Cerny et al., 2006 - Google Patents
Cytochrome P450-catalyzed oxidation of N-benzyl-N-cyclopropylamine generates both cyclopropanone hydrate and 3-hydroxypropionaldehyde via hydrogen …Cerny et al., 2006
- Document ID
- 14507425718093087712
- Author
- Cerny M
- Hanzlik R
- Publication year
- Publication venue
- Journal of the American Chemical Society
External Links
Snippet
The suicide substrate activity of N-benzyl-N-cyclopropylamine (1) and N-benzyl-N-(1 '- methylcyclopropyl) amine (2) toward cytochrome P450 and other enzymes has been explained by a mechanism involving single electron transfer (SET) oxidation, followed by …
- 238000007254 oxidation reaction 0 title abstract description 55
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/26—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Cerny et al. | Cytochrome P450-catalyzed oxidation of N-benzyl-N-cyclopropylamine generates both cyclopropanone hydrate and 3-hydroxypropionaldehyde via hydrogen abstraction, not single electron transfer | |
Yoshimoto et al. | Mechanism of the third oxidative step in the conversion of androgens to estrogens by cytochrome P450 19A1 steroid aromatase | |
Fitzpatrick | Substrate dehydrogenation by flavoproteins | |
Jonsson et al. | Experimental evidence for extensive tunneling of hydrogen in the lipoxygenase reaction: implications for enzyme catalysis | |
Jiang et al. | Menaquinone biosynthesis in Escherichia coli: identification of 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate as a novel intermediate and re-evaluation of MenD activity | |
Stivers et al. | Catalytic role of the amino-terminal proline in 4-oxalocrotonate tautomerase: affinity labeling and heteronuclear NMR studies | |
Ralph et al. | Insights into the mechanism of flavoprotein-catalyzed amine oxidation from nitrogen isotope effects on the reaction of N-methyltryptophan oxidase | |
Pfeiffer et al. | Catechol formation: A novel pathway in the metabolism of sterigmatocystin and 11-methoxysterigmatocystin | |
Koehn et al. | Discovery of hydroxylase activity for PqqB provides a missing link in the pyrroloquinoline quinone biosynthetic pathway | |
Walker et al. | Determination of degradation pathways and kinetics of acyl glucuronides by NMR spectroscopy | |
Sun et al. | In vitro metabolism of a model cyclopropylamine to reactive intermediate: insights into trovafloxacin-induced hepatotoxicity | |
Bhakta et al. | Microsomal P450-Catalyzed N-Dealkylation of N, N-Dialkylanilines: Evidence for a Cα− H Abstraction Mechanism | |
Rothman et al. | Type II isopentenyl diphosphate isomerase: irreversible inactivation by covalent modification of flavin | |
Henderson et al. | Pre-steady-state kinetic analysis of 2-hydroxy-6-keto-nona-2, 4-diene-1, 9-dioic acid 5, 6-hydrolase: kinetic evidence for enol/keto tautomerization | |
Mutlib et al. | P450-Mediated Metabolism of 1-[3-(Aminomethyl) phenyl]-N-[3-fluoro-2 ‘-(methylsulfonyl)-[1, 1 ‘-biphenyl]-4-yl]-3-(trifluoromethyl)-1 H-pyrazole-5-carboxamide (DPC 423) and Its Analogues to Aldoximes. Characterization of Glutathione Conjugates of Postulated Intermediates Derived from Aldoximes | |
Van Vleet et al. | Carbon Isotope Effect Study on Orotidine 5 ‘-Monophosphate Decarboxylase: Support for an Anionic Intermediate | |
Charan et al. | Dioxapyrrolomycin Biosynthesis in Streptomyces f umanus | |
Li et al. | Mechanism of benzylsuccinate synthase probed by substrate and isotope exchange | |
Li et al. | Deuterium isotope effects in the unusual addition of toluene to fumarate catalyzed by benzylsuccinate synthase | |
Ni et al. | Reduction of fluorinated cyclopropene by nitrogenase | |
Marques-Soares et al. | Sulfaphenazole derivatives as tools for comparing cytochrome P450 2C5 and human cytochromes P450 2Cs: identification of a new high affinity substrate common to those enzymes | |
Cheng et al. | Isotope effects for deuterium transfer between substrate and coenzyme in adenosylcobalamin-dependent glutamate mutase | |
Zhang et al. | Evidence for Dramatic Acceleration of a C− H Bond Ionization Rate in Thiamin Diphosphate Enzymes by the Protein Environment | |
Chen et al. | Delineating novel metabolic pathways of DPC 963, a non-nucleoside reverse transcriptase inhibitor, in rats. Characterization of glutathione conjugates of postulated oxirene and benzoquinone imine intermediates by LC/MS and LC/NMR | |
Sun et al. | Chemical and kinetic reaction mechanisms of quinohemoprotein amine dehydrogenase from Paracoccus denitrificans |