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370 related items for PubMed ID: 9250416
1. 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; 10(7):811-9. PubMed ID: 9250416 [Abstract] [Full Text] [Related]
2. 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; 283(3):1544-51. PubMed ID: 9400032 [Abstract] [Full Text] [Related]
3. 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; 9(4):696-702. PubMed ID: 8831812 [Abstract] [Full Text] [Related]
4. Cysteine conjugate beta-lyase-dependent metabolism of compound A (2-[fluoromethoxy]-1,1,3,3,3-pentafluoro-1-propene) in human subjects anesthetized with sevoflurane and in rats given compound A. Iyer RA, Frink EJ, Ebert TJ, Anders MW. Anesthesiology; 1998 Mar; 88(3):611-8. PubMed ID: 9523802 [Abstract] [Full Text] [Related]
5. 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]
6. Cysteine conjugate beta-lyase-catalyzed bioactivation of bromine-containing cysteine S-conjugates: stoichiometry and formation of 2,2-difluoro-3-halothiiranes. Finkelstein MB, Dekant W, Anders MW. Chem Res Toxicol; 1996 Oct 01; 9(1):227-31. PubMed ID: 8924595 [Abstract] [Full Text] [Related]
7. Cysteine conjugate beta-lyase-dependent biotransformation of the cysteine S-conjugates of the sevoflurane degradation product compound A in human, nonhuman primate, and rat kidney cytosol and mitochondria. Iyer RA, Anders MW. Anesthesiology; 1996 Dec 01; 85(6):1454-61. PubMed ID: 8968194 [Abstract] [Full Text] [Related]
8. Reactive intermediate formation from the 2-(Fluoromethoxy)-1,1,3,3,3-pentafluoro-1-propene (compound A)-derived cysteine S-conjugate S-[2-(Fluoromethoxy)-1,1,3,3,3-pentafluoropropyl]-L-cysteine in pyridoxal model systems. Tong Z, Anders MW. Chem Res Toxicol; 2002 May 01; 15(5):623-8. PubMed ID: 12018982 [Abstract] [Full Text] [Related]
10. 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]
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 01; 30(2):148-54. PubMed ID: 11792683 [Abstract] [Full Text] [Related]
12. Fate and toxicity of 2-(fluoromethoxy)-1,1,3,3,3-pentafluoro-1-propene (compound A)-derived mercapturates in male, Fischer 344 rats. Uttamsingh V, Iyer RA, Baggs RB, Anders MW. Anesthesiology; 1998 Nov 01; 89(5):1174-83. PubMed ID: 9822006 [Abstract] [Full Text] [Related]
13. 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 01; 9(2):555-61. PubMed ID: 8839062 [Abstract] [Full Text] [Related]
14. Bioactivation of the cysteine-S-conjugate and mercapturic acid of tetrafluoroethylene to acylating reactive intermediates in the rat: dependence of activation and deactivation activities on acetyl coenzyme A availability. Commandeur JN, De Kanter FJ, Vermeulen NP. Mol Pharmacol; 1989 Oct 01; 36(4):654-63. PubMed ID: 2811861 [Abstract] [Full Text] [Related]
15. 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]
16. Role of renal cysteine conjugate beta-lyase in the mechanism of compound A nephrotoxicity in rats. Kharasch ED, Thorning D, Garton K, Hankins DC, Kilty CG. Anesthesiology; 1997 Jan 01; 86(1):160-71. PubMed ID: 9009951 [Abstract] [Full Text] [Related]
17. 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]