Search Results - "HOLLENBERG, Paul F"
-
1
Oxidation of the endogenous cannabinoid arachidonoyl ethanolamide by the cytochrome P450 monooxygenases: physiological and pharmacological implications
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…”
Get full text
Journal Article -
2
Heme Modification Contributes to the Mechanism-Based Inactivation of Human Cytochrome P450 2J2 by Two Terminal Acetylenic Compounds
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),…”
Get full text
Journal Article -
3
Mechanism-Based Inactivation of Human Cytochromes P450s: Experimental Characterization, Reactive Intermediates, and Clinical Implications
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…”
Get full text
Journal Article -
4
Mechanism-Based Inactivation of Human Cytochrome P450 2B6 by Chlorpyrifos
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…”
Get full text
Journal Article -
5
Polymorphic variants of cytochrome P450 2B6 (CYP2B6.4-CYP2B6.9) exhibit altered rates of metabolism for bupropion and efavirenz: a charge-reversal mutation in the K139E variant (CYP2B6.8) impairs formation of a functional cytochrome p450-reductase complex
Published in The Journal of pharmacology and experimental therapeutics (01-09-2011)“…In this study, metabolism of bupropion, efavirenz, and 7-ethoxy-4-trifluoromethylcoumarin (7-EFC) by CYP2B6 wild type (CYP2B6.1) and six polymorphic variants…”
Get more information
Journal Article -
6
The inactivation of human CYP2E1 by phenethyl isothiocyanate, a naturally occurring chemopreventive agent, and its oxidative bioactivation
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…”
Get full text
Journal Article -
7
Inhibition of bupropion metabolism by selegiline: mechanism-based inactivation of human CYP2B6 and characterization of glutathione and peptide adducts
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…”
Get full text
Journal Article -
8
Uncovering the Role of Hydrophobic Residues in Cytochrome P450−Cytochrome P450 Reductase Interactions
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…”
Get full text
Journal Article -
9
A cytochrome P450-derived epoxygenated metabolite of anandamide is a potent cannabinoid receptor 2-selective agonist
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…”
Get more information
Journal Article -
10
Formation of the thiol conjugates and active metabolite of clopidogrel by human liver microsomes
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…”
Get more information
Journal Article -
11
Multiple mechanisms and multiple oxidants in P450-catalyzed hydroxylations
Published in Archives of Biochemistry and Biophysics (2003)“…Cytochrome P450 enzymes catalyze a number of oxidations in nature including the difficult hydroxylations of unactivated positions in an alkyl group. The…”
Get full text
Book Review Journal Article -
12
SILYBIN INACTIVATES CYTOCHROMES P450 3A4 AND 2C9 AND INHIBITS MAJOR HEPATIC GLUCURONOSYLTRANSFERASES
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)…”
Get full text
Journal Article -
13
The endocannabinoid anandamide is a substrate for the human polymorphic cytochrome P450 2D6
Published in The Journal of pharmacology and experimental therapeutics (01-11-2008)“…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…”
Get more information
Journal Article -
14
Anandamide metabolism by human liver and kidney microsomal cytochrome p450 enzymes to form hydroxyeicosatetraenoic and epoxyeicosatrienoic acid ethanolamides
Published in The Journal of pharmacology and experimental therapeutics (01-05-2007)“…The endocannabinoid anandamide is an arachidonic acid derivative that is found in most tissues where it acts as an important signaling mediator in…”
Get more information
Journal Article -
15
Role of the Highly Conserved Threonine in Cytochrome P450 2E1: Prevention of H2O2‑Induced Inactivation during Electron Transfer
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…”
Get full text
Journal Article -
16
Gender Dimorphic Formation of Mouse Mallory–Denk Bodies and the Role of Xenobiotic Metabolism and Oxidative Stress
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…”
Get full text
Journal Article -
17
Characteristics and common properties of inhibitors, inducers, and activators of CYP enzymes
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…”
Get full text
Journal Article -
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
Published in The Journal of pharmacology and experimental therapeutics (01-04-2005)“…Bergamottin (BG), a component of grapefruit juice, is a mechanism-based inactivator of cytochromes P450 (P450) 2B6 and 3A5 in the reconstituted system. The…”
Get more information
Journal Article -
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
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…”
Get full text
Journal Article -
20
Cross-linking of human cytochrome P450 2B6 to NADPH-cytochrome P450 reductase: Identification of a potential site of interaction
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…”
Get full text
Journal Article