An Efficient Synthesis of Cyclic RGD Peptides as Antithrombotic Agents
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 61 (15) , 5180-5185
- https://doi.org/10.1021/jo9603284
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Facile detosylation of cyclic peptides. An effective synthesis of platelet glycoprotein IIb/IIIa inhibitorsTetrahedron Letters, 1994
- Template-Constrained Cyclic Peptides: Design of High-Affinity Ligands for GPIIb/IIIaJournal of the American Chemical Society, 1994
- Structural Studies of a Family of High Affinity Ligands for GPIIb/IIIaJournal of the American Chemical Society, 1994
- Cyclo(dipeptide)s as low-molecular-mass gelling agents to harden organic fluidsJournal of the Chemical Society, Chemical Communications, 1994
- Development of a small RGD peptide fibrinogen receptor antagonist with potent antiaggregatory activity in vitroJournal of Medicinal Chemistry, 1991
- Polymer-supported acidolysis of protecting groups used in the synthesis of large peptidesJournal of the Chemical Society, Chemical Communications, 1991
- Synthesis and structure-activity relationships of (MeTyr1, MeArg7)-Dynorphin A(1-8)-OH analogues with substitution at position 8.CHEMICAL & PHARMACEUTICAL BULLETIN, 1990
- Trimethylsilyl trifluoromethanesulphonate as a useful deprotecting reagent in both solution and solid phase peptide synthesesJournal of the Chemical Society, Chemical Communications, 1987
- A murine monoclonal antibody that completely blocks the binding of fibrinogen to platelets produces a thrombasthenic-like state in normal platelets and binds to glycoproteins IIb and/or IIIa.Journal of Clinical Investigation, 1983
- Synthèses de la Phé2‐arginine‐vasopressine et de la Phé2‐arginine‐vasotocine et nouvelles synthèses de l'argininevasopressine et de l'arginine‐vasotocineHelvetica Chimica Acta, 1962