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Marbostat-100 Defines a New Class of Potent and Selective Antiinflammatory and Antirheumatic Histone Deacetylase 6 Inhibitors

Authors :
Andreas Sellmer
Sigurd Elz
Emerich Eichhorn
Michel Leonhardt
Oliver H. Krämer
Rainer H. Straub
Elisabeth Grünstein
Hubert Stangl
Herwig Pongratz
Siavosh Mahboobi
Birgit Striegl
Mandy Beyer
Stefan Dove
Zsuzsa Jenei-Lanzl
Source :
Journal of Medicinal Chemistry. 61:3454-3477
Publication Year :
2018
Publisher :
American Chemical Society (ACS), 2018.

Abstract

Epigenetic modifiers of the histone deacetylase (HDAC) family contribute to autoimmunity, cancer, HIV infection, inflammation, and neurodegeneration. Hence, histone deacetylase inhibitors (HDACi), which alter protein acetylation, gene expression patterns, and cell fate decisions, represent promising new drugs for the therapy of these diseases. Whereas pan-HDACi inhibit all 11 Zn2+-dependent histone deacetylases (HDACs) and cause a broad spectrum of side effects, specific inhibitors of histone deacetylase 6 (HDAC6i) are supposed to have less side effects. We present the synthesis and biological evaluation of Marbostats, novel HDAC6i that contain the hydroxamic acid moiety linked to tetrahydro-β-carboline derivatives. Our lead compound Marbostat-100 is a more potent and more selective HDAC6i than previously established well-characterized compounds in vitro as well as in cells. Moreover, Marbostat-100 is well tolerated by mice and effective against collagen type II induced arthritis. Thus, Marbostat-100 repr...

Details

ISSN :
15204804 and 00222623
Volume :
61
Database :
OpenAIRE
Journal :
Journal of Medicinal Chemistry
Accession number :
edsair.doi.dedup.....0149487923fb5d81cf6dcb58e4a3fca5
Full Text :
https://doi.org/10.1021/acs.jmedchem.7b01593