Highly Potent Inhibitors of Proprotein Convertase Furin as Potential Drugs for Treatment of Infectious Diseases
Open Access
- 1 June 2012
- journal article
- Published by Elsevier BV in Online Journal of Public Health Informatics
- Vol. 287 (26), 21992-22003
- https://doi.org/10.1074/jbc.m111.332643
Abstract
No abstract availableThis publication has 67 references indexed in Scilit:
- Cleavage of Influenza Virus Hemagglutinin by Airway Proteases TMPRSS2 and HAT Differs in Subcellular Localization and Susceptibility to Protease InhibitorsJournal of Virology, 2010
- Potent Inhibitors of Furin and Furin-like Proprotein Convertases Containing Decarboxylated P1 Arginine MimeticsJournal of Medicinal Chemistry, 2009
- Inhibition of Furin/Proprotein Convertase-catalyzed Surface and Intracellular Processing by Small MoleculesOnline Journal of Public Health Informatics, 2009
- Substrate Cleavage Analysis of Furin and Related Proprotein ConvertasesOnline Journal of Public Health Informatics, 2008
- Differential P 1 arginine and lysine recognition in the prototypical proprotein convertase Kex2Proceedings of the National Academy of Sciences of the United States of America, 2007
- Synthetic small molecule furin inhibitors derived from 2,5-dideoxystreptamineProceedings of the National Academy of Sciences of the United States of America, 2006
- Stearylated octaarginine and artificial virus-like particles for transfection of siRNA into primary rat neuronsRNA, 2006
- Proprotein Convertase Models based on the Crystal Structures of Furin and Kexin: Explanation of their SpecificityJournal of Molecular Biology, 2005
- Furin at the cutting edge: From protein traffic to embryogenesis and diseaseNature Reviews Molecular Cell Biology, 2002
- Refined structure of the Hirudin-thrombin complexJournal of Molecular Biology, 1991