Structural basis for the design and synthesis of selective HDAC inhibitors-Reference-Cited by-同舟云学术

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Structural basis for the design and synthesis of selective HDAC inhibitors

Published:2013-07 Issue:13 Volume:21 Page:3795-3807
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Di Micco Simone,Chini Maria Giovanna,Terracciano Stefania,Bruno Ines,Riccio Raffaele,Bifulco Giuseppe

Funder

Ministero dell’Istruzione, dell’Università e della Ricerca (MIUR), PRIN 2009

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference70 articles.

1. The language of covalent histone modifications

2. Histone deacetylases (HDACs): characterization of the classical HDAC family

3. Evolutionarily Conserved and Nonconserved Cellular Localizations and Functions of Human SIRT Proteins

4. Inside HDAC with HDAC inhibitors

5. HDAC family: What are the cancer relevant targets?

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1. A Review on Molecular Docking on HDAC Isoforms: Novel Tool for Designing Selective Inhibitors;Pharmaceuticals;2023-11-22

2. Are inhibitors of histone deacetylase 8 (HDAC8) effective in hematological cancers especially acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL)?;European Journal of Medicinal Chemistry;2023-10

3. 2-Substituted 1,5-benzothiazepine-based HDAC inhibitors exert anticancer activities on human solid and acute myeloid leukemia cell lines;Bioorganic & Medicinal Chemistry;2023-10

4. Identification of potent histone deacetylase 2 (HDAC2) inhibitors through combined structure and ligand-based designs and molecular modelling approach;Journal of Biomolecular Structure and Dynamics;2023-06-12

5. Synthesis and biological evaluation of novel N-benzyltriazolyl-hydroxamate derivatives as selective histone deacetylase 6 inhibitors;Bioorganic & Medicinal Chemistry;2023-02

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