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413 related items for PubMed ID: 8839062
1. Identification in rat bile of glutathione conjugates of fluoromethyl 2,2-difluoro-1-(trifluoromethyl)vinyl ether, a nephrotoxic degradate of the anesthetic agent sevoflurane. Jin L, Davis MR, Kharasch ED, Doss GA, Baillie TA. Chem Res Toxicol; 1996 Mar; 9(2):555-61. PubMed ID: 8839062 [Abstract] [Full Text] [Related]
2. Glutathione S-conjugation of the sevoflurane degradation product, fluoromethyl-2,2-difluoro-1-(trifluoromethyl)vinyl ether (compound A) in human liver, kidney, and blood in vitro. Altuntas TG, Kharasch ED. Toxicol Appl Pharmacol; 2001 Dec 01; 177(2):85-93. PubMed ID: 11740907 [Abstract] [Full Text] [Related]
3. Role of cytochrome P4503A in cysteine S-conjugates sulfoxidation and the nephrotoxicity of the sevoflurane degradation product fluoromethyl-2,2-difluoro-1-(trifluoromethyl)vinyl ether (compound A) in rats. Sheffels P, Schroeder JL, Altuntas TG, Liggitt HD, Kharasch ED. Chem Res Toxicol; 2004 Sep 01; 17(9):1177-89. PubMed ID: 15377151 [Abstract] [Full Text] [Related]
4. Dose-dependent metabolism of fluoromethyl-2,2-difluoro-1-(trifluoromethyl)vinyl ether (compound A), an anesthetic degradation product, to mercapturic acids and 3,3,3-trifluoro-2-(fluoromethoxy)propanoic acid in rats. Kharasch ED, Jubert C, Spracklin DK, Hoffman GM. Toxicol Appl Pharmacol; 1999 Oct 01; 160(1):49-59. PubMed ID: 10502502 [Abstract] [Full Text] [Related]
5. Evidence for metabolism of fluoromethyl 2,2-difluoro-1-(trifluoromethyl)vinyl ether (compound A), a sevoflurane degradation product, by cysteine conjugate beta-lyase. Spracklin DK, Kharasch ED. Chem Res Toxicol; 1996 Jun 01; 9(4):696-702. PubMed ID: 8831812 [Abstract] [Full Text] [Related]
6. Sulfoxidation of cysteine and mercapturic acid conjugates of the sevoflurane degradation product fluoromethyl-2,2-difluoro-1-(trifluoromethyl)vinyl ether (compound A). Altuntas TG, Park SB, Kharasch ED. Chem Res Toxicol; 2004 Mar 01; 17(3):435-45. PubMed ID: 15025515 [Abstract] [Full Text] [Related]
7. Nephrotoxicity of the glutathione and cysteine S-conjugates of the sevoflurane degradation product 2-(fluoromethoxy)-1,1,3,3, 3-pentafluoro-1-propene (Compound A) in male Fischer 344 rats. Iyer RA, Baggs RB, Anders MW. J Pharmacol Exp Ther; 1997 Dec 01; 283(3):1544-51. PubMed ID: 9400032 [Abstract] [Full Text] [Related]
8. Cytotoxicity of S-conjugates of the sevoflurane degradation product fluoromethyl-2,2-difluoro-1-(trifluoromethyl) vinyl ether (Compound A) in a human proximal tubular cell line. Altuntas TG, Zager RA, Kharasch ED. Toxicol Appl Pharmacol; 2003 Nov 15; 193(1):55-65. PubMed ID: 14613716 [Abstract] [Full Text] [Related]
9. Nephrotoxicity of sevoflurane compound A [fluoromethyl-2,2-difluoro-1-(trifluoromethyl)vinyl ether] in rats: evidence for glutathione and cysteine conjugate formation and the role of renal cysteine conjugate beta-lyase. Jin L, Baillie TA, Davis MR, Kharasch ED. Biochem Biophys Res Commun; 1995 May 16; 210(2):498-506. PubMed ID: 7755627 [Abstract] [Full Text] [Related]
10. Cysteine conjugate beta-lyase-dependent biotransformation of the cysteine S-conjugates of the sevoflurane degradation product 2-(fluoromethoxy)-1,1,3,3,3-pentafluoro-1-propene (compound A). Iyer RA, Anders MW. Chem Res Toxicol; 1997 Jul 16; 10(7):811-9. PubMed ID: 9250416 [Abstract] [Full Text] [Related]
11. Biotransformation of L-cysteine S-conjugates and N-acetyl-L-cysteine S-conjugates of the sevoflurane degradation product fluoromethyl-2,2-difluoro-1-(trifluoromethyl)vinyl ether (compound A) in human kidney in vitro: interindividual variability in N-acetylation, N-deacetylation, and beta-lyase-catalyzed metabolism. Gul Altuntas T, Kharasch ED. Drug Metab Dispos; 2002 Feb 16; 30(2):148-54. PubMed ID: 11792683 [Abstract] [Full Text] [Related]
12. Conjugation of glutathione with a toxic metabolite of valproic acid, (E)-2-propyl-2,4-pentadienoic acid, catalyzed by rat hepatic glutathione-S-transferases. Tang W, Borel AG, Abbott FS. Drug Metab Dispos; 1996 Apr 16; 24(4):436-46. PubMed ID: 8801059 [Abstract] [Full Text] [Related]
13. P450-dependent and nonenzymatic human liver microsomal defluorination of fluoromethyl-2,2-difluoro-1-(trifluoromethyl)vinyl ether (compound A), a sevoflurane degradation product. Kharasch ED, Hankins DC. Drug Metab Dispos; 1996 Jun 16; 24(6):649-54. PubMed ID: 8781780 [Abstract] [Full Text] [Related]
14. Metabolism of the chemoprotective agent diallyl sulfide to glutathione conjugates in rats. Jin L, Baillie TA. Chem Res Toxicol; 1997 Mar 16; 10(3):318-27. PubMed ID: 9084912 [Abstract] [Full Text] [Related]
15. Formation and biliary excretion of glutathione conjugates of bile acids in the rat as shown by liquid chromatography/electrospray ionization-linear ion trap mass spectrometry. Mitamura K, Watanabe S, Mitsumoto Y, Sakai T, Sogabe M, Wakamiya T, Ikegawa S. Anal Biochem; 2009 Jan 15; 384(2):224-30. PubMed ID: 18938128 [Abstract] [Full Text] [Related]
16. Gene expression profiling of nephrotoxicity from the sevoflurane degradation product fluoromethyl-2,2-difluoro-1-(trifluoromethyl)vinyl ether ("compound A") in rats. Kharasch ED, Schroeder JL, Bammler T, Beyer R, Srinouanprachanh S. Toxicol Sci; 2006 Apr 15; 90(2):419-31. PubMed ID: 16384817 [Abstract] [Full Text] [Related]
17. Identification of bile acid S-acyl glutathione conjugates in rat bile by liquid chromatography/electrospray ionization-linear ion trap mass spectrometry. Mitamura K, Hori N, Iida T, Hofmann AF, Ikegawa S. Steroids; 2011 Jan 15; 76(1-2):68-77. PubMed ID: 20837038 [Abstract] [Full Text] [Related]
18. Determination of enzyme kinetics and glutathione conjugates of chlortetracycline and chloroacetanilides using liquid chromatography-mass spectrometry. Farkas M, Berry JO, Aga DS. Analyst; 2007 Jul 15; 132(7):664-71. PubMed ID: 17592585 [Abstract] [Full Text] [Related]
19. Bioactivation of a toxic metabolite of valproic acid, (E)-2-propyl-2,4-pentadienoic acid, via glucuronidation. LC/MS/MS characterization of the GSH-glucuronide diconjugates. Tang W, Abbott FS. Chem Res Toxicol; 1996 Mar 15; 9(2):517-26. PubMed ID: 8839057 [Abstract] [Full Text] [Related]
20. Glutathione S-transferase conjugation of organophosphorus pesticides yields S-phospho-, S-aryl-, and S-alkylglutathione derivatives. Fujioka K, Casida JE. Chem Res Toxicol; 2007 Aug 15; 20(8):1211-7. PubMed ID: 17645302 [Abstract] [Full Text] [Related] Page: [Next] [New Search]