Design, synthesis, and biological activity of a novel series of human sirtuin-2-selective inhibitors
| Autor: | Natsuko Tokuda, Katsura Yamatsuta, Hidehiko Nakagawa, Takuya Seko, Hideyuki Sawada, Mohammed Naseer Ahmed Khan, Naoki Miyata, Yukihiro Itoh, Takayoshi Suzuki, Jun Takeuchi, Erika Imai |
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| Rok vydání: | 2012 |
| Předmět: |
Models
Molecular Protein Conformation Chemistry Techniques Synthetic Pharmacology SIRT2 Homology (biology) law.invention Substrate Specificity Inhibitory Concentration 50 Protein structure Sirtuin 2 law Drug Discovery Humans Enzyme Inhibitors biology Chemistry Biological activity Enzyme assay Biochemistry Acetylation Drug Design Sirtuin Benzamides biology.protein Recombinant DNA Molecular Medicine |
| Zdroj: | Journal of medicinal chemistry. 55(12) |
| ISSN: | 1520-4804 |
| Popis: | Selective inhibitors of human sirtuin 2 (SIRT2), a deacetylase, are candidate therapeutic agents for neurodegenerative diseases such as Parkinson's disease and Huntington's disease as well as potential tools for elucidating the biological functions of SIRT2. On the basis of homology models of SIRT1 and SIRT2, we designed and prepared a series of 2-anilinobenzamide analogues. Enzyme assays using recombinant SIRT1 and SIRT2 revealed that 3'-phenethyloxy-2-anilinobenzamide analogues such as 33a and 33i are potent and selective SIRT2 inhibitors, showing more than 3.5-fold greater SIRT2-inhibitory activity and more than 35-fold greater SIRT2-selectivity compared with AGK2 (3), a previously reported SIRT2-selective inhibitor. Compound 33a also induced a dose-dependent selective increase of α-tubulin acetylation in human colon cancer HCT116 cells, indicating selective inhibition of SIRT2 in the cells. These 3'-phenethyloxy-2-anilinobenzamide derivatives represent an entry into a new class of SIRT2-selective inhibitors. |
| Databáze: | OpenAIRE |
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