메뉴 건너뛰기




Volumn 11, Issue 5, 1998, Pages 454-463

Reactivity of haloketenes and halothioketenes with nucleobases: Chemical characterization of reaction products

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; ALKENE; CYTOSINE; GUANINE; KETENE DERIVATIVE; NUCLEIC ACID BASE; THYMINE;

EID: 0039991859     PISSN: 0893228X     EISSN: None     Source Type: Journal    
DOI: 10.1021/tx9701438     Document Type: Article
Times cited : (15)

References (24)
  • 1
    • 0006366992 scopus 로고
    • Toxizität chlororganischer Verbindungen: Einfluβ der Einführung von Chlor in organische Moleküle. (Toxicity of chloro-organic compounds: the effect of a chloro-atom to organic molecules.)
    • Henschler, D. (1994) Toxizität chlororganischer Verbindungen: Einfluβ der Einführung von Chlor in organische Moleküle. (Toxicity of chloro-organic compounds: the effect of a chloro-atom to organic molecules.) Angew. Chem. 106, 1997-2012.
    • (1994) Angew. Chem. , vol.106 , pp. 1997-2012
    • Henschler, D.1
  • 2
    • 0024514780 scopus 로고
    • Metabolism of the nephrotoxin dichloroacetylene by glutathione conjugation
    • Kanhai, W., Dekant, W., and Henschler, D. (1989) Metabolism of the nephrotoxin dichloroacetylene by glutathione conjugation. Chem. Res. Toxicol. 2, 51-56.
    • (1989) Chem. Res. Toxicol. , vol.2 , pp. 51-56
    • Kanhai, W.1    Dekant, W.2    Henschler, D.3
  • 4
    • 0000666578 scopus 로고
    • Thioketene formation from α-haloalkenyl 2-nitrophenyl disulfides: Models for biological reactive intermediates of cytotoxic S-conjugates
    • Dekant, W., Urban, G., Görsman, C., and Anders, M. W. (1991) Thioketene formation from α-haloalkenyl 2-nitrophenyl disulfides: models for biological reactive intermediates of cytotoxic S-conjugates. J. Am. Chem. Soc. 113, 5120-5122.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 5120-5122
    • Dekant, W.1    Urban, G.2    Görsman, C.3    Anders, M.W.4
  • 5
    • 0017009654 scopus 로고
    • Chemical reactivity, biotransformation, and toxicity of polychlorinated aliphatic compounds
    • Bonse, G., and Henschler, D. (1976) Chemical reactivity, biotransformation, and toxicity of polychlorinated aliphatic compounds. Crit. Rev. Toxicol. 4, 395-409.
    • (1976) Crit. Rev. Toxicol. , vol.4 , pp. 395-409
    • Bonse, G.1    Henschler, D.2
  • 6
    • 0020473257 scopus 로고
    • Oxidation of trichloroethylene by liver microsomal cytochrome P-450: Evidence for chlorine migration in a transition state not involving trichloroethylene oxide
    • Miller, R. E., and Guengerich, F. P. (1982) Oxidation of trichloroethylene by liver microsomal cytochrome P-450: evidence for chlorine migration in a transition state not involving trichloroethylene oxide. Biochemistry 21, 1090-1097.
    • (1982) Biochemistry , vol.21 , pp. 1090-1097
    • Miller, R.E.1    Guengerich, F.P.2
  • 8
    • 0342626039 scopus 로고
    • Bioactivation of halogenated xenobiotics by S-conjugate formation
    • Anders, M. W., Dekant, W., Henschler, D., Oberleithner, H., and Silbernagl, S., Eds., Academic Press, San Diego
    • Dekant, W., Anders, M. W., and Monks, J. (1993) Bioactivation of halogenated xenobiotics by S-conjugate formation. In Renal Disposition and Nephrotoxicity of Xenobiotics (Anders, M. W., Dekant, W., Henschler, D., Oberleithner, H., and Silbernagl, S., Eds.) pp 187-215, Academic Press, San Diego.
    • (1993) Renal Disposition and Nephrotoxicity of Xenobiotics , pp. 187-215
    • Dekant, W.1    Anders, M.W.2    Monks, J.3
  • 9
    • 0020997740 scopus 로고
    • New pathways of trichloroethylene metabolism
    • Hayes, A. W., Schnell, R. C., and Miya, T. S., Eds., Elsevier Science Publishers, Amsterdam
    • Dekant, W., and Henschler, D. (1983) New pathways of trichloroethylene metabolism. In Developments in the Science and Practice of Toxicology (Hayes, A. W., Schnell, R. C., and Miya, T. S., Eds.) pp 399-402, Elsevier Science Publishers, Amsterdam.
    • (1983) Developments in the Science and Practice of Toxicology , pp. 399-402
    • Dekant, W.1    Henschler, D.2
  • 12
    • 0023034215 scopus 로고
    • Quantitation of etheno adducts by fluorescence detection
    • Bedell, M. A., Dyroff, M. C., Doerjer, G., and Swenberg, J. A. (1986) Quantitation of etheno adducts by fluorescence detection. IARC Sci. Pub. 70, 425-434.
    • (1986) IARC Sci. Pub. , vol.70 , pp. 425-434
    • Bedell, M.A.1    Dyroff, M.C.2    Doerjer, G.3    Swenberg, J.A.4
  • 13
    • 85065121461 scopus 로고
    • Halogenated ketenes: Valuable intermediates in organic synthesis
    • Brady, W. T. (1971) Halogenated ketenes: valuable intermediates in organic synthesis. Synthesis 415-422.
    • (1971) Synthesis , pp. 415-422
    • Brady, W.T.1
  • 14
    • 84918061692 scopus 로고
    • Herstellung und Umwandlung von Ketenen
    • Müller, Eu., Ed. VII/4, Georg Thieme Verlag, Stuttgart, New York
    • Bormann, D. (1968) Herstellung und Umwandlung von Ketenen. In Houben Weyl, Methoden der Organischen Chemie, 4th ed. (Müller, Eu., Ed.) VII/4, p 65, Georg Thieme Verlag, Stuttgart, New York.
    • (1968) Houben Weyl, Methoden der Organischen Chemie, 4th Ed. , pp. 65
    • Bormann, D.1
  • 15
    • 0345329665 scopus 로고
    • The chemistry of thioketenes - Tetrahedron Report No. 231
    • Schaumann, E. (1988) The chemistry of thioketenes - Tetrahedron Report No. 231. Tetrahedron 44, 1827-1871.
    • (1988) Tetrahedron , vol.44 , pp. 1827-1871
    • Schaumann, E.1
  • 16
    • 0017786671 scopus 로고
    • 2,3-ethenoguanine. Synthesis and comparison of the electronic spectral properties of these linear and angular triheterocycles related to the Y bases
    • 2,3-ethenoguanine. Synthesis and comparison of the electronic spectral properties of these linear and angular triheterocycles related to the Y bases. J. Org. Chem. 42, 3292-3296.
    • (1977) J. Org. Chem. , vol.42 , pp. 3292-3296
    • Sattsangi, P.D.1    Leonard, N.J.2    Frihart, C.R.3
  • 17
    • 2642614515 scopus 로고
    • Effect of acid concentration on the partitioning of the tetrahedral intermediate in the hydrolysis of thioacetanilide
    • Edward, J. T., and Wong, S. C. (1979) Effect of acid concentration on the partitioning of the tetrahedral intermediate in the hydrolysis of thioacetanilide. J. Org. Chem. 101, 1807-1809.
    • (1979) J. Org. Chem. , vol.101 , pp. 1807-1809
    • Edward, J.T.1    Wong, S.C.2
  • 19
    • 0015220685 scopus 로고
    • The preparation and properties of some cytosine derivatives
    • Goody, R. S., and Walker, R. T. (1970) The preparation and properties of some cytosine derivatives. J. Org. Chem. 36, 727-730.
    • (1970) J. Org. Chem. , vol.36 , pp. 727-730
    • Goody, R.S.1    Walker, R.T.2
  • 20
    • 0014607194 scopus 로고
    • 6-(α-aminoacyl)adenines into N-(6-purinyl)amino acids
    • 6-(α-aminoacyl)adenines into N-(6-purinyl)amino acids. J. Org. Chem. 34, 3498-3502.
    • (1968) J. Org. Chem. , vol.34 , pp. 3498-3502
    • Chheda, G.B.1    Hall, R.H.2
  • 21
    • 0013915716 scopus 로고
    • 6-(α-aminoacyl)adenines into N-(6-purinyl)amino acids
    • 6-(α-aminoacyl)adenines into N-(6-purinyl)amino acids. Biochemistry 5, 2082-2091.
    • (1966) Biochemistry , vol.5 , pp. 2082-2091
    • Chheda, G.B.1    Hall, R.H.2
  • 22
    • 0014607289 scopus 로고
    • 6-(α-aminoacyl)adenines to-N-(6-purinyl)-amino acids. Application to adenosine analogue
    • 6-(α-aminoacyl)adenines to-N-(6-purinyl)-amino acids. Application to adenosine analogue. J. Org. Chem. 34, 2082-2091.
    • (1968) J. Org. Chem. , vol.34 , pp. 2082-2091
    • Chheda, G.B.1    Hall, R.H.2
  • 23
    • 0022960951 scopus 로고
    • Substituted ethenoadenosines and ethenocytidines
    • Leonard, N. J., and Cruickshank, K. A. (1986) Substituted ethenoadenosines and ethenocytidines. IARC Sci. Pub. 70, 33-36.
    • (1986) IARC Sci. Pub. , vol.70 , pp. 33-36
    • Leonard, N.J.1    Cruickshank, K.A.2
  • 24
    • 0028216653 scopus 로고
    • Formation, detection, and role in carcinogenesis of ethenobases in DNA
    • Bartsch, H., Barbin, A., Marion, M.-J., Nair, J., and Guichard, Y. (1994) Formation, detection, and role in carcinogenesis of ethenobases in DNA. Drug Metab. Rev. 26, 349-372.
    • (1994) Drug Metab. Rev. , vol.26 , pp. 349-372
    • Bartsch, H.1    Barbin, A.2    Marion, M.-J.3    Nair, J.4    Guichard, Y.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.