50 articles for thisTarget
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Article Title
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Design and synthesis of 1,2,3-triazole-containing N-acyl zanamivir analogs as potent neuraminidase inhibitors.
National Tsing Hua University
A Novel Potent and Highly Specific Inhibitor against Influenza Viral N1-N9 Neuraminidases: Insight into Neuraminidase-Inhibitor Interactions.
Thammasat University
Peramivir Phosphonate Derivatives as Influenza Neuraminidase Inhibitors.
National Taiwan University
Identification, synthesis and evaluation of SARS-CoV and MERS-CoV 3C-like protease inhibitors.
Academia Sinica
Design, synthesis, and biological evaluation of crenatoside analogues as novel influenza neuraminidase inhibitors.
Central South University
Development of oseltamivir phosphonate congeners as anti-influenza agents.
The Genomics Research Center
Analogs of zanamivir with modified C4-substituents as the inhibitors against the group-1 neuraminidases of influenza viruses.
National Taiwan University
Synergistic effect of zanamivir-porphyrin conjugates on inhibition of neuraminidase and inactivation of influenza virus.
National Taiwan University
Total synthesis of dryocrassin ABBA and its analogues with potential inhibitory activity against drug-resistant neuraminidases.
Chinese Academy of Sciences
Discovery of novel acylhydrazone neuraminidase inhibitors.
Shanghai Institute of Technology
1,2,3-Triazolyl-4-oxoquinolines: A feasible beginning for promising chemical structures to inhibit oseltamivir-resistant influenza A and B viruses.
Universidade Federal Fluminense
Anti-influenza activities of polyphenols from the medicinal mushroom Phellinus baumii.
Chonbuk National University
Flavonoids from Matteuccia struthiopteris and Their Anti-influenza Virus (H1N1) Activity.
Shenyang Pharmaceutical University
Exploring human parainfluenza virus type-1 hemagglutinin-neuraminidase as a target for inhibitor discovery.
Griffith University
Design and synthesis of 6-oxo-1,4,5,6-tetrahydropyrimidine-5-carboxylate derivatives as neuraminidase inhibitors.
Wuhan University School of Pharmaceutical Sciences
Oseltamivir analogues bearing N-substituted guanidines as potent neuraminidase inhibitors.
Utrecht University
Computer-guided approach to access the anti-influenza activity of licorice constituents.
University of Innsbruck
Development of novel potent orally bioavailable oseltamivir derivatives active against resistant influenza A.
Christian-Albrechts University of Kiel
Further discovery of caffeic acid derivatives as novel influenza neuraminidase inhibitors.
Shandong University
Caffeic acid derivatives: a new type of influenza neuraminidase inhibitors.
Shandong University
Structure-based design and synthesis of C-1- and C-4-modified analogs of zanamivir as neuraminidase inhibitors.
Chinese Academy of Sciences
Enhanced anti-influenza agents conjugated with anti-inflammatory activity.
National Taiwan University
Synthesis of C-4-modified zanamivir analogs as neuraminidase inhibitors and their anti-AIV activities.
Chinese Academy of Sciences
Xanthones from Polygala karensium inhibit neuraminidases from influenza A viruses.
Chosun University
Synthesis and in vitro study of novel neuraminidase inhibitors against avian influenza virus.
Chulalongkorn University
Intramolecular ion-pair prodrugs of zanamivir and guanidino-oseltamivir.
National Taiwan University
Design, synthesis and biological activity of thiazolidine-4-carboxylic acid derivatives as novel influenza neuraminidase inhibitors.
Shandong University
Chalcones as novel influenza A (H1N1) neuraminidase inhibitors from Glycyrrhiza inflata.
Chosun University
CS-8958, a prodrug of the new neuraminidase inhibitor R-125489, shows long-acting anti-influenza virus activity.
Daiichi Sankyo
New stilbenoid with inhibitory activity on viral neuraminidases from Erythrina addisoniae.
Chosun University
Carbocycles related to oseltamivir as influenza virus group-1-specific neuraminidase inhibitors. Binding to N1 enzymes in the context of virus-like particles.
Simon Fraser University
C-Methylated Flavonoids from Cleistocalyx operculatus and Their Inhibitory Effects on Novel Influenza A (H1N1) Neuraminidase.
Chosun University
Structure-activity relationship of flavonoids as influenza virus neuraminidase inhibitors and their in vitro anti-viral activities.
Peking Union Medical College
Ensemble-based virtual screening reveals potential novel antiviral compounds for avian influenza neuraminidase.
University of California
Design, synthesis, inhibitory activity, and SAR studies of hydrophobic p-aminosalicylic acid derivatives as neuraminidase inhibitors.
Shandong University
QSAR study of neuraminidase inhibitors based on heuristic method and radial basis function network.
Lanzhou University
Quantitative structure activity relationship studies on thiourea analogues as influenza virus neuraminidase inhibitors.
National Institute of Pharmaceutical Education and Research (NIPER)
Design, synthesis, inhibitory activity, and SAR studies of pyrrolidine derivatives as neuraminidase inhibitors.
Shandong University
Design, synthesis, and evaluation of carboxyl-modified oseltamivir derivatives with improved lipophilicity as neuraminidase inhibitors.
Shenyang Pharmaceutical University
Peramivir conjugates as orally available agents against influenza H275Y mutant.
National Taiwan University
Acylguanidine derivatives of zanamivir and oseltamivir: Potential orally available prodrugs against influenza viruses.
National Taiwan University
Optimization of N-Substituted Oseltamivir Derivatives as Potent Inhibitors of Group-1 and -2 Influenza A Neuraminidases, Including a Drug-Resistant Variant.
Shandong University
Discovery of C-1 modified oseltamivir derivatives as potent influenza neuraminidase inhibitors.
Shandong University
Discovery of (E)-1-amino-4-phenylbut-3-en-2-ol derivatives as novel neuraminidase inhibitors.
Shanghai Institute of Technology