Synthesis and cytotoxicity of novel 6H-indolo[2,3-b]quinoxaline derivatives-Reference-Cited by-同舟云学术

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Synthesis and cytotoxicity of novel 6H-indolo[2,3-b]quinoxaline derivatives

Published:2012-12-01 Issue:8 Volume:22 Page:3712-3718
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Avula Sreenivas,Komsani Jayaram Reddy,Koppireddi Satish,Yadla Rambabu,Kanugula Anantha KoteswaraRao,Kotamraju Srigiridhar

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/content/pdf/10.1007/s00044-012-0373-7.pdf

Reference22 articles.

1. Abadi AH (1998) 5-Substituted 2-bromo indolo[3,2-b]quinoxalines, a class of potential anti-tumor agents with cdc25 phosphatase inhibitory properties. Arch Pharm 331:352–358

2. Allais A, Meier J (Roussele Uclaf) (1969) Novel quinolines. DE Patent 1815467

3. Bergman JOE, Akerfeldt SG (Lundblad Leif) (1987) Indoloquinoxalines with substitutents in 6-position containing cyclic groups. EP Patent 0231159

4. Bergman J, Engqvist R, Stalhandske C, Wallberg H (2003) Studies of the reactions between indole-2,3-diones (isatins) and 2-aminobenzylamine. Tetrahedron 59:1033–1048

5. Brown DJ (2004) Quinoxalines. Wiley, New York

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