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NB 06: From a simple lysosomotropic aSMase inhibitor to tools for elucidating the role of lysosomes in signaling apoptosis and LPS-induced inflammation.

Abstract
Ceramide generation is involved in signal transduction of cellular stress response, in particular during stress-induced apoptosis in response to stimuli such as minimally modified Low-density lipoproteins, TNFalpha and exogenous C6-ceramide. In this paper we describe 48 diverse synthetic products and evaluate their lysosomotropic and acid sphingomyelinase inhibiting activities in macrophages. A stimuli-induced increase of C16-ceramide in macrophages can be almost completely suppressed by representative compound NB 06 providing an effective protection of macrophages against apoptosis. Compounds like NB 06 thus offer highly interesting fields of application besides prevention of apoptosis of macrophages in atherosclerotic plaques in vessel walls. Most importantly, they can be used for blocking pH-dependent lysosomal processes and enzymes in general as well as for analyzing lysosomal dependent cellular signaling. Modulation of gene expression of several prominent inflammatory messengers IL1B, IL6, IL23A, CCL4 and CCL20 further indicate potentially beneficial effects in the field of (systemic) infections involving bacterial endotoxins like LPS or infections with influenza A virus.
AuthorsMarkus Blaess, Nelly Bibak, Ralf A Claus, Matthias Kohl, Gabriel A Bonaterra, Ralf Kinscherf, Stefan Laufer, Hans-Peter Deigner
JournalEuropean journal of medicinal chemistry (Eur J Med Chem) Vol. 153 Pg. 73-104 (Jun 10 2018) ISSN: 1768-3254 [Electronic] France
PMID29031494 (Publication Type: Journal Article)
CopyrightCopyright © 2017 Elsevier Masson SAS. All rights reserved.
Chemical References
  • Ceramides
  • Enzyme Inhibitors
  • Lipopolysaccharides
  • Sphingomyelin Phosphodiesterase
Topics
  • Apoptosis (drug effects)
  • Cell Line
  • Cells, Cultured
  • Ceramides (immunology)
  • Enzyme Inhibitors (chemistry, pharmacology)
  • Humans
  • Inflammation (drug therapy, immunology)
  • Lipopolysaccharides (immunology)
  • Lysosomes (drug effects, immunology)
  • Macrophages (drug effects, immunology)
  • Signal Transduction (drug effects)
  • Sphingomyelin Phosphodiesterase (antagonists & inhibitors, immunology)

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