Abstract
In the binding of Fgn to GP IIb/IIIa, RGD is the key sequence. In the present paper, RGDS, RGDV and RGDF were synthesized by use of solution method. Bioassay indicated that the C-terminal amino acid residues were very important for their antithrombosis effects. Conformational studies showed that their antithrombosis potency may depend on their total energies. The observation of their vasodilation effects suggests that this kind of function is worthy to be further studied.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Fibrinolytic Agents / chemical synthesis
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Fibrinolytic Agents / pharmacology
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Male
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Oligopeptides / chemical synthesis*
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Oligopeptides / pharmacology
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Platelet Aggregation Inhibitors / chemical synthesis
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Platelet Aggregation Inhibitors / pharmacology
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Rats
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Rats, Wistar
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Vasodilation / drug effects
Substances
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Fibrinolytic Agents
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Oligopeptides
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Platelet Aggregation Inhibitors
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arginyl-glycyl-aspartyl-phenylalanine
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arginyl-glycyl-aspartyl-valine
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arginyl-glycyl-aspartyl-serine