n-phenylacrylamide and Huntington-Disease

n-phenylacrylamide has been researched along with Huntington-Disease* in 1 studies

Other Studies

1 other study(ies) available for n-phenylacrylamide and Huntington-Disease

ArticleYear
Discovery and structure-activity relationship of potent and selective covalent inhibitors of transglutaminase 2 for Huntington's disease.
    Journal of medicinal chemistry, 2012, Feb-09, Volume: 55, Issue:3

    Tissue transglutaminase 2 (TG2) is a multifunctional protein primarily known for its calcium-dependent enzymatic protein cross-linking activity via isopeptide bond formation between glutamine and lysine residues. TG2 overexpression and activity have been found to be associated with Huntington's disease (HD); specifically, TG2 is up-regulated in the brains of HD patients and in animal models of the disease. Interestingly, genetic deletion of TG2 in two different HD mouse models, R6/1 and R6/2, results in improved phenotypes including a reduction in neuronal death and prolonged survival. Starting with phenylacrylamide screening hit 7d, we describe the SAR of this series leading to potent and selective TG2 inhibitors. The suitability of the compounds as in vitro tools to elucidate the biology of TG2 was demonstrated through mode of inhibition studies, characterization of druglike properties, and inhibition profiles in a cell lysate assay.

    Topics: Acrylamides; Animals; Caco-2 Cells; Cell Membrane Permeability; GTP-Binding Proteins; HEK293 Cells; Humans; Huntington Disease; In Vitro Techniques; Male; Mice; Microsomes, Liver; Models, Molecular; Piperazines; Protein Glutamine gamma Glutamyltransferase 2; Pyridines; Pyrimidines; Rats; Structure-Activity Relationship; Sulfonamides; Transglutaminases

2012