Polyacrylamides Bearing Pendant .alpha.-Sialoside Groups Strongly Inhibit Agglutination of Erythrocytes by Influenza A Virus: Multivalency and Steric Stabilization of Particulate Biological Systems

Watson J. Lees, Andrew Spaltenstein, Jill Kingery-Wood, +1

Journal of Medicinal Chemistry

The agglutination of erythrocytes by influenza virus is strongly inhibited by liposomes incorporating an analog of sialyl gangliosides

Jill Kingery-Wood, Kevin W. Williams, George B. Sigal, +1

Journal of the American Chemical Society

Microbial PathogensEmerging Infectious DiseasesSialyl GangliosidesDonut IconMedicine +9

Secondary Interactions Significantly Removed from the Sulfonamide Binding Pocket of Carbonic Anhydrase II Influence Inhibitor Binding Constants

P. Ann Boriack, David W. Christianson, Jill Kingery-Wood, +1

Journal of Medicinal Chemistry

Ethylene GlycolBioorganic ChemistryCarbonic Anhydrase IiChemical BiologyPharmaceutical Chemistry +16

Indole diterpene synthetic studies. 8. The total synthesis of (+)-paspalicine and (+)-paspalinine

Amos B. Smith, Jill Kingery-Wood, Tamara L. Leenay, +2

Journal of the American Chemical Society

Bioorganic ChemistryEngineeringBiochemistryNatural SciencesChemical Derivative +10

Discovery of heterocyclic ureas as a new class of raf kinase inhibitors: identification of a second generation lead by a combinatorial chemistry approach

Roger A. Smith, J A Barbosa, Cheri L. Blum, +15

Bioorganic & Medicinal Chemistry Letters

Combinatorial ChemistryMedicinal ChemistryDrug TargetBioorganic ChemistryBiochemistry +10

Total syntheses of (+)-paspalicine and (+)-paspalinine

Amos B. Smith, Toshiaki Sunazuka, Tamara L. Leenay, +1

Journal of the American Chemical Society

BiosynthesisEngineeringChemical MeasurementChemical AnalysisDonut Icon +13

Discovery of a new class of p38 kinase inhibitors

Jacques Dumas, Robert Sibley, Bernd Riedl, +15

Bioorganic & Medicinal Chemistry Letters

Medicinal ChemistryDrug TargetP38 Kinase InhibitorsMedicineRational Drug Design +3

p38 Kinase inhibitors for the treatment of arthritis and osteoporosis: thienyl, furyl, and pyrrolyl ureas

Anikó M. Redman, Jeffrey S. Johnson, Robert Dally, +19

Bioorganic & Medicinal Chemistry Letters

Pharmaceutical ChemistryP38 Kinase InhibitorsMedicineOsteoarthritisPharmacological Agent +7

Omega-carboxypyridyl substituted ureas as Raf kinase inhibitors

Uday R. Khire, Donald Bankston, J A Barbosa, +23

Bioorganic & Medicinal Chemistry Letters

Molecular PharmacologyBiochemistryMedicineRaf Kinase InhibitorsMechanism Of Action +3

Resolution of anti-3-Oxotricyclo[2.2.1.0]heptane-7-carboxylic acid by Candidia antartica Lipase A

Jill Kingery-Wood, Jeffrey S. Johnson

Tetrahedron Letters

BiosynthesisBiochemistryNatural SciencesBiocatalysisNatural Product Biosynthesis +1