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Structure-based screening and optimization of cytisine derivatives as inhibitors of the menin–MLL interaction

  • Hai Jing Zhong
  • , Bo Ra Lee
  • , Joshua William Boyle
  • , Wanhe Wang
  • , Dik Lung Ma*
  • , Philip Wai Hong Chan*
  • , Chung Hang Leung*
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

34 Citations (Scopus)

Abstract

The natural product-like compound 1 was identified as a direct inhibitor of the menin-MLL interaction by in silico screening. Structure-based optimization furnished analogue 1a, which showed significantly higher potency than both the lead structure 1 and the reference compound MI-2.

Original languageEnglish
Pages (from-to)5788-5791
Number of pages4
JournalChemical Communications
Volume52
Issue number34
Early online date10 Mar 2016
DOIs
Publication statusPublished - 30 Apr 2016

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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