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双呋喃类霉菌毒素的生物活性中间体。

Biological reactive intermediates of bisfuranoid mycotoxins.

作者信息

Hsieh D P

机构信息

Department of Environmental Toxicology, University of California, Davis 95616.

出版信息

J Toxicol Sci. 1990 Dec;15 Suppl 4:152-8. doi: 10.2131/jts.15.supplementiv_152.

Abstract

Based on the mode of action of AFB1 and the activities of its biologically active intermediates, one may conclude that: 1. The mode of toxic action of the bisfuranoid mycotoxin is through epoxidation of the vinyl ether double bond of their dihydrobisfuran functionality. 2. The DNA and plasma albumin adducts formed in vivo may be useful in the molecular dosimetry of these environmental carcinogens. 3. Monitoring of these adducts of AFB1 in biological samples so far indicates that aflatoxin is likely involved in the etiology of human liver cancer.

摘要

基于黄曲霉毒素B1(AFB1)的作用模式及其生物活性中间体的活性,可以得出以下结论:1. 双呋喃类霉菌毒素的毒性作用模式是通过其二氢双呋喃官能团的乙烯基醚双键环氧化。2. 体内形成的DNA和血浆白蛋白加合物可能有助于这些环境致癌物的分子剂量测定。3. 迄今为止,对生物样品中AFB1这些加合物的监测表明,黄曲霉毒素可能与人类肝癌的病因有关。

相似文献

1
Biological reactive intermediates of bisfuranoid mycotoxins.双呋喃类霉菌毒素的生物活性中间体。
J Toxicol Sci. 1990 Dec;15 Suppl 4:152-8. doi: 10.2131/jts.15.supplementiv_152.
7
Biological reactive intermediates of mycotoxins.霉菌毒素的生物反应中间体。
Adv Exp Med Biol. 1986;197:597-610. doi: 10.1007/978-1-4684-5134-4_56.

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