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19 articles for DA Griffith


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

PMID
Data
Article Title
Organization
Helixconstraints and amino acid substitution in GLP-1 increase cAMP and insulin secretion but not beta-arrestin 2 signaling.EBI
The University of Queensland
Cyclic alpha-conotoxin peptidomimetic chimeras as potent GLP-1R agonists.EBI
The University of Queensland
Discovery of spirocyclic-diamine inhibitors of mammalian acetyl CoA-carboxylase.EBI
Pfizer
Short Hydrophobic Peptides with Cyclic Constraints Are Potent Glucagon-like Peptide-1 Receptor (GLP-1R) Agonists.EBI
University of Queensland
Decreasing the rate of metabolic ketone reduction in the discovery of a clinical acetyl-CoA carboxylase inhibitor for the treatment of diabetes.EBI
Pfizer
Spirolactam-based acetyl-CoA carboxylase inhibitors: toward improved metabolic stability of a chromanone lead structure.EBI
Pfizer
Identification of novel series of pyrazole and indole-urea based DFG-out PYK2 inhibitors.EBI
Pfizer
Discovery and evaluation of pyrazolo[1,5-a]pyrimidines as neuropeptide Y1 receptor antagonists.EBI
Pfizer
Bioisosteric replacement of the hydrazide pharmacophore of the cannabinoid-1 receptor antagonist SR141716A. Part I: potent, orally-active 1,4-disubstituted imidazoles.EBI
Pfizer
6-Azaspiro[2.5]octanes as small molecule agonists of the human glucagon-like peptide-1 receptor.EBI
Pfizer
A Small-Molecule Oral Agonist of the Human Glucagon-like Peptide-1 Receptor.EBI
Pfizer
New bicyclic cannabinoid receptor-1 (CB1-R) antagonists.EBI
Pfizer
Optimizing the Benefit/Risk of Acetyl-CoA Carboxylase Inhibitors through Liver Targeting.EBI
Pfizer
BCL-2 InhibitorsBDB
Eil Therapeutics
MCL-1 inhibitorsBDB
Gilead Sciences
Aryl and heteroaryl-fused tetrahydro-1,4-oxazepine amides as somatostatin receptor subtype 4 (SSTR4) agonistsBDB
Boehringer Ingelheim International
Synthesis and anticholinesterase activity of new substituted benzo[d]oxazole-based derivatives.BDB
Shahid Bahonar University of Kerman
Carbonic anhydrase inhibitors. The mitochondrial isozyme VB as a new target for sulfonamide and sulfamate inhibitors.BDB
Kochi Medical School