Search Results - "HOLLENBERG, Paul F"

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  1. 1

    Oxidation of the endogenous cannabinoid arachidonoyl ethanolamide by the cytochrome P450 monooxygenases: physiological and pharmacological implications by Snider, Natasha T, Walker, Vyvyca J, Hollenberg, Paul F

    Published in Pharmacological reviews (01-03-2010)
    “…Arachidonoyl ethanolamide (anandamide) is an endogenous amide of arachidonic acid and an important signaling mediator of the endocannabinoid system. Given its…”
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    Journal Article
  2. 2

    Heme Modification Contributes to the Mechanism-Based Inactivation of Human Cytochrome P450 2J2 by Two Terminal Acetylenic Compounds by Lin, Hsia-Lien, Zhang, Haoming, Walker, Vyvyca J, D'Agostino, Jaime, Hollenberg, Paul F

    Published in Drug metabolism and disposition (01-09-2017)
    “…The mechanism-based inactivation of human CYP2J2 by three terminal acetylenic compounds: -(methylsulfonyl)-6-(2-propargyloxyphenyl)hexanamide (MS),…”
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    Journal Article
  3. 3

    Mechanism-Based Inactivation of Human Cytochromes P450s: Experimental Characterization, Reactive Intermediates, and Clinical Implications by Hollenberg, Paul F, Kent, Ute M, Bumpus, Namandjé N

    Published in Chemical research in toxicology (01-01-2008)
    “…The P450 type cytochromes are responsible for the metabolism of a wide variety of xenobiotics and endogenous compounds. Although P450-catalyzed reactions are…”
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    Journal Article
  4. 4

    Mechanism-Based Inactivation of Human Cytochrome P450 2B6 by Chlorpyrifos by D’Agostino, Jaime, Zhang, Haoming, Kenaan, Cesar, Hollenberg, Paul F

    Published in Chemical research in toxicology (20-07-2015)
    “…Chlorpyrifos (CPS) is a commonly used pesticide which is metabolized by P450s into the toxic metabolite chlorpyrifos-oxon (CPO). Metabolism also results in the…”
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    Journal Article
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  6. 6

    The inactivation of human CYP2E1 by phenethyl isothiocyanate, a naturally occurring chemopreventive agent, and its oxidative bioactivation by Yoshigae, Yasushi, Sridar, Chitra, Kent, Ute M, Hollenberg, Paul F

    Published in Drug metabolism and disposition (01-04-2013)
    “…Phenethylisothiocyanate (PEITC), a naturally occurring isothiocyanate and potent cancer chemopreventive agent, works by multiple mechanisms, including the…”
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    Journal Article
  7. 7

    Inhibition of bupropion metabolism by selegiline: mechanism-based inactivation of human CYP2B6 and characterization of glutathione and peptide adducts by Sridar, Chitra, Kenaan, Cesar, Hollenberg, Paul F

    Published in Drug metabolism and disposition (01-12-2012)
    “…Selegiline, the R-enantiomer of deprenyl, is used in the treatment of Parkinson's disease. Bupropion, an antidepressant, often used to treat patients in…”
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    Journal Article
  8. 8

    Uncovering the Role of Hydrophobic Residues in Cytochrome P450−Cytochrome P450 Reductase Interactions by Kenaan, Cesar, Zhang, Haoming, Shea, Erin V, Hollenberg, Paul F

    Published in Biochemistry (Easton) (17-05-2011)
    “…Cytochrome P450 (CYP or P450)-mediated drug metabolism requires the interaction of P450s with their redox partner, cytochrome P450 reductase (CPR). In this…”
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    Journal Article
  9. 9

    A cytochrome P450-derived epoxygenated metabolite of anandamide is a potent cannabinoid receptor 2-selective agonist by Snider, Natasha T, Nast, James A, Tesmer, Laura A, Hollenberg, Paul F

    Published in Molecular pharmacology (01-04-2009)
    “…Oxidation of the endocannabinoid anandamide by cytochrome P450 (P450) enzymes has the potential to affect signaling pathways within the endocannabinoid system…”
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    Journal Article
  10. 10

    Formation of the thiol conjugates and active metabolite of clopidogrel by human liver microsomes by Zhang, Haoming, Lau, Wei C, Hollenberg, Paul F

    Published in Molecular pharmacology (01-08-2012)
    “…We reported previously the formation of a glutathionyl conjugate of the active metabolite (AM) of clopidogrel and the covalent modification of a cysteinyl…”
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    Journal Article
  11. 11

    Multiple mechanisms and multiple oxidants in P450-catalyzed hydroxylations by Newcomb, Martin, Hollenberg, Paul F, Coon, Minor J

    “…Cytochrome P450 enzymes catalyze a number of oxidations in nature including the difficult hydroxylations of unactivated positions in an alkyl group. The…”
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    Book Review Journal Article
  12. 12

    SILYBIN INACTIVATES CYTOCHROMES P450 3A4 AND 2C9 AND INHIBITS MAJOR HEPATIC GLUCURONOSYLTRANSFERASES by SRIDAR, Chitra, GOOSEN, Theunis C, KENT, Ute M, WILLIAMS, J. Andrew, HOLLENBERG, Paul F

    Published in Drug metabolism and disposition (01-06-2004)
    “…Silybin, a major constituent of the milk thistle, is used to treat several liver disorders. Silybin inactivated purified, recombinant cytochromes P450 (P450)…”
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    Journal Article
  13. 13

    The endocannabinoid anandamide is a substrate for the human polymorphic cytochrome P450 2D6 by Snider, Natasha T, Sikora, Matthew J, Sridar, Chitra, Feuerstein, Thomas J, Rae, James M, Hollenberg, Paul F

    “…Members of the cytochrome P450 (P450) family of drug-metabolizing enzymes are present in the human brain, and they may have important roles in the oxidation of…”
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    Journal Article
  14. 14

    Anandamide metabolism by human liver and kidney microsomal cytochrome p450 enzymes to form hydroxyeicosatetraenoic and epoxyeicosatrienoic acid ethanolamides by Snider, Natasha T, Kornilov, Andrei M, Kent, Ute M, Hollenberg, Paul F

    “…The endocannabinoid anandamide is an arachidonic acid derivative that is found in most tissues where it acts as an important signaling mediator in…”
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    Journal Article
  15. 15

    Role of the Highly Conserved Threonine in Cytochrome P450 2E1: Prevention of H2O2‑Induced Inactivation during Electron Transfer by Yoshigae, Yasushi, Kent, Ute M, Hollenberg, Paul F

    Published in Biochemistry (Easton) (09-07-2013)
    “…A highly conserved threonine in the I-helix of cytochrome P450s has been suggested to play an important role in dioxygen activation, a critical step for…”
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    Journal Article
  16. 16

    Gender Dimorphic Formation of Mouse Mallory–Denk Bodies and the Role of Xenobiotic Metabolism and Oxidative Stress by Hanada, Shinichiro, Snider, Natasha T, Brunt, Elizabeth M, Hollenberg, Paul F, Omary, M. Bishr

    Published in Gastroenterology (New York, N.Y. 1943) (01-04-2010)
    “…Background & Aims Mallory–Denk bodies (MDBs) are keratin (K)-rich cytoplasmic hepatocyte inclusions commonly associated with alcoholic steatohepatitis. Given…”
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    Journal Article
  17. 17

    Characteristics and common properties of inhibitors, inducers, and activators of CYP enzymes by Hollenberg, Paul F.

    Published in Drug metabolism reviews (01-01-2002)
    “…Many inhibitors of the CYP enzymes have been identified and although some are inhibitory for a number of different CYPs, a fair number are very selective for…”
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    Journal Article
  18. 18

    The grapefruit juice effect is not limited to cytochrome P450 (P450) 3A4: evidence for bergamottin-dependent inactivation, heme destruction, and covalent binding to protein in P450s 2B6 and 3A5 by Lin, Hsia-lien, Kent, Ute M, Hollenberg, Paul F

    “…Bergamottin (BG), a component of grapefruit juice, is a mechanism-based inactivator of cytochromes P450 (P450) 2B6 and 3A5 in the reconstituted system. The…”
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    Journal Article
  19. 19

    Effect of Conformational Dynamics on Substrate Recognition and Specificity as Probed by the Introduction of a de Novo Disulfide Bond into Cytochrome P450 2B1 by Zhang, Haoming, Kenaan, Cesar, Hamdane, Djemel, Hoa, Gaston Hui Bon, Hollenberg, Paul F.

    Published in The Journal of biological chemistry (18-09-2009)
    “…The conformational dynamics of cytochrome P450 2B1 (CYP2B1) were investigated through the introduction of a disulfide bond to link the I- and K-helices by…”
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    Journal Article
  20. 20

    Cross-linking of human cytochrome P450 2B6 to NADPH-cytochrome P450 reductase: Identification of a potential site of interaction by Bumpus, Namandjé N., Hollenberg, Paul F.

    Published in Journal of inorganic biochemistry (01-04-2010)
    “…Isotopic labeling of cross-linked peptides coupled with mass spectrometry was used to identify P450 2B6 residues that potentially interact with…”
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    Journal Article