19 articles for EA Peterson
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Sulfonamides as Selective Na

Amgen
Sulfonamides as Selective Na

Amgen
Sulfonamides as Selective Na

Amgen
Discovery of (R)-6-(1-(8-Fluoro-6-(1-methyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)ethyl)-3-(2-methoxyethoxy)-1,6-naphthyridin-5(6H)-one (AMG 337), a Potent and Selective Inhibitor of MET with High Unbound Target Coverage and Robust In Vivo Antitumor Activity.

Amgen
Discovery of potent and selective 8-fluorotriazolopyridine c-Met inhibitors.

Amgen
Discovery and optimization of potent and selective imidazopyridine and imidazopyridazine mTOR inhibitors.

Amgen
Discovery of triazine-benzimidazoles as selective inhibitors of mTOR.

Amgen
A Tiny Pocket Packs a Punch: Leveraging Pyridones for the Discovery of CNS-Penetrant Aza-indazole IRAK4 Inhibitors.

Biogen
The Discovery of 7-Isopropoxy-2-(1-methyl-2-oxabicyclo[2.1.1]hexan-4-yl)-N-(6-methylpyrazolo[1,5-a]pyrimidin-3-yl)imidazo[1,2-a]pyrimidine-6-carboxamide (BIO-7488), a Potent, Selective, and CNS-Penetrant IRAK4 Inhibitor for the Treatment of Ischemic Stroke.

Biogen
Discovery of BIO-8169─A Highly Potent, Selective, and Brain-Penetrant IRAK4 Inhibitor for the Treatment of Neuroinflammation.

Biogen Inc.
Discovery of Phospholipase D Inhibitors with Improved Drug-like Properties and Central Nervous System Penetrance.

Biogen
1,2,4-Triazolsulfone: A novel isosteric replacement of acylsulfonamides in the context of Na

Amgen
Discovery of a biarylamide series of potent, state-dependent Na

Amgen
The discovery of benzoxazine sulfonamide inhibitors of Na

Amgen
Benzo[5,6][1,4]dioxino[2,3-b]pyridine compounds useful as IRAK4 inhibitors

Bristol-Myers Squibb
NEW SPIRO[3H-INDOLE-3,2'-PYRROLIDIN]-2(1H)-ONE COMPOUNDS AND DERIVATIVES AS MDM2-P53 INHIBITORS

Boehringer Ingelheim International
Substituted 3-haloallylamine inhibitors of ASSAO and uses thereof

Boehringer Ingelheim International
Effect of N-methyl substitution of the peptide bonds in luteinizing hormone-releasing hormone agonists.

Abbott Laboratories