期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 26, 期 47, 页码 10682-10689出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202002153
关键词
lead discovery; metal carbenoids; molecular diversity; protein-protein interactions; scaffold hopping
资金
- EPSRC [EP/N013573/1]
- Established Career Fellowship [EP/N025652/1]
- GSK (iCASE studentship)
- Leverhulme Trust [SRF\R1\191087]
- EPSRC [EP/N025652/1, EP/N013573/1] Funding Source: UKRI
Protein-protein interactions (PPIs) provide a rich source of potential targets for drug discovery and biomedical science research. However, the identification of structural-diverse starting points for discovery of PPI inhibitors remains a significant challenge. Activity-directed synthesis (ADS), a function-driven discovery approach, was harnessed in the discovery of the p53/hDM2 PPI. Over two rounds of ADS, 346 microscale reactions were performed, with prioritisation on the basis of the activity of the resulting product mixtures. Four distinct and novel series of PPI inhibitors were discovered that, through biophysical characterisation, were shown to have promising ligand efficiencies. It was thus shown that ADS can facilitate ligand discovery for a target that does not have a defined small-molecule binding site, and can provide distinctive starting points for the discovery of PPI inhibitors.
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