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Volumn 17, Issue 12, 2004, Pages 1652-1658

Characterization of the adducts formed in the reactions of glycidamide with thymidine and cytidine

Author keywords

[No Author keywords available]

Indexed keywords

ACRYLAMIDE DERIVATIVE; AMIDE; CYTIDINE; EPOXIDE; GLYCIDAMIDE; N3 (2 CARBAMOYL 2 HYDROXYETHYL)THYMIDINE; N3 (2 CARBOXY 2 HYDROXYETHYL)CYTIDINE; N3 (2 CARBOXY 2 HYDROXYETHYL)URIDINE; THYMIDINE; UNCLASSIFIED DRUG; URIDINE DERIVATIVE;

EID: 10844219851     PISSN: 0893228X     EISSN: None     Source Type: Journal    
DOI: 10.1021/tx049823i     Document Type: Article
Times cited : (16)

References (21)
  • 3
    • 0037015489 scopus 로고    scopus 로고
    • Acrylamide is formed in the Maillard reaction
    • Mottram, D. S., Wedzicha, B. L., and Dodson, A. T. (2002) Acrylamide is formed in the Maillard reaction. Nature 419, 448-449.
    • (2002) Nature , vol.419 , pp. 448-449
    • Mottram, D.S.1    Wedzicha, B.L.2    Dodson, A.T.3
  • 4
    • 0025000669 scopus 로고
    • Acrylamide is metabolized to glycidamide in the rat: Evidence from hemoglobin adduct formation
    • Calleman, C. J., Bergmark, E., and Costa, L. G. (1990) Acrylamide is metabolized to glycidamide in the rat: Evidence from hemoglobin adduct formation. Chem. Res. Toxicol. 3 (5), 406-412.
    • (1990) Chem. Res. Toxicol. , vol.3 , Issue.5 , pp. 406-412
    • Calleman, C.J.1    Bergmark, E.2    Costa, L.G.3
  • 5
    • 0029903973 scopus 로고    scopus 로고
    • The metabolism and pharmacokinetics of acrylamide: Implications for mechanisms of toxicity and human risk estimation
    • Calleman, C. J. (1996) The metabolism and pharmacokinetics of acrylamide: Implications for mechanisms of toxicity and human risk estimation. Drug Metab. Rev. 28 (4), 527-590.
    • (1996) Drug Metab. Rev. , vol.28 , Issue.4 , pp. 527-590
    • Calleman, C.J.1
  • 6
    • 0025840203 scopus 로고
    • Formation of hemoglobin adducts of acrylamide and its epoxide metabolite glycidamide in the rat
    • Bergmark, E., Calleman, C. J., and Costa, L. G. (1991) Formation of hemoglobin adducts of acrylamide and its epoxide metabolite glycidamide in the rat. Toxicol. Appl. Pharmacol. 111, 352-363.
    • (1991) Toxicol. Appl. Pharmacol. , vol.111 , pp. 352-363
    • Bergmark, E.1    Calleman, C.J.2    Costa, L.G.3
  • 7
    • 0026893695 scopus 로고
    • Linear versus nonlinear models for hemoglobin adduct formation by acrylamide and its metabolite glycidamide: Implications for risk estimation
    • Calleman, C. J., Stern, L. G., Bergmark, E., and Costa, L. G. (1992) Linear versus nonlinear models for hemoglobin adduct formation by acrylamide and its metabolite glycidamide: Implications for risk estimation. Cancer Epidemiol. Biomarkers Prev. 1, 361-368.
    • (1992) Cancer Epidemiol. Biomarkers Prev. , vol.1 , pp. 361-368
    • Calleman, C.J.1    Stern, L.G.2    Bergmark, E.3    Costa, L.G.4
  • 8
    • 0022412486 scopus 로고
    • Mutagenicity of acrylamide and its analogues in Salmonella typhimurium
    • Hashimoto, K., and Tanii, H. (1985) Mutagenicity of acrylamide and its analogues in Salmonella typhimurium. Mutat. Res. 158, 129-133.
    • (1985) Mutat. Res. , vol.158 , pp. 129-133
    • Hashimoto, K.1    Tanii, H.2
  • 9
    • 0021932011 scopus 로고
    • Direct alkylation of 2′-deoxynucleosides and DNA following in vitro reaction with acrylamide
    • Solomon, J. J., Fedyk, J., Mukai, F., and Segal, A. (1985) Direct alkylation of 2′-deoxynucleosides and DNA following in vitro reaction with acrylamide. Cancer Res. 45, 3465-3470.
    • (1985) Cancer Res. , vol.45 , pp. 3465-3470
    • Solomon, J.J.1    Fedyk, J.2    Mukai, F.3    Segal, A.4
  • 12
    • 0031408197 scopus 로고    scopus 로고
    • Characterization of four N-3-thymidine adducts formed in vitro by the reaction of thymidine and butadiene monoxide
    • Selzer, R. R., and Elfarra, A. A. (1997) Characterization of four N-3-thymidine adducts formed in vitro by the reaction of thymidine and butadiene monoxide. Carcinogenesis 18 (10), 1993-1998.
    • (1997) Carcinogenesis , vol.18 , Issue.10 , pp. 1993-1998
    • Selzer, R.R.1    Elfarra, A.A.2
  • 13
    • 0026507888 scopus 로고
    • Roles of the vinyl chloride oxidation products 2-chlorooxirane and 2-chloroacetaldehyde in the in vitro formation of etheno adducts of nucleic acid bases
    • Guengerich, F. P. (1992) Roles of the vinyl chloride oxidation products 2-chlorooxirane and 2-chloroacetaldehyde in the in vitro formation of etheno adducts of nucleic acid bases. Chem. Res. Toxicol. 5, 2-5.
    • (1992) Chem. Res. Toxicol. , vol.5 , pp. 2-5
    • Guengerich, F.P.1
  • 14
    • 0030614916 scopus 로고    scopus 로고
    • 2-ethenoguanine and 5,6,7,9-tetrahydro-7- hydroxy-9-oxoimidazo[1,2-a]purine in DNA treated with 2-chlorooxirane by high-performance liquid chroamtography/electrospray mass spectrometry and comparison of amounts to other DNA adducts
    • 2-ethenoguanine and 5,6,7,9-tetrahydro-7-hydroxy-9- oxoimidazo[1,2-a]purine in DNA treated with 2-chlorooxirane by high-performance liquid chroamtography/electrospray mass spectrometry and comparison of amounts to other DNA adducts. Chem. Res. Toxicol. 10, 242-247.
    • (1997) Chem. Res. Toxicol. , vol.10 , pp. 242-247
    • Muller, M.1    Belas, F.J.2    Blair, I.A.3    Guengerich, F.P.4
  • 15
    • 12244302243 scopus 로고    scopus 로고
    • Identification of adducts derived from reactions of (1-chloroethenyl) oxirane with nucleosides and calf thymus DNA
    • Munter, T., Cottrell, L., Hill, S., Kronberg, L., Watson, W. P., and Golding, B. T. (2002) Identification of adducts derived from reactions of (1-chloroethenyl)oxirane with nucleosides and calf thymus DNA. Chem. Res. Toxicol. 15, 1549-1560.
    • (2002) Chem. Res. Toxicol. , vol.15 , pp. 1549-1560
    • Munter, T.1    Cottrell, L.2    Hill, S.3    Kronberg, L.4    Watson, W.P.5    Golding, B.T.6
  • 19
    • 0023787141 scopus 로고
    • Reactions of propylene oxide with 2′-deoxynucleosides and in vitro with calf thymus DNA
    • Solomon, J. J., Mukai, F., Fedyk, J., and Segal, A. (1988) Reactions of propylene oxide with 2′-deoxynucleosides and in vitro with calf thymus DNA. Chem.-Biol. Interact. 67, 275-294.
    • (1988) Chem.-Biol. Interact. , vol.67 , pp. 275-294
    • Solomon, J.J.1    Mukai, F.2    Fedyk, J.3    Segal, A.4
  • 20
    • 0026773508 scopus 로고
    • In vitro reaction of ethylene oxide with DNA and characterization of DNA adducts
    • Li, F., Segal, A., and Solomon, J. J. (1992) In vitro reaction of ethylene oxide with DNA and characterization of DNA adducts. Chem.-Biol. Interact. 83, 35-54.
    • (1992) Chem.-Biol. Interact. , vol.83 , pp. 35-54
    • Li, F.1    Segal, A.2    Solomon, J.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.