| Literature DB >> 28944578 |
Martina Bigatti1, Alberto Dal Corso2, Sara Vanetti1, Samuele Cazzamalli2, Ulrike Rieder1, Jörg Scheuermann2, Dario Neri2, Filippo Sladojevich1.
Abstract
The screening of encoded self-assembling chemical libraries allows the identification of fragment pairs that bind to adjacent pockets on target proteins of interest. For practical applications, it is necessary to link these ligand pairs into discrete organic molecules, devoid of any nucleic acid component. Here we describe the discovery of a synergistic binding pair for acid alpha-1 glycoprotein and a chemical strategy for the identification of optimal linkers, connecting the two fragments. The procedure yielded a set of small organic ligands, the best of which exhibited a dissociation constant of 9.9 nm, as measured in solution by fluorescence polarization.Keywords: DNA-encoded libraries; encoded self-assembling chemical libraries (ESAC); fragment linking; fragment-based drug discovery; polymer-supported synthesis
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Year: 2017 PMID: 28944578 DOI: 10.1002/cmdc.201700569
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466