Design, synthesis and antitumour activity of novel 5(6)-amino-benzimidazolequinones containing a fused morpholine
Author:
Funder
National Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Pharmacology,General Medicine
Reference29 articles.
1. Design of Highly Active Analogues of the Pyrrolo[1,2-a]benzimidazole Antitumor Agents
2. A Comprehensive Study of the Active Site Residues of DT-Diaphorase: Rational Design of Benzimidazolediones as DT-Diaphorase Substrates
3. Chemistry of the Pyrrolo[1,2-a]benzimidazole Antitumor Agents: Influence of the 7-Substituent on the Ability To Alkylate DNA and Inhibit Topoisomerase II
4. Synthesis by Radical Cyclization and Cytotoxicity of Highly Potent Bioreductive Alicyclic Ring Fused [1,2-a]Benzimidazolequinones
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1. Synthesis and SAR of morpholine and its derivatives: A review update;E3S Web of Conferences;2024
2. Design, synthesis, and anti-respiratory syncytial virus potential of novel 3-(1,2,3-triazol-1-yl)furoxazine-fused benzimidazole derivatives;European Journal of Medicinal Chemistry;2023-12
3. Synthesis of condensed morpholine-containing systems by reductive or oxidative heterocyclisation;From Chemistry Towards Technology Step-By-Step;2023-09-23
4. Synthesis of condensed morpholine-containing systems by reductive or oxidative heterocyclisation;From Chemistry Towards Technology Step-By-Step;2023-09-23
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