24 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Imidazo[4,5-C]pyridine derived SSAO inhibitors

Proximagen
Compounds

Inflazome
Analogs for the treatment of disease

Insilico Medicine Ip
Compositions and methods for treating infections

Vyera Pharmaceuticals
Analogs for the treatment of disease

Insilico Medicine Ip
Protacs targeting coronavirus 3CL protease and preparation method and application thereof

Shaanxi Panlong Pharmaceutical
Kinase inhibitors

University of Manchester
Piperidinone formyl peptide 2 receptor and formyl peptide 1 receptor agonists

Bristol-Myers Squibb
Alpha-5 beta-1 inhibitors

University of California
Development of Selective Inhibitors for Human Aldehyde Dehydrogenase 3A1 (ALDH3A1) for the Enhancement of Cyclophosphamide Cytotoxicity.

Indiana University
Long residence times revealed by Aurora A kinase-targeting fluorescent probes derived from inhibitors MLN8237 and VX-689.

University of Tartu
Thiazolyl mGluR5 antagonists and methods for their use

Merck Sharp & Dohme
Heterocyclic inhibitors of glutaminase

Calithera Biosciences
Substituted imidazopyridinyl-aminopyridine compounds

Arqule
Compositions for preventing and/or treating degenerative disorders of the central nervous system

Amicus Therapeutics
Compound, a process for its preparation, a pharmaceutical composition, use of a compound, a method for modulating or regulating serine/threonine kinases and a serine/threonine kinases modulating agent

Selvita
Substituted piperidine spiro pyrrolidinone and piperidinone, preparation and therapeutic use thereof

Sanofi
Purine derivatives as adenosine A1 receptor agonists and methods of use thereof

Inotek Pharmaceuticals
Glucagon receptor antagonists, preparation and therapeutic uses

Eli Lilly
Methods and compositions for sleep disorders and other disorders

Intra-Cellular Therapies
Development of fragment-based n-FABS NMR screening applied to the membrane enzyme FAAH.

Fondazione Istituto Italiano Di Tecnologia
DXP synthase-catalyzed C-N bond formation: nitroso substrate specificity studies guide selective inhibitor design.

The Johns Hopkins University
New insights into the pharmacological chaperone activity of c2-substituted glucoimidazoles for the treatment of Gaucher disease.

Nankai University
Substituted dihydropteridin-6-one derivatives, process for their preparation and their use as kinase inhibitors

Nerviano Medical Sciences