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Metabolism of CJ-036878, N-(3-phenethoxybenzyl)-4-hydroxybenzamide, in liver microsomes and recombinant cytochrome P450 enzymes: metabolite identification by LC-UV/MS(n) and (1)H-NMR.

Metabolism of CJ-036878, N-(3-phenethoxybenzyl)-4-hydroxybenzamide, in liver microsomes and recombinant cytochrome P450 enzymes: metabolite identification by LC-UV/MS(n) and (1)H-NMR. Research Abstract Details 

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  • Metabolism of CJ-036878, N-(3-phenethoxybenzyl)-4-hydroxybenzamide, in liver microsomes and recombinant cytochrome P450 enzymes: metabolite identification by LC-UV/MS(n) and (1)H-NMR. Abstract Text:

    h nishidaH Nishida,h hiraiH Hirai,c emotoC Emoto,k iwasakiK Iwasaki,h nishidaH Nishida,h hiraiH Hirai,c emotoC Emoto,k iwasakiK Iwasaki,

    The identification of metabolites in the early stages of drug discovery is important not only for guiding structure-activity relationships (SAR) and structure-metabolism relationships (SMR) strategies, but also for predicting the potential for adverse events. The present study investigated the phase I metabolism of CJ-036878 (N-(3-phenethoxybenzyl)-4-hydroxybenzamide), a potent antagonist of the N-methyl-D-asparatate (NMDA) receptor, using liver microsomes and representative recombinant cytochrome P450 enzymes. The structures of the oxidative metabolites M1-M11 were confirmed by LC-UV/MS(n) and/or (1)H-nuclear magnetic resonance (NMR). It was found that CJ-036878 is metabolized through three routes: (1) aliphatic hydroxylation that generates M1 and M2; (2) aromatic hydroxylation that produces M3-M5, M7 and M8; and (3) dimerization through an oxidative phenol coupling reaction that yields M10 and M11. The use of recombinant human cytochrome P450 enzymes suggested that CYP3A4 is the major enzyme involved in the oxidative metabolism of CJ-036878, with minor contributions from CYP1A2, CYP2C19, and CYP2D6.

    Metabolism of CJ-036878, N-(3-phenethoxybenzyl)-4-hydroxybenzamide, in liver microsomes and recombinant cytochrome P450 enzymes: metabolite identification by LC-UV/MS(n) and (1)H-NMR. Publishing Authors By Initials

    h nishidaH Nishida,h hiraiH Hirai,c emotoC Emoto,k iwasakiK Iwasaki,h nishidaH Nishida,h hiraiH Hirai,c emotoC Emoto,k iwasakiK Iwasaki,

    For similar abstracts research abstracts see: abstracts research

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    Metabolism of CJ-036878, N-(3-phenethoxybenzyl)-4-hydroxybenzamide, in liver microsomes and recombinant cytochrome P450 enzymes: metabolite identification by LC-UV/MS(n) and (1)H-NMR. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Xenobiotica; the fate of foreign compounds in biol

    VOLUME: 37

    Page Numbers: 1394-407

    Journal Abbreviation: Xenobiotica

    ISSN: 0049-8254

    DAY: 22

    MONTH: Dec

    YEAR: 2007

    Metabolism of CJ-036878, N-(3-phenethoxybenzyl)-4-hydroxybenzamide, in liver microsomes and recombinant cytochrome P450 enzymes: metabolite identification by LC-UV/MS(n) and (1)H-NMR. Information

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    LANGUAGE: eng

    NlmUniqueID: 1306665

    Metabolism of CJ-036878, N-(3-phenethoxybenzyl)-4-hydroxybenzamide, in liver microsomes and recombinant cytochrome P450 enzymes: metabolite identification by LC-UV/MS(n) and (1)H-NMR. Keywords Mesh Terms:

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    Chemical & Substance for Abstract: Metabolism of CJ-036878, N-(3-phenethoxybenzyl)-4-hydroxybenzamide, in liver microsomes and recombinant cytochrome P450 enzymes: metabolite identification by LC-UV/MS(n) and (1)H-NMR. Information

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    Grant and Affiliation Information for Metabolism of CJ-036878, N-(3-phenethoxybenzyl)-4-hydroxybenzamide, in liver microsomes and recombinant cytochrome P450 enzymes: metabolite identification by LC-UV/MS(n) and (1)H-NMR.

    AFFILIATION: Department of Discovery Chemistry Research, Dynamics and Metabolism, Pfizer Global Research and Development, Aichi, Japan.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Xenobiotica

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