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Volumn 45, Issue 11, 2007, Pages 2260-2265

Synthesis and antioxidant properties of fullero-steroidal covalent conjugates

Author keywords

[No Author keywords available]

Indexed keywords

BIOACTIVITY; COVALENT BONDS; FULLERENES; OXIDANTS; SYNTHESIS (CHEMICAL);

EID: 34548500386     PISSN: 00086223     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carbon.2007.06.027     Document Type: Article
Times cited : (31)

References (34)
  • 1
    • 33751386072 scopus 로고
    • Solubility of fullerene (C60) in a variety of solvents
    • Ruoff R.S., Tse D.S., Malhotra R., and Lorents D.C. Solubility of fullerene (C60) in a variety of solvents. J Phys Chem 97 13 (1993) 3379-3383
    • (1993) J Phys Chem , vol.97 , Issue.13 , pp. 3379-3383
    • Ruoff, R.S.1    Tse, D.S.2    Malhotra, R.3    Lorents, D.C.4
  • 2
    • 0028185194 scopus 로고
    • Purification of C60 and C70 by selective complexation with calixarenes
    • Atwood J.L., Koutsantonis G.A., and Raston C.L. Purification of C60 and C70 by selective complexation with calixarenes. Nature 368 6468 (1994) 229-231
    • (1994) Nature , vol.368 , Issue.6468 , pp. 229-231
    • Atwood, J.L.1    Koutsantonis, G.A.2    Raston, C.L.3
  • 3
    • 0028450551 scopus 로고
    • Photoinduced electron transfer properties of porous polymer membranes doped with the fullerene C60 associated with phospholipids
    • Garaud J.L., Janot J.M., Miquel G., and Seta P. Photoinduced electron transfer properties of porous polymer membranes doped with the fullerene C60 associated with phospholipids. J Membrane Sci 91 3 (1994) 259-264
    • (1994) J Membrane Sci , vol.91 , Issue.3 , pp. 259-264
    • Garaud, J.L.1    Janot, J.M.2    Miquel, G.3    Seta, P.4
  • 4
    • 0008524112 scopus 로고
    • Incorporation of C60 into artificial lipid membranes
    • Hungerbühler H., Guldi D.M., and Asmus K.D. Incorporation of C60 into artificial lipid membranes. J Am Chem Soc 115 8 (1993) 3386-3387
    • (1993) J Am Chem Soc , vol.115 , Issue.8 , pp. 3386-3387
    • Hungerbühler, H.1    Guldi, D.M.2    Asmus, K.D.3
  • 9
    • 0021964203 scopus 로고
    • Prooxidant states and tumor promotion
    • Cerutti P.A. Prooxidant states and tumor promotion. Science 227 4685 (1985) 375-381
    • (1985) Science , vol.227 , Issue.4685 , pp. 375-381
    • Cerutti, P.A.1
  • 10
    • 0017118879 scopus 로고
    • Identification of singlet oxygen as the cytotoxic agent in photoinactivation of a murine tumor
    • Weishaupt K.R., Gomer C.J., and Dougherty T.J. Identification of singlet oxygen as the cytotoxic agent in photoinactivation of a murine tumor. Cancer Res 36 7part1 (1976) 2326-2329
    • (1976) Cancer Res , vol.36 , Issue.7 part1 , pp. 2326-2329
    • Weishaupt, K.R.1    Gomer, C.J.2    Dougherty, T.J.3
  • 11
    • 0026935528 scopus 로고
    • Importance of type I and type II mechanisms in the photodynamic inactivation of viruses in blood with aluminium phthalocyanine derivatives
    • Rywkin S., Leny L., Goldstein J., Geacintov N.E., Margolis-Nunno H., and Horowitz B. Importance of type I and type II mechanisms in the photodynamic inactivation of viruses in blood with aluminium phthalocyanine derivatives. Photochem Photobiol 56 4 (1992) 463-469
    • (1992) Photochem Photobiol , vol.56 , Issue.4 , pp. 463-469
    • Rywkin, S.1    Leny, L.2    Goldstein, J.3    Geacintov, N.E.4    Margolis-Nunno, H.5    Horowitz, B.6
  • 13
    • 7544226477 scopus 로고    scopus 로고
    • The differential cytotoxicity of water-soluble fullerenes
    • Sayes C.M., Fortner J.D., Guo W., Lyon D., Boyd A.M., Ausman K.D., et al. The differential cytotoxicity of water-soluble fullerenes. Nano Lett 4 10 (2004) 1881-1887
    • (2004) Nano Lett , vol.4 , Issue.10 , pp. 1881-1887
    • Sayes, C.M.1    Fortner, J.D.2    Guo, W.3    Lyon, D.4    Boyd, A.M.5    Ausman, K.D.6
  • 14
    • 10744226839 scopus 로고    scopus 로고
    • Detection of 1270 nm emission from singlet oxygen and photocytotoxic property of sugar-pendant [60]fullerenes
    • Mikata Y., Takagi S., Tanahashi M., Ishii S., Obata M., Miayamoto Y., et al. Detection of 1270 nm emission from singlet oxygen and photocytotoxic property of sugar-pendant [60]fullerenes. Biorg Med Chem Lett 13 19 (2003) 3289-3292
    • (2003) Biorg Med Chem Lett , vol.13 , Issue.19 , pp. 3289-3292
    • Mikata, Y.1    Takagi, S.2    Tanahashi, M.3    Ishii, S.4    Obata, M.5    Miayamoto, Y.6
  • 15
    • 20444494391 scopus 로고    scopus 로고
    • Fullerene-pyropheophorbide a complexes as sensitizer for photodynamic therapy: Uptake and photo-induced cytotoxicity on Jurkat cells
    • Rancan F., Helmreich M., Mölich A., Jux N., Hirsch A., Roder B., et al. Fullerene-pyropheophorbide a complexes as sensitizer for photodynamic therapy: Uptake and photo-induced cytotoxicity on Jurkat cells. J Photochem Photobiol B 80 1 (2005) 1-7
    • (2005) J Photochem Photobiol B , vol.80 , Issue.1 , pp. 1-7
    • Rancan, F.1    Helmreich, M.2    Mölich, A.3    Jux, N.4    Hirsch, A.5    Roder, B.6
  • 16
    • 24644507264 scopus 로고    scopus 로고
    • Photodynamic effect of hydrophilic C60-derived nanostructures for catalytic antitumoral antibacterial applications
    • Yu C., Canteenwala T., Chiang L.Y., Wilson B., and Pritzker K. Photodynamic effect of hydrophilic C60-derived nanostructures for catalytic antitumoral antibacterial applications. Synthetic Metals 153 1-3 (2005) 37-40
    • (2005) Synthetic Metals , vol.153 , Issue.1-3 , pp. 37-40
    • Yu, C.1    Canteenwala, T.2    Chiang, L.Y.3    Wilson, B.4    Pritzker, K.5
  • 17
    • 34548476415 scopus 로고    scopus 로고
    • Kronholm DL, Hummelen JC, Sieval AB. High efficiency fullerene-based radical scavengers. US pat WO2005058002 A2, 2005.
  • 18
    • 0033523845 scopus 로고    scopus 로고
    • C60 and water-soluble fullerene derivatives as antioxidants against radical-initiated lipid peroxidation
    • Wang I.C., Tai L.A., Lee D.D., Kanakamma P.P., Shen C.K.F., Luh T.Y., et al. C60 and water-soluble fullerene derivatives as antioxidants against radical-initiated lipid peroxidation. J Med Chem 42 22 (1999) 4614-4620
    • (1999) J Med Chem , vol.42 , Issue.22 , pp. 4614-4620
    • Wang, I.C.1    Tai, L.A.2    Lee, D.D.3    Kanakamma, P.P.4    Shen, C.K.F.5    Luh, T.Y.6
  • 19
    • 1542509424 scopus 로고    scopus 로고
    • Different radical scavenging activity of water soluble β-alanine C60 adducts
    • Sun T., Jia Z., and Xu Z. Different radical scavenging activity of water soluble β-alanine C60 adducts. Bioorg Med Chem Lett 14 7 (2004) 1779-1781
    • (2004) Bioorg Med Chem Lett , vol.14 , Issue.7 , pp. 1779-1781
    • Sun, T.1    Jia, Z.2    Xu, Z.3
  • 20
    • 0036452073 scopus 로고    scopus 로고
    • Interaction of a water soluble fullerene derivative with reactive oxygen species and model enzymatic systems
    • Foley S., Curtis A.D.M., Hirsch A., Brettreich M., Pelegrin A., Seta P., et al. Interaction of a water soluble fullerene derivative with reactive oxygen species and model enzymatic systems. Full Nanotubes Carb Nanostruc 10 1 (2002) 49-67
    • (2002) Full Nanotubes Carb Nanostruc , vol.10 , Issue.1 , pp. 49-67
    • Foley, S.1    Curtis, A.D.M.2    Hirsch, A.3    Brettreich, M.4    Pelegrin, A.5    Seta, P.6
  • 21
    • 33845890057 scopus 로고    scopus 로고
    • Antioxidant activity of supramolecular water-soluble fullerenes evaluated by β-carotene bleaching assay
    • Takada H., Kokubo K., Matsubayashi K., and Oshima T. Antioxidant activity of supramolecular water-soluble fullerenes evaluated by β-carotene bleaching assay. Biosci Biotechnol Biochem 70 12 (2006) 3088-3093
    • (2006) Biosci Biotechnol Biochem , vol.70 , Issue.12 , pp. 3088-3093
    • Takada, H.1    Kokubo, K.2    Matsubayashi, K.3    Oshima, T.4
  • 26
    • 0343924391 scopus 로고    scopus 로고
    • The synthesis and biological evaluation of A-ring substituted steroidal p-quinones
    • Milić D., Gašić M.J., Muster W., Csanadi J.J., and Šolaja B.A. The synthesis and biological evaluation of A-ring substituted steroidal p-quinones. Tetrahedron 53 41 (1997) 14073-14084
    • (1997) Tetrahedron , vol.53 , Issue.41 , pp. 14073-14084
    • Milić, D.1    Gašić, M.J.2    Muster, W.3    Csanadi, J.J.4    Šolaja, B.A.5
  • 27
    • 0035921015 scopus 로고    scopus 로고
    • Synthesis and antiproliferative activity of epoxy and bromo compounds derived from estrone
    • Milić D.R., Kop T., Juranić Z., Gašić M.J., and Solaja B.A. Synthesis and antiproliferative activity of epoxy and bromo compounds derived from estrone. Bioorg Med Chem Lett 11 16 (2001) 2197-2200
    • (2001) Bioorg Med Chem Lett , vol.11 , Issue.16 , pp. 2197-2200
    • Milić, D.R.1    Kop, T.2    Juranić, Z.3    Gašić, M.J.4    Solaja, B.A.5
  • 28
    • 27844533964 scopus 로고    scopus 로고
    • Synthesis and antiproliferative activity of A-ring aromatised and conduritol-like steroidal compounds
    • Milić D., Kop T., Juranić Z., Gašić M.J., Tinant B., Pocsfalvi G., et al. Synthesis and antiproliferative activity of A-ring aromatised and conduritol-like steroidal compounds. Steroids 70 14 (2005) 922-932
    • (2005) Steroids , vol.70 , Issue.14 , pp. 922-932
    • Milić, D.1    Kop, T.2    Juranić, Z.3    Gašić, M.J.4    Tinant, B.5    Pocsfalvi, G.6
  • 29
    • 0342677835 scopus 로고
    • Addition of azomethine ylides to C60: synthesis, characterization, and functionalization of fullerene pyrrolidines
    • Maggini M., Scorrano G., and Prato M. Addition of azomethine ylides to C60: synthesis, characterization, and functionalization of fullerene pyrrolidines. J Am Chem Soc 115 21 (1993) 9798-9799
    • (1993) J Am Chem Soc , vol.115 , Issue.21 , pp. 9798-9799
    • Maggini, M.1    Scorrano, G.2    Prato, M.3
  • 30
    • 23844497142 scopus 로고    scopus 로고
    • Preparation of highly stable organic steps with a fullerene-based molecule
    • GABA-OtBu can also be obtained by one-step esterification of the unprotected amino acid with iso-butene over 24 h in low yield (32%):
    • GABA-OtBu can also be obtained by one-step esterification of the unprotected amino acid with iso-butene over 24 h in low yield (32%):. Burghardt S., Hirsch A., Medard N., Kachfhe R.A., Ausseré D., Valignat M.P., et al. Preparation of highly stable organic steps with a fullerene-based molecule. Langmuir 21 16 (2005) 7540-7544
    • (2005) Langmuir , vol.21 , Issue.16 , pp. 7540-7544
    • Burghardt, S.1    Hirsch, A.2    Medard, N.3    Kachfhe, R.A.4    Ausseré, D.5    Valignat, M.P.6
  • 31
    • 10744225610 scopus 로고    scopus 로고
    • Synthesis of a proline-rich [60]fullerene peptide with potential biological activity
    • Sofou P., Elemes Y., Panou-Pomonis E., Stavrakoudis A., Tsikaris V., Sakarellos C., et al. Synthesis of a proline-rich [60]fullerene peptide with potential biological activity. Tetrahedron 60 12 (2004) 2823-2828
    • (2004) Tetrahedron , vol.60 , Issue.12 , pp. 2823-2828
    • Sofou, P.1    Elemes, Y.2    Panou-Pomonis, E.3    Stavrakoudis, A.4    Tsikaris, V.5    Sakarellos, C.6
  • 32
    • 0031805269 scopus 로고    scopus 로고
    • Antioxidant activity of extracts obtained by different isolation procedures from some aromatic herbs grown in Lithuania
    • Dapkevicius A., Venskutonis R., Van Beek T.A., and Linssen J.P.H. Antioxidant activity of extracts obtained by different isolation procedures from some aromatic herbs grown in Lithuania. J Sci Food Agricult 77 1 (1998) 140-146
    • (1998) J Sci Food Agricult , vol.77 , Issue.1 , pp. 140-146
    • Dapkevicius, A.1    Venskutonis, R.2    Van Beek, T.A.3    Linssen, J.P.H.4
  • 34
    • 0031176960 scopus 로고    scopus 로고
    • Quantitative spectroscopic studies of the photoexcited state properties of methano- and pyrrolidino-[60]fullerene derivatives
    • Ma B., Bunker C.E., Guduru R., Zhang X., and Sun Y.P. Quantitative spectroscopic studies of the photoexcited state properties of methano- and pyrrolidino-[60]fullerene derivatives. J Phys Chem A 101 31 (1997) 5626-5632
    • (1997) J Phys Chem A , vol.101 , Issue.31 , pp. 5626-5632
    • Ma, B.1    Bunker, C.E.2    Guduru, R.3    Zhang, X.4    Sun, Y.P.5


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