37 articles for JJ Chen
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Oxopyrido[2,3-d]pyrimidines as Covalent L858R/T790M Mutant Selective Epidermal Growth Factor Receptor (EGFR) Inhibitors.

Amgen
An Orally Available BACE1 Inhibitor That Affords Robust CNS Aß Reduction without Cardiovascular Liabilities.

Amgen
Development of 2-aminooxazoline 3-azaxanthenes as orally efficaciousß-secretase inhibitors for the potential treatment of Alzheimer's disease.

Amgen
Discovery of 2-methylpyridine-based biaryl amides as¿-secretase modulators for the treatment of Alzheimer's disease.

Amgen
Development of pyrimidine-based inhibitors of Janus tyrosine kinase 3.

Procter and Gamble Pharmaceuticals
Discovery of dehydro-oxopiperazine acetamides as novel bradykinin B1 receptor antagonists with enhanced in vitro potency.

Amgen
3-Oxo-2-piperazinyl acetamides as potent bradykinin B1 receptor antagonists for the treatment of pain and inflammation.

Amgen
Aryl sulfonamides containing tetralin allylic amines as potent and selective bradykinin B1 receptor antagonists.

Amgen
Identification of a new class of small molecule C5a receptor antagonists.

Wyeth Research
Synthesis and activity of conformationally-constrained macrocyclic norstatine-based inhibitors of HIV protease

TBA
Design, synthesis, activity, and structure of a novel class of matrix metalloproteinase inhibitors containing a heterocyclic P
2′-P
3′ amide bond isostere

TBA
Design, synthesis, and activity of conformationally-constrained macrocyclic peptide-based inhibitors of HIV protease

TBA
Aryl sulfones as novel bradykinin B1 receptor antagonists for treatment of chronic pain.

Amgen
Discovery of dihydroquinoxalinone acetamides containing bicyclic amines as potent Bradykinin B1 receptor antagonists.

Amgen
Potent nonpeptide antagonists of the bradykinin B1 receptor: structure-activity relationship studies with novel diaminochroman carboxamides.

Amgen
Discovery of CMX990: A Potent SARS-CoV-2 3CL Protease Inhibitor Bearing a Novel Warhead.

Calibr At Scripps Research Institute
Identification of a nonpeptidic and conformationally restricted bradykinin B1 receptor antagonist with anti-inflammatory activity.

Amgen
Targeting the Mitotic Kinesin KIF18A in Chromosomally Unstable Cancers: Hit Optimization Toward an In Vivo Chemical Probe.

Amgen Research
A new class of bradykinin 1 receptor antagonists containing the piperidine acetic acid tetralin core.

Amgen
Synthesis and biological evaluation of paeoveitol D derivatives as new melatonin receptor agonists with antidepressant activities.

Chinese Academy of Sciences
Polybenzyls from Gastrodia elata, their agonistic effects on melatonin receptors and structure-activity relationships.

Chinese Academy of Sciences
Design, synthesis, biological evaluation of benzoyl amide derivatives containing nitrogen heterocyclic ring as potential VEGFR-2 inhibitors.

Zhengzhou Children'S Hospital
Discovery of a Covalent Inhibitor of KRAS

TBA
Synthesis and biological evaluation of magnolol derivatives as melatonergic receptor agonists with potential use in depression.

Chinese Academy of Sciences
Discovery of TRPM8 Antagonist ( S)-6-(((3-Fluoro-4-(trifluoromethoxy)phenyl)(3-fluoropyridin-2-yl)methyl)carbamoyl)nicotinic Acid (AMG 333), a Clinical Candidate for the Treatment of Migraine.

TBA
IRAK4 PROTACS

Astrazeneca
COMBINATION OF A T CELL THERAPY AND A DGK INHIBITOR

Juno Therapeutics
S6K1 protein kinase inhibitors as cancer therapeutics

Xavier University Of Louisiana
KDM1A inhibitors for the treatment of disease

Imago Biosciences
Fused bicyclic 1,2,4-triazine compounds as TAM inhibitors

Incyte
Nitrogen-containing condensed heterocyclic compound

Taisho Pharmaceutical
Pyridopyrazines as highly selective ras-Raf-Mek-Erk signal transduction pathway inhibitors

Aeterna Zentaris
Ligand binding to thromboxane receptors on human platelets: correlation with biological activity.

University of Edinburgh
Thermodynamic analysis of the binding of the polyglutamate chain of 5-formyltetrahydropteroylpolyglutamates to serine hydroxymethyltransferase.

Virginia Commonwealth University