Discovery of N-(2-oxoethyl) sulfanilamide-derived inhibitors of KAT6A (MOZ) against leukemia by an isostere strategy-Reference-Cited by-同舟云学术

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Discovery of N-(2-oxoethyl) sulfanilamide-derived inhibitors of KAT6A (MOZ) against leukemia by an isostere strategy

Published:2023-11 Issue: Volume:260 Page:115770
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Duan Yongtao,Zhao Yabiao,Li Zhenzhen,Liu Zhenling,Wang Mingzhu,Wang Xuan,Sun Moran^ORCID,Song Chuanjun,Yao Yongfang

Funder

National Natural Science Foundation of China

Natural Science Foundation of Henan Province

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference35 articles.

1. Epigenetics in cancer: targeting chromatin modifications;Ellis;Mol. Cancer Therapeut.,2009

2. Epigenetics and human disease: translating basic biology into clinical applications;Rodenhiser;Can. Med. Assoc. J.,2006

3. An efficient high-throughput screening method for MYST family acetyltransferases, a new class of epigenetic drug targets;Falk;J. Biomol. Screen,2011

4. The MYST family of histone acetyltransferases and their intimate links to cancer;Avvakumov;Oncogene,2007

5. Global levels of histone modifications predict prognosis in different cancers;Seligson;Am. J. Pathol.,2009

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1. Current Scenario of Pyridine/Quinoline-Sulfonamide Hybrids with Anticancer Potential (A Review);Russian Journal of General Chemistry;2024-04

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