25 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Pyrimidinopyrimidine inhibitors of ketohexokinase: exploring the ring C2 group that interacts with Asp-27B in the ligand binding pocket.

Janssen Pharmaceutical Companies of Johnson & Johnson
Inhibitors of Ketohexokinase: Discovery of Pyrimidinopyrimidines with Specific Substitution that Complements the ATP-Binding Site.

TBA
Optimization of a pyrazole hit from FBDD into a novel series of indazoles as ketohexokinase inhibitors.

Johnson & Johnson Pharmaceutical Research and Development
Novel Cyanopyridine Compounds as KHK Inhibitors for Treating NAFLD, NASH, and Type II Diabetes.

Smith, Gambrell & Russell
Identification of LY3522348: A Highly Selective and Orally Efficacious Ketohexokinase Inhibitor.

Eli Lilly
Discovery of a Novel Ketohexokinase Inhibitor with Improved Drug Distribution in Target Tissue for the Treatment of Fructose Metabolic Disease.

Tuojie Biotech (Shanghai) Co.
Oxetanes in Drug Discovery Campaigns.

Imperial College London
Small-Molecule Kinase Inhibitors for the Treatment of Nononcologic Diseases.

Hefei University of Technology
Discovery of PF-06835919: A Potent Inhibitor of Ketohexokinase (KHK) for the Treatment of Metabolic Disorders Driven by the Overconsumption of Fructose.

Pfizer
The Race to Bash NASH: Emerging Targets and Drug Development in a Complex Liver Disease.

Terns Pharmaceuticals
Discovery of Fragment-Derived Small Molecules for in Vivo Inhibition of Ketohexokinase (KHK).

Pfizer
Pyrimidine Derivatives As Modulators of the 5-HT2A Serotonin Receptor Useful For The Treatment of Disorders Related Thereto

Arena Pharmaceuticals
Cyclin-dependent kinase degraders and methods of use

Dana-Farber Cancer Institute
SUBSTITUTED TRIAZOLE DERIVATIVE, PREPARATION METHOD THEREFOR, PHARMACEUTICAL COMPOSITION THEREOF, AND USE THEREOF

Shanghai Simr Biotechnology
Methods of Treating Lymphedema

Celltaxis
HETEROCYCLIC SPIRO COMPOUNDS AND METHODS OF USE

Amgen
Uracil compound as c-MET/AXL inhibitor

Medshine Discovery
Apoptosis signal-regulating kinase inhibitors

Gilead Sciences
5-membered and bicyclic heterocyclic amides as inhibitors of rock

Bristol-Myers Squibb
Imidazopyrrolopyridine as inhibitors of the JAK family of kinases

Janssen Pharmaceutica
Heteroaryl compounds useful as inhibitors of SUMO activating enzyme

Millennium Pharmaceuticals
Cyclin dependent kinase inhibitors

Pfizer
Selective inhibitors of human corticosteroid synthases

Universitat Des Saarlandes
Spirocyclic molecules as protein kinase inhibitors

Nanjing Allgen Pharma