BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 9660853)

  • 1. (R)-(+)-Menthofuran is a potent, mechanism-based inactivator of human liver cytochrome P450 2A6.
    Khojasteh-Bakht SC; Koenigs LL; Peter RM; Trager WF; Nelson SD
    Drug Metab Dispos; 1998 Jul; 26(7):701-4. PubMed ID: 9660853
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mechanism-based inactivation of human liver cytochrome P450 2A6 by 8-methoxypsoralen.
    Koenigs LL; Peter RM; Thompson SJ; Rettie AE; Trager WF
    Drug Metab Dispos; 1997 Dec; 25(12):1407-15. PubMed ID: 9394031
    [TBL] [Abstract][Full Text] [Related]  

  • 3. In vitro inhibition of cytochrome P450 enzymes in human liver microsomes by a potent CYP2A6 inhibitor, trans-2-phenylcyclopropylamine (tranylcypromine), and its nonamine analog, cyclopropylbenzene.
    Taavitsainen P; Juvonen R; Pelkonen O
    Drug Metab Dispos; 2001 Mar; 29(3):217-22. PubMed ID: 11181487
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inhibition and inactivation of cytochrome P450 2A6 and cytochrome P450 2A13 by menthofuran, β-nicotyrine and menthol.
    Kramlinger VM; von Weymarn LB; Murphy SE
    Chem Biol Interact; 2012 May; 197(2-3):87-92. PubMed ID: 22486895
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Metabolism of (R)-(+)-pulegone and (R)-(+)-menthofuran by human liver cytochrome P-450s: evidence for formation of a furan epoxide.
    Khojasteh-Bakht SC; Chen W; Koenigs LL; Peter RM; Nelson SD
    Drug Metab Dispos; 1999 May; 27(5):574-80. PubMed ID: 10220485
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inhibition of coumarin 7-hydroxylase activity in human liver microsomes.
    Draper AJ; Madan A; Parkinson A
    Arch Biochem Biophys; 1997 May; 341(1):47-61. PubMed ID: 9143352
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inhibition of human cytochrome P450 enzymes by the natural hepatotoxin safrole.
    Ueng YF; Hsieh CH; Don MJ
    Food Chem Toxicol; 2005 May; 43(5):707-12. PubMed ID: 15778010
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mechanism-based inactivation of P450 2A6 by furanocoumarins.
    Koenigs LL; Trager WF
    Biochemistry; 1998 Jul; 37(28):10047-61. PubMed ID: 9665710
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluation of methoxsalen, tranylcypromine, and tryptamine as specific and selective CYP2A6 inhibitors in vitro.
    Zhang W; Kilicarslan T; Tyndale RF; Sellers EM
    Drug Metab Dispos; 2001 Jun; 29(6):897-902. PubMed ID: 11353760
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mechanism-based inactivation of cytochrome P450 2A6 by decursinol angelate isolated from Angelica Gigas.
    Yoo HH; Lee MW; Kim YC; Yun CH; Kim DH
    Drug Metab Dispos; 2007 Oct; 35(10):1759-65. PubMed ID: 17620343
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synthetic models related to methoxalen and menthofuran-cytochrome P450 (CYP) 2A6 interactions. benzofuran and coumarin derivatives as potent and selective inhibitors of CYP2A6.
    Yamaguchi Y; Akimoto I; Motegi K; Yoshimura T; Wada K; Nishizono N; Oda K
    Chem Pharm Bull (Tokyo); 2013; 61(10):997-1001. PubMed ID: 23902929
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mechanism-based inactivation of cytochrome P450 3A4 by 4-ipomeanol.
    Alvarez-Diez TM; Zheng J
    Chem Res Toxicol; 2004 Feb; 17(2):150-7. PubMed ID: 14967002
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Baculovirus-mediated expression and characterization of rat CYP2A3 and human CYP2a6: role in metabolic activation of nasal toxicants.
    Liu C; Zhuo X; Gonzalez FJ; Ding X
    Mol Pharmacol; 1996 Oct; 50(4):781-8. PubMed ID: 8863822
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Competitive interactions between cytochromes P450 2A6 and 2E1 for NADPH-cytochrome P450 oxidoreductase in the microsomal membranes produced by a baculovirus expression system.
    Tan Y; Patten CJ; Smith T; Yang CS
    Arch Biochem Biophys; 1997 Jun; 342(1):82-91. PubMed ID: 9185616
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Screening of organosulfur compounds as inhibitors of human CYP2A6.
    Fujita K; Kamataki T
    Drug Metab Dispos; 2001 Jul; 29(7):983-9. PubMed ID: 11408364
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expression of cytochrome P450 2A6 in Escherichia coli: purification, spectral and catalytic characterization, and preparation of polyclonal antibodies.
    Soucek P
    Arch Biochem Biophys; 1999 Oct; 370(2):190-200. PubMed ID: 10510277
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An evaluation of potential mechanism-based inactivation of human drug metabolizing cytochromes P450 by monoamine oxidase inhibitors, including isoniazid.
    Polasek TM; Elliot DJ; Somogyi AA; Gillam EM; Lewis BC; Miners JO
    Br J Clin Pharmacol; 2006 May; 61(5):570-84. PubMed ID: 16669850
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterization of CYP2A6 involved in 3'-hydroxylation of cotinine in human liver microsomes.
    Nakajima M; Yamamoto T; Nunoya K; Yokoi T; Nagashima K; Inoue K; Funae Y; Shimada N; Kamataki T; Kuroiwa Y
    J Pharmacol Exp Ther; 1996 May; 277(2):1010-5. PubMed ID: 8627511
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inhibition of human drug metabolizing cytochromes P450 by anastrozole, a potent and selective inhibitor of aromatase.
    Grimm SW; Dyroff MC
    Drug Metab Dispos; 1997 May; 25(5):598-602. PubMed ID: 9152599
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Human reductive halothane metabolism in vitro is catalyzed by cytochrome P450 2A6 and 3A4.
    Spracklin DK; Thummel KE; Kharasch ED
    Drug Metab Dispos; 1996 Sep; 24(9):976-83. PubMed ID: 8886607
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.