The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
22677529 |
3 |
Pyrrolidinobenzoic acid inhibitors of influenza virus neuraminidase: the hydrophobic side chain influences type A subtype selectivity. |
University Of Alabama At Birmingham |
18694948 |
17 |
Limited inhibitory effects of oseltamivir and zanamivir on human sialidases. |
Miyagi Cancer Center Research Institute |
15214773 |
76 |
Fragment-based drug discovery. |
Sunesis Pharmaceuticals |
11000002 |
10 |
BCX-1812 (RWJ-270201): discovery of a novel, highly potent, orally active, and selective influenza neuraminidase inhibitor through structure-based drug design. |
Biocryst Pharmaceuticals |
10602699 |
15 |
Binding constants of neuraminidase inhibitors: An investigation of the linear interaction energy method. |
University Of Southampton |
9526556 |
18 |
Dihydropyrancarboxamides related to zanamivir: a new series of inhibitors of influenza virus sialidases. 2. Crystallographic and molecular modeling study of complexes of 4-amino-4H-pyran-6-carboxamides and sialidase from influenza virus types A and B. |
Glaxo Wellcome Research And Development |
8126701 |
3 |
Molecular modeling studies on ligand binding to sialidase from influenza virus and the mechanism of catalysis. |
Monash University |
11266166 |
36 |
Sialidase inhibitors related to zanamivir. Further SAR studies of 4-amino-4H-pyran-2-carboxylic acid-6-propylamides. |
Glaxowellcome Medicines Research Centre |
| 22 |
Novel inhibitors of influenza sialidases related to zanamivir. Heterocyclic replacements of the glycerol sidechain |
TBA |
| 51 |
Novel inhibitors of influenza sialidases related to GG167 structure-activity, crystallographic and Molecular dynamics studies with 4H-pyran-2-carboxylic acid 6-carboxamides |
TBA |
| 16 |
Novel inhibitors of influenza sialidase related to GG167 Synthesis of 4-amino and guanidino-4H-pyran-2-carboxylic acid-6-propylamides; selective inhibitors of influenza a virus sialidase |
TBA |
22100261 |
12 |
Synthesis and biological evaluation of sialic acid derivatives containing a long hydrophobic chain at the anomeric position and their C-5 linked polymers as potent influenza virus inhibitors. |
Saitama University |
21843936 |
35 |
3D QSAR and docking study of flavone derivatives as potent inhibitors of influenza H1N1 virus neuraminidase. |
Chinese Academy Of Medical Sciences |
20014777 |
6 |
Antiviral potential and molecular insight into neuraminidase inhibiting diarylheptanoids from Alpinia katsumadai. |
University Of Innsbruck |
15828835 |
6 |
Dimeric zanamivir conjugates with various linking groups are potent, long-lasting inhibitors of influenza neuraminidase including H5N1 avian influenza. |
Glaxosmithkline |
15582424 |
6 |
Design, synthesis, and structural analysis of inhibitors of influenza neuraminidase containing a 2,3-disubstituted tetrahydrofuran-5-carboxylic acid core. |
Abbott Laboratories |
11312919 |
22 |
Design, synthesis, and structural analysis of influenza neuraminidase inhibitors containing pyrrolidine cores. |
Abbott Laboratories |
10395473 |
19 |
Potent inhibition of influenza sialidase by a benzoic acid containing a 2-pyrrolidinone substituent. |
University Of Alabama At Birmingham |
16621549 |
40 |
Novel 5-azaindole factor VIIa inhibitors. |
Celera |
14561087 |
27 |
Structure-activity relationships of the p38alpha MAP kinase inhibitor 1-(5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[4-(2-morpholin-4-yl-ethoxy)naph- thalen-1-yl]urea (BIRB 796). |
Boehringer Ingelheim Pharmaceuticals |
11896401 |
3 |
Inhibition of p38 MAP kinase by utilizing a novel allosteric binding site. |
Boehringer Ingelheim Pharmaceuticals |
15857116 |
5 |
1-(5-Chloro-2-alkoxyphenyl)-3-(5-cyanopyrazin-2-yl)ureas [correction of cyanopyrazi] as potent and selective inhibitors of Chk1 kinase: synthesis, preliminary SAR, and biological activities. |
Abbott Laboratories |
16303309 |
31 |
Bicyclic and tricyclic thiophenes as protein tyrosine phosphatase 1B inhibitors. |
Wyeth Research |
10694412 |
15 |
Thermodynamics of substrate binding to the chaperone SecB. |
Indian Institute Of Science |