Relationships between the chemical constitution of aggregation inhibitors and human blood platelet response profile
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Biochemistry,Biophysics
Reference28 articles.
1. Human Blood Platelet Aggregation-inhibitory Target Sites Assumed to Involve Membrane Phospholipids
2. Surface activity and human blood platelet aggregation-inhibitory potency
3. Interaction of human blood platelet aggregation inhibitors with phospholipid films
4. Relationships between the chemical constitution of carbamoylpiperidines and related compounds, and their inhibition of ADP-induced human blood platelet aggregation
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1. Investigation of platelet aggregation inhibitory activity by phenyl amides and esters of piperidinecarboxylic acids;Bioorganic & Medicinal Chemistry;2003-04
2. Inhibition of PAF-induced human platelet aggregation by antithrombotic nipecotamides;Prostaglandins, Leukotrienes and Essential Fatty Acids;1995-05
3. Design and Synthesis of Piperidine-3-carboxamides as Human Platelet Aggregation Inhibitors;Journal of Medicinal Chemistry;1995-01
4. Antiplatelet Activity of Nipecotamides in Experimental Thrombosis in Mice;Journal of Pharmaceutical Sciences;1994-02
5. Depth-dependent change in membrane fluidity by phenolic compounds in bovine platelets and its relationship with their effects on aggregation and adenylate cyclase activity;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;1993-11
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