14 articles for A Nagata
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Discovery of 1-{(3R,4R)-3-[({5-Chloro-2-[(1-methyl-1H-pyrazol-4-yl)amino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}oxy)methyl]-4-methoxypyrrolidin-1-yl}prop-2-en-1-one (PF-06459988), a Potent, WT Sparing, Irreversible Inhibitor of T790M-Containing EGFR Mutants.

Pfizer
Design of oxobenzimidazoles and oxindoles as novel androgen receptor antagonists.

Pfizer
Discovery of 3-aryloxy-lactam analogs as potent androgen receptor full antagonists for treating castration resistant prostate cancer.

Pfizer
Discovery of aryloxy tetramethylcyclobutanes as novel androgen receptor antagonists.

Pfizer
Discovery of PF-06873600, a CDK2/4/6 Inhibitor for the Treatment of Cancer.

Pfizer
Discovery of Allosteric, Potent, Subtype Selective, and Peripherally Restricted TrkA Kinase Inhibitors.

Pfizer
Discovery of Potent, Selective, and Peripherally Restricted Pan-Trk Kinase Inhibitors for the Treatment of Pain.

Pfizer
Discovery of N-((3R,4R)-4-Fluoro-1-(6-((3-methoxy-1-methyl-1H-pyrazol-4-yl)amino)-9-methyl-9H-purin-2-yl)pyrrolidine-3-yl)acrylamide (PF-06747775) through Structure-Based Drug Design: A High Affinity Irreversible Inhibitor Targeting Oncogenic EGFR Mutants with Selectivity over Wild-Type EGFR.

Wuxi Apptec
RET inhibitors, pharmaceutical compositions and uses thereof

Sunshine Lake Pharma Co.
2,4,5-trisubstituted 1,2,4-triazolones useful as inhibitors of DHODH

Bayer Aktiengesellschaft
Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors

Incyte
Dihydropyrrolopyridine inhibitors of ROR-gamma

Vitae Pharmaceuticals
Conjugate comprising a neurotensin receptor ligand and use thereof

3B Pharmaceuticals
The preparation, in vitro screening and molecular docking of symmetrical bisquaternary cholinesterase inhibitors containing a but-(2E)-en-1,4-diyl connecting linkage.

University of Defence