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Research Article
Primary structure and function of novel O-glycosylated hirudins from the leech Hirudinaria manillensis
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Biochemistry, 1992, 31 (8), pp 2294–2298
DOI: 10.1021/bi00123a012
Publication Date: March 1992
Note: In lieu of an abstract, this is the article's first page.
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This article has been cited by 3 ACS Journal articles (3 most recent appear below).
Leech-Derived Thrombin Inhibitors: From Structures to Mechanisms to Clinical Applications
María Ángeles Corral-Rodríguez, Sandra Macedo-Ribeiro, Pedro José Barbosa Pereira and Pablo Fuentes-PriorJournal of Medicinal Chemistry2010 53 (10), 3847-3861Leech-Derived Thrombin Inhibitors: From Structures to Mechanisms to Clinical Applications
María Ángeles Corral-Rodríguez, Sandra Macedo-Ribeiro, Pedro José Barbosa Pereira and Pablo Fuentes-PriorJournal of Medicinal Chemistry2010 53 (10), 3847-3861
Structural Investigations of Glycoconjugates at High Sensitivity
Yehia Mechref and Milos V. NovotnyChemical Reviews2002 102 (2), 321-370Structural Investigations of Glycoconjugates at High Sensitivity
Yehia Mechref and Milos V. NovotnyChemical Reviews2002 102 (2), 321-370
Rational Design of True Hirudin Mimetics: Synthesis and Characterization of Multisite-Directed α-Thrombin Inhibitors1
Angela Lombardi, Flavia Nastri, Rossella Della Morte, Armando Rossi, Alfredo De Rosa, Norma Staiano, Carlo Pedone, and Vincenzo PavoneJournal of Medicinal Chemistry1996 39 (10), 2008-2017Rational Design of True Hirudin Mimetics: Synthesis and Characterization of Multisite-Directed α-Thrombin Inhibitors1
Angela Lombardi, Flavia Nastri, Rossella Della Morte, Armando Rossi, Alfredo De Rosa, Norma Staiano, Carlo Pedone, and Vincenzo PavoneJournal of Medicinal Chemistry1996 39 (10), 2008-2017We describe here the design, synthesis, and activity of a novel class of -thrombin inhibitors named hirunorms. They were rationally designed to interact through their N-terminal end with the -thrombin active site in a nonsubstrate mode and to ...
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