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12 articles for M Martinson


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

PMID
Data
Article Title
Organization
Discovery of highly potent, selective, and efficacious small molecule inhibitors of ERK1/2.EBI
Array Biopharma
Discovery of 5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine inhibitors of Erk2.EBI
Array Biopharma
Discovery and preclinical pharmacology of a selective ATP-competitive Akt inhibitor (GDC-0068) for the treatment of human tumors.EBI
Array Biopharma
Non-oxime pyrazole based inhibitors of B-Raf kinase.EBI
Array Biopharma
Discovery of spirocyclic sulfonamides as potent Akt inhibitors with exquisite selectivity against PKA.EBI
Array Biopharma
Discovery and SAR of spirochromane Akt inhibitors.EBI
Array Biopharma
Non-oxime inhibitors of B-Raf(V600E) kinase.EBI
Array Biopharma
The discovery of furo[2,3-c]pyridine-based indanone oximes as potent and selective B-Raf inhibitors.EBI
Array Biopharma, 3200 Walnut Street, Boulder, Co 80301, Usa.
Discovery of dihydrothieno- and dihydrofuropyrimidines as potent pan Akt inhibitors.EBI
Array Biopharma
Discovery of pyrrolopyrimidine inhibitors of Akt.EBI
Array Biopharma
Discovery of (S)-1-(1-(4-Chloro-3-fluorophenyl)-2-hydroxyethyl)-4-(2-((1-methyl-1H-pyrazol-5-yl)amino)pyrimidin-4-yl)pyridin-2(1H)-one (GDC-0994), an Extracellular Signal-Regulated Kinase 1/2 (ERK1/2) Inhibitor in Early Clinical Development.EBI
Array Biopharma
1-(3-aminopropyl) substituted cyclic amine compounds, preparation method therefor, and pharmaceutical compositions and uses thereofBDB
Shanghai Institute of Material Medica, Chinese Academy of Sciences