Imidazoquinoline derivatives: Potent inhibitors of platelet cAMP phosphodiesterase which elevate cAMP levels and activate protein kinase in platelets

Author:

Seiler S.,Gillespie E.,Arnold A.J.,Brassard C.L.,Meanwell N.A.,Fleming J.S.

Publisher

Elsevier BV

Subject

Hematology

Reference28 articles.

1. 1,3-Dihydro-2H-Imidazo[4,5-b]Quinolin-2-Ones — Inhibitors of blood platelet aggregation and cAMP phosphodiesterase;Meanwell,1987

2. Pharmacology of a potent, new antithrombotic agent, 1,3-dihydro-7,8-dimethyl-2H-imidazo[4,5-b]quinolin-2-one (BMY-20844);Buchanan;Throm. Res.,1989

3. BMY-21638, a new, potent, broad-spectrum inhibitor of blood platelet aggregation and experimental thrombosis;Fleming;Thromb. Haemostasis,1989

4. Regulation of blood platelet function by cyclic nucleotides;Haslam;Adv. in Cyclic Nucleotide Res.,1978

5. The influence on platelet aggregation of drugs that affect the accumulation of adenosine 3′: 5′-cyclic monophosphate in platelets;Mills;Biochem. J.,1971

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