Design and Synthesis of E7820/Tasisulam Hybrids as Potential DCAF15 Binders

We describe the design and synthesis of a series of N-[arylsulfonyl]-1H-pyrrole-2-carboxamides as hybrid analogs of the DCAF15 binders E7820 and tasisulam, two representative SPLAMs (sulfonamide-containing molecular glues). These hybrid molecules were designed to combine the key interactions of both parent ligands within the DCAF15 binding site, as supported by docking studies. Binding affinity was evaluated using fluorescence polarization assays, and structure–activity relationships were established, highlighting the importance of dichlorinated pyrrole moieties. Selected compounds were also tested in HCT116 cells to assess in vitro activity.

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Reactions
Published
2025-05-20
DOI
https://doi.org/10.3390/reactions6020034
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
0.00

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article

Design and Synthesis of E7820/Tasisulam Hybrids as Potential DCAF15 Binders

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Reactions
Protein Degradation and Inhibitors
article

Design and Synthesis of E7820/Tasisulam Hybrids as Potential DCAF15 Binders

Sébastien Triboulet, Sofiane Hocine, Stephen Hanessian, András Herner, Timea Baló, Laurence Klipfel, Victor Cosson, Remi Calandrino, Jayson Alves Bordelo, Laure Caruana
article en

Abstract

We describe the design and synthesis of a series of N-[arylsulfonyl]-1H-pyrrole-2-carboxamides as hybrid analogs of the DCAF15 binders E7820 and tasisulam, two representative SPLAMs (sulfonamide-containing molecular glues). These hybrid molecules were designed to combine the key interactions of both parent ligands within the DCAF15 binding site, as supported by docking studies. Binding affinity was evaluated using fluorescence polarization assays, and structure–activity relationships were established, highlighting the importance of dichlorinated pyrrole moieties. Selected compounds were also tested in HCT116 cells to assess in vitro activity.

ReactionsVol. 6(2)
Eötvös Loránd University (HU), University of California, Irvine (US), Servier (France) (FR), Université de Montréal (CA), Institut des Hautes Études Scientifiques (FR)
Servier, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 90%
Protein Degradation and Inhibitors
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