In contrast, even at 1 mg kg −1 QD, OXS008474 and OXS008255 showed a trend to reduced tumour growth compared to vehicle treated controls.
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Lead optimisation of OXS007417: <i>in vivo</i> PK profile and hERG liability modulation to optimise a small molecule differentiation agent for the potential treatment of acute myeloid leukaemia.
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