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187 related items for PubMed ID: 20836985
21. Structures of cytochrome P450 2B6 bound to 4-benzylpyridine and 4-(4-nitrobenzyl)pyridine: insight into inhibitor binding and rearrangement of active site side chains. Shah MB, Pascual J, Zhang Q, Stout CD, Halpert JR. Mol Pharmacol; 2011 Dec; 80(6):1047-55. PubMed ID: 21875942 [Abstract] [Full Text] [Related]
22. Quantitative structure-activity relationships (QSARs) for inhibitors and substrates of CYP2B enzymes: importance of compound lipophilicity in explanation of potency differences. Lewis DF, Ito Y, Lake BG. J Enzyme Inhib Med Chem; 2010 Oct; 25(5):679-84. PubMed ID: 20100069 [Abstract] [Full Text] [Related]
23. Mechanism-based inactivation of cytochromes P450 2E1 and 2E1 T303A by tert-butyl acetylenes: characterization of reactive intermediate adducts to the heme and apoprotein. Blobaum AL, Kent UM, Alworth WL, Hollenberg PF. Chem Res Toxicol; 2002 Dec; 15(12):1561-71. PubMed ID: 12482238 [Abstract] [Full Text] [Related]
24. Peroxynitrite inactivation of human cytochrome P450s 2B6 and 2E1: heme modification and site-specific nitrotyrosine formation. Lin HL, Myshkin E, Waskell L, Hollenberg PF. Chem Res Toxicol; 2007 Nov; 20(11):1612-22. PubMed ID: 17907788 [Abstract] [Full Text] [Related]
25. Elucidation of amino acid residues critical for unique activities of rabbit cytochrome P450 2B5 using hybrid enzymes and reciprocal site-directed mutagenesis with rabbit cytochrome P450 2B4. Szklarz GD, He YQ, Kedzie KM, Halpert JR, Burnett VL. Arch Biochem Biophys; 1996 Mar 15; 327(2):308-18. PubMed ID: 8619620 [Abstract] [Full Text] [Related]
26. Coumarin Derivatives as Substrate Probes of Mammalian Cytochromes P450 2B4 and 2B6: Assessing the Importance of 7-Alkoxy Chain Length, Halogen Substitution, and Non-Active Site Mutations. Liu J, Shah MB, Zhang Q, Stout CD, Halpert JR, Wilderman PR. Biochemistry; 2016 Apr 05; 55(13):1997-2007. PubMed ID: 26982502 [Abstract] [Full Text] [Related]
27. Identification of 17-alpha-ethynylestradiol-modified active site peptides and glutathione conjugates formed during metabolism and inactivation of P450s 2B1 and 2B6. Kent UM, Lin HL, Mills DE, Regal KA, Hollenberg PF. Chem Res Toxicol; 2006 Feb 05; 19(2):279-87. PubMed ID: 16485904 [Abstract] [Full Text] [Related]
28. Thiophene derivatives as new mechanism-based inhibitors of cytochromes P-450: inactivation of yeast-expressed human liver cytochrome P-450 2C9 by tienilic acid. López-Garcia MP, Dansette PM, Mansuy D. Biochemistry; 1994 Jan 11; 33(1):166-75. PubMed ID: 8286335 [Abstract] [Full Text] [Related]
29. Rational engineering of cytochromes P450 2B6 and 2B11 for enhanced stability: Insights into structural importance of residue 334. Talakad JC, Wilderman PR, Davydov DR, Kumar S, Halpert JR. Arch Biochem Biophys; 2010 Feb 15; 494(2):151-8. PubMed ID: 19944064 [Abstract] [Full Text] [Related]
30. Formation of a novel reversible cytochrome P450 spectral intermediate: role of threonine 303 in P450 2E1 inactivation. Blobaum AL, Lu Y, Kent UM, Wang S, Hollenberg PF. Biochemistry; 2004 Sep 28; 43(38):11942-52. PubMed ID: 15379534 [Abstract] [Full Text] [Related]
31. Mechanism-based inactivators as probes of cytochrome P450 structure and function. Kent UM, Juschyshyn MI, Hollenberg PF. Curr Drug Metab; 2001 Sep 28; 2(3):215-43. PubMed ID: 11513328 [Abstract] [Full Text] [Related]
32. Kinetics of oxidation of benzphetamine by compounds I of cytochrome P450 2B4 and its mutants. Sheng X, Zhang H, Im SC, Horner JH, Waskell L, Hollenberg PF, Newcomb M. J Am Chem Soc; 2009 Mar 04; 131(8):2971-6. PubMed ID: 19209859 [Abstract] [Full Text] [Related]
33. Catalytic selectivity and mechanism-based inactivation of stably expressed and hepatic cytochromes P450 2B4 and 2B5: implications of the cytochrome P450 2B5 polymorphism. Grimm SW, Dyroff MC, Philpot RM, Halpert JR. Mol Pharmacol; 1994 Dec 04; 46(6):1090-9. PubMed ID: 7808429 [Abstract] [Full Text] [Related]
34. Crystal structure of a cytochrome P450 2B6 genetic variant in complex with the inhibitor 4-(4-chlorophenyl)imidazole at 2.0-A resolution. Gay SC, Shah MB, Talakad JC, Maekawa K, Roberts AG, Wilderman PR, Sun L, Yang JY, Huelga SC, Hong WX, Zhang Q, Stout CD, Halpert JR. Mol Pharmacol; 2010 Apr 04; 77(4):529-38. PubMed ID: 20061448 [Abstract] [Full Text] [Related]
35. Mechanism-based inactivation of CYP2B1 and its F-helix mutant by two tert-butyl acetylenic compounds: covalent modification of prosthetic heme versus apoprotein. Lin HL, Zhang H, Noon KR, Hollenberg PF. J Pharmacol Exp Ther; 2009 Nov 04; 331(2):392-403. PubMed ID: 19700628 [Abstract] [Full Text] [Related]
36. Progress in cytochrome P450 active site modeling. Kemp CA, Maréchal JD, Sutcliffe MJ. Arch Biochem Biophys; 2005 Jan 15; 433(2):361-8. PubMed ID: 15581592 [Abstract] [Full Text] [Related]
37. Mechanism-based inactivation of human cytochrome P450 2B6 by clopidogrel: involvement of both covalent modification of cysteinyl residue 475 and loss of heme. Zhang H, Amunugama H, Ney S, Cooper N, Hollenberg PF. Mol Pharmacol; 2011 Nov 15; 80(5):839-47. PubMed ID: 21862689 [Abstract] [Full Text] [Related]
38. Investigation of the mechanisms underlying the differential effects of the K262R mutation of P450 2B6 on catalytic activity. Bumpus NN, Hollenberg PF. Mol Pharmacol; 2008 Oct 15; 74(4):990-9. PubMed ID: 18621926 [Abstract] [Full Text] [Related]
39. Differential behavior of the sub-sites of cytochrome 450 active site in binding of substrates, and products (implications for coupling/uncoupling). Narasimhulu S. Biochim Biophys Acta; 2007 Mar 15; 1770(3):360-75. PubMed ID: 17134838 [Abstract] [Full Text] [Related]
40. The mechanism-based inactivation of human cytochrome P450 2B6 by phencyclidine. Jushchyshyn MI, Kent UM, Hollenberg PF. Drug Metab Dispos; 2003 Jan 15; 31(1):46-52. PubMed ID: 12485952 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]