Free Radical Intermediates in the Reduction of Quinoxaline N-Oxide Antitumor Drugs: Redox and Prototropic Reactions-Reference-Cited by-同舟云学术

Free Radical Intermediates in the Reduction of Quinoxaline N-Oxide Antitumor Drugs: Redox and Prototropic Reactions

Published:1996-01-01 Issue:24 Volume:118 Page:5648-5654
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Priyadarsini K. Indira¹,Dennis Madeleine F.¹,Naylor Matthew A.¹,Stratford Michael R. L.¹,Wardman Peter¹

Affiliation:

1. Contribution from the Gray Laboratory Cancer Research Trust, Mount Vernon Hospital, P.O. Box 100, Northwood, Middlesex HA6 2JR, U.K., Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai-400085, India, and MRC Radiobiology Unit, Chilton, Didcot, Oxon OX11 ORD, U.K.

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja953761o

Reference31 articles.

1. Bioreductive drugs for cancer therapy: The search for tumor specificity

2. High levels of expression of the NAD(P)H:Quinone oxidoreductase (NQO1) gene in tumor cells compared to normal cells of the same origin

3. Induction of Hypoxia in the KHT Sarcoma by Tumour Necrosis Factor and Flavone Acetic Acid

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