Aurone derivatives as Vps34 inhibitors that modulate autophagy
Acta Pharmaceutica Sinica B
; (6): 537-544, 2019.
Article
em En
| WPRIM
| ID: wpr-774970
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WPRO
ABSTRACT
We report in this study the identification of a natural product-like antagonist () of Vps34 as a potent autophagy modulator structure-based virtual screening. Aurone derivative strongly inhibited Vps34 activity in cell-free and cell-based assays. Significantly, prevents autophagy in human cells induced either by starvation or by an mTOR inhibitor. modeling and kinetic data revealed that could function as an ATP-competitive inhibitor of Vps34. Moreover, it suppressed autophagy and without inducing heart or liver damage in mice. could be utilized as a new motif for more selective and efficacious antagonists of Vps34 for the potential treatment of autophagy-related human diseases.
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WPRIM
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En
Revista:
Acta Pharmaceutica Sinica B
Ano de publicação:
2019
Tipo de documento:
Article