Design and synthesis of 4-amino-2-phenylquinazolines as novel topoisomerase I inhibitors with molecular modeling-Reference-Cited by-同舟云学术

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Design and synthesis of 4-amino-2-phenylquinazolines as novel topoisomerase I inhibitors with molecular modeling

Published:2011-07 Issue:14 Volume:19 Page:4399-4404
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Le Thanh Nguyen,Yang Su Hui,Khadka Daulat Bikram,Van Hue Thi My,Cho Suk Hee,Kwon Youngjoo,Lee Eung-Seok,Lee Kyung-Tae,Cho Won-Jea

Funder

Korea Research Foundation

Publisher

Elsevier BV

Subject

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

Reference28 articles.

1. DNA TOPOISOMERASES

2. DNA TOPOISOMERASE POISONS AS ANTITUMOR DRUGS

3. Design, Synthesis and Development of Novel Camptothecin Drugs

4. Novel E-ring camptothecin keto analogues (S38809 and S39625) are stable, potent, and selective topoisomerase I inhibitors without being substrates of drug efflux transporters

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2. p-Toluenesulfonic acid-catalyzed regioselective C4–H iodination of isoquinolin-1(2H)-ones;New Journal of Chemistry;2022

3. Reaction Outcome Critically Dependent on the Method of Workup: An Example from the Synthesis of 1-Isoquinolones;The Journal of Organic Chemistry;2021-05-25

4. Therapeutic progression of quinazolines as targeted chemotherapeutic agents;European Journal of Medicinal Chemistry;2021-02

5. Mn-mediated oxidative radical cyclization of 2-(azidomethyl)phenyl isocyanides with carbazate: access to quinazoline-2-carboxylates;New Journal of Chemistry;2020

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