75 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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NUCLEOTIDE AND NUCLEOSIDE THERAPEUTIC COMPOSITIONS, COMBINATIONS AND USES RELATED THERETO
Emory University
2,3-DIHYDROBENZO[B][1,4]DIOXIN-6-YL CONTAINING COMPOUNDS USEFUL AS IMMUNOMODULATORS
Bristol-Myers Squibb
PYRIDO[4,3-b]INDOLE DERIVATIVES AND THEIR USE AS PHARMACEUTICALS
Ventus Therapeutics U.S.
COMBINATION OF AN ALPHA2-ADRENOCEPTOR SUBTYPE C (ALPHA-2C) ANTAGONIST WITH A TASK1/3 CHANNEL BLOCKER FOR THE TREATMENT OF SLEEP APNEA
Bayer Aktiengesellschaft
Compound having KDM5 inhibitory activity and pharmaceutical use thereof
Ono Pharmaceutical
Fluorinated tetrahydronaphthyridinyl nonanoic acid derivatives and uses thereof
Ocuterra Therapeutics
Pyrimidine derivative having effect of inhibiting cancer cell growth and pharmaceutical composition containing same
Oncobix
Heterocyclic derivatives and their use in the treatment of neurological disorders
Novartis
Tetrahydroisoquinoline derivatives useful as inhibitors of diacylglyceride O-acyltransferase 2
Merck Sharp & Dohme
Compounds as inhibitors of DNA methyltransferases
FundaciÓN Para La InvestigaciÓN MÉDica Aplicada
Fused pyrimidine compound, and preparation method, intermediate, composition, and uses thereof
Shanghai Yingli Pharmaceutical
Compound having ability to inhibit 11Beta-HSD1 enzyme or pharmaceutically acceptable salt thereof, method for producing same, and pharmaceutical composition containing same as active ingredient
Ahn-Gook Pharmaceutical
Substituted phenyl cycloalkyl pyrrolidine (piperidine) spirolactams and amides, preparation and therapeutic use thereof
Sanofi
Interaction of superoxide dismutase with the glycine zipper regions of ß-amyloid peptides: is there an implication towards Alzheimer's disease and oxidative stress?
Rhodes University
Inhibition of acetylpolyamine and spermine oxidases by the polyamine analogue chlorhexidine.
University Roma Tre
Inhibition of mammalian carbonic anhydrase isoforms I, II and VI with thiamine and thiamine-like molecules.
Kirklareli University
Nantenine as an acetylcholinesterase inhibitor: SAR, enzyme kinetics and molecular modeling investigations.
City University of New York Hunter College
New antihyperglycemic, alpha-glucosidase inhibitory, and cytotoxic derivatives of benzimidazoles.
Indian Institute of Chemical Technology
Ellagitannin and flavonoid constituents from Agrimonia pilosa Ledeb. with their protein tyrosine phosphatase and acetylcholinesterase inhibitory activities
Catholic University of Daegu
Synthesis and preliminary biological assay of uridine glycoconjugate derivatives containing amide and/or 1,2,3-triazole linkers.
Silesian University of Technology
Substituted [1,2,4]triazolo[4,3-a]pyrazines as PARP-1 inhibitors
Shanghai Institute of Material Medica, Chinese Academy of Sciences
Cardioprotective effect of novel sulphonamides-1,3,5-triazine conjugates against ischaemic-reperfusion injury via selective inhibition of MMP-9.
Zhejiang Hospital
Development of hydroxylated naphthylchalcones as polyphenol oxidase inhibitors: Synthesis, biochemistry and molecular docking studies.
University of Technology Sydney
Direct Staudinger-Phosphonite Reaction Provides Methylphosphonamidates as Inhibitors of CE4 De-N-acetylases.
University of Toronto
Cyclic inhibitors of 11β-hydroxysteroid dehydrogenase 1 based on the 1,3-oxazinan-2-one structure
Vitae Pharmaceuticals
2,3,4,5-tetrahydro-benzo{B}{1,4}diazepine-comprising compounds of formula(III) for treating pain
Purde Pharma
Boron-based inhibitors of acyl protein thioesterases 1 and 2.
Technical University of Dortmund
Inactivation of glucosamine-6-phosphate synthase by N3-oxoacyl derivatives of L-2,3-diaminopropanoic acid.
Gda£?Sk University of Technology
Effects of pyridine ring substitutions on affinity, efficacy, and subtype selectivity of neuronal nicotinic receptor agonist epibatidine.
University of Miami
A novel phenylaminotetralin radioligand reveals a subpopulation of histamine H(1) receptors.
University of North Carolina at Chapel Hill
Molecular and pharmacological characterization of muscarinic receptor subtypes in a rat parotid gland cell line: comparison with native parotid gland.
Creighton University
Expression and characterization of the rat D3 dopamine receptor: pharmacologic properties and development of antibodies.
University of Pennsylvania