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Corrigendum to “1,4-Naphthoquinones as inhibitors of Itch, a HECT domain-E3 ligase, and tumor growth suppressors in multiple myeloma” [Eur. J. Med. Chem. 140 (2017) 84–91](S0223523417306931)(10.1016/j.ejmech.2017.09.011)

研究成果: 雜誌貢獻評論/辯論同行評審

2   連結會在新分頁中開啟 引文 斯高帕斯(Scopus)

摘要

The authors regret that the information of concentration unit of the Table 2 and 3 and the name of synthesized compound 10e in 4.1.1.5 was incorrect. The correct version should be: The concentration unit of the Table 2 and 3 is μM. The name of synthesized compound 10e is 4-(((3-Chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)amino)methyl)-N-(pyridin-4-yl)benzamide (10e) in 4.1.1.5. The authors would like to apologise for any inconvenience caused.

原文英語
文章編號112633
期刊European Journal of Medicinal Chemistry
202
DOIs
出版狀態已發佈 - 9月 15 2020

ASJC Scopus subject areas

  • 藥理
  • 藥物發現
  • 有機化學

指紋

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