From the configurational preference of dihydroceramide desaturase-1 towards Δ6-unsaturated substrates to the discovery of a new inhibitor

Ana Pou, José Luís Abad, Yadira F. Ordóñez, Maria Garrido, Josefina Casas, Gemma Fabriàs*, Antonio Delgado

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Dihydroceramide desaturase 1 (Des1) catalyzes the last step of ceramide synthesis de novo, thus regulating the physiologically relevant balance between dihydrosphingolipids and sphingolipids. Here we report on the configurational preference of Des1 towards isomeric Δ6-unsaturated dihydroceramide analogs and the discovery of a potent Des1 inhibitor.

Original languageEnglish
Pages (from-to)4394-4397
Number of pages4
JournalChemical Communications
Volume53
Issue number31
DOIs
StatePublished - 2017
Externally publishedYes

Bibliographical note

Publisher Copyright:
© The Royal Society of Chemistry.

Funding

This work was partially supported by the Spanish Ministry of Economy and Competitiveness through Grant CTQ2014-54743- R. Predoctoral fellowships from the Spanish Ministry of Economy and Competitiveness (BES-2012-056019, to A. P.), CSIC (to M. G.) and SENESCYT-Ecuador (to Y. F. O.) are also acknowledged.

FundersFunder number
Spanish Ministry of Economy and CompetitivenessCTQ2014-54743, BES-2012-056019
Consejo Superior de Investigaciones Científicas

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