双二氧代哌嗪ICRF 159和ICRF 154对镉中毒大鼠尿镉排泄的影响（作者译） - Suppr

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超能文献

[Effect of the bis-dioxopiperazines ICRF 159 and ICRF 154 on the urinary excretion of cadmium in cadmium-poisoned rats (author's transl)].

作者信息

Witting U, Bertram H P, Schumacher E, Ritter G

出版信息

Int Arch Occup Environ Health. 1979 Jan 15;42(3-4):365-73. doi: 10.1007/BF00377792.

DOI:10.1007/BF00377792

PMID:217839

Abstract

摘要

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[Effect of the bis-dioxopiperazines ICRF 159 and ICRF 154 on the urinary excretion of cadmium in cadmium-poisoned rats (author's transl)].双二氧代哌嗪ICRF 159和ICRF 154对镉中毒大鼠尿镉排泄的影响（作者译）

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引用本文的文献

Metal binding by pharmaceuticals. Part 2. Interactions of Ca(II), Cu(II), Fe(II), Mg(II), Mn(II) and Zn(II) with the intracellular hydrolysis products of the antitumour agent ICRF 159 and its inactive homologue ICRF 192.药物与金属的结合。第2部分。Ca(II)、Cu(II)、Fe(II)、Mg(II)、Mn(II)和Zn(II)与抗肿瘤药物ICRF 159及其无活性同系物ICRF 192的细胞内水解产物的相互作用。

Agents Actions. 1982 Oct;12(4):536-42. doi: 10.1007/BF01965940.

Lead elimination of ICRF 158 in rats after chronic lead exposure.慢性铅暴露后大鼠体内ICRF 158的铅清除情况。

Int Arch Occup Environ Health. 1981;48(1):89-98. doi: 10.1007/BF00405935.

Metal binding by pharmaceuticals. Part 5. Interaction of Cd(II), Ni(II) and Pb(II) with the intracellular hydrolysis products of the anti-tumour agent ICRF 159 and its inactive homologue ICRF 192.药物与金属的结合。第5部分。镉（II）、镍（II）和铅（II）与抗肿瘤药物ICRF 159及其无活性同系物ICRF 192的细胞内水解产物的相互作用。

Agents Actions. 1984 Oct;15(3-4):448-53. doi: 10.1007/BF01972386.

本文引用的文献

Edathamil calcium-disodium in cadmium poisoning; a study of the excretion, distribution, and toxicity of cadmium in animals.

AMA Arch Ind Health. 1956 Jan;13(1):18-23.

[Effects of CaEDTA and CaDTPA in cadmium poisoning].[依地酸钙钠和二乙烯三胺五乙酸钙在镉中毒中的作用]

Acta Biol Med Ger. 1966;17(2):178-85.

Studies on the stability and cellular distribution of dioxopiperazines in cultured BHK-21S cells.

Biochem Pharmacol. 1975 Dec 15;24(24):2249-53. doi: 10.1016/0006-2952(75)90262-2.

Commentary. New developments in metal antidotal properties of chelating agents.述评。螯合剂金属解毒特性的新进展。

Biochem Pharmacol. 1975 Sep 1;24(17):1557-62. doi: 10.1016/0006-2952(75)90078-7.

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