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Marbostat-100 Defines a New Class of Potent and Selective Antiinflammatory and Antirheumatic Histone Deacetylase 6 Inhibitors
- 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...
- Subjects :
- Male
0301 basic medicine
Anti-Inflammatory Agents
Histone Deacetylase 6
Hydroxamic Acids
Arthritis, Rheumatoid
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Cell Line, Tumor
Drug Discovery
Gene expression
Animals
Humans
Epigenetics
Collagen Type II
Zebrafish
Binding Sites
Hydroxamic acid
biology
HEK 293 cells
HDAC6
Arthritis, Experimental
In vitro
Histone Deacetylase Inhibitors
Molecular Docking Simulation
HEK293 Cells
030104 developmental biology
Histone
chemistry
Mice, Inbred DBA
Antirheumatic Agents
030220 oncology & carcinogenesis
Benzamides
Cancer research
biology.protein
Molecular Medicine
Histone deacetylase
Carbolines
Subjects
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