Xenobiotica 1988-10-01

Biotransformation of 1,4-cineole, a monoterpene ether.

Y Asakawa, M Toyota, T Ishida

Index: Xenobiotica 18(10) , 1129-34, (1988)

Full Text: HTML

Abstract

1. The metabolism of 1,4-cineole, a monoterpene ether, was studied in the rabbit. 2. Four neutral and one acidic metabolites were isolated from the urine and shown to be 9-hydroxy-1,4-cineole, 3,8-dihydroxy-1,4-cineole, 8,9-dihydroxy-1,4-cineole, 1,4-cineole-8-en-9-ol and 1,4-cineole-9-carboxylic acid.


Related Compounds

Related Articles:

Inhibition by menthol and its related chemicals of compound action potentials in frog sciatic nerves.

2013-03-14

[Life Sci. 92(6-7) , 359-67, (2013)]

1,8-cineole, a TRPM8 agonist, is a novel natural antagonist of human TRPA1.

2012-01-01

[Mol. Pain 8 , 86, (2012)]

[Analysis of the chemical constituents of essential oil from Chimonanthus zhejiangensis by GC-MS].

2010-03-01

[Zhong Yao Cai 33(3) , 385-7, (2010)]

[GC-MS analysis of constituents of essential oils from stems of Ephedra sinica Stapf, E. intermedia Schrenk et C.A. Mey. and E. equisetina Bge].

1997-08-01

[Zhongguo Zhong Yao Za Zhi 22(8) , 489-92, 512, (1997)]

A soluble Bacillus cereus cytochrome P-450cin system catalyzes 1,4-cineole hydroxylations.

1993-11-01

[Appl. Environ. Microbiol. 59(11) , 3889-93, (1993)]

More Articles...