44 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Synthesis and evaluation of 2-pyridinone derivatives as HIV-1-specific reverse transcriptase inhibitors. 4. 3-[2-(Benzoxazol-2-yl)ethyl]-5-ethyl-6-methylpyridin-2(1H)-one and analogues.

Merck Reserch Laboratories
Synergistic combination of immunologic inhibitors for the treatment of cancer

The University of Chicago
Indole carboxamide derivatives as P2X7 receptor antagonists

Actelion Pharmaceuticals
Therapeutic hydroxyquinolones

Rutgers, The State University of New Jersey
Azabenzimidazole derivatives

Boehringer Ingelheim International
Dihydrooxazine or oxazepine derivatives having BACE1 inhibitory activity

Shionogi
7-hydroxy-indolinyl antagonists of P2Y1 receptor

Bristol-Myers Squibb
Pyrrole six-membered heteroaryl ring derivative, preparation method thereof, and medicinal uses thereof

Jiangsu Hengrui Medicine
Substituted 1,7-naphthyridines as dopamine D1 ligands

Pfizer
Fused thiazin-3-ones as KCA3.1 inhibitors

Boehringer Ingelheim International
Substituted N-heteroaryl spirolactam bipyrrolidines, preparation and therapeutic use thereof

Sanofi
Modified biotin, mutant streptavidin, and use thereof

Savid Therapeutics
Fused tricyclic amide compounds as multiple kinase inhibitors

Beigene
Heteroaryl compounds and methods of use thereof

Sunovion Pharmaceuticals
5-HT3 receptor antagonists

Takeda Pharmaceutical
Toll-like receptor 2-agonistic lipopeptides, and method of making the same

University of Kansas
Pyrimido-diazepinone compounds and methods of treating disorders

Dana-Farber Cancer Institute
Pharmacologically active compounds

The University of Liverpool
Method of treatment using substituted pyrazolo[1,5-A] pyrimidine compounds

Array Biopharma
Substituted pyrazolo[1,5-a]pyrazines as negative allosteric modulators of metabotropic glutamate receptor 3

Vanderbilt University
Aza-oxo-indoles for the treatment and prophylaxis of respiratory syncytial virus infection

Hoffmann-La Roche
Muscarinic agonists

Acadia Pharmaceuticals
Serine/threonine kinase inhibitors

Array Biopharma
Compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders

Galapagos
Fused tricyclic urea compounds as Raf kinase and/or Raf kinase dimer inhibitors

Beigene
Substituted triazolopyridines

Bayer Pharma Aktiengesellschaft
Methyl- and trifluoromethyl-substituted pyrrolopyridine modulators of RORC2 and methods of use thereof

Pfizer
Thiazole-substituted aminoheteroaryls as Spleen Tyrosine Kinase inhibitors

Merck Sharp & Dohme
Trifluoromethyl-oxadiazole derivatives and their use in the treatment of disease

Novartis
Pyridyl-and pyrimidinyl-substituted pyrrole-, thiophene- and furane-derivatives as kinase inhibitors

Nerviano Medical Sciences
Substituted 6,7-dialkoxy-3-isoquinolinol derivatives as inhibitors of phosphodiesterase 10 (PDE 10A)

Allergan
Substituted bicyclic dihydropyrimidinones and their use as inhibitors of neutrophil elastase activity

Boehringer Ingelheim International
Cyclosporin analogues for preventing or treating hepatitis C infection

Enanta Pharmaceuticals
4-aryl-N-phenyl-1,3,5-triazin-2-amines containing a sulfoximine group

Bayer Intellectual Property
Substituted biaryl compound

Ube Industries
Cyclopropylamine derivatives useful as LSD1 inhibitors

Oryzon Genomics
Arylaminoalcohol-substituted 2,3-dihydroimidazo[1,2-C]quinolines

Bayer Intellectual Property
Substituted tetrazolo[1,5-a]pyrazines as ROR-gamma inhibitors

Merck Patent
Substituted condensed pyrimidine compounds

GrÜNenthal
Macrocyclic urea and sulfamide derivatives as inhibitors of TAFIa

Sanofi
Novel modifications in the alkenyldiarylmethane (ADAM) series of non-nucleoside reverse transcriptase inhibitors.

Purdue University
Compulsory order of substrate binding to herpes simplex virus type 1 thymidine kinase. A calorimetric study.

Swiss Federal Institute of Technology
Thermodynamics of substrate binding to the chaperone SecB.

Indian Institute of Science
Energetic roles of hydrogen bonds at the ureido oxygen binding pocket in the streptavidin-biotin complex.

University of Washington