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Volumn 35, Issue 12, 2005, Pages 1121-1133

Characterization of the enzymes involved in the in vitro metabolism of amrubicin hydrochloride

Author keywords

Amrubicin hydrochloride; Carbonyl reductase; Cisplatin; NADPH cytochrome P450 reductase; NADPH:quinone oxidoreductase

Indexed keywords

AMRUBICIN; AMRUBICINOL; ANTINEOPLASTIC ANTIBIOTIC; CARBONYL REDUCTASE; CISPLATIN; DICOUMAROL; OXIDOREDUCTASE; QUERCETIN; QUINONE DERIVATIVE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE FERRIHEMOPROTEIN REDUCTASE; UNCLASSIFIED DRUG;

EID: 31544435787     PISSN: 00498254     EISSN: 13665928     Source Type: Journal    
DOI: 10.1080/00498250500342746     Document Type: Article
Times cited : (26)

References (18)
  • 1
    • 0032979405 scopus 로고    scopus 로고
    • Five-day intravenous comparative toxicity study on amrubicin hydrochloride (SM-5887) and doxorubicin hydrochloride (DXR) in male rats
    • Adachi H, Nakayama K, Ozaki M, Uwagawa S, Seki T, Matsuo M. 1999. Five-day intravenous comparative toxicity study on amrubicin hydrochloride (SM-5887) and doxorubicin hydrochloride (DXR) in male rats. Japanese Pharmacology and Therapy 27S:221-239.
    • (1999) Japanese Pharmacology and Therapy , vol.27 S , pp. 221-239
    • Adachi, H.1    Nakayama, K.2    Ozaki, M.3    Uwagawa, S.4    Seki, T.5    Matsuo, M.6
  • 2
    • 0039483056 scopus 로고    scopus 로고
    • Metabolic activation of adriamycin by NADPH-cytochrome P450 reductase; overview of its biological and biochemical effects
    • Bartoszek A. 2002. Metabolic activation of adriamycin by NADPH-cytochrome P450 reductase; overview of its biological and biochemical effects. Acta Biochemica Polonica 49:323-331.
    • (2002) Acta Biochemica Polonica , vol.49 , pp. 323-331
    • Bartoszek, A.1
  • 3
    • 0026757021 scopus 로고
    • Metabolism of 2,6-dinitro[3-3H]toluene by human and rat liver microsomal and cytosolic fractions
    • Chapman DE, Michener SR, Powis G. 1992. Metabolism of 2,6-dinitro[3-3H]toluene by human and rat liver microsomal and cytosolic fractions. Xenobiotica 22:1015-1028.
    • (1992) Xenobiotica , vol.22 , pp. 1015-1028
    • Chapman, D.E.1    Michener, S.R.2    Powis, G.3
  • 5
    • 0023899593 scopus 로고
    • Quantitative analysis of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine metabolism in isolated rat hepatocytes
    • Di MD, Shinka T, Sandy MS, Castagnoli N Jr, Smith MT. 1988. Quantitative analysis of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine metabolism in isolated rat hepatocytes. Drug Metabolism and Disposition 16:250-255.
    • (1988) Drug Metabolism and Disposition , vol.16 , pp. 250-255
    • Di, M.D.1    Shinka, T.2    Sandy, M.S.3    Castagnoli Jr., N.4    Smith, M.T.5
  • 6
    • 0034665414 scopus 로고    scopus 로고
    • Human carbonyl reductase overexpression in the heart advances the development of doxorubicin-induced cardiotoxicity in transgenic mice
    • Forrest GL, Gonzalez B, Tseng W, Li X, Mann J. 2000. Human carbonyl reductase overexpression in the heart advances the development of doxorubicin-induced cardiotoxicity in transgenic mice. Cancer Research 60:5158-5164.
    • (2000) Cancer Research , vol.60 , pp. 5158-5164
    • Forrest, G.L.1    Gonzalez, B.2    Tseng, W.3    Li, X.4    Mann, J.5
  • 7
    • 0029018690 scopus 로고
    • Comparative resistance of idarubicin, doxorubicin and their C-13 alcohol metabolites in human MDR1 transfected NIH-3T3 cells
    • Kuffel MJ, Ames MM. 1995. Comparative resistance of idarubicin, doxorubicin and their C-13 alcohol metabolites in human MDR1 transfected NIH-3T3 cells. Cancer Chemotherapy and Pharmacology 36:223-226.
    • (1995) Cancer Chemotherapy and Pharmacology , vol.36 , pp. 223-226
    • Kuffel, M.J.1    Ames, M.M.2
  • 8
    • 0041694227 scopus 로고    scopus 로고
    • Anthracycline secondary alcohol metabolite formation in human or rabbit heart: Biochemical aspects and pharmacologic implications
    • Mordente A, Minotti G, Martorana GE, Silvestrini A, Giardina B, Meucci E. 2003. Anthracycline secondary alcohol metabolite formation in human or rabbit heart: Biochemical aspects and pharmacologic implications. Biochemistry and Pharmacology 66:989-998.
    • (2003) Biochemistry and Pharmacology , vol.66 , pp. 989-998
    • Mordente, A.1    Minotti, G.2    Martorana, G.E.3    Silvestrini, A.4    Giardina, B.5    Meucci, E.6
  • 10
    • 31544458791 scopus 로고    scopus 로고
    • Studies on the metabolic fate of amrubicin hydrochloride (SM-5887), a novel antitumor agent (IV): Metabolism of SM-5887 in rats and dogs
    • Nakai S, Akao K, Ito M, Kanamaru H, Nakatsuka I. 1998. Studies on the metabolic fate of amrubicin hydrochloride (SM-5887), a novel antitumor agent (IV): Metabolism of SM-5887 in rats and dogs. Xenobiotic Metabolism and Disposition 13:100-112.
    • (1998) Xenobiotic Metabolism and Disposition , vol.13 , pp. 100-112
    • Nakai, S.1    Akao, K.2    Ito, M.3    Kanamaru, H.4    Nakatsuka, I.5
  • 11
    • 0033011860 scopus 로고    scopus 로고
    • Studies on the metabolic fate of amrubicin hydrochloride (SM-5887), a novel antitumor agent (6) - Pharmacokinetic studies of amrubicinol, the major bioactive metabolite of amrubicin, in rats
    • Nakai S, Akao K, Ito M, Kanamaru H, Nakatsuka I. 1999. Studies on the metabolic fate of amrubicin hydrochloride (SM-5887), a novel antitumor agent (6) - pharmacokinetic studies of amrubicinol, the major bioactive metabolite of amrubicin, in rats. Japanese Pharmacology and Therapy 278:521-543.
    • (1999) Japanese Pharmacology and Therapy , vol.278 , pp. 521-543
    • Nakai, S.1    Akao, K.2    Ito, M.3    Kanamaru, H.4    Nakatsuka, I.5
  • 12
    • 0032978954 scopus 로고    scopus 로고
    • Studies on the metabolic fate of amrubicin hydrochloride (SM-5887), a novel antitumor agent (9) - In vitro chiral conversion of SM-5887 and stereoselectivity of reduction of the carbonyl group at the C-13 position
    • Nakai S, Ito M, Kanamaru H, Nakatsuka I. 1999. Studies on the metabolic fate of amrubicin hydrochloride (SM-5887), a novel antitumor agent (9) - in vitro chiral conversion of SM-5887 and stereoselectivity of reduction of the carbonyl group at the C-13 position. Japanese Pharmacology and Therapy 278:557-568.
    • (1999) Japanese Pharmacology and Therapy , vol.278 , pp. 557-568
    • Nakai, S.1    Ito, M.2    Kanamaru, H.3    Nakatsuka, I.4
  • 14
    • 0024355564 scopus 로고
    • Comparative activity of anthracycline 13-dihydrometabolites against rat glioblastoma cells in culture
    • Schott B, Robert J. 1989. Comparative activity of anthracycline 13-dihydrometabolites against rat glioblastoma cells in culture. Biochemistry and Pharmacology 38:4069-4074.
    • (1989) Biochemistry and Pharmacology , vol.38 , pp. 4069-4074
    • Schott, B.1    Robert, J.2
  • 16
    • 0017258828 scopus 로고
    • Adriamycin metabolism in man. Evidence from urinary metabolites
    • Takanashi S, Bachur NR. 1976. Adriamycin metabolism in man. Evidence from urinary metabolites. Drug Metabolism and Disposition 4:79-87.
    • (1976) Drug Metabolism and Disposition , vol.4 , pp. 79-87
    • Takanashi, S.1    Bachur, N.R.2
  • 17
    • 0026515575 scopus 로고
    • Metabolism by rat liver cytosol of illudin S, a toxic substance of Lampteromyces japonicus. II. Characterization of illudin S-metabolizing enzyme
    • Tanaka K, Inoue T, Kadota S, Kikuchi T. 1992. Metabolism by rat liver cytosol of illudin S, a toxic substance of Lampteromyces japonicus. II. Characterization of illudin S-metabolizing enzyme. Xenobiotica 22:33-39.
    • (1992) Xenobiotica , vol.22 , pp. 33-39
    • Tanaka, K.1    Inoue, T.2    Kadota, S.3    Kikuchi, T.4
  • 18
    • 0031786266 scopus 로고    scopus 로고
    • Cytotoxicity of amrubicin, a novel 9-aminoanthracycline, and its active metabolite amrubicinol on human tumor cells
    • Yamaoka T, Hanada M, Ichii S, Morisada S, Noguchi T, Yanagi Y. 1998. Cytotoxicity of amrubicin, a novel 9-aminoanthracycline, and its active metabolite amrubicinol on human tumor cells. Japanese Journal of Cancer Research 89:1067-1073.
    • (1998) Japanese Journal of Cancer Research , vol.89 , pp. 1067-1073
    • Yamaoka, T.1    Hanada, M.2    Ichii, S.3    Morisada, S.4    Noguchi, T.5    Yanagi, Y.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.