Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractSexual pheromone induces diffusion of the pheromone-homologous polypeptide in the extracellular matrix of Volvox carteri    Next AbstractVoltage-gated channel properties of epithelial cells in porcine vomeronasal organ »

J Pharm Sci


Title:"Terpenoids biotransformation in mammals III: Biotransformation of alpha-pinene, beta-pinene, pinane, 3-carene, carane, myrcene, and p-cymene in rabbits"
Author(s):Ishida T; Asakawa Y; Takemoto T; Aratani T;
Address:
Journal Title:J Pharm Sci
Year:1981
Volume:70
Issue:4
Page Number:406 - 415
DOI: 10.1002/jps.2600700417
ISSN/ISBN:0022-3549 (Print) 0022-3549 (Linking)
Abstract:"The biotransformation of (+)-, (-)-, and (+-)-alpha-pinenes, (-)-beta-pinene (nopinene), (-)-cis-pinane, (+)-3-carene, (-)-cis-carane, myrcene, and p-cymene in rabbits was investigated. The major metabolites were as follows: (-)-trans-verbenol from (+)-, (-)-, and (+/-)-alpha-pinenes; (-)-10-pinanol and (-)-1-p-menthene-7,8-diol from (-)-beta-pinene; (-)-alpha-terpineol and (-)-trans-sobrerol from (-)-cis-pinane; (-)-m-mentha-4,6-dien-8-ol, 3-caren-9-ol, (-)-3-carene-9-carboxylic acid, and 3-carene-9,10-dicarboxylic acid from (+)-3-carene; carane-9,10-dicarboxylic acid from (-)-cis-carane; and myrcene-3(10)-glycol, myrcene-1,2-glycol, uroterpenol, and p-cymene-9-carboxylic acid from p-cymene. These metabolisms include allylic oxidation, epoxidation, stereoselective gem-dimethyl hydroxylation and its oxidation, cleavage of a conjugated double bond by epoxidation, and regioselective oxidation, some of which are not found usually in chemical reactions, and due to which various new compounds were determined. This biotransformation of the monoterpene hydrocarbons gave some insect pheromones in high yield.U"
Keywords:Acyclic Monoterpenes Animals Bicyclic Monoterpenes Biotransformation Bridged Bicyclo Compounds/metabolism Cymenes Male *Monoterpenes Rabbits Terpenes/*metabolism;
Notes:"MedlineIshida, T Asakawa, Y Takemoto, T Aratani, T eng 1981/04/01 J Pharm Sci. 1981 Apr; 70(4):406-15. doi: 10.1002/jps.2600700417"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 21-09-2024