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Volumn 27, Issue 12, 1999, Pages 1519-1522

CYP2C9 is a principal low-affinity phenacetin O-deethylase: Fluvoxamine is not a specific CYP1A2 inhibitor (multiple letters)

Author keywords

[No Author keywords available]

Indexed keywords

FLUVOXAMINE; PHENACETIN O DEETHYLASE;

EID: 0032751543     PISSN: 00909556     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter
Times cited : (13)

References (15)
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  • 3
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  • 4
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  • 5
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    • Involvement of CYP2E1 as a low-affinity enzyme in phenacetin O-deethylation in human liver microsomes
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  • 6
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  • 7
    • 0030056594 scopus 로고    scopus 로고
    • Specificity of substrate and inhibitor probes for cytochrome P450s: Evaluation of in vitro metabolism using cDNA-expressed human P450s and human liver microsomes
    • Ono S, Hatanaka T, Hotta H, Satoh T, Gonzalez FJ and Tsutsui M (1996) Specificity of substrate and inhibitor probes for cytochrome P450s: Evaluation of in vitro metabolism using cDNA-expressed human P450s and human liver microsomes. Xenobiotica 26:681-693.
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  • 8
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  • 9
    • 0030706197 scopus 로고    scopus 로고
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    • Schmider J, Greenblatt DJ, von Moltke LL, Karsov D and Shader RI (1997) Inhibition of CYP2C9 by selective serotonin reuptake inhibitors in vitro: Studies of phenytoin parahydroxylation. Br J Clin Pharmacol 44:495-498.
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  • 10
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.