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-Reference-Cited by-同舟云学术

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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

Published:1987-05 Issue:10 Volume:36 Page:1583-1588
ISSN:0006-2952
Container-title:Biochemical Pharmacology
language:en
Short-container-title:Biochemical Pharmacology

Author:

Armarego Wilfred L.F.,Altin Joseph G.,Weir Ronald C.,Bygrave Fyfe L.

Publisher

Elsevier BV

Subject

Pharmacology,Biochemistry

Reference29 articles.

1. Binding characteristics of 3H-prazosin to rat brain α-adrenergic receptors

2. New directions in adrenergic receptor research part II

3. Alpha-adrenergic receptors in liver membranes: Delineation with subtype selective radioligands

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. References;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02

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