(R)-BAY1238097 |
Catalog No.GC34443 |
(R)-BAY1238097 est l'isomère R avec une activité plus faible de BAY1238097. BAY1238097 est un inhibiteur puissant et sélectif de la liaison BET aux histones et possède une forte activité anti-proliférative dans différents modèles AML (leucémie myéloÏde aiguë) et MM (myélome multiple) grÂce À la régulation À la baisse des niveaux de c-Myc et de son transcriptome en aval.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 1564269-85-7
Sample solution is provided at 25 µL, 10mM.
(R)-BAY1238097 is the R-isomer with lower activity of BAY1238097. BAY1238097 is a potent and selective inhibitor of BET binding to histones and has strong anti-proliferative activity in different AML (acute myeloid leukemia) and MM (multiple myeloma) models through down-regulation of c-Myc levels and its downstream transcriptome[1][2]. BET[1].
[1]. Lejeune, P., et al. (2015) Abstract 3524: BAY 1238097, a novel BET inhibitor with strong efficacy in hematological tumor models. Cancer Research, 75(15 Suppl), 884. [2]. Bernasconi E, et al. Preclinical evaluation of the BET bromodomain inhibitor BAY 1238097 for the treatment of lymphoma. Br J Haematol. 2017 Sep;178(6):936-948.
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