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Xenobiotica
the fate of foreign compounds in biological systems
Volume 15, 1985 - Issue 4
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Research Article

Further studies of trans-sobrerol metabolism: rat, dog and human urine

P. Ventura Analytical Chemistry Department, Camillo Corvi S.p.A., Stradone Farnese 118, 29100, Piacenza, Italy
,
M. Schiavi Analytical Chemistry Department, Camillo Corvi S.p.A., Stradone Farnese 118, 29100, Piacenza, Italy
,
S. Serafini Analytical Chemistry Department, Camillo Corvi S.p.A., Stradone Farnese 118, 29100, Piacenza, Italy
&
A. Selva C.N.R., Centro di Studio per le Sostanze Organiche Naturali, Dipartimento di Chimica del Politecnico, P. zza L. de Vinci 32, 20133, Milano, Italy
Pages 317-325 | Received 18 May 1984, Published online: 22 Sep 2008

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M. Schiavi, S. Serafini, A. Italia & P. Ventura. (1992) Metabolism of (-)-6(S)-hydroxy-4(R)-(1-hydroxy-1-methylethyl)-1-cyclohexene-1-ethanol in rat and dog. Xenobiotica 22:1, pages 41-49.
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A. Lippi, P. G. Gervasi, G. Bellucci, F. Marioni, F. Luzzani & P. Ventura. (1991) Effect of a terpenoid, (—)-6-Hydroxy-4-(1-hydroxy-1-methylethyl)-1-cyclohexene-1-ethanol, on drug-metabolizing enzymes and glutathione content in rat liver and lung. Xenobiotica 21:2, pages 141-145.
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A. Lippi, P. G. Gervasi, G. Bellucci, F. Marioni, F. Luzzani & P. Ventura. (1989) Effects of trans-sobrerol on drug metabolizing enzymes in the rat. Xenobiotica 19:8, pages 823-832.
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P. Ventura, R. Pellegata, M. Schiavi & S. Serafini. (1986) Biotransformation of trans-sobrerol. III. Metabolites of 8-hydroxycarvotanacetone in the rat. Xenobiotica 16:4, pages 317-323.
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Päivi Mäki‐Arvela, Irina L. Simakova, Tapio Salmi & Dmitry Yu. Murzin. 2013. Catalytic Process Development for Renewable Materials. Catalytic Process Development for Renewable Materials 309 339 .
. (2013) Scientific Opinion on Flavouring Group Evaluation 23, Revision 4 (FGE.23Rev4): Aliphatic, alicyclic and aromatic ethers including anisole derivatives from chemical groups 15, 16, 22, 26 and 30. EFSA Journal 11:2.
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. (2011) Scientific Opinion on Flavouring Group Evaluation 23, Revision 3 (FGE.23Rev3): Aliphatic, alicyclic and aromatic ethers including anisole derivatives from chemical groups 15, 16, 22, 26 and 30. EFSA Journal 9:10, pages 2398.
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. (2011) Scientific Opinion on Flavouring Group Evaluation 23, Revision 2 (FGE.23Rev2): Aliphatic, alicyclic and aromatic ethers including anisole derivatives from chemical groups 15, 16, 22, 26 and 30. EFSA Journal 9:2.
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. (2008) Flavouring Group Evaluation 23, Revision 1 (FGE.23Rev1): Aliphatic, alicyclic and aromatic ethers including anisole derivatives from chemical groups 15, 16, 26 and 30 ‐ Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food. EFSA Journal 6:10.
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. (2007) Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 23 (FGE.23): Aliphatic, alicyclic and aromatic ethers including anisole derivatives From chemical groups 15, 16 and 26 (Commission Regulation (EC) No 1565/2000 of 18 July 2000. EFSA Journal 5:5.
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Raymond A. Kemper, Diane L. Nabb, Shawn A. Gannon, Timothy A. Snow & Anne Marie Api. (2006) COMPARATIVE METABOLISM OF GERANYL NITRILE AND CITRONELLYL NITRILE IN MOUSE, RAT, AND HUMAN HEPATOCYTES. Drug Metabolism and Disposition 34:6, pages 1019-1029.
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Alison Li Lin, Nandita Shangari, Tom S. Chan, Diadelas Remirez & Peter J. O'Brien. (2006) Herbal monoterpene alcohols inhibit propofol metabolism and prolong anesthesia time. Life Sciences 79:1, pages 21-29.
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Wolfgang Engel. (2001) In Vivo Studies on the Metabolism of the Monoterpenes S -(+)- and R -(−)-Carvone in Humans Using the Metabolism of Ingestion-Correlated Amounts (MICA) Approach . Journal of Agricultural and Food Chemistry 49:8, pages 4069-4075.
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T.B. Adams, J.B. Hallagan, J.M. Putnam, T.L. Gierke, J. Doull, I.C. Munro, P. Newberne, P.S. Portoghese, R.L. Smith, B.M. Wagner, C.S. Weil, L.A. Woods & R.A. Ford. (1996) The FEMA GRAS assessment of alicyclic substances used as flavour ingredients. Food and Chemical Toxicology 34:9, pages 763-828.
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J. D. Connolly & R. A. HillJ. D. Connolly & R. A. Hill. 1991. Dictionary of Terpenoids. Dictionary of Terpenoids 7 152 .
J. Elks & C. R. Ganellin. 1990. Dictionary of Drugs. Dictionary of Drugs 617 672 .
K. Madhava Madyastha & V. Srivatsan. (1988) Biotransformations of α-terpineol in the rat: Its effects on the liver microsomal cytochrome P-450 system. Bulletin of Environmental Contamination and Toxicology 41:1, pages 17-25.
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Antonio Selva, Francesco Ferrario, Paolo Ventura & Renato Pellegata. (2005) Stereocontrolled regiospecificity of the water loss from trans ‐sobrerol radical cation upon electron ionization . Organic Mass Spectrometry 22:8, pages 523-529.
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Renato Pellegata, Ivana Dosi, Paolo Ventura, Maurizio Villa, Giordano Lesma & Giovanni Palmisano. (1987) Monoterpenoid chemistry. Part 3.. Stereoselective synthesis of the major oxygenated metabolites oftrans-sobrerol. Helvetica Chimica Acta 70:1, pages 71-78.
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A. L. Burlingame, Thomas A. Baillie & Peter J. Derrick. (2002) Mass spectrometry. Analytical Chemistry 58:5, pages 165-211.
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