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Title

Discovery of deoxyceramide analogs as highly selective ACER3 inhibitors in live cells

AuthorsBielsa, Núria; Casasampere, Mireia; Aseeri, Mazen; Casas, Josefina CSIC ORCID ; Delgado Cirilo, Antonio; Abad, José Luis CSIC ORCID ; Fabriàs, Gemma CSIC ORCID
KeywordsCeramide
Ceramidase
Sphingolipid
Inhibition
Therapeutic target
Enzyme activity
Issue Date24-Feb-2021
PublisherElsevier
CitationEuropean Journal of Medicinal Chemistry: 113296 (2021)
AbstractAcid (AC), neutral (NC) and alkaline ceramidase 3 (ACER3) are the most ubiquitous ceramidases and their therapeutic interest as targets in cancer diseases has been well sustained. This supports the importance of discovering potent and specific inhibitors for further use in combination therapies. Although several ceramidase inhibitors have been reported, most of them target AC and a few focus on NC. In contrast, well characterized ACER3 inhibitors are lacking. Here we report on the synthesis and screening of two series of 1-deoxy(dihydro)ceramide analogs on the three enzymes. Activity was determined using fluorogenic substrates in recombinant human NC (rhNC) and both lysates and intact cells enriched in each enzyme. None of the molecules elicited a remarkable AC inhibitory activity in either experimental setup, while using rhNC, several compounds of both series were active as non-competitive inhibitors with Ki values between 1 and 5 μM. However, a dramatic loss of potency occurred in NC-enriched cell lysates and no activity was elicited in intact cells. Interestingly, several compounds of Series 2 inhibited ACER3 dose-dependently in both cell lysates and intact cells with IC50‘s around 20 μM. In agreement with their activity in live cells, they provoked a significant increase in the amounts of ceramides. Overall, this study identifies highly selective ACER3 activity blockers in intact cells, opening the door to further medicinal chemistry efforts aimed at developing more potent and specific compounds.
Publisher version (URL)https://doi.org/10.1016/j.ejmech.2021.113296
URIhttp://hdl.handle.net/10261/230805
DOIhttp://dx.doi.org/10.1016/j.ejmech.2021.113296
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