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Rational Design and Simple Chemistry Yield a Superior, Neuroprotective HDAC6 Inhibitor, Tubastatin A
- Publication Year :
- 2010
-
Abstract
- Structure-based drug design combined with homology modeling techniques were used to develop potent inhibitors of HDAC6 that display superior selectivity for the HDAC6 isozyme compared to other inhibitors. These inhibitors can be assembled in a few synthetic steps, and thus are readily scaled up for in vivo studies. An optimized compound from this series, designated Tubastatin A, was tested in primary cortical neuron cultures in which it was found to induce elevated levels of acetylated alpha-tubulin, but not histone, consistent with its HDAC6 selectivity. Tubastatin A also conferred dose-dependent protection in primary cortical neuron cultures against glutathione depletion-induced oxidative stress. Importantly, when given alone at all concentrations tested, this hydroxamate-containing HDAC6-selective compound displayed no neuronal toxicity, thus, forecasting the potential application of this agent and its analogues to neurodegenerative conditions.
- Subjects :
- Models, Molecular
Indoles
medicine.disease_cause
Histone Deacetylase 6
Hydroxamic Acids
Biochemistry
Neuroprotection
Catalysis
Article
Histone Deacetylases
chemistry.chemical_compound
Structure-Activity Relationship
Colloid and Surface Chemistry
In vivo
medicine
Structure–activity relationship
Humans
Anilides
Enzyme Inhibitors
Homocysteine
Neurons
Cell Death
Dose-Response Relationship, Drug
Molecular Structure
Chemistry
Rational design
Stereoisomerism
General Chemistry
Glutathione
HDAC6
Isoenzymes
Oxidative Stress
Neuroprotective Agents
Acetylation
Drug Design
Oxidative stress
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....4ea3d77c4a74847e67e1a3c1a1d67a59