A water-soluble derivative of prazosin prazosinamine hydrochloride [1-(4′-amino-6′,7′-dimethoxyquinazolin-2′-yl)-4-(6″-aminohexanoyl) piperazine hydrochloride], reversibly inhibits the calcium-mobilizing action of α1-adrenergic agonists in the perfused rat liver
Wilfred L.F. Armarego, Joseph G. Altin, Ronald C. Weir, Fyfe L. BygraveVolume:
36
Year:
1987
Language:
english
Pages:
1589
DOI:
10.1016/0006-2952(87)90040-2
File:
PDF, 626 KB
english, 1987