https://www.selleckchem.com/products/nvl-655.html
Importantly, all compounds were non-cytotoxic per se. A transactivation experiment showed that only the carbonitriles are partial agonists of PPARγ, which does not seem to be involved in the mode of action. Yet, immunoassays revealed a suppression of the STAT5 phosphorylation status by co-application of the most active derivatives with imatinib. This mechanism consequently resulted in reduced cell proliferation and induction of cell death in resistant CML cells. To use advanced medical technologies (AMTs) correctly and safely requires b
Curtir
Comentario
Compartilhar
