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.

Aventis Pharma
Non-steroidal glucocorticoid agonists: the discovery of aryl pyrazoles as A-ring mimetics.

Glaxosmithkline
Design and synthesis of new nonsteroidal glucocorticoid modulators through application of an"agreement docking" method.

Glaxosmithkline
Discovery of a potent series of non-steroidal nona-trifluoromethyl carbinol glucocorticoid receptor agonists with reduced lipophilicity.

Glaxosmithkline
Synthesis and structure-activity relationships of long-acting beta2 adrenergic receptor agonists incorporating metabolic inactivation: an antedrug approach.

Glaxosmithkline
Highly tractable, sub-nanomolar non-steroidal glucocorticoid receptor agonists.

Glaxosmithkline
Synthesis and structure-activity relationships of long-acting beta2 adrenergic receptor agonists incorporating arylsulfonamide groups.

Glaxosmithkline
Nonsteroidal glucocorticoid agonists: tetrahydronaphthalenes with alternative steroidal A-ring mimetics possessing dissociated (transrepression/transactivation) efficacy selectivity.

Glaxosmithkline
Dissociated nonsteroidal glucocorticoid receptor modulators; discovery of the agonist trigger in a tetrahydronaphthalene-benzoxazine series.

Glaxosmithkline
Selective endothelin A receptor antagonists. 3. Discovery and structure-activity relationships of a series of 4-phenoxybutanoic acid derivatives.

Rh£Ne-Poulenc Rorer
The discovery of potent and long-acting oral factor Xa inhibitors with tetrahydroisoquinoline and benzazepine P4 motifs.

Glaxosmithkline
New non peptidic C5a receptor antagonists

TBA
Aryl aminopyrazole benzamides as oral non-steroidal selective glucocorticoid receptor agonists.

Medicines Research Centre
Drug rings database with web interface. A tool for identifying alternative chemical rings in lead discovery programs.

Glaxosmithkline
Selective ET(A) antagonists. 5. Discovery and structure-activity relationships of phenoxyphenylacetic acid derivatives.

RhôNe-Poulenc Rorer
Selective endothelin A receptor antagonists. 4. Discovery and structure-activity relationships of stilbene acid and alcohol derivatives.

RhôNe-Poulenc Rorer
An algorithm-directed two-component library synthesized via solid-phase methodology yielding potent and orally bioavailable p38 MAP kinase inhibitors.

Aventis Pharma