23 articles for HJ Dyke
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
7-Methoxyfuro[2,3-c]pyridine-4-carboxamides as PDE4 inhibitors: a potential treatment for asthma.

Celltech R&D
Synthesis and profile of SCH351591, a novel PDE4 inhibitor.

Schering-Plough
8-Methoxyquinolines as PDE4 inhibitors.

Schering-Plough
8-Methoxyquinoline-5-carboxamides as PDE4 inhibitors: a potential treatment for asthma.

Celltech R&D
Synthesis and structure-activity relationships of guanine analogues as phosphodiesterase 7 (PDE7) inhibitors.

Celltech R&D
7-Methoxybenzofuran-4-carboxamides as PDE 4 inhibitors: a potential treatment for asthma.

Celltech-Chiroscience
PDE4 inhibitors: new xanthine analogues.

Chiroscience
Novel triazolo-pyrrolopyridines as inhibitors of Janus kinase 1.

Argenta Discovery
Increasing selectivity of CC chemokine receptor 8 antagonists by engineering nondesolvation related interactions with the intended and off-target binding sites.

Astrazeneca
Identification of imidazo-pyrrolopyridines as novel and potent JAK1 inhibitors.

Argenta Discovery
Identification and hit-to-lead exploration of a novel series of histamine H4 receptor inverse agonists.

Argenta Discovery
1H-Pyrazolo[3,4-g]hexahydro-isoquinolines as selective glucocorticoid receptor antagonists with high functional activity.

Corcept Therapeutics
2-Benzenesulfonyl-8a-benzyl-hexahydro-2H-isoquinolin-6-ones as selective glucocorticoid receptor antagonists.

Corcept Therapeutics
Modulation of 11beta-hydroxysteroid dehydrogenase type 1 activity by 1,5-substituted 1H-tetrazoles.

University of Edinburgh
Discovery and optimization of novel, non-steroidal glucocorticoid receptor modulators.

Argenta Discovery
Quinazoline and benzimidazole MCH-1R antagonists.

Argenta Discovery
Identification and optimisation of a series of substituted 5-pyridin-2-yl-thiophene-2-hydroxamic acids as potent histone deacetylase (HDAC) inhibitors.

Argenta Discovery
Identification and optimisation of a series of substituted 5-(1H-pyrazol-3-yl)-thiophene-2-hydroxamic acids as potent histone deacetylase (HDAC) inhibitors.

Argenta Discovery
Novel 7-methoxy-6-oxazol-5-yl-2,3-dihydro-1H-quinazolin-4-ones as IMPDH inhibitors.

Ucb Pharma
Quinazolinethiones and quinazolinediones, novel inhibitors of inosine monophosphate dehydrogenase: synthesis and initial structure-activity relationships.

Celltech R and D
A virtual screening approach to finding novel and potent antagonists at the melanin-concentrating hormone 1 receptor.

Argenta Discovery
Structure-activity relationships of a novel series of melanin-concentrating hormone (MCH) receptor antagonists.

Argenta Discovery
Aryl sulfonamides as selective PDE4 inhibitors.

Chiroscience