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Circulation|August 2, 2006
Inhibition of urokinase-type plasminogen activator or matrix metalloproteinases prevents cardiac injury and dysfunction during viral myocarditisStephane Heymans, Matthias Pauschinger, Armando De Palma, et al.Gastroenterology|November 24, 2024
A Pangenotypic Hepatitis E Virus Replication Inhibitor With High Potency in a Rat Infection ModelXin Zhang, Mara Klöhn, Sivi Ouwerkerk-Mahadevan, et al.Journal of Medicinal Chemistry|March 6, 2007
N-(3,3a,4,4a,5,5a,6,6a-Octahydro-1,3-dioxo-4,6- ethenocycloprop[f]isoindol-2-(1H)-yl)carboxamides: Identification of novel orthopoxvirus egress inhibitorsThomas R Bailey, Susan R Rippin, Elizabeth Opsitnick, et al.Antiviral Research|July 11, 2009
Identification of allosteric inhibitors blocking the hepatitis C virus polymerase NS5B in the RNA synthesis initiation stepStéphane Betzi, Cécilia Eydoux, Cécile Bussetta, et al.Antimicrobial Agents and Chemotherapy|January 24, 2008
Inhibition of human immunodeficiency virus type 1 replication in human cells by Debio-025, a novel cyclophilin binding agentRoger G Ptak, Philippe A Gallay, Dirk Jochmans, et al.European Journal of Medicinal Chemistry|December 9, 2014
New 1-phenyl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides inhibit hepatitis C virus replication via suppression of cyclooxygenase-2Dinesh Manvar, Sveva Pelliccia, Giuseppe La Regina, et al.Journal of Medicinal Chemistry|September 30, 2022
Diastereomeric Resolution Yields Highly Potent Inhibitor of SARS-CoV-2 Main ProteaseMark S Cooper, Linlin Zhang, Mohamed Ibrahim, et al.ACS Medicinal Chemistry Letters|May 16, 2022
Discovery of 2-Phenylquinolines with Broad-Spectrum Anti-coronavirus ActivityMaria Giulia Nizi, Leentje Persoons, Angela Corona, et al.Hepatology (Baltimore, Md.)|October 20, 2012
The postbinding activity of scavenger receptor class B type I mediates initiation of hepatitis C virus infection and viral disseminationMuhammad N Zahid, Marine Turek, Fei Xiao, et al.Journal of Virology|August 10, 2007
The imidazopyrrolopyridine analogue AG110 is a novel, highly selective inhibitor of pestiviruses that targets the viral RNA-dependent RNA polymerase at a hot spot for inhibition of viral replicationJan Paeshuyse, Jean-Michel Chezal, Matheus Froeyen, et al.Pageof 62