Metabolism of the anti-tumour drugsN2-methyl-9-hydroxyellipticinium acetate (NSC 264137) andN2-methyl-9-hydroxyolivacinium acetate in the rat: preliminary identification of biliary 9-(O)-glucuronide and 10-(S)-glutathione conjugates-Reference-Cited by-同舟云学术

Metabolism of the anti-tumour drugsN2-methyl-9-hydroxyellipticinium acetate (NSC 264137) andN2-methyl-9-hydroxyolivacinium acetate in the rat: preliminary identification of biliary 9-(O)-glucuronide and 10-(S)-glutathione conjugates

Published:1983-01 Issue:5 Volume:13 Page:303-310
ISSN:0049-8254
Container-title:Xenobiotica
language:en
Short-container-title:Xenobiotica

Author:

Maftouh M.,Meunier G.,Dugue B.,Monsarrat B.,Meunier B.,Paoletti C.

Publisher

Informa UK Limited

Subject

Health, Toxicology and Mutagenesis,Pharmacology,Toxicology,Biochemistry,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/00498258309052268

Reference11 articles.

1. Bioactivation of the antitumor drugs 9-hydroxyellipticine and derivatives by a peroxidase-hydrogen peroxide system

2. The Synthesis of Aryl-D-glucopyranosiduronic Acids1

3. N-Hydroxyacetaminophen: a postulated toxic metabolite of acetaminophen

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1. A Versatile Construction of the 8H-Quino[4,3-b]carbazole Ring System as a Potential DNA Binder;The Journal of Organic Chemistry;1995-04

2. Nephrotoxicity of an Ellipticine Derivative (N2-Methyl-9-Hydroxyellipticinium Acetate) in Rat: a Defect of Urinary Concentrating Ability;Renal Failure;1991-01

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