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11 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Cmpds
Data
Article Title
Organization
7
Exploiting subsite S1 of trypsin-like serine proteases for selectivity: potent and selective inhibitors of urokinase-type plasminogen activator.EBI
Axys Pharmaceuticals
30
Monocharged inhibitors of mast cell tryptase derived from potent and selective dibasic inhibitors.EBI
Axys Pharmaceuticals
14
Optimization of a screening lead for factor VIIa/TF.EBI
Axys Pharmaceuticals
33
Development of serine protease inhibitors displaying a multicentered short (<2.3 A) hydrogen bond binding mode: inhibitors of urokinase-type plasminogen activator and factor Xa.EBI
Axys Pharmaceuticals
23
Development of potent and selective factor Xa inhibitors.EBI
Axys Pharmaceuticals
17
Dibasic inhibitors of human mast cell tryptase. Part 3: identification of a series of potent and selective inhibitors containing the benzamidine functionality.EBI
Axys Pharmaceuticals
59
Dibasic inhibitors of human mast cell tryptase. Part 2: structure-activity relationships and requirements for potent activity.EBI
Axys Pharmaceuticals
18
Dibasic inhibitors of human mast cell tryptase. Part 1: synthesis and optimization of a novel class of inhibitors.EBI
Axys Pharmaceuticals
4
Structural basis for selectivity of a small molecule, S1-binding, submicromolar inhibitor of urokinase-type plasminogen activator.BDB
Axys Pharmaceuticals
18
Engineering inhibitors highly selective for the S1 sites of Ser190 trypsin-like serine protease drug targets.BDB
Axys Pharmaceuticals
10
A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site.BDB
Axys Pharmaceuticals