Design and synthesis of a new generation of substituted purine hydroxamate analogs as histone deacetylase inhibitors-Reference-Cited by-同舟云学术

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Design and synthesis of a new generation of substituted purine hydroxamate analogs as histone deacetylase inhibitors

Published:2016-04 Issue:7 Volume:24 Page:1446-1454
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Liu Renshuai,Wang Junhua,Tang Weiping,Fang Hao

Funder

National Natural Foundation Research Grant

Shandong Natural Science Fund for Distinguished Young Scholars

Publisher

Elsevier BV

Subject

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

Reference20 articles.

1. Histone deacetylase inhibitors in the treatment of cancer: overview and perspectives

2. New and emerging HDAC inhibitors for cancer treatment

3. FDA Approval Summary: Vorinostat for Treatment of Advanced Primary Cutaneous T-Cell Lymphoma

4. StatBite: FDA Oncology Drug Product Approvals in 2009

5. FDA Approval: Belinostat for the Treatment of Patients with Relapsed or Refractory Peripheral T-cell Lymphoma

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4. Design, Synthesis, and Biological Evaluation of New Urushiol Derivatives as Potent Class I Histone Deacetylase Inhibitors;ChemBioChem;2023-08-11

5. Synthesis and Cytotoxic Activity of the Derivatives of N-(Purin-6-yl)aminopolymethylene Carboxylic Acids and Related Compounds;Molecules;2023-02-15

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