LIPINSKI C. A.; STAM J. G.; PEREIRA J. N.; ACHERMAN N. R.; HESS H.-J., J. MED. CHEM., 1980, 23, NO 9, 1026-1031
作者:LIPINSKI C. A.、 STAM J. G.、 PEREIRA J. N.、 ACHERMAN N. R.、 HESS H.-J.
DOI:——
日期:——
Bronchodilator and antiulcer phenoxypyrimidinones
作者:C. A. Lipinski、J. G. Stam、J. N. Pereira、N. R. Ackerman、H. J. Hess
DOI:10.1021/jm00183a012
日期:1980.9
was found in both the 2(1H)- and 4(3H)-pyrimidinone series and was most prominent in analogues containing either an electron-withdrawing or -donating substituent in the para position of the phenoxy ring. Significant antiulcer activity was observed only in the 2(1H)-pyrimidinone series among three closely related analogues. One of these, 5-(m-methylphenoxy)-2(1H)-pyrimidinone (3), exhibited more potent