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Volumn 2, Issue 11, 2003, Pages 1200-1204

Steady-state and time-resolved studies on the formation of skatolyl radicals photosensitized by 2-benzoylthiophene

Author keywords

[No Author keywords available]

Indexed keywords

2 BENZOYLTHIOPHENE DERIVATIVE; DIMER; SKATOLE;

EID: 19844382412     PISSN: 1474905X     EISSN: 14749092     Source Type: Journal    
DOI: 10.1039/b307346g     Document Type: Article
Times cited : (4)

References (24)
  • 1
    • 0030050265 scopus 로고    scopus 로고
    • Mechanistic studies on the cytochrome P450 catalysed dehydrogenation of 3-methylindole
    • and references therein
    • (a) G. L. Skiles and G. S. Yost, Mechanistic studies on the cytochrome P450 catalysed dehydrogenation of 3-methylindole, Chem. Res. Toxicol., 1996, 9, 291-297 and references therein;
    • (1996) Chem. Res. Toxicol. , vol.9 , pp. 291-297
    • Skiles, G.L.1    Yost, G.S.2
  • 2
    • 0028359812 scopus 로고
    • Identification of 3-MI-derived N-centered radicals obtained from incubation of 3-MI with micromosomal-NADPH system by EPR-HPLC spin trapping
    • (b) G. Chen, E. G. Janzen and T. M. Bray, Identification of 3-MI-derived N-centered radicals obtained from incubation of 3-MI with micromosomal-NADPH system by EPR-HPLC spin trapping, Free-Radical Biol. Med., 1994, 17, 19-25.
    • (1994) Free-Radical Biol. Med. , vol.17 , pp. 19-25
    • Chen, G.1    Janzen, E.G.2    Bray, T.M.3
  • 3
    • 0036015564 scopus 로고    scopus 로고
    • Indole-3-acetic acids and horseradish peroxidase: A new prodrug/enzyme combination for targeted cancer therapy
    • P. Wardman, Indole-3-acetic acids and horseradish peroxidase: a new prodrug/enzyme combination for targeted cancer therapy, Curr. Pharm. Des., 2002, 8, 1363-1374.
    • (2002) Curr. Pharm. Des. , vol.8 , pp. 1363-1374
    • Wardman, P.1
  • 4
    • 0029410838 scopus 로고
    • Enhancement of lipid peroxidation by indole-3-acetic acid and derivatives: Substituent effects
    • L. P. Candeias, L. K. Folkes, M. Porssa, J. Parrick and P. Wardman, Enhancement of lipid peroxidation by indole-3-acetic acid and derivatives: substituent effects, Free Radical Res., 1995, 23, 403-418.
    • (1995) Free Radical Res. , vol.23 , pp. 403-418
    • Candeias, L.P.1    Folkes, L.K.2    Porssa, M.3    Parrick, J.4    Wardman, P.5
  • 5
    • 84981669996 scopus 로고
    • Quenching of triplet states of aromatic ketones by indole and 3-methylindole in benzene solution. Evidence for hydrogen-atom abstraction, for quenching due to favourable charge transfer interaction and for the lack of electronic energy transfer
    • F. Wilkinson and A. Garner, Quenching of triplet states of aromatic ketones by indole and 3-methylindole in benzene solution. Evidence for hydrogen-atom abstraction, for quenching due to favourable charge transfer interaction and for the lack of electronic energy transfer, Photochem. Photobiol., 1978, 27, 659-670.
    • (1978) Photochem. Photobiol. , vol.27 , pp. 659-670
    • Wilkinson, F.1    Garner, A.2
  • 6
    • 0026219295 scopus 로고
    • Reactivity of tert-butoxyl radicals towards substituted indole derivatives
    • M. V. Encinas, E. A. Lissi and C. Majmud, Reactivity of tert-butoxyl radicals towards substituted indole derivatives, Int. J. Chem. Kinet., 1991, 23, 761-766.
    • (1991) Int. J. Chem. Kinet. , vol.23 , pp. 761-766
    • Encinas, M.V.1    Lissi, E.A.2    Majmud, C.3
  • 7
    • 0035526568 scopus 로고    scopus 로고
    • Photoreactivity of the nonsteroidal anti-inflammatory 2-arylpropionic acids with photosensitizing side effects
    • F. Boscá, M. L. Marín and M. A. Miranda, Photoreactivity of the nonsteroidal anti-inflammatory 2-arylpropionic acids with photosensitizing side effects, Photochem. Photobiol., 2001, 74, 637-655.
    • (2001) Photochem. Photobiol. , vol.74 , pp. 637-655
    • Boscá, F.1    Marín, M.L.2    Miranda, M.A.3
  • 8
    • 0028003309 scopus 로고
    • Photodynamic lipid peroxidation by the photosensitizing nonsteroidal antiinflammatory drugs suprofen and tiaprofenic acid
    • J. V. Castell, M. J. Gómez-Lechón, C. Grassa, L. Martínez, M. A. Miranda and P. Tarrega, Photodynamic lipid peroxidation by the photosensitizing nonsteroidal antiinflammatory drugs suprofen and tiaprofenic acid, Photochem. Photobiol., 1994, 59, 35-39.
    • (1994) Photochem. Photobiol. , vol.59 , pp. 35-39
    • Castell, J.V.1    Gómez-Lechón, M.J.2    Grassa, C.3    Martínez, L.4    Miranda, M.A.5    Tarrega, P.6
  • 10
    • 0032215524 scopus 로고    scopus 로고
    • Photobinding of tiaprofenic acid and suprofen to proteins and cells: A combined study using radiolabeling, antibodies and laser flash photolysis of model bichromophores
    • J. V. Castell, D. Hernández, M. J. Gómez-Lechón, A. Lahoz, M. A. Miranda, I. M. Morera, J. Pérez-Prieto and Z. Sarabia, Photobinding of tiaprofenic acid and suprofen to proteins and cells: a combined study using radiolabeling, antibodies and laser flash photolysis of model bichromophores, Photochem. Photobiol., 1998, 68, 660-665.
    • (1998) Photochem. Photobiol. , vol.68 , pp. 660-665
    • Castell, J.V.1    Hernández, D.2    Gómez-Lechón, M.J.3    Lahoz, A.4    Miranda, M.A.5    Morera, I.M.6    Pérez-Prieto, J.7    Sarabia, Z.8
  • 11
    • 0031889244 scopus 로고    scopus 로고
    • Drug-photosensitized protein modification: Identification of the reactive sites and elucidation of the reaction mechanisms with tiaprofenic acid albumin as model system
    • (a) M. A. Miranda, J. V. Castell, D. Hernández, M. J. Gómez-Lechón, F. Bosca, I. M. Morera and Z. Sarabia, Drug-photosensitized protein modification: identification of the reactive sites and elucidation of the reaction mechanisms with tiaprofenic acid albumin as model system, Chem. Res. Toxicol., 1998, 11, 172-177;
    • (1998) Chem. Res. Toxicol. , vol.11 , pp. 172-177
    • Miranda, M.A.1    Castell, J.V.2    Hernández, D.3    Gómez-Lechón, M.J.4    Bosca, F.5    Morera, I.M.6    Sarabia, Z.7
  • 14
    • 0034286911 scopus 로고    scopus 로고
    • Sequence specificity of alkali-labile DNA damage photosensitized by suprofen
    • (b) S. M. Starrs and R. J. H. Davies, Sequence specificity of alkali-labile DNA damage photosensitized by suprofen, Photochem. Photobiol., 2000, 72, 291-297;
    • (2000) Photochem. Photobiol. , vol.72 , pp. 291-297
    • Starrs, S.M.1    Davies, R.J.H.2
  • 15
    • 0026201398 scopus 로고
    • Mechanism of DNA cleavage mediated by photoexcited nonsteroidal antiinflammatory drugs
    • T. Artuso, J. Bernadou, B. Meunier, J. Piette and N. Paillous, Mechanism of DNA cleavage mediated by photoexcited nonsteroidal antiinflammatory drugs, Photochem. Photobiol., 1991, 54, 205-213.
    • (1991) Photochem. Photobiol. , vol.54 , pp. 205-213
    • Artuso, T.1    Bernadou, J.2    Meunier, B.3    Piette, J.4    Paillous, N.5
  • 16
    • 33751154998 scopus 로고
    • Photophysical properties of some thienyl ketones: An experimental and theoretical study
    • (a) R. S. Becker, G. Favaro, G. Poggi and A. Romani, Photophysical properties of some thienyl ketones: an experimental and theoretical study, J. Phys. Chem., 1995, 99, 1410-1417;
    • (1995) J. Phys. Chem. , vol.99 , pp. 1410-1417
    • Becker, R.S.1    Favaro, G.2    Poggi, G.3    Romani, A.4
  • 17
    • 0001243456 scopus 로고
    • Photochemical reactivity of some benzoylthiophenes. Electronic absorption and emission spectra
    • (b) D. R. Arnold and R. J. Birtwell, Photochemical reactivity of some benzoylthiophenes. Electronic absorption and emission spectra, J. Am. Chem. Soc., 1973, 95, 4599-4605.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 4599-4605
    • Arnold, D.R.1    Birtwell, R.J.2
  • 19
    • 0000226127 scopus 로고
    • Substituent effects on the spectral, acid-base, and redox properties of indolyl radicals - A pulse-radiolysis study
    • S. V. Jovanovic and S. J. Steenken, Substituent effects on the spectral, acid-base, and redox properties of indolyl radicals - a pulse-radiolysis study, J. Phys. Chem., 1992, 96, 6674-6679.
    • (1992) J. Phys. Chem. , vol.96 , pp. 6674-6679
    • Jovanovic, S.V.1    Steenken, S.J.2
  • 20
    • 27944485095 scopus 로고
    • Réduction électrochimique sur électrode de mercure du benzoyl-2-thiophène dans l'acétonitrile
    • (a) P. Foulatier, J. P. Salaun and C. Caullet, Réduction électrochimique sur électrode de mercure du benzoyl-2- thiophène dans l'acétonitrile, C. R. Seances Acad. Sci., Ser. C, 1974, 279, 779-783;
    • (1974) C. R. Seances Acad. Sci., Ser. C , vol.279 , pp. 779-783
    • Foulatier, P.1    Salaun, J.P.2    Caullet, C.3
  • 21
    • 0038370686 scopus 로고
    • The pinacol rearrangement in the heterocyclic series. II. Thiophene and furan analogs of benzopinacol
    • (b) M. R. Kegelman and E. V. Brown, The pinacol rearrangement in the heterocyclic series. II. Thiophene and furan analogs of benzopinacol, J. Am. Chem. Soc., 1953, 75, 5961-5963.
    • (1953) J. Am. Chem. Soc. , vol.75 , pp. 5961-5963
    • Kegelman, M.R.1    Brown, E.V.2
  • 22
    • 84952487948 scopus 로고
    • A novel N-amination method and its application to the preparation of N-aminoheterocycles
    • M. Somei, M. Matsuraba, Y. Kanda and M. Natsume, A novel N-amination method and its application to the preparation of N-aminoheterocycles, Chem. Pharm. Bull., 1978, 26, 2522-2534.
    • (1978) Chem. Pharm. Bull. , vol.26 , pp. 2522-2534
    • Somei, M.1    Matsuraba, M.2    Kanda, Y.3    Natsume, M.4
  • 23
    • 7944238142 scopus 로고
    • 2-(Indol-3′-yl)-2-hydroxy-N,N-dimethylethylamine (4) and 2-(indol-3′-yl)-2-(3″-[2‴-N,N-dimethyl-amino-ethyl] indol-2″-yl)-N,N-dimethylethylamine (1), by products in the LAH reduction of 3-indoleglyoxyl-N,N-dimethylamide
    • D. Crookes, K. Parry and G. Smith, 2-(Indol-3′-yl)-2-hydroxy-N,N- dimethylethylamine (4) and 2-(indol-3′-yl)-2-(3″-[2‴-N,N- dimethyl-amino-ethyl]indol-2″-yl)-N,N-dimethylethylamine (1), by products in the LAH reduction of 3-indoleglyoxyl-N,N-dimethylamide, Pol. J. Chem., 1979, 53, 73-78.
    • (1979) Pol. J. Chem. , vol.53 , pp. 73-78
    • Crookes, D.1    Parry, K.2    Smith, G.3
  • 24
    • 27944476175 scopus 로고
    • Stoichiometrically sensitized decarboxylation occurring in a molecular crystal composed of phenanthridine and 3-indoleacetic acid
    • H. Hoshima, K. Ding and T. Matsuura, Stoichiometrically sensitized decarboxylation occurring in a molecular crystal composed of phenanthridine and 3-indoleacetic acid, J. Chem. Soc., Chem. Commun., 1995, 2053-2054.
    • (1995) J. Chem. Soc., Chem. Commun. , pp. 2053-2054
    • Hoshima, H.1    Ding, K.2    Matsuura, T.3


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