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ChemicalBook--->CAS DataBase List--->1018830-99-3

1018830-99-3

1018830-99-3 Structure

1018830-99-3 Structure
IdentificationBack Directory
[Name]

Methanone, [2-amino-4-[3-(trifluoromethyl)phenyl]-3-thienyl]phenyl-
[CAS]

1018830-99-3
[Synonyms]

VCP171
VPC171
Methanone, [2-amino-4-[3-(trifluoromethyl)phenyl]-3-thienyl]phenyl-
(2-Amino-4-(3-(trifluoromethyl)phenyl)thiophen-3-yl)(phenyl)methanone
[Molecular Formula]

C18H12F3NOS
[MDL Number]

MFCD34601853
[MOL File]

1018830-99-3.mol
[Molecular Weight]

347.35
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 30 mg/ml,DMSO: 30 mg/ml,DMSO:PBS (pH 7.2) (1:6): 0.14 mg/ml,Ethanol: 10 mg/ml
[form ]

A crystalline solid
Spectrum DetailBack Directory
[Spectrum Detail]

Methanone, [2-amino-4-[3-(trifluoromethyl)phenyl]-3-thienyl]phenyl-(1018830-99-3)1HNMR
Hazard InformationBack Directory
[Biological Activity]

VCP171 is a positive allosteric modulator of adenosine A1 receptors (EC50 = 15.8 μM in a kinetic assay measuring agonist dissociation).1. It reduces AMPA receptor-mediated evoked excitatory postsynaptic currents (eEPSCs) in lamina I and lamina II neurons in a rat model of neuropathic pain (EC50s = 1.995 and 0.251 μM, respectively) to a greater extent than in sham control animals (EC50s = 2.512 and 0.631 μM, respectively).2
[storage]

Store at -20°C
[References]

1.Aurelio, L., Figler, H., Flynn, B.L., et al.5-Substituted 2-aminothiophenes as A1 adenosine receptor allosteric enhancersBioorg. Med. Chem.16(3)1319-1327(2008) 2.Imlach, W.L., Bhola, R.F., May, L.T., et al.A positive allosteric modulator of the adenosine A1 receptor selectively inhibits primary afferent synaptic transmission in a neuropathic pain modelMol. Pharm.88(3)460-468(2015)
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