23 articles for MC Bryan
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Pyridones as Highly Selective, Noncovalent Inhibitors of T790M Double Mutants of EGFR.

Genentech
4-Aminoindazolyl-dihydrofuro[3,4-d]pyrimidines as non-covalent inhibitors of mutant epidermal growth factor receptor tyrosine kinase.

Genentech
Lead optimization and modulation of hERG activity in a series of aminooxazoline xantheneß-site amyloid precursor protein cleaving enzyme (BACE1) inhibitors.

Amgen
Discovery of selective and noncovalent diaminopyrimidine-based inhibitors of epidermal growth factor receptor containing the T790M resistance mutation.

Genentech
Small molecule disruptors of the glucokinase-glucokinase regulatory protein interaction: 1. Discovery of a novel tool compound for in vivo proof-of-concept.

Amgen
N-substituted azaindoles as potent inhibitors of Cdc7 kinase.

Amgen
Rapid development of piperidine carboxamides as potent and selective anaplastic lymphoma kinase inhibitors.

Amgen
High-throughput identification of fucosyltransferase inhibitors using carbohydrate microarrays.

The Scripps Research Institute
Chromenones as potent bradykinin B1 antagonists.

Amgen
Phospshoinositide 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) dual inhibitors: discovery and structure-activity relationships of a series of quinoline and quinoxaline derivatives.

Amgen
Discovery of potent, orally bioavailable phthalazinone bradykinin B1 receptor antagonists.

Amgen
Discovery of Selective Tertiary Amide Inhibitors of Cyclin-Dependent Kinase 2 (CDK2).

Genentech
Discovery of a Noncovalent, Mutant-Selective Epidermal Growth Factor Receptor Inhibitor.

Charles River Laboratories
Development of Potent and Selective Pyrazolopyrimidine IRAK4 Inhibitors.

Genentech
Discovery of Potent Benzolactam IRAK4 Inhibitors with Robust in Vivo Activity.

Genentech
Kinase Inhibitors for the Treatment of Immunological Disorders: Recent Advances.

Genentech
Noncovalent Mutant Selective Epidermal Growth Factor Receptor Inhibitors: A Lead Optimization Case Study.

Argenta Discovery
Substituted quinolines useful as kinase inhibitors

Teligene
Therapeutic compounds and methods of use thereof

Genentech
Isoindolinone inhibitors of the MDM2-p53 interaction having anticancer activity

Astex Therapeutics
Heteroarylbenzimidazole compounds

Bayer Pharma Aktiengesellschaft
Modulators of P97 AAA ATPase activity

University of Pittsburgh