An efficient synthesis of SK-658 and its analogs as potent histone deacetylase inhibitors-Reference-Cited by-同舟云学术

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An efficient synthesis of SK-658 and its analogs as potent histone deacetylase inhibitors

Published:2015-04 Issue: Volume:59 Page:145-150
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Shahidul Islam Md.,Nurul Islam Md.,Ashraful Hoque Md.,Nishino Norikazu,Kato Tamaki,Kim Hyun-Jung,Ito Akihiro,Yoshida Minoru

Funder

Kitakyushu Foundation for the Advancement of Industry, Science and Technology

Japan Student Services Organization

Saneyoshi Scholarship Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference27 articles.

1. Chemical Origins of Isoform Selectivity in Histone Deacetylase Inhibitors

2. R. Breslow, P.A. Marks, R.A. Rifkind, B. Jursic, PTC Int. Appl. WO 93/07148, April 15, 1993.

3. Highly Potent and Selective Histone Deacetylase 6 Inhibitors Designed Based on a Small-Molecular Substrate

4. Thiol-based SAHA analogues as potent histone deacetylase inhibitors

5. Non-Peptide Macrocyclic Histone Deacetylase Inhibitors Derived from Tricyclic Ketolide Skeleton

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2. HDAC as onco target: Reviewing the synthetic approaches with SAR study of their inhibitors;European Journal of Medicinal Chemistry;2018-10

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4. Inside HDACs with more selective HDAC inhibitors;European Journal of Medicinal Chemistry;2016-10

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