Design, synthesis, biological evaluation and molecular docking study of novel chalcone-based hydroxamic acids possessing a central 2, 4-dimethy pyrrole linker as potential HDAC (Histone Deacetylase) inhibitors and anticancer agents-Reference-Cited by-同舟云学术

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Design, synthesis, biological evaluation and molecular docking study of novel chalcone-based hydroxamic acids possessing a central 2, 4-dimethy pyrrole linker as potential HDAC (Histone Deacetylase) inhibitors and anticancer agents

Published:2024-06 Issue: Volume:1305 Page:137749
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Yousefian Mozhdeh,Hashemi Maryam,Eskandarpour Vahid^ORCID,Hadizadeh Farzin^ORCID,Zarghi Afshin,Ghodsi Razieh

Funder

Mashhad University of Medical Sciences

Publisher

Elsevier BV

Reference36 articles.

1. The unique physiology of solid tumors: opportunities (and problems) for cancer therapy;Brown;Cancer Res.,1998

2. Histone deacetylase inhibitors as anticancer drugs;Eckschlager;Int. J. Mol. Sci.,2017

3. Highly compacted chromatin formed in vitro reflects the dynamics of transcription activation in vivo;Li;Mol. Cell,2010

4. Epigenetics: the Science of Change;Weinhold,2006

5. Epigenetics—An epicenter of gene regulation: histones and histone-modifying enzymes;Biel;Angew. Chem. Int. Ed.,2005

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Green synthesis, structure–activity relationships, in silico molecular docking, and antifungal activities of novel prenylated chalcones;Frontiers in Chemistry;2024-04-26

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