ChemicalBook--->CAS DataBase List--->354812-16-1

354812-16-1

354812-16-1 Structure

354812-16-1 Structure
IdentificationBack Directory
[Name]

3-amino-5-(4-methoxyphenyl)-2-Thiophenecarboxamide
[CAS]

354812-16-1
[Synonyms]

AA43279, CID 4278270
3-amino-5-(4-methoxyphenyl)-2-Thiophenecarboxamide
2-Thiophenecarboxamide, 3-amino-5-(4-methoxyphenyl)-
3-Amino-5-(4-Methoxyphenyl)-2-Thiophenecarboxamide(WXC03635)
[Molecular Formula]

C12H12N2O2S
[MDL Number]

MFCD00277422
[MOL File]

354812-16-1.mol
[Molecular Weight]

248.3
Chemical PropertiesBack Directory
[Boiling point ]

456.7±45.0 °C(Predicted)
[density ]

1.312±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C
[solubility ]

Soluble in DMSO (up to 35 mg/ml)
[form ]

solid
[pka]

15.71±0.50(Predicted)
[color ]

Tan
[Stability:]

Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
Hazard InformationBack Directory
[Description]

AA43279 (354812-16-1) is a selective Nav1.1 activator. In HEK-293 cells expressing human Nav1.1 channels AA43279 increased the Nav1.1-mediated current in a concentration dependent manner (EC50=9.5 μM). In rat hippocampal brain slices it increased the firing activity of parvalbumin-expressing, fast-spiking GABAergic interneurons and increased the spontaneous inhibitory post-synaptic currents recorded from pyramidal neurons. It displayed anticonvulsant activity in vivo. Important tool compound for exploring the physiology of Nav1.1 channels.1
[Uses]

AA43279 is an in gamma-aminobutyric acid (GABA) fast-firing interneurons located activator for Nav1.1 channel (SCN1A) with an EC50 of 9.5 μM. AA43279 enhances specific neuronal firing activity in vitro, and exhibits anticonvulsant activity in rat MEST model[1].
[IC 50]

Nav1.1: 9.5 μM (IC50); Nav1.6: 11.6 μM (IC50); Nav1.5: 14.4 μM (IC50); Nav1.2: 22.8 μM (IC50)
[References]

1) Frederiksen et al. (2017), A small molecule activator of Nav 1.1 channels increases fast-spiking interneuron excitability and GABAergic transmission in vitro and has anti-convulsive effects in vivo.; Eur. J. Neuroscience, 46 1887
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