4.4 Article

A Novel Inhibitor of the Obesity-Related Protein FTO

Journal

BIOCHEMISTRY
Volume 55, Issue 10, Pages 1516-1522

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.biochem.6b00023

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Funding

  1. National Natural Science Foundation of China [81330075, 21403199]
  2. China Postdoctoral Science Foundation [2014M552010]

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Fe-II and alpha-ketoglutarate-dependent fat mass and obesity associated protein (FTO)-dependent demethylation of m(6)A is important for regulation of mRNA splicing and adipogenesis. Developing FTO-specific inhibitors can help probe the biology of FTO and unravel novel therapeutic targets for treatment of obesity or obesity-associated diseases. In the present paper, we have identified that 4-chloro-6-(6'-chloro-7'-hydroxy-2',4',4'-trimethyl-chroman-2'-yl)benzene-1,3-diol (CHTB) is an inhibitor of FTO. The crystal structure of CHTB complexed with human FTO reveals that the novel small molecule binds to FTO in a specific manner. The identification of the novel small molecule offers opportunities for further development of more selective and potent FTO inhibitors.

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