16 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Understanding the structure-activity relationship of the human ether-a-go-go-related gene cardiac K+ channel. A model for bad behavior.

Aventis Pharmaceuticals
Potent small molecule inhibitors of spleen tyrosine kinase (Syk).

Aventis Pharmaceuticals
Characterization of HERG potassium channel inhibition using CoMSiA 3D QSAR and homology modeling approaches.

Aventis Pharmaceuticals
Design, synthesis, and biological activity of potent and selective inhibitors of mast cell tryptase.

Aventis Pharmaceuticals
Design of bivalent ligands using hydrogen bond linkers: synthesis and evaluation of inhibitors for human beta-tryptase.

Aventis Pharmaceuticals
Novel pyrazinone inhibitors of mast cell tryptase: synthesis and SAR evaluation.

Aventis Pharmaceuticals
Mapping the kinase domain of Janus Kinase 3.

Aventis Pharmaceuticals
Potent quinoxaline-based inhibitors of PDGF receptor tyrosine kinase activity. Part 2: the synthesis and biological activities of RPR127963 an orally bioavailable inhibitor.

Aventis Pharmaceuticals
Potent quinoxaline-based inhibitors of PDGF receptor tyrosine kinase activity. Part 1: SAR exploration and effective bioisosteric replacement of a phenyl substituent.

Aventis Pharmaceuticals
Discovery of an orally efficacious inhibitor of coagulation factor Xa which incorporates a neutral P1 ligand.

Aventis Pharmaceuticals
Optimization of the beta-aminoester class of factor Xa inhibitors. Part 2: Identification of FXV673 as a potent and selective inhibitor with excellent In vivo anticoagulant activity.

Aventis Pharmaceuticals
Optimization of the beta-aminoester class of factor Xa inhibitors. Part 1: P(4) and side-chain modifications for improved in vitro potency.

Aventis Pharmaceuticals
Benzimidazoles and isosteric compounds as potent and selective factor Xa inhibitors.

Aventis Pharmaceuticals
Nonbenzamidine compounds as selective factor Xa inhibitors.

Aventis Pharmaceuticals
FXR (NR1H4) modulating compounds

Gilead Sciences
Lead identification to generate 3-cyanoquinoline inhibitors of insulin-like growth factor receptor (IGF-1R) for potential use in cancer treatment.

Wyeth Research