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Exhibits antifungal and cytotoxic activity against some tumor cell lines partly attributed to inhibition of Ras-inducible genes. Inhibits proliferation of mouse and human T cells and modulates production of cytokines during T cell activation. Facilitates the ubiquitinylation process of cyclin D1. Has been identified as a potent and selective inhibitor of threonine/tyrosine-specific kinase, MEK, and other protein kinases that contain a conserved cysteine residue in the ATP-binding site in both in vitro and in vivo studies. HCT-116: IC50=0,0026 µM; PSN1 : IC50=0,26 µM; T98G : IC50=2,6 µM; A549 : IC50=0,26 µM (preliminary laboratory results). Journal of Natural Products (2011), 74(5), 1126-1131. Potential mode of action/Key words: Kinase inhibitor, Cytotoxic, Antitumoral, Kinase inhibitor
Cfm Oskar Tropitzsch GmbH supplies unique molecules - in this case the cytotoxins for antibodies. These payloads are ultra-toxic drugs, i.e. cytotoxic and/or cytostatic molecules, effective at a low dosage and ...