Highly Ligand Efficient and SelectiveN-2-(Thioethyl)picolinamide Histone Deacetylase Inhibitors Inspired by the Natural Product Psammaplin A-Reference-Cited by-同舟云学术

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Highly Ligand Efficient and SelectiveN-2-(Thioethyl)picolinamide Histone Deacetylase Inhibitors Inspired by the Natural Product Psammaplin A

Published:2012-11-26 Issue:1 Volume:8 Page:149-156
ISSN:1860-7179
Container-title:ChemMedChem
language:en
Short-container-title:ChemMedChem

Author:

Baud Matthias G. J.,Haus Patricia,Leiser Thomas,Meyer-Almes Franz-Josef,Fuchter Matthew J.

Publisher

Wiley

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics,Molecular Medicine,Drug Discovery,Biochemistry,Pharmacology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/cmdc.201200450/fullpdf

Reference57 articles.

1. Epigenetic therapy of cancer: past, present and future

2. Histone-deacetylase inhibitors: novel drugs for the treatment of cancer

3. Histone deacetylase inhibitors: molecular mechanisms of action

4. Characterisation of the in vitro activity of the depsipeptide histone deacetylase inhibitor spiruchostatin A

5. Histone Deacetylase Inhibitors

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1. Psammaplin A and Its Analogs Attenuate Oxidative Stress in Neuronal Cells through Peroxisome Proliferator-Activated Receptor γ Activation;Journal of Natural Products;2024-04-18

2. Non-Hydroxamate Zinc-Binding Groups as Warheads for Histone Deacetylases;Molecules;2021-08-25

3. Natural Products Impacting DNA Methyltransferases and Histone Deacetylases;Frontiers in Pharmacology;2020-08-13

4. Class I HDAC Inhibitors Display Different Antitumor Mechanism in Leukemia and Prostatic Cancer Cells Depending on Their p53 Status;Journal of Medicinal Chemistry;2018-03-02

5. Hydroxyl Ketone-Based Histone Deacetylase Inhibitors To Gain Insight into Class I HDAC Selectivity versus That of HDAC6;ACS Omega;2017-04-20

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