Identification and Preliminary Structure-Activity Relationship Studies of 1,5-Dihydrobenzo[e][1,4]oxazepin-2(3H)-ones That Induce Differentiation of Acute Myeloid Leukemia Cells In Vitro.
Laia Josa-CulleréThomas J CogswellIrene GeorgiouMorgan Jay-SmithThomas R JacksonCarole J R BatailleStephen G DaviesParesh VyasThomas A MilneGraham M WynneAngela J RussellPublished in: Molecules (Basel, Switzerland) (2021)
Acute myeloid leukemia (AML) is the most aggressive type of blood cancer, and there is a continued need for new treatments that are well tolerated and improve long-term survival rates in patients. Induction of differentiation has emerged as a promising alternative to conventional cytotoxic chemotherapy, but known agents lack efficacy in genetically distinct patient populations. Previously, we established a phenotypic screen to identify small molecules that could stimulate differentiation in a range of AML cell lines. Utilising this strategy, a 1,5-dihydrobenzo[e][1,4]oxazepin-2(3H)-one hit compound was identified. Herein, we report the hit validation in vitro, structure-activity relationship (SAR) studies and the pharmacokinetic profiles for selected compounds.
Keyphrases
- acute myeloid leukemia
- structure activity relationship
- allogeneic hematopoietic stem cell transplantation
- end stage renal disease
- ejection fraction
- chronic kidney disease
- induced apoptosis
- newly diagnosed
- prognostic factors
- papillary thyroid
- peritoneal dialysis
- case report
- signaling pathway
- squamous cell carcinoma
- cell death
- single cell