The present disclosure relates to novel heterotricyclic derivative compounds and the use thereof, and more particularly, to novel heterotricyclic derivative compounds having inhibitory activity against EZH1 (enhancer of zeste homolog 1) and/or EZH2 (enhancer of zeste homolog 2) activity, pharmaceutically acceptable salts thereof, or pharmaceutical compositions containing these compounds.
本公开涉及新型杂环衍
生物化合物及其用途,更具体地说,涉及对 EZH1(zeste 同源体 1 的增强子)和/或 EZH2(zeste 同源体 2 的增强子)活性具有抑制活性的新型杂环衍
生物化合物、其药学上可接受的盐或含有这些化合物的药物组合物。