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A-967079

SIGMA/SML0085 - ≥98% (HPLC)

Synonym: (1E,3E)-1-(4-Fluorophenyl)-2-methyl-1-penten-3-one oxime

CAS Number: 1170613-55-4
Empirical Formula (Hill Notation): C12H14FNO
Molecular Weight: 207.24
MDL Number: MFCD20488058
Linear Formula: C12H14FNO
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-SML0085-5MG 5 mg
$142.00
1/EA
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45-SML0085-25MG 25 mg
$538.00
1/EA
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assay ≥98% (HPLC)
color white to tan
form powder
InChI 1S/C12H14FNO/c1-3-12(14-15)9(2)8-10-4-6-11(13)7-5-10/h4-8,15H,3H2,1-2H3/b9-8+,14-12+
InChI key HKROEBDHHKMNBZ-CHBKHGQFSA-N
originator Abbott
Quality Level 100 
SMILES string CCC(=N/O)C(C)=Cc1ccc(F)cc1
solubility DMSO: ≥12 mg/mL
storage temp. 2-8°C
Application: A-967079 has been used in blocking miR-711-induced TRPA1 (transient receptor potential cation channel subfamily A member 1) channel.
Biochem/physiol Actions: A-967079 is a potent and selective antagonist of Transient Receptor Potential Anykrin 1 (TRPA1) with IC50′s of 67 nM and 289 nM at human and rat TRPA1 receptors, respectively, and minimal or no activity at other TRP channels or G-protein-coupled receptors, enzymes, transporters, and ion channels out of 89 tested. A-967079 blocks TRPA1 activation in human and rat cell lines and has been shown to reduce the responses of wide dynamic range (WDR) and nociceptive specific (NS) neurons to high-intensity mechanical stimulation.
Features and Benefits: This compound was developed by Abbott . To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here .
General description: A-967079 prevents neuropathic and inflammatory pain. It reduces cold allodynia, which is produced by nerve injury.
Packaging: 5, 25 mg in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
Storage Temp. 2-8°C
UNSPSC 12352200

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