Abstract |
Ceramides are lipid-derived intracellular messengers involved in the control of senescence, inflammation, and apoptosis. The cysteine amidase, acid ceramidase (AC), hydrolyzes these substances into sphingosine and fatty acid and, by doing so, regulates their signaling activity. AC inhibitors may be useful in the treatment of pathological conditions, such as cancer, in which ceramide levels are abnormally reduced. Here, we present a systematic SAR investigation of the benzoxazolone carboxamides, a recently described class of AC inhibitors that display high potency and systemic activity in mice. We examined a diverse series of substitutions on both benzoxazolone ring and carboxamide side chain. Several modifications enhanced potency and stability, and one key compound with a balanced activity-stability profile (14) was found to inhibit AC activity in mouse lungs and cerebral cortex after systemic administration. The results expand our arsenal of AC inhibitors, thereby facilitating the use of these compounds as pharmacological tools and their potential development as drug leads.
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Authors | Anders Bach, Daniela Pizzirani, Natalia Realini, Valentina Vozella, Debora Russo, Ilaria Penna, Laurin Melzig, Rita Scarpelli, Daniele Piomelli |
Journal | Journal of medicinal chemistry
(J Med Chem)
Vol. 58
Issue 23
Pg. 9258-72
(Dec 10 2015)
ISSN: 1520-4804 [Electronic] United States |
PMID | 26560855
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Benzoxazoles
- Enzyme Inhibitors
- benzoxazolone
- Acid Ceramidase
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Topics |
- Acid Ceramidase
(antagonists & inhibitors, metabolism)
- Animals
- Benzoxazoles
(chemical synthesis, chemistry, pharmacology)
- Brain
(drug effects, enzymology)
- Enzyme Inhibitors
(administration & dosage, chemical synthesis, chemistry, pharmacology)
- Humans
- Lung
(drug effects, enzymology)
- Male
- Mice
- Mice, Inbred C57BL
- Structure-Activity Relationship
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