22 articles for DJ Burdick
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
Fragment-based discovery of potent ERK2 pyrrolopyrazine inhibitors.

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

Genentech
Discovery of highly potent, selective, and brain-penetrant aminopyrazole leucine-rich repeat kinase 2 (LRRK2) small molecule inhibitors.

Genentech
Discovery of a Highly Selective, Brain-Penetrant Aminopyrazole LRRK2 Inhibitor.

Genentech
Discovery of highly potent, selective, and brain-penetrable leucine-rich repeat kinase 2 (LRRK2) small molecule inhibitors.

Genentech
Discovery of selective LRRK2 inhibitors guided by computational analysis and molecular modeling.

Genentech
Cyclic RGD peptide analogues as antiplatelet antithrombotics.

Genentech
N-Benzoyl amino acids as LFA-1/ICAM inhibitors 1: amino acid structure-activity relationship.

Genentech
Structure-based design of thienobenzoxepin inhibitors of PI3-kinase.

Genentech
Stereochemistry of the benzodiazepine based Ras farnesyltransferase inhibitors

TBA
N-Benzoyl amino acids as ICAM/LFA-1 inhibitors. Part 2: structure-activity relationship of the benzoyl moiety.

Genentech
Diving into the Water: Inducible Binding Conformations for BRD4, TAF1(2), BRD9, and CECR2 Bromodomains.

Genentech
GNE-371, a Potent and Selective Chemical Probe for the Second Bromodomains of Human Transcription-Initiation-Factor TFIID Subunit 1 and Transcription-Initiation-Factor TFIID Subunit 1-like.

Genentech
GNE-886: A Potent and Selective Inhibitor of the Cat Eye Syndrome Chromosome Region Candidate 2 Bromodomain (CECR2).

Genentech
2-amino 3,5,5-trifluoro-3,4,5,6-tetrahydropyridines as BACE1 inhibitors for treatment of Alzheimer's disease

H. Lundbeck
Validation of flavonoids as potential dipeptidyl peptidase III inhibitors: Experimental and computational approach.

Josip Juraj Strossmayer University of Osijek
Design and synthesis of quinazoline-3,4-(4H)-diamine endowed with thiazoline moiety as new class for DPP-4 and DPPH inhibitor.

Jamia Hamdard (Hamdard University)
Kinase inhibitors

Allergan
Quinazoline-7-ether compounds and methods of use

Newgen Therapeutics
Kinetic properties and inhibition of the dimeric dUTPase-dUDPase from Campylobacter jejuni.

Instituto De Parastiologia Y Biomedicina "Lopez-Neyra