29 articles for thisTarget
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N-(2-Benzoylphenyl)-L-tyrosine PPARgamma agonists. 1. Discovery of a novel series of potent antihyperglycemic and antihyperlipidemic agents.

Glaxo Wellcome Research and Development
Discovery of 1,5-benzodiazepines with peripheral cholecystokinin (CCK-A) receptor agonist activity (II): Optimization of the C3 amino substituent.

Glaxo Wellcome Research and Development
3-[2-(N-phenylacetamide)]-1,5-benzodiazepines: orally active, binding selective CCK-A agonists.

Glaxo Wellcome Research and Development
3-(1H-indazol-3-ylmethyl)-1,5-benzodiazepines: CCK-A agonists that demonstrate oral activity as satiety agents.

Glaxo Wellcome Research and Development
Dihydropyrancarboxamides related to zanamivir: a new series of inhibitors of influenza virus sialidases. 2. Crystallographic and molecular modeling study of complexes of 4-amino-4H-pyran-6-carboxamides and sialidase from influenza virus types A and B.

Glaxo Wellcome Research and Development
N-Phenylamidines as selective inhibitors of human neuronal nitric oxide synthase: structure-activity studies and demonstration of in vivo activity.

Glaxo Wellcome Research and Development
Substituted N-phenylisothioureas: potent inhibitors of human nitric oxide synthase with neuronal isoform selectivity.

Glaxo Wellcome Research and Development
Inhibition of inducible nitric oxide synthase by acetamidine derivatives of hetero-substituted lysine and homolysine.

Glaxo Wellcome Research and Development
Conversion of acyclic nonpeptide CCK antagonists into CCK agonists

Glaxo Wellcome Research and Development
Isolation of translactone-containing triterpenes with thrombin inhibitory activities from the leaves of Lantana camara.

Glaxo Wellcome Research and Development
2-Amino-4,6-diarylpyridines as novel ligands for the estrogen receptor.

Glaxo Wellcome Research and Development
Novel glucocorticoid antedrugs possessing a 17beta-(gamma-lactone) ring.

Glaxo Wellcome Research and Development
Design and synthesis of pyrrolidine-5,5-trans-lactams (5-oxo-hexahydro-pyrrolo[3,2-b]pyrroles) as novel mechanism-based inhibitors of human cytomegalovirus protease. 1. The alpha-methyl-trans-lactam template.

Glaxo Wellcome Research and Development
Synthesis and SAR of 4-aryl-2-hydroxy-4-oxobut-2-enoic acids and esters and 2-amino-4-aryl-4-oxobut-2-enoic acids and esters: potent inhibitors of kynurenine-3-hydroxylase as potential neuroprotective agents.

Glaxo Wellcome Research and Development
Selective plasma hydrolysis of glucocorticoid gamma-lactones and cyclic carbonates by the enzyme paraoxonase: an ideal plasma inactivation mechanism.

Glaxo Wellcome Research and Development
Synthesis and biological activity of a novel series of indole-derived PPARgamma agonists.

Glaxo Wellcome Research and Development
Thrombin inhibitors based on [5,5] trans-fused indane lactams.

Glaxo Wellcome Research and Development
Synthetic [5,5] trans-fused indane lactones as inhibitors of thrombin.

Glaxo Wellcome Research and Development
Differential activity of rosiglitazone enantiomers at PPAR gamma.

Glaxo Wellcome Research and Development
5,5-trans lactone-containing inhibitors of serine proteases: identification of a novel, acylating thrombin inhibitor.

Glaxo Wellcome Research and Development
Design and synthesis of monocyclic beta-lactams as mechanism-based inhibitors of human cytomegalovirus protease.

Glaxo Wellcome Research and Development
S-aryl cysteine S,S-dioxides as inhibitors of mammalian kynureninase.

Glaxo Wellcome Research and Development
The squalestatins: inhibitors of squalene synthase. Enzyme inhibitory activities and in vivo evaluation of C3-modified analogues.

Glaxo Wellcome Research and Development
The structure-activity relationship between peroxisome proliferator-activated receptor gamma agonism and the antihyperglycemic activity of thiazolidinediones.

Glaxo Wellcome Research and Development
N-(2-Benzoylphenyl)-L-tyrosine PPARgamma agonists. 3. Structure-activity relationship and optimization of the N-aryl substituent.

Glaxo Wellcome Research and Development
N-(2-Benzoylphenyl)-L-tyrosine PPARgamma agonists. 2. Structure-activity relationship and optimization of the phenyl alkyl ether moiety.

Glaxo Wellcome Research and Development