Free radical modulation by N-substituted dehydroalanines, a new way to improve therapeutic activity of anticancer drugs-Reference-Cited by-同舟云学术

Free radical modulation by N-substituted dehydroalanines, a new way to improve therapeutic activity of anticancer drugs

Published:1987-12 Issue:3-4 Volume:14 Page:379-382
ISSN:0305-7372
Container-title:Cancer Treatment Reviews
language:en
Short-container-title:Cancer Treatment Reviews

Author:

Buc-Calderon P.,Praet M.,Ruysschaert J.M.,Roberfroid M.

Publisher

Elsevier BV

Subject

Radiology, Nuclear Medicine and imaging,Oncology,General Medicine

Reference6 articles.

1. A general mechanism for microsomal activation of quinone anticancer agents to free radicals;Bachur,1979

2. N-substituted dehydroalanine derivatives, a new class of radicophiles, reduce enzymatic and chemical production of superoxyde anion and hydroxyl radical;Buc-Calderon;Arch. Internat. Physiol. Biochim.,1986

3. Anthracycline glycoside-membrane interactions;Goormaghtigh;Biochim. Biophys. Acta,1984

4. The capto-dative effect;Viehe;Acc. Chem. Res.,1985

5. Capdo-dative substituent effects in synthesis with radicals and radicophiles;Viehe;Agnew. Chem.,1979

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4. Amino acids and their derivatives as radioprotective agents;Amino Acids;1992

5. Increase in the survival time of mice exposed to ionizing radiation by a new class of free radical scavengers;Experientia;1990-07