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Discovery of an MLLT1/3 YEATS Domain Chemical Probe

Authors :
Gennady Poda
Ioanna Panagakou
Thomas Christott
Apirat Chaikuad
Laura Diaz Saez
Vicki Gamble
Stefan Knapp
Rima Al-awar
Nadia Halidi
Oleg Fedorov
Gillian Farnie
Octovia P. Monteiro
Nenad Manevski
Carina Gileadi
Jim Bennett
Paul Smith
Moses Moustakim
Paul Brennan
Charline Giroud
Kilian Huber
Jennifer Ward
Jag Paul Heer
David Heidenreich
Suet Ling Felce
Catherine Rogers
Darren J. Dixon
Source :
Angewandte Chemie (International Ed. in English)
Publication Year :
2018
Publisher :
American Chemical Society (ACS), 2018.

Abstract

YEATS domain (YD) containing proteins are an emerging class of epigenetic targets in drug discovery. Dysregulation of these modified lysine binding proteins has been linked to the onset and progression of cancers. We herein report the discovery and characterisation of the first small molecule chemical probe, SGC-iMLLT, for the YD of MLLT1 (ENL/YEATS1) and MLLT3 (AF9/YEATS3). SGC-iMLLT is a potent and selective inhibitor of MLLT1/3 -histone interactions. Excellent selectivity over other human YD proteins (YEATS2/4) and bromodomains was observed. Furthermore, our probe displays cellular target engagement of MLLT1 and MLLT3. The first small molecule X-ray co-crystal structures with the MLLT1 YD are also reported. This first in class probe molecule can be used to understand MLLT1/3 associated biology and the therapeutic potential of small molecule YD inhibitors.

Details

Database :
OpenAIRE
Journal :
Angewandte Chemie (International Ed. in English)
Accession number :
edsair.doi.dedup.....5a40f419ca25006585e6111920806a14
Full Text :
https://doi.org/10.26434/chemrxiv.7090547