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Journal Abstract Search


302 related items for PubMed ID: 8886604

  • 1. Ropivacaine, a new amide-type local anesthetic agent, is metabolized by cytochromes P450 1A and 3A in human liver microsomes.
    Ekström G, Gunnarsson UB.
    Drug Metab Dispos; 1996 Sep; 24(9):955-61. PubMed ID: 8886604
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  • 2. Tolterodine, a new muscarinic receptor antagonist, is metabolized by cytochromes P450 2D6 and 3A in human liver microsomes.
    Postlind H, DanielsonA, Lindgren A, Andersson SH.
    Drug Metab Dispos; 1998 Apr; 26(4):289-93. PubMed ID: 9531513
    [Abstract] [Full Text] [Related]

  • 3. Stereoselective metabolism of cibenzoline, an antiarrhythmic drug, by human and rat liver microsomes: possible involvement of CYP2D and CYP3A.
    Niwa T, Shiraga T, Mitani Y, Terakawa M, Tokuma Y, Kagayama A.
    Drug Metab Dispos; 2000 Sep; 28(9):1128-34. PubMed ID: 10950860
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  • 4. Metabolism of a new local anesthetic, ropivacaine, by human hepatic cytochrome P450.
    Oda Y, Furuichi K, Tanaka K, Hiroi T, Imaoka S, Asada A, Fujimori M, Funae Y.
    Anesthesiology; 1995 Jan; 82(1):214-20. PubMed ID: 7832304
    [Abstract] [Full Text] [Related]

  • 5. Human cytochrome P450 3A (CYP3A) mediated midazolam metabolism: the effect of assay conditions and regioselective stimulation by alpha-naphthoflavone, terfenadine and testosterone.
    Mäenpää J, Hall SD, Ring BJ, Strom SC, Wrighton SA.
    Pharmacogenetics; 1998 Apr; 8(2):137-55. PubMed ID: 10022752
    [Abstract] [Full Text] [Related]

  • 6. Metabolism of phencyclidine by human liver microsomes.
    Laurenzana EM, Owens SM.
    Drug Metab Dispos; 1997 May; 25(5):557-63. PubMed ID: 9152594
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  • 8. Identification and characterization of the cytochrome P450 enzymes involved in N-dealkylation of propafenone: molecular base for interaction potential and variable disposition of active metabolites.
    Botsch S, Gautier JC, Beaune P, Eichelbaum M, Kroemer HK.
    Mol Pharmacol; 1993 Jan; 43(1):120-6. PubMed ID: 8423765
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  • 11. Oxidative metabolism of bupivacaine into pipecolylxylidine in humans is mainly catalyzed by CYP3A.
    Gantenbein M, Attolini L, Bruguerolle B, Villard PH, Puyoou F, Durand A, Lacarelle B, Hardwigsen J, Le-Treut YP.
    Drug Metab Dispos; 2000 Apr; 28(4):383-5. PubMed ID: 10725304
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  • 14. Identification of the human liver cytochrome P450 isoenzyme responsible for the 6-methylhydroxylation of the novel anticancer drug 5,6-dimethylxanthenone-4-acetic acid.
    Zhou S, Paxton JW, Tingle MD, Kestell P.
    Drug Metab Dispos; 2000 Dec; 28(12):1449-56. PubMed ID: 11095582
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  • 15. Metabolism and excretion of ropivacaine in humans.
    Halldin MM, Bredberg E, Angelin B, Arvidsson T, Askemark Y, Elofsson S, Widman M.
    Drug Metab Dispos; 1996 Sep; 24(9):962-8. PubMed ID: 8886605
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  • 17. Metabolism of DHEA by cytochromes P450 in rat and human liver microsomal fractions.
    Fitzpatrick JL, Ripp SL, Smith NB, Pierce WM, Prough RA.
    Arch Biochem Biophys; 2001 May 15; 389(2):278-87. PubMed ID: 11339818
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  • 18. Overlapping substrate specificities of cytochrome P450 3A and P-glycoprotein for a novel cysteine protease inhibitor.
    Zhang Y, Guo X, Lin ET, Benet LZ.
    Drug Metab Dispos; 1998 Apr 15; 26(4):360-6. PubMed ID: 9531525
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  • 19. Metabolism of alfentanil by cytochrome p4503a (cyp3a) enzymes.
    Klees TM, Sheffels P, Dale O, Kharasch ED.
    Drug Metab Dispos; 2005 Mar 15; 33(3):303-11. PubMed ID: 15557344
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