30 articles for CH Wong
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Peramivir Phosphonate Derivatives as Influenza Neuraminidase Inhibitors.
National Taiwan University
Oseltamivir hydroxamate and acyl sulfonamide derivatives as influenza neuraminidase inhibitors.
TBA
Chemical constituents of Plectranthus amboinicus and the synthetic analogs possessing anti-inflammatory activity.
National Defense Medical Center, Taiwan
Development of oseltamivir phosphonate congeners as anti-influenza agents.
The Genomics Research Center
Evaluation of sulfatase-directed quinone methide traps for proteomics.
Bielefeld University
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
High-throughput identification of fucosyltransferase inhibitors using carbohydrate microarrays.
The Scripps Research Institute
Synthesis of sialyl Lewis X mimetics using the Ugi four-component reaction.
Scripps Research Institute
Enhancement of capillary leakage and restoration of lymphocyte egress by a chiral S1P1 antagonist in vivo.
The Scripps Research Institute
Design, synthesis, and biological evaluation of HIV/FIV protease inhibitors incorporating a conformationally constrained macrocycle with a small P3' residue.
The Scripps Research Institute
Acceptor substrate-based selective inhibition of galactosyltransferases.
Scripps Research Institute
Chemoenzymatic synthesis of iminocyclitol derivatives: a useful library strategy for the development of selective fucosyltransfer enzymes inhibitors.
Scripps Research Institute
Development of selective tight-binding inhibitors of leukotriene A4 hydrolase.
Scripps Research Institute
Enhanced anti-influenza agents conjugated with anti-inflammatory activity.
National Taiwan University
Intramolecular ion-pair prodrugs of zanamivir and guanidino-oseltamivir.
National Taiwan University
A copper(I)-catalyzed 1,2,3-triazole azide-alkyne click compound is a potent inhibitor of a multidrug-resistant HIV-1 protease variant.
The Scripps Research Institute
High-throughput screening for human lysosomal beta-N-Acetyl hexosaminidase inhibitors acting as pharmacological chaperones.
Research Institute, Hospital For Sick Children
Isoquinoline-pyridine-based protein kinase B/Akt antagonists: SAR and in vivo antitumor activity.
Abbott Laboratories