메뉴 건너뛰기




Volumn 61, Issue 10, 2009, Pages 1309-1318

In-vitro and in-vivo metabolic studies of the candidate chemopreventative pentamethylchromanol using liquid chromatography/tandem mass spectrometry

Author keywords

CYP450; Drug metabolism; Liquid chromatography tandem mass spectrometry; Pentamethylchromanol

Indexed keywords

ANTIOXIDANT; CYTOCHROME P450; PENTAMETHYLCHROMANOL; UNCLASSIFIED DRUG; 2,2,5,7,8 PENTAMETHYL 1 HYDROXYCHROMAN; 2,2,5,7,8-PENTAMETHYL-1-HYDROXYCHROMAN; CHROMAN DERIVATIVE; ISOENZYME;

EID: 85047681307     PISSN: 00223573     EISSN: None     Source Type: Journal    
DOI: 10.1211/jpp.61.10.0006     Document Type: Article
Times cited : (5)

References (20)
  • 3
    • 75749139011 scopus 로고    scopus 로고
    • Farrell P, Roberts R. Vitamin E. In: Shils M, et al. eds. Modern Nutrition in Health and Disease. 8th edn. Philadelphia: Lea and Febiger, 326-341.
    • Farrell P, Roberts R. Vitamin E. In: Shils M, et al. eds. Modern Nutrition in Health and Disease. 8th edn. Philadelphia: Lea and Febiger, 326-341.
  • 4
    • 0033037413 scopus 로고    scopus 로고
    • Vitamin E: Function and metabolism
    • Brigelius-Flohe R, Traber MG. Vitamin E: function and metabolism. J FASEB 1999; 13: 1145-1155.
    • (1999) J FASEB , vol.13 , pp. 1145-1155
    • Brigelius-Flohe, R.1    Traber, M.G.2
  • 5
    • 0025315455 scopus 로고
    • Vitamin E: Antioxidant activity, biokinetics and bioavailability
    • Burton GW, Traber MG. Vitamin E: antioxidant activity, biokinetics and bioavailability. Annu Rev Nutr 1990; 10: 357-382.
    • (1990) Annu Rev Nutr , vol.10 , pp. 357-382
    • Burton, G.W.1    Traber, M.G.2
  • 6
    • 2342573753 scopus 로고    scopus 로고
    • Thompson TA, Wilding G. Androgen antagonist activity by the antioxidant moiety of vitamin E, 2,2,5,7,8-pentamethyl-6-chromanol in human prostate carcinoma cells. Mol Cancer Ther 2003; 8: 797-803.
    • Thompson TA, Wilding G. Androgen antagonist activity by the antioxidant moiety of vitamin E, 2,2,5,7,8-pentamethyl-6-chromanol in human prostate carcinoma cells. Mol Cancer Ther 2003; 8: 797-803.
  • 7
    • 0026636615 scopus 로고
    • The importance of steroid hormones in prostate cancer
    • Wilding G. The importance of steroid hormones in prostate cancer. Cancer Surv 1992; 14: 113-130.
    • (1992) Cancer Surv , vol.14 , pp. 113-130
    • Wilding, G.1
  • 8
    • 0031887611 scopus 로고    scopus 로고
    • Expression and characterization of a novel thyroid hormone-sulfating form of cytosolic sulfotransferase from human liver
    • Wang J et al. Expression and characterization of a novel thyroid hormone-sulfating form of cytosolic sulfotransferase from human liver. Mol Pharmacol 1998; 53: 274-282.
    • (1998) Mol Pharmacol , vol.53 , pp. 274-282
    • Wang, J.1
  • 9
    • 75749140968 scopus 로고    scopus 로고
    • Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions
    • Bertz RJ, Granneman GR. Use of in vitro and in vivo data to estimate the likelihood of metabolic pharmacokinetic interactions. Clin Pharmacokinet 1997; 37: 1150-1159.
    • (1997) Clin Pharmacokinet , vol.37 , pp. 1150-1159
    • Bertz, R.J.1    Granneman, G.R.2
  • 10
    • 0030799001 scopus 로고    scopus 로고
    • The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data
    • Obach RS et al. The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data. J Pharmacol Exp Ther 1997; 283: 46-58.
    • (1997) J Pharmacol Exp Ther , vol.283 , pp. 46-58
    • Obach, R.S.1
  • 11
    • 0031974059 scopus 로고    scopus 로고
    • In vitro approaches to predicting drug interactions in vivo
    • von Moltke LL et al. In vitro approaches to predicting drug interactions in vivo. Biochem Pharmacol 1998; 55: 113-122.
    • (1998) Biochem Pharmacol , vol.55 , pp. 113-122
    • von Moltke, L.L.1
  • 12
    • 0028968479 scopus 로고
    • Gender differences in drug metabolism regulated by growth hormone
    • Shapiro BH et al. Gender differences in drug metabolism regulated by growth hormone. Int J Biochem Cell Biol 1995; 27: 9-20.
    • (1995) Int J Biochem Cell Biol , vol.27 , pp. 9-20
    • Shapiro, B.H.1
  • 13
    • 0037562873 scopus 로고    scopus 로고
    • Cytochrome P450 genes are differently expressed in female and male hepatocyte retinoid X receptor α-deficient mice
    • Cai Y et al. Cytochrome P450 genes are differently expressed in female and male hepatocyte retinoid X receptor α-deficient mice. Endocrinology 2003; 144: 2311-2318.
    • (2003) Endocrinology , vol.144 , pp. 2311-2318
    • Cai, Y.1
  • 14
    • 0028237729 scopus 로고
    • Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: Studies with liver microsomes of 30 Japanese and 30 caucasians
    • Shimada T et al. Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: studies with liver microsomes of 30 Japanese and 30 caucasians. J Pharmacol Exp Ther 1994; 270: 414-423.
    • (1994) J Pharmacol Exp Ther , vol.270 , pp. 414-423
    • Shimada, T.1
  • 15
    • 0035887386 scopus 로고    scopus 로고
    • Human cytochrome P450 2A6 is a major enzyme involved in the metabolism of three alkoxy ethers used as oxyfuels
    • Le Gal A et al. Human cytochrome P450 2A6 is a major enzyme involved in the metabolism of three alkoxy ethers used as oxyfuels. Toxicol Lett 2001; 124: 47-58.
    • (2001) Toxicol Lett , vol.124 , pp. 47-58
    • Le Gal, A.1
  • 16
    • 0036266180 scopus 로고    scopus 로고
    • Quantitative structure activity relationships for the glucuronidation of simple phenols by expressed human UGT1A6 and UGT1A9
    • Ethell B et al. Quantitative structure activity relationships for the glucuronidation of simple phenols by expressed human UGT1A6 and UGT1A9. Drug Metab Dispos 2002; 30: 734-738.
    • (2002) Drug Metab Dispos , vol.30 , pp. 734-738
    • Ethell, B.1
  • 17
    • 0027394069 scopus 로고
    • The expression of UDP-glucuronosyltransferases of the UGT1 family in human liver and kidney and in response to drugs
    • Sutherland L et al. The expression of UDP-glucuronosyltransferases of the UGT1 family in human liver and kidney and in response to drugs. Biochem Pharmacol 1993; 45: 295-301.
    • (1993) Biochem Pharmacol , vol.45 , pp. 295-301
    • Sutherland, L.1
  • 18
    • 0032055273 scopus 로고    scopus 로고
    • Drug glucuronidation by human renal UDP-glucuronosyltransferases
    • McGurk KA et al. Drug glucuronidation by human renal UDP-glucuronosyltransferases. Biochem. Pharmacol 1998; 55: 1005-1012.
    • (1998) Biochem. Pharmacol , vol.55 , pp. 1005-1012
    • McGurk, K.A.1
  • 19
    • 0031022419 scopus 로고    scopus 로고
    • Human UGT2B7 catalyzes morphine glucuronidation
    • Coffman BL et al. Human UGT2B7 catalyzes morphine glucuronidation. Drug Metab Dispos 1997; 25: 1-4.
    • (1997) Drug Metab Dispos , vol.25 , pp. 1-4
    • Coffman, B.L.1
  • 20
    • 75749122702 scopus 로고    scopus 로고
    • Glucuronidation of catechols by human hepatic, gastric, and intestinal microsomal UDP-glucuronosyltransferases (UGT) and recombinant UGT1A6, UGT1A9, and UGT2B7
    • Antonio L et al. Glucuronidation of catechols by human hepatic, gastric, and intestinal microsomal UDP-glucuronosyltransferases (UGT) and recombinant UGT1A6, UGT1A9, and UGT2B7. Arch Biochem Biophys 2003; 478: 127-212.
    • (2003) Arch Biochem Biophys , vol.478 , pp. 127-212
    • Antonio, L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.