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 language | English |
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Pages (from-to) | 4394-4397 |
Number of pages | 4 |
Journal | Chemical Communications |
Volume | 53 |
Issue number | 31 |
DOIs | |
State | Published - 2017 |
Externally published | Yes |
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.
Funders | Funder number |
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Spanish Ministry of Economy and Competitiveness | CTQ2014-54743, BES-2012-056019 |
Consejo Superior de Investigaciones Científicas |