23 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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Development of the First Generation of Disulfide-Based Subtype-Selective and Potent Covalent Pyruvate Dehydrogenase Kinase 1 (PDK1) Inhibitors.

East China University of Science and Technology
 
Application of Off-Rate Screening in the Identification of Novel Pan-Isoform Inhibitors of Pyruvate Dehydrogenase Kinase.

Vernalis (R&D)
 
Development of Dihydroxyphenyl Sulfonylisoindoline Derivatives as Liver-Targeting Pyruvate Dehydrogenase Kinase Inhibitors.

National Institute of Biological Science
 
Discovery and optimization of 4,5-diarylisoxazoles as potent dual inhibitors of pyruvate dehydrogenase kinase and heat shock protein 90.

Chinese Academy of Sciences
 
Design and synthesis of novel fluorene derivatives as inhibitors of pyruvate dehydrogenase kinase.

Japan Tobacco
 
Targeting the pyruvate dehydrogenase complex/pyruvate dehydrogenase kinase (PDC/PDK) axis to discover potent PDK inhibitors through structure-based virtual screening and pharmacological evaluation.

Chongqing Medical and Pharmaceutical College
 
Structure-based drug design of novel and highly potent pyruvate dehydrogenase kinase inhibitors.

Central Pharmaceutical Research Institute
 
Fragment-based lead discovery to identify novel inhibitors that target the ATP binding site of pyruvate dehydrogenase kinases.

Japan Tobacco
 
High-throughput screening of novel pyruvate dehydrogenase kinases inhibitors and biological evaluation of their in vitro and in vivo antiproliferative activity.

Jiangsu Normal University
 
Identification of Novel Resorcinol Amide Derivatives as Potent and Specific Pyruvate Dehydrogenase Kinase (PDHK) Inhibitors.

Korea University
 
In vitro cytotoxicity screening to identify novel anti-osteosarcoma therapeutics targeting pyruvate dehydrogenase kinase 2.

Capital Medical University
 
Discovery of novel pyruvate dehydrogenase kinases inhibitors by screening of an in-house small molecule library for anti-lung cancer therapeutics.

Shaanxi Province Tuberculosis Prevention and Treatment Institute
 
Identification of pyruvate dehydrogenase kinase 1 inhibitors with anti-osteosarcoma activity.

Sichuan University
 
Human dihydroorotate dehydrogenase (hDHODH) inhibitors and their use in targeting oncological diseases sensitive to pyrimidine starvation

Drug Discovery And Clinic
 
Pyrimidine derivative having effect of inhibiting cancer cell growth and pharmaceutical composition containing same

Oncobix
 
Pyrazolopyrimidine compounds and uses thereof

Incyte
 
Substituted aminoquinazoline compounds as A2A antagonist

Merck Sharp & Dohme
 
Arylpropionyl-triketone antibacterial agents

TBA
 
KDM1A inhibitors for the treatment of disease

Imago Biosciences
 
Pyrazolopyridine compounds and uses thereof

Incyte
 
Quinoxaline inhibitors of phosphoinositide-3-kinases (PI3Ks)

Merck Serono
 
Somatostatin receptor subtype specificity in human fetal pituitary cultures. Differential role of SSTR2 and SSTR5 for growth hormone, thyroid-stimulating hormone, and prolactin regulation.

Cedars-Sinai Research Institute
 
Receptor occupancy and adenylate cyclase activation in AR 4-2J rat pancreatic acinar cell membranes by analogs of pituitary adenylate cyclase-activating peptides amino-terminally shortened or modified at position 1, 2, 3, 20, or 21.

Universit&Acute