102151-93-9Relevant articles and documents
Substituted benzylamino-6-(trifluoromethyl)pyrimidin-4(1H)-ones: A novel class of selective human A-FABP inhibitors
Ringom, Rune,Axen, Eva,Uppenberg, Jonas,Lundb?ck, Thomas,Rondahl, Lena,Barf, Tjeerd
, p. 4449 - 4452 (2007/10/03)
The synthesis and evaluation of novel human A-FABP inhibitors based on the 6-(trifluoromethyl)pyrimidine-4(1H)-one scaffold is described. Two series of compounds, bearing either an amino or carbon substituent in the 2-position of the pyrimidine ring were