Free shipping on all orders over $ 500

A-967079

Cat. No. M6380

All AbMole products are for research use only, cannot be used for human consumption.

A-967079 Structure
Synonym:

A967079

Size Price Availability Quantity
5mg USD 70 In stock
10mg USD 120 In stock
25mg USD 240 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

A-967079 is a selective TRPA1 channel blocker (IC50 values are 67 and 289 nM at human and rat TRPA1 receptors respectively). A 967079 displays 1000-fold selectivity for TRPA1 over other TRP channels, and is >150-fold selective over 75 other ion channels, enzymes and G-protein-coupled receptors. A 967079 exhibits analgesic effects in a rat osteoarthritic pain model.

Chemical Information
Molecular Weight 207.24
Formula C12H14FNO
CAS Number 1170613-55-4
Solubility (25°C) DMSO 20.72 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Jianhua Zhao, et al. Irritant-evoked activation and calcium modulation of the TRPA1 receptor

[2] Obed A Gyamfi, et al. Analysis of TRPA1 antagonist, A-967079, in plasma using high-performance liquid chromatography tandem mass-spectrometry

[3] Stefan Heber, et al. A Human TRPA1-Specific Pain Model

[4] Hoai T Ton, et al. Identification of a putative binding site critical for general anesthetic activation of TRPA1

[5] Ari Koivisto, et al. TRPA1: a transducer and amplifier of pain and inflammation

Related TRP Channel Products
SB-705498

SB-705498 is a potent, selective and orally bioavailable transient receptor potential vanilloid 1 (TRPV1) receptor antagonist with a pIC50 of 7.1.

HC-030031

HC-030031 is a selective TRPA1 blocker, antagonizing TRPA1-mediated calcium influx induced by AITC and formalin (IC50 = 6.2 and 5.3 μM, respectively).

AMG-517

AMG 517 is a potent and selective TRPV1 antagonist, antagonizes capsaicin, proton, and heat activation of TRPV1 with IC50 of 0.76 nM, 0.62 nM and 1.3 nM.

Icilin

Icilin is a synthetic super-agonist of the transient receptor potential M8 (TRPM8) ion channel.

Phenazopyridine hydrochloride

Phenazopyridine HCl is a competitive SARM1 inhibitor as well as a TRPM8 antagonist with an IC50 for SARM1 inhibition of 145 μM. It has local anesthetic/analgesic activity and can be used in studies related to traumatic brain injury, peripheral neuropathy, and neurodegenerative diseases.

  Catalog
Abmole Inhibitor Catalog




Keywords: A-967079, A967079 supplier, TRP Channel, inhibitors, activators

All AbMole products are for research use only, cannot be used for human consumption or veterinary use. We do not provide products or services to individuals. Please comply with the intended use and do not use AbMole products for any other purpose.



Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2026 AbMole BioScience. All Rights Reserved.