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17 articles for IM McLay


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

PMID
Data
Article Title
Organization
RPR203494 a pyrimidine analogue of the p38 inhibitor RPR200765A with an improved in vitro potency.EBI
Aventis Pharma
Non-steroidal glucocorticoid agonists: the discovery of aryl pyrazoles as A-ring mimetics.EBI
Glaxosmithkline
Design and synthesis of new nonsteroidal glucocorticoid modulators through application of an"agreement docking" method.EBI
Glaxosmithkline
Discovery of a potent series of non-steroidal nona-trifluoromethyl carbinol glucocorticoid receptor agonists with reduced lipophilicity.EBI
Glaxosmithkline
Synthesis and structure-activity relationships of long-acting beta2 adrenergic receptor agonists incorporating metabolic inactivation: an antedrug approach.EBI
Glaxosmithkline
Highly tractable, sub-nanomolar non-steroidal glucocorticoid receptor agonists.EBI
Glaxosmithkline
Synthesis and structure-activity relationships of long-acting beta2 adrenergic receptor agonists incorporating arylsulfonamide groups.EBI
Glaxosmithkline
Nonsteroidal glucocorticoid agonists: tetrahydronaphthalenes with alternative steroidal A-ring mimetics possessing dissociated (transrepression/transactivation) efficacy selectivity.EBI
Glaxosmithkline
Dissociated nonsteroidal glucocorticoid receptor modulators; discovery of the agonist trigger in a tetrahydronaphthalene-benzoxazine series.EBI
Glaxosmithkline
Selective endothelin A receptor antagonists. 3. Discovery and structure-activity relationships of a series of 4-phenoxybutanoic acid derivatives.EBI
Rh£Ne-Poulenc Rorer
The discovery of potent and long-acting oral factor Xa inhibitors with tetrahydroisoquinoline and benzazepine P4 motifs.EBI
Glaxosmithkline
 
New non peptidic C5a receptor antagonistsEBI
TBA
Aryl aminopyrazole benzamides as oral non-steroidal selective glucocorticoid receptor agonists.EBI
Medicines Research Centre
Drug rings database with web interface. A tool for identifying alternative chemical rings in lead discovery programs.EBI
Glaxosmithkline
Selective ET(A) antagonists. 5. Discovery and structure-activity relationships of phenoxyphenylacetic acid derivatives.EBI
RhôNe-Poulenc Rorer
Selective endothelin A receptor antagonists. 4. Discovery and structure-activity relationships of stilbene acid and alcohol derivatives.EBI
RhôNe-Poulenc Rorer
An algorithm-directed two-component library synthesized via solid-phase methodology yielding potent and orally bioavailable p38 MAP kinase inhibitors.EBI
Aventis Pharma