The synthesis of 6-(N-Arylamino)-7-chloro-5,8-quinolinedione derivatives for evaluation of antifungal activities-Reference-Cited by-同舟云学术

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The synthesis of 6-(N-Arylamino)-7-chloro-5,8-quinolinedione derivatives for evaluation of antifungal activities

Published:1994-06 Issue:3 Volume:17 Page:139-144
ISSN:0253-6269
Container-title:Archives of Pharmacal Research
language:en
Short-container-title:Arch. Pharm. Res.

Author:

Ryu Chung-Kyu,Kim Hee-Jeong

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Drug Discovery,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF02974248.pdf

Reference24 articles.

1. Bowman, C. M., Porter, T. H., Skelton, F. S. and Folkers, K., 5,8-Quinolinequinone analogs which inhibit mitocondrial succinoxidase.J. Med. Chem., 14, 206–209 (1973).

2. Clark, N. G., The fungicidal activity of substituted 1,4-naphthoquinones.Pestic. Sci., 15, 235–40 (1984).

3. Cadenas, E. and Ernster, L., Effect of superoxide dismutase on the autoxidation of hydroquinones formed during DT-diaphorase catalysis and glutathione nucleophilic addition: Emerit, I., Packer, L. and Auclair, C. (Eds.),Antioxidants in therapy and preventive medicine-Advances in experimental medicine and biology, Vol. 264, Plenum, New York, 1990, pp. 37–44.

4. Hafuri, Y., Takemori, E., Oogose, K., Inouye, Y. and Nakamura, S., Mechanism of inhibition of reverse transcriptase by quinone antibiotics.J. Antibiotics, 41, 1471–1478 (1988).

5. Hassan, H. M. and Fridovich, I., Enzymatic defense against the toxicity of oxygen and of streptonigrin inE. coli.J. Bacterol., 129(3), 1574–1579 (1977).

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