Search Count: 2
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Discovery Of Potent, Highly Selective, And Orally Bioavailable Pyridine Carboxamide C-Jun Nh2-Terminal Kinase Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 2006-07-25 Classification: TRANSCRIPTION Ligands: SO4, 893, GOL |
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Solution Structure Of The Amino Terminal Fragment Of Urokinase-Type Plasminogen Activator
Organism: Homo sapiens
Method: SOLUTION NMR Release Date: 1995-05-08 Classification: PLASMINOGEN ACTIVATION Ligands: FUC |