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使用鼠伤寒沙门氏菌TA1535/pSK1002 Umu试验,研究具有对薄荷烷骨架的单萜类化合物对糠基糠酰胺诱导的SOS反应的抑制作用。

Suppression of the furylfuramide-induced SOS response by monoterpenoids with a p-menthane skeleton using the Salmonella typhimurium TA1535/pSK1002 Umu test.

作者信息

Miyazawa M, Okuno Y, Nakamura S i, Kosaka H

机构信息

Department of Applied Chemistry, Faculty of Science and Engineering, Kinki University, Kowakae, Higashiosaka-shi, Osaka 577-8502, Japan.

出版信息

J Agric Food Chem. 2000 Nov;48(11):5440-3. doi: 10.1021/jf0002544.

Abstract

Suppression of the furylfuramide-induced SOS response by 25 kinds monoterpenoids (hydrocarbons, alcohols, ketones, and aldehydes) with a p-menthane skeleton was studied. Suppression of the SOS-inducing activity by monoterpenoids was determined in the umu test using Salmonella typhimurium TA1535/pSK1002. The terpene alcohols, ketones, and aldehydes had potent suppressive effects, but the hydrocarbons did not. Especially, (+)-menthol, (+)-pulegone, piperitenone, and cuminaldehyde were shown to have the most potent suppressive effects, and the ID(50) (dose for 50% inhibition) was 0.52 micromol/mL.

摘要

研究了25种具有对薄荷烷骨架的单萜类化合物(烃类、醇类、酮类和醛类)对糠基糠酰胺诱导的SOS反应的抑制作用。使用鼠伤寒沙门氏菌TA1535/pSK1002在umu试验中测定单萜类化合物对SOS诱导活性的抑制作用。萜烯醇类、酮类和醛类具有较强的抑制作用,而烃类则没有。特别是,(+)-薄荷醇、(+)-胡薄荷酮、胡椒酮和枯茗醛显示出最强的抑制作用,半数抑制剂量(ID50)为0.52微摩尔/毫升。

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