O-benzyl hydroxyproline as a bioisostere for Phe-Pro: Novel dipeptide thrombin inhibitors
- 1 September 1996
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 6 (18) , 2225-2230
- https://doi.org/10.1016/0960-894x(96)00404-0
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Chapter 8. Anticoagulant Strategies Targeting Thrombin and Factor XaPublished by Elsevier ,1995
- Direct thrombin inhibitors in cardiovascular medicine.Circulation, 1994
- Superior Activity of a Thromboxane Receptor Antagonist as Compared with Aspirin in Rat Models of Arterial and Venous ThrombosisJournal of Cardiovascular Pharmacology, 1993
- Lasting safe interruption of endarterectomy thrombosis by transiently infused antithrombin peptide D-Phe-Pro-ArgCH2Cl in baboonsBlood, 1993
- Refined 2·3ÅX-ray crystal structure of bovine thrombin complexes formed with the benzamidine and arginine-based thrombin inhibitors NAPAP, 4-TAPAP and MQPA: A starting point for improving antithromboticsJournal of Molecular Biology, 1992
- The refined 1.9‐Å X‐ray crystal structure of d‐Phe‐Pro‐Arg chloromethylketone‐inhibited human α‐thrombin: Structure analysis, overall structure, electrostatic properties, detailed active‐site geometry, and structure‐function relationshipsProtein Science, 1992
- Pharmacologic Aspects of the Development of Selective Synthetic Thrombin Inhibitors as AnticoagulantsSeminars in Thrombosis and Hemostasis, 1992
- Thrombin structure and functionBlood Coagulation & Fibrinolysis, 1991
- ThrombinaAnnals of the New York Academy of Sciences, 1986
- D-PHE-PRO-ARGCH2Cl-A selective affinity label for thrombinThrombosis Research, 1979