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Evodiamine-inspired dual inhibitors of histone deacetylase 1 (HDAC1) and topoisomerase 2 (TOP2) with potent antitumor activity

A great challenge in multi-targeting drug discovery is to identify drug-like lead compounds with therapeutic advantages over single target inhibitors and drug combinations. Inspired by our previous efforts in designing antitumor evodiamine derivatives, herein selective histone deacetylase 1 (HDAC1)...

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Dades bibliogràfiques
Publicat a:Acta Pharm Sin B
Autors principals: Huang, Yahui, Chen, Shuqiang, Wu, Shanchao, Dong, Guoqiang, Sheng, Chunquan
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2020
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7452071/
https://ncbi.nlm.nih.gov/pubmed/32874829
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.apsb.2019.11.011
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