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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

✍ Scribed by Wilfred L.F. Armarego; Joseph G. Altin; Ronald C. Weir; Fyfe L. Bygrave


Book ID
115779432
Publisher
Elsevier Science
Year
1987
Tongue
English
Weight
626 KB
Volume
36
Category
Article
ISSN
0006-2952

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