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Xenobiotica
the fate of foreign compounds in biological systems
Volume 24, 1994 - Issue 2
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Original Article

Fate of dipropyl sulphide and dipropyl sulphoxide in rat

R. M. Nickson Department of Pharmacology and Toxicology, St Mary's Hospital Medical School, Imperial College of Science, Technology and Medicine, London, W2 1PG, UK
&
S. C. Mitchell Department of Pharmacology and Toxicology, St Mary's Hospital Medical School, Imperial College of Science, Technology and Medicine, London, W2 1PG, UK
Pages 157-168 | Received 01 Nov 1993, Published online: 27 Aug 2009

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Evita Vandenbossche, Christopher Lucas, Lata Mistry, Emma Garfield, Stephen C. Mitchell & Glyn B. Steventon. (2016) Phenylalanine monooxygenase and the sulfur oxygenation of S-carboxymethyl-l-cysteine in mice. Xenobiotica 46:4, pages 379-384.
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E. Germain, E. Semon, M.-H. Siess & C. Teyssier. (2008) Disposition and metabolism of dipropyl disulphide in vivo in rat. Xenobiotica 38:1, pages 87-97.
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Hang Xiao & Kirk L. Parkin. (2006) Induction of Phase II Enzyme Activity by Various Selenium Compounds. Nutrition and Cancer 55:2, pages 210-223.
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R. M. Nickson, S. C. Mitchell & A. Q. Zhang. (1995) Fate of dipropyl sulphone in rat. Xenobiotica 25:12, pages 1391-1398.
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Articles from other publishers (22)

Daniela Nedelcheva, Stoyanka Stoeva, Sabcho Dimitrov, Ann Detroyer, Aziz Fadli, Reine Note, Delphine Blanchet & Ovanes Mekenyan. (2019) In silico mechanistically-based profiling module for acute oral toxicity. Computational Toxicology 12, pages 100109.
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. (2012) Scientific Opinion on Flavouring Group Evaluation 08, Revision 5 (FGE.08Rev5): Aliphatic and alicyclic mono‐, di‐, tri‐, and polysulphides with or without additional oxygenated functional groups from chemical groups 20 and 30. EFSA Journal 10:7.
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. (2012) Scientific Opinion on Flavouring Group Evaluation 08, Revision 4 (FGE.08Rev4): Aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups from chemical groups 20 and 30. EFSA Journal 10:2, pages 2455.
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. (2011) Scientific Opinion on Flavouring Group Evaluation 17, Revision 3 (FGE.17Rev3): Pyrazine derivatives from chemical group 24. EFSA Journal 9:11.
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. (2011) Scientific Opinion on Flavouring Group Evaluation 13, Revision 2 (FGE.13Rev2): Furfuryl and furan derivatives with and without additional side-chain substituents and heteroatoms from chemical group 14. EFSA Journal 9:8, pages 2313.
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. (2011) Scientific Opinion on Flavouring Group Evaluation 8, Revision 3 (FGE.08Rev3): Aliphatic and alicyclic mono‐, di‐, tri‐, and polysulphides with or without additional oxygenated functional groups from chemical groups 20 and 30. EFSA Journal 9:5.
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. (2011) Scientific Opinion on Flavouring Group Evaluation 17, Revision 2 (FGE.17Rev2): Pyrazine derivatives from chemical group 24. EFSA Journal 9:5.
Crossref
Chia-Wen Tsai, Kai-Li Liu, Chia-Yuan Lin, Haw-Wen Chen & Chong-Kuei Lii. (2011) Structure and Function Relationship Study of Allium Organosulfur Compounds on Upregulating the Pi Class of Glutathione S -Transferase Expression . Journal of Agricultural and Food Chemistry 59:7, pages 3398-3405.
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. (2010) Flavouring Group Evaluation 08 Rev2 (FGE.08 Rev2): Aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups from chemical groups 20 and 30. EFSA Journal 8:11, pages 1408.
Crossref
. (2010) Flavouring Group Evaluation 8, Revision 1 (FGE.08Rev1): Aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups from chemical groups 20 and 30. EFSA Journal 8:7, pages 1021.
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. (2010) Scientific Opinion on Flavouring Group Evaluation 13Rev1: Furfuryl and furan derivatives with and without additional side‐chain substituents and heteroatoms from chemical group 14. EFSA Journal 8:4.
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. (2009) Application (Reference EFSA‐GMO‐NL‐2008‐51) for the placing on the market of glyphosate tolerant genetically modified cotton GHB614, for food and feed uses, import and processing under Regulation (EC) No 1829/2003 from Bayer CropScience. EFSA Journal 7:3.
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. (2008) Flavouring Group Evaluation 17, Revision 1 (FGE.17Rev1): Pyrazine derivatives from chemical group 24 - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC). EFSA Journal 6:9, pages 812.
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. (2006) Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) on a request from the Commission related to Flavouring Group Evaluation 17 (FGE.17): Pyrazine derivatives from chemical group 24 (Comm. EFSA Journal 4:1, pages 295.
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. (2005) Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 13 (FGE.13); Furfuryl and furan derivatives with and without additional side-chain substituents. EFSA Journal 3:7, pages 215.
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Peter Rose, Matt Whiteman, Philip K. Moore & Yi Zhun Zhu. (2005) Bioactive S-alk(en)yl cysteine sulfoxide metabolites in the genus Allium: the chemistry of potential therapeutic agents. Natural Product Reports 22:3, pages 351.
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T.B Adams, J Doull, V.J Feron, J.I Goodman, L.J Marnett, I.C Munro, P.M Newberne, P.S Portoghese, R.L Smith, W.J Waddell & B.M Wagner. (2002) The FEMA GRAS assessment of pyrazine derivatives used as flavor ingredients. Food and Chemical Toxicology 40:4, pages 429-451.
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Brian M. Fox, Jeffrey A. Vroman, Phillip E. Fanwick & Mark Cushman. (2001) Preparation and Evaluation of Sulfide Derivatives of the Antibiotic Brefeldin A as Potential Prodrug Candidates with Enhanced Aqueous Solubilities. Journal of Medicinal Chemistry 44:23, pages 3915-3924.
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Ankush B. ArgadeRajesh DevrajJeffrey A. VromanRudiger D. HaugwitzMelinda HollingsheadMark Cushman. (1998) Design and Synthesis of Brefeldin A Sulfide Derivatives as Prodrug Candidates with Enhanced Aqueous Solubilities. Journal of Medicinal Chemistry 41:18, pages 3337-3346.
Crossref
Marie-Hélène Siess, Anne-Marie Le Bon, Marie-Chantal Canivenc-Lavier & Marc Suschetet. (1997) Modification of hepatic drug-metabolizing enzymes in rats treated with alkyl sulfides. Cancer Letters 120:2, pages 195-201.
Crossref
R.M. Nickson & S.C. Mitchell. (1996) Role of Bile in the Elimination of Dipropyl Sulphone from the Male Rat. Drug Metabolism and Drug Interactions 13:2.
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R.M. Nickson & S.C. Mitchell. (1995) Distribution of Dipropyl [35S]-Sulphoxide in the Rat. Drug Metabolism and Drug Interactions 12:1.
Crossref

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