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Differential mechanism of retention of Cu-pyruvaldehyde-bis(N4-methylthiosemicarbazone) (Cu-PTSM) by brain and tumor: a novel radiopharmaceutical for positron emission tomography imaging.

作者信息

Fujibayashi Y, Taniuchi H, Wada K, Yonekura Y, Konishi J, Yokoyama A

机构信息

Department of Radiopharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University, Japan.

出版信息

Ann Nucl Med. 1995 Feb;9(1):1-5. doi: 10.1007/BF03165001.

DOI:10.1007/BF03165001
PMID:7779524
Abstract

The reductive retention of 62Cu-PTSM was comparatively studied in the brain and Ehrlich ascites tumor cells by electron spin resonance spectrometry and nonradioactive Cu-PTSM. In the brain, only the mitochondrial fraction showed the ability to reduce Cu-PTSM, and the other subcellular fractions did not. In contrast, the cytosolic fraction of Ehrlich ascites tumor cells was the specific site of Cu-PTSM reduction. It was therefore considered that the retention of Cu-PTSM in the brain is closely related to mitochondrial reduction, most probably involving the mitochondrial electron transport system.

摘要

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THE ANTI-TUMOR ACTIVITY OF 2-KETO-3-ETHOXYBUTYRALDEHYDE BIS(THIOSEMICARBAZONE) AND RELATED COMPOUNDS.2-酮-3-乙氧基丁醛双(硫代半卡巴腙)及相关化合物的抗肿瘤活性
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Effect of heavy metals on the in vitro cytotoxicity of 3-ethoxy-2-oxobutyraldehyde bis (thiosemicarbazone) and related compounds.重金属对3-乙氧基-2-氧代丁醛双(硫代氨基脲)及相关化合物体外细胞毒性的影响。
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J Nucl Med. 1988 Sep;29(9):1549-57.
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