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Structure-activity relationships for the direct toxic action of trichothecenes on rat brain.

作者信息

Bergmann F, Yagen B

机构信息

Department of Pharmacology, Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

Arch Toxicol. 1989;63(2):155-6. doi: 10.1007/BF00316439.

DOI:10.1007/BF00316439
PMID:2730341
Abstract

Three classes of 12,13-epoxytrichothecenes, differing in the number of hydroxy or acetoxy substituents, were implanted or injected into rat brain to establish structure-toxicity relationships. A free 3 alpha-hydroxy group increases toxicity more than 10-fold, when compared to trichothecenes lacking this substituent. The 8 alpha-hydroxy group enhances toxicity about 4-fold.

摘要

相似文献

1
Structure-activity relationships for the direct toxic action of trichothecenes on rat brain.
Arch Toxicol. 1989;63(2):155-6. doi: 10.1007/BF00316439.
2
Comparison of the toxicity of two trichothecenes applied topically to brain and liver of rats.
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3
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The toxicity of macrocyclic trichothecenes administered directly into the rat brain.直接注入大鼠脑内的大环单端孢霉烯族毒素的毒性。
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Chemical interconversion of T-2 and HT-2 toxins and related compounds.T-2毒素和HT-2毒素及相关化合物的化学相互转化
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Cerebral toxicity of the trichothecene toxin T-2, of the products of its hydrolysis and of some related toxins.单端孢霉烯族毒素T-2、其水解产物及某些相关毒素的脑毒性。
Toxicon. 1988;26(10):923-30. doi: 10.1016/0041-0101(88)90257-7.
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Metabolism of trichothecene mycotoxins. II. Substrate specificity of microsomal deacetylation of trichothecenes.单端孢霉烯族霉菌毒素的代谢。II. 单端孢霉烯族霉菌毒素微粒体脱乙酰作用的底物特异性。
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