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15 articles for EM Doherty


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

PMID
Data
Article Title
Organization
N-substituted azaindoles as potent inhibitors of Cdc7 kinase.EBI
Amgen
2-Phenylamino-6-cyano-1H-benzimidazole-based isoform selective casein kinase 1 gamma (CK1¿) inhibitors.EBI
Amgen
Rapid development of piperidine carboxamides as potent and selective anaplastic lymphoma kinase inhibitors.EBI
Amgen
4-Aminopyrimidine tetrahydronaphthols: a series of novel vanilloid receptor-1 antagonists with improved solubility properties.EBI
Amgen
Design of a new peptidomimetic agonist for the melanocortin receptors based on the solution structure of the peptide ligand, Ac-Nle-cyclo[Asp-Pro-DPhe-Arg-Trp-Lys]-NH(2).EBI
Amgen
Discovery of pyridazinopyridinones as potent and selective p38 mitogen-activated protein kinase inhibitors.EBI
Amgen
Design and synthesis of peripherally restricted transient receptor potential vanilloid 1 (TRPV1) antagonists.EBI
Amgen
Developing HDAC4-Selective Protein Degraders To Investigate the Role of HDAC4 in Huntington's Disease Pathology.EBI
Charles River Laboratories
Discovery of potent, orally available vanilloid receptor-1 antagonists. Structure-activity relationship of N-aryl cinnamides.EBI
Amgen
Discovery of 5-hydroxyalkyl-4-phenylpyridines as a new class of glucagon receptor antagonists.EBI
Bayer Research Center
Inhibitors of HIV-1 protease containing the novel and potent (R)-(hydroxyethyl)sulfonamide isostere.EBI
Searle Discovery Research
Phosphorus-substituted quinoxaline-type piperidine compounds and uses thereofBDB
Purdue Pharma
Amino compounds for treatment of complement mediated disordersBDB
Achillion Pharmaceuticals
A novel class of carbonic anhydrase inhibitors: glycoconjugate benzene sulfonamides prepared by "click-tailing".BDB
Griffith University
Synthesis and biological activity of 2-anilino-4-(1H-pyrrol-3-yl) pyrimidine CDK inhibitors.BDB
Cyclacel