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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)].

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

相似文献

1
[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)
Int Arch Occup Environ Health. 1979 Jan 15;42(3-4):365-73. doi: 10.1007/BF00377792.
2
[Significance of cadmium excretion in the urine by a long-term cadmium administration to rats. I. Changes in the urinary cadmium level (author's transl)].长期给大鼠施用镉后尿镉排泄的意义。I. 尿镉水平的变化(作者译)
Sangyo Igaku. 1977 Jul;19(4):198-9.
3
Inhibition of cardiotoxic, nephrotoxic and neurotoxic effects of doxorubicin by ICRF-159.ICRF - 159对阿霉素心脏毒性、肾毒性和神经毒性作用的抑制
Pharmacology. 1983;26(4):210-20. doi: 10.1159/000137804.
4
[Significance of cadmium excretion in the urine by a long-term cadmium administration to rats. II. Changes of cadmium distribution in the urine (author's transl)].长期给大鼠施用镉后尿镉排泄的意义。II. 尿中镉分布的变化(作者译)
Sangyo Igaku. 1977 Jul;19(4):200-1.
5
Role of (+-)-1,2-bis(3,5-dioxopiperazinyl-1-yl)propane (ICRF-187) in modulating free radical scavenging enzymes in doxorubicin-induced cardiomyopathy.(±)-1,2-双(3,5-二氧代哌嗪基-1-基)丙烷(ICRF-187)在调节阿霉素诱导的心肌病中自由基清除酶的作用
Cancer Res. 1990 Aug 15;50(16):5136-42.
6
Effects of ICRF 159 on adriamycin-induced cardiomyopathy in rats.ICRF 159对阿霉素诱导的大鼠心肌病的影响。
Cancer Lett. 1983 May;19(1):77-83. doi: 10.1016/0304-3835(83)90139-8.
7
Effect of razoxane (ICRF 159) on daunomycin (NSC 82151) metabolism and DNA complexation.丙亚胺(ICRF 159)对柔红霉素(NSC 82151)代谢及DNA络合的影响。
Drug Chem Toxicol. 1980;3(2):213-25. doi: 10.3109/01480548009108284.
8
Influence of ICRF-159 or ICRF-186 on cytotoxicity of daunorubicin and doxorubicin.ICRF - 159或ICRF - 186对柔红霉素和阿霉素细胞毒性的影响。
Tumori. 1984 Apr 30;70(2):121-6. doi: 10.1177/030089168407000202.
9
[Pharmacological studies on bimolane (AT-1727), a new antineoplastic agent (author's transl)].新型抗肿瘤药丙亚胺(AT-1727)的药理研究(作者译)
Yao Xue Xue Bao. 1980 Oct;15(10):577-83.
10
Biological properties of ICRF-159 and related bis(dioxopiperazine) compounds.ICRF-159及相关双(二氧代哌嗪)化合物的生物学特性。
Adv Pharmacol Chemother. 1982;19:249-90. doi: 10.1016/s1054-3589(08)60025-3.

引用本文的文献

1
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.
2
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.
3

本文引用的文献

1
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.
2
[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.
3
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.
4
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.
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.