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Targeting dihydroceramide desaturase 1 (Des1): Syntheses of ceramide analogues with a rigid scaffold, inhibitory assays, and AlphaFold2-assisted structural insights reveal cyclopropenone PR280 as a potent inhibitor.
Rivero P, Ivanova V, Barril X, Casampere M, Casas J, Fabriàs G, Díaz Y, Matheu MI. Rivero P, et al. Among authors: matheu mi. Bioorg Chem. 2024 Apr;145:107233. doi: 10.1016/j.bioorg.2024.107233. Epub 2024 Feb 23. Bioorg Chem. 2024. PMID: 38422591 Free article.
Revealing 2-dimethylhydrazino-2-alkyl alkynyl sphingosine derivatives as sphingosine kinase 2 inhibitors: Some hints on the structural basis for selective inhibition.
Corro-Morón M, Granell A, Ivanova V, Domingo E, Beltrán-Debón R, Barril X, Sanz MJ, Matheu MI, Castillón S, Díaz Y. Corro-Morón M, et al. Among authors: matheu mi. Bioorg Chem. 2022 Apr;121:105668. doi: 10.1016/j.bioorg.2022.105668. Epub 2022 Feb 12. Bioorg Chem. 2022. PMID: 35219046 Free article.
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