QSAR Study of Novel Benzofuran Derivatives as Potent LSD1 Inhibitors-Reference-Cited by-同舟云学术

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QSAR Study of Novel Benzofuran Derivatives as Potent LSD1 Inhibitors

Published:2023 Issue:05 Volume:13 Page:8769-8781
ISSN:2161-8712
Container-title:Advances in Clinical Medicine
language:
Short-container-title:ACM

Author:

张渝琪

Publisher

Hans Publishers

Subject

General Engineering

Reference42 articles.

1. 倪娜, 袁宜耘, 陈秋荣, 等. 表观遗传学抗肿瘤药物的临床研究进展[J]. 世界临床药物, 2022, 43(7): 831-838.

2. Histone Demethylation Mediated by the Nuclear Amine Oxidase Homolog LSD1

3. High-Throughput Virtual Screening Identifies Novel N′-(1-Phenylethylidene)-benzohydrazides as Potent, Specific, and Reversible LSD1 Inhibitors

4. Triazole–Dithiocarbamate Based Selective Lysine Specific Demethylase 1 (LSD1) Inactivators Inhibit Gastric Cancer Cell Growth, Invasion, and Migration

5. Discovery of a Novel Inhibitor of Histone Lysine-Specific Demethylase 1A (KDM1A/LSD1) as Orally Active Antitumor Agent

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