
CAS 33469-36-2: 2-Phenyl-4-(trifluoromethyl)-1H-imidazole
Formula:C10H7F3N2
InChI:InChI=1/C10H7F3N2/c11-10(12,13)8-6-14-9(15-8)7-4-2-1-3-5-7/h1-6H,(H,14,15)
SMILES:c1ccc(cc1)c1ncc(C(F)(F)F)[nH]1
Synonyms:- 1H-imidazole, 2-phenyl-4-(trifluoromethyl)-
- 2-phenyl-5-(trifluoromethyl)-1H-imidazole
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Found 4 products.
2-Phenyl-4-(trifluoromethyl)-1H-imidazole
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:212.17500305175782-Phenyl-4-(trifluoromethyl)-1H-imidazole
CAS:Formula:C10H7F3N2Purity:97%Color and Shape:SolidMolecular weight:212.17122-Phenyl-4-(trifluoromethyl)-1H-imidazole
CAS:2-Phenyl-4-(trifluoromethyl)-1H-imidazolePurity:97%Molecular weight:212.17g/mol2-Phenyl-4-(trifluoromethyl)-1H-imidazole
CAS:2-Phenyl-4-(trifluoromethyl)-1H-imidazole is an extracellular control agent that binds to cytosolic Ca2+ and inhibits the elevation of camp levels. 2-Phenyl-4-(trifluoromethyl)-1H-imidazole has been shown to reduce oxidative DNA damage in vitro, which may be due to its ability to inhibit intracellular Ca2+ release from the sarcoplasmic reticulum. This drug has been shown to be effective against high blood pressure and heart rate in both wild-type mice and mice with elevated concentrations of phenylephrine. 2-Phenyl-4-(trifluoromethyl)-1H-imidazole also has the potential mechanism of inhibiting the activity of phosphodiesterase enzymes, which are responsible for deactivating cyclic adenosine monophosphate (cAMP).Formula:C10H7F3N2Purity:Min. 95%Molecular weight:212.17 g/mol