Design, synthesis, cytotoxicity, and molecular docking studies of novel thiazolyl–hydrazone derivatives as histone lysine acetyl‐transferase inhibitors and apoptosis inducers-Reference-Cited by-同舟云学术

Design, synthesis, cytotoxicity, and molecular docking studies of novel thiazolyl–hydrazone derivatives as histone lysine acetyl‐transferase inhibitors and apoptosis inducers

Published:2022-04-08 Issue:7 Volume:355 Page:2200076
ISSN:0365-6233
Container-title:Archiv der Pharmazie
language:en
Short-container-title:Archiv der Pharmazie

Author:

Abbas Eman M. H.¹,Farghaly Thoraya A.²^ORCID,Sabour Rehab³,Shaaban Mohamed R.⁴,Abdallah Zeinab A.²

Affiliation:

1. Department of Chemistry, Natural and Microbial Products National Research Center Dokki Cairo Egypt

2. Department of Chemistry, Faculty of Science Cairo University Giza Egypt

3. Department of Pharmaceutical Chemistry, Faculty of Pharmacy (Girls) Al‐Azhar University Cairo Egypt

4. Department of Chemistry, Faculty of Applied Science Umm Al‐Qura University Makkah Almukkarramah Saudi Arabia

Publisher

Wiley

Subject

Drug Discovery,Pharmaceutical Science

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ardp.202200076

Reference56 articles.

1. CPTH6, a Thiazole Derivative, Induces Histone Hypoacetylation and Apoptosis in Human Leukemia Cells

2. The complex language of chromatin regulation during transcription

3. Acetylation of Histones and Transcription-Related Factors

4. Acetylated Lysine 56 on Histone H3 Drives Chromatin Assembly after Repair and Signals for the Completion of Repair

5. GCN5 Is a Positive Regulator of Origins of DNA Replication in Saccharomyces cerevisiae

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