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Design, synthesis, and cytotoxicity evaluation of novel indole-acylhydrazone derivatives of 4-pyridinone as potential histone deacetylase-2 inhibitors
BACKGROUND AND PURPOSE: Histone deacetylation is one of the essential cellular pathways in the growth and spread of cancer, so the design of histone deacetylase (HDAC) inhibitors as anticancer agents is of great importance in pharmaceutical chemistry. Here, a series of indole acylhydrazone derivativ...
Autores principales: | Naghi-Ganji, Niloofar, Saghaei, Lotfollah, Tavakoli, Farial, Azimian, Vajihe, Mirian, Mina, Sirous, Hajar, Rostami, Mahboubeh |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661679/ https://www.ncbi.nlm.nih.gov/pubmed/36386484 http://dx.doi.org/10.4103/1735-5362.355214 |
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