

357.8 Da

Molecular formula

C<sub>1</sub><sub>9</sub>H<sub>1</sub><sub>6</sub>ClNO<sub>4</sub>

PubChem

16038374

Nature

Synthetic

Solubility

Soluble in DMSO to 100 mM and in ethanol to 25 mM

Biochemical name

5-(4-chlorophenyl)-N-(3,5-dimethoxyphenyl)furan-2-carboxamide

Biological description

Selective blocker of NaV1.8 channels (IC50 = 8 nM for human NaV1.8 ). Shows greater than 100-fold selectivity over human NaV1.2, NaV1.3, NaV1.5, and NaV1.7 (IC50 values =1 μM). Shows no significant activity against TRPV1, P2X2/3, CaV2.2 and KCNQ2/3 channels. Antinociceptive.

Canonical smiles

COC1=CC(=CC(=C1)NC(=O)C2=CC=C(O2)C3=CC=C(C=C3)Cl)OC

InChi

InChI=1S/C19H16ClNO4/c1-23-15-9-14(10-16(11-15)24-2)21-19(22)18-8-7-17(25-18)12-3-5-13(20)6-4-12/h3-11H,1-2H3,(H,21,22)

InChiKey

VHKBTPQDHDSBSP-UHFFFAOYSA-N

IUPAC Name

5-(4-chlorophenyl)-N-(3,5-dimethoxyphenyl)furan-2-carboxamide

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
Ambient
Appropriate long-term storage conditions
Ambient
Storage information
Store under desiccating conditions|The product can be stored for up to 12 months

Product protocols

Publications (4)

Recent publications for all applications. Explore the full list and refine your search

Pain 161:1100-1108 PubMed31929383

2020

An unbiased and efficient assessment of excitability of sensory neurons for analgesic drug discovery.

Applications

Unspecified application

Species

Unspecified reactive species

Zainab A Mohammed,Katerina Kaloyanova,Mohammed A Nassar

Journal of neuroinflammation 12:219 PubMed26597700

2015

SDF1-CXCR4 signaling contributes to persistent pain and hypersensitivity via regulating excitability of primary nociceptive neurons: involvement of ERK-dependent Nav1.8 up-regulation.

Applications

Unspecified application

Species

Unspecified reactive species

Fei Yang,Wei Sun,Yan Yang,Yan Wang,Chun-Li Li,Han Fu,Xiao-Liang Wang,Fan Yang,Ting He,Jun Chen

American journal of physiology. Cell physiology 304:C739-47 PubMed23364266

2013

Effective contractile response to voltage-gated Na+ channels revealed by a channel activator.

Applications

Unspecified application

Species

Unspecified reactive species

W-S Vanessa Ho,Alison J Davis,Preet S Chadha,Iain A Greenwood

Journal of neurophysiology 108:2230-41 PubMed22855776

2012

Tetrodotoxin-resistant voltage-dependent sodium channels in identified muscle afferent neurons.

Applications

Unspecified application

Species

Unspecified reactive species

Renuka Ramachandra,Stephanie Y McGrew,James C Baxter,Esad Kiveric,Keith S Elmslie
View all publications

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