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Bioorg Med Chem Lett ; 23(11): 3300-3, 2013 Jun 01.
Article in English | MEDLINE | ID: mdl-23602399

ABSTRACT

The p38α mitogen-activated protein kinase (MAPK) inhibitor SB203580 had been reported to enhance the cardiomyogenesis of human embryonic stem cells (hESCs). To investigate if tri-substituted imidazole analogues of SB203580 are equally effective inducers for cardiomyogenesis of hESCs, and if there is a correlation between p38α MAPK inhibition and cardiomyogenesis, we designed and synthesized a series of novel tri-substituted imidazoles with a range of p38α MAPK inhibitory activities. Our studies demonstrated that suitably designed analogues of SB203580 can also be inducers of cardiomyogenesis in hESCs and that cell growth is affected by changes in the imidazole structures.


Subject(s)
Embryonic Stem Cells/cytology , Imidazoles/chemistry , Pyridines/chemistry , Cell Differentiation/drug effects , Humans , Imidazoles/metabolism , Imidazoles/pharmacology , Mitogen-Activated Protein Kinase 14/antagonists & inhibitors , Mitogen-Activated Protein Kinase 14/metabolism , Myocytes, Cardiac/cytology , Protein Binding , Pyridines/metabolism
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