51 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
METHIONINE ADENOSYLTRANSFERASE 2a (MAT2A) INHIBITORS AND USES THEREOF
Insilico Medicine IP
Derivatives of 4-aminoantipyrine as anti-Alzheimers butyrylcholinesterase inhibitors
Individual
Substituted dihydrothienopyrimidines and their use as phosphodiesterase inhibitors
Union Therapeutics
Design of SARS-CoV-2 PLpro Inhibitors for COVID-19 Antiviral Therapy Leveraging Binding Cooperativity.
University of Illinois At Chicago
Amino, amido and heterocyclic compounds as modulators of RAGE activity and uses thereof
The State University of New York
Compositions and methods for treating toxoplasmosis, cryptosporidiosis and other apicomplexan protozoan related diseases
University of Washington
Cardiac glycoside analogs and their use in methods for inhibition of viral infection
The John Hopkins University
Six-membered ring benzo derivatives as DPP-4 inhibitor and use thereof
East China University of Science and Technology
Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors
Array Biopharma
Heterocyclylmethyl-thienouracile as antagonists of the adenosine-A2B-receptor
Bayer Pharma Aktiengesellschaft
Substituted [1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists
Euroscreen
Synthesis and biological evaluation of novel N, N'-disubstituted urea and thiourea derivatives as potential anti-melanoma agents.
Nanjing University
Serendipitous discovery of light-induced (In Situ) formation of an Azo-bridged dimeric sulfonated naphthol as a potent PTP1B inhibitor.
Concordia University of Wisconsin
Substituted pyrazolo[1,5-a]pyrazines as mGluR5 receptor modulators
Vanderbilt University
4-amino-6-alkyloxy-2-alkylthiopyrimidine derivatives as novel non-nucleoside agonists for the adenosine A1 receptor.
Universit�� Di Napoli Federico Ii
Hypophosphorous acid derivatives having antihyperalgic activity and biological applications thereof
Universite Paris Descartes
Transcriptional Profiling of a Selective CREB Binding Protein Bromodomain Inhibitor Highlights Therapeutic Opportunities.
Pfizer
Hybrid benzothiazole analogs as antiurease agent: Synthesis and molecular docking studies.
Universiti Teknologi Mara (Uitm), Puncak Alam Campus
Na/K-ATPase ligands, ouabain antagonists, assays and uses thereof
The University of Toledo
3-Oxo-2,3-dihydro-1H-indazole-4-carboxamide derivatives as PARP-1 inhibitors
Nerviano Medical Sciences
Synthesis and biological evaluation of kojic acid derivatives containing 1,2,4-triazole as potent tyrosinase inhibitors.
Hunan University of Science and Technology
Novel synthesis of dihydropyrimidines for a-glucosidase inhibition to treat type 2 diabetes: in vitro biological evaluation and in silico docking.
Comsats Institute of Information Technology