Isoindolo[2,1-a]quinoxaline Derivatives, Novel Potent Antitumor Agents with Dual Inhibition of Tubulin Polymerization and Topoisomerase I-Reference-Cited by-同舟云学术

Isoindolo[2,1-a]quinoxaline Derivatives, Novel Potent Antitumor Agents with Dual Inhibition of Tubulin Polymerization and Topoisomerase I

Published:2008-03-27 Issue:8 Volume:51 Page:2387-2399
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Diana Patrizia¹,Martorana Annamaria¹,Barraja Paola¹,Montalbano Alessandra¹,Dattolo Gaetano¹,Cirrincione Girolamo¹,Dall’Acqua Francesco¹,Salvador Alessia¹,Vedaldi Daniela¹,Basso Giuseppe¹,Viola Giampietro¹

Affiliation:

1. Dipartimento Farmacochimico Tossicologico e Biologico, Università degli Studi di Palermo, Via Archirafi 32, 90123 Palermo, Italy, Dipartimento di Scienze Farmaceutiche, Università degli Studi di Padova, Via Marzolo 5, 35131 Padova, Italy, and Dipartimento di Pediatria, Università degli Studi di Padova, Via Giustiniani 3, 35131 Padova, Italy

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm070834t

Reference46 articles.

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2. Quinoxaline chemistry. Part 16. 4-Substituted anilino and 4-substituted phenoxymethyl pyrrolo[1,2-a]quinoxalines and N-[4-(pyrrolo[1,2-a]quinoxalin-4-yl)amino and hydroxymethyl]benzoyl glutamates. Synthesis and evaluation of in vitro biological activity

3. An Efficient and Expeditious Synthesis of a Novel 5H-Naphth[1',2':5,6][1,4]oxazino[2,3-b]quinoxalin-5-one and Its Unique Inhibitory Activity against a Panel of Human Cancer Cell Lines

4. Structure−Activity Studies of Substituted Quinoxalinones as Multiple-Drug-Resistance Antagonists

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