Pure and Applied Chemistry, 2011, Volume 83, No. 4, pp. 801-811, References

Pure Appl. Chem., 2011, Vol. 83, No. 4, pp. 801-811

http://dx.doi.org/10.1351/PAC-CON-10-08-22

Published online 2010-12-15

Production and quenching of reactive oxygen species by pterin derivatives, an intriguing class of biomolecules

Esther Oliveros¹*, Maria Laura Dántola², Mariana Vignoni², Andrés H. Thomas² and Carolina Lorente²*

¹ IMRCP Laboratory, UMR CNRS/UPS 5623, Paul Sabatier University (Toulouse III), 118 route de Narbonne, F-31062 Toulouse cédex 9, France
² INIFTA, Department of Chemistry, Faculty of Sciences, National University of La Plata, -CCT La Plata-CONICET, Casilla de Correo 16, Sucursal 4, (1900) La Plata, Argentina

References

1. W. Pfleiderer. In Chemistry and Biology of Pteridines and Folates, J. E. Ayling, M. G. Nair, C. M. Baugh (Eds.), pp. 1–16, Plenum Press, New York (1993).
2. T. J. Kappock, J. P. Caradonna. Chem. Rev. 96, 2659 (1996). (http://dx.doi.org/10.1021/cr9402034)
3. G. Maharaj, B. S. Selinsky, J. R. Appleman, M. Perlman, R. E. London, R. L. Bakley. Biochemistry 29, 4554 (1990). (http://dx.doi.org/10.1021/bi00471a008)
4. A. Albert. Biochem. J. 54, 646 (1953).
5. R. L. Blakley. The Biochemistry of Folic Acid and Related Pteridines, North-Holland, Amsterdam (1969).
6. C. A. Nichol, G. K. Smith, D. Duch. Annu. Rev. Biochem. 54, 729 (1985). (http://dx.doi.org/10.1146/annurev.bi.54.070185.003501)
7. J. M. Hevel, M. A. Marletta. Biochemistry 31, 7160 (1992). (http://dx.doi.org/10.1021/bi00146a019)
8. C. Huber, J. R. Batchelor, D. Fuchs, A. Hausen, A. Lang, D. Niederwieser, G. Reibnegger, P. Swetly, J. Troppmair, H. Wachter. J. Exp. Med. 160, 310 (1984). (http://dx.doi.org/10.1084/jem.160.1.310)
9. C. Huber, D. Fuchs, A. Hausen, R. Margreiter, G. Reibnegger, M. Spielberger, H. Wachter. J. Immunol. 130, 1047 (1983).
10. D. Fuchs, G. Weiss, H. Wachter. Crit. Rev. Clin. Lab. Sci. 29, 307 (1992). (http://dx.doi.org/10.3109/10408369209114604)
11. D. Fuchs, G. Weiss, H. Wachter. Int. Arch. Allergy Immunol. 101, 1 (1993). (http://dx.doi.org/10.1159/000236491)
12. C. Lorente, A. H. Thomas. Acc. Chem. Res. 39, 395 (2006). (http://dx.doi.org/10.1021/ar050151c)
13. K. U. Schallreuter, J. Moore, J. M. Wood, W. D. Beazley, E. M. Peters, L. K. Marles, S. C. Behrens-Williams, R. Dummer, N. Blau, B. Thöny. J. Invest. Dermatol. 116, 167 (2001). (http://dx.doi.org/10.1046/j.1523-1747.2001.00220.x)
14. K. U. Schallreuter, J. M. Wood, M. R. Pittelkow, M. Gütlich, K. R. Lemke, W. Rödl, N. N. Swanson, K. Hitzemann, I. Ziegler. Science 263, 1444 (1994). (http://dx.doi.org/10.1126/science.8128228)
15. R. F. Branda, J. W. Eaton. Science 201, 625 (1978). (http://dx.doi.org/10.1126/science.675247)
16. J. E. Hearst Science 268, 1858 (1995). (http://dx.doi.org/10.1126/science.7604259)
17. P. Galland, H. Senger. Photochem. Photobiol. 48, 811 (1988). (http://dx.doi.org/10.1111/j.1751-1097.1988.tb02896.x)
18. R. C. Fuller, G. W. Kidder, N. A. Nugent, V. C. Dewey, N. Rigopoulos. Photochem. Photobiol. 14, 359 (1971). (http://dx.doi.org/10.1111/j.1751-1097.1971.tb06179.x)
19. M. C. DeRosa, R. J. Crutchley. Coord. Chem. Rev. 233-234, 351 (2002). (http://dx.doi.org/10.1016/S0010-8545(02)00034-6)
20. J. Cadet, J. L. Ravanat, G. R. Martinez, M. H. G. Medeiros, P. Di Mascio. Photochem. Photobiol. 82, 1219 (2006). (http://dx.doi.org/10.1562/2006-06-09-IR-914)
21. M. Tarr, D. P. Valenzeno. Photochem. Photobiol. Sci. 2, 355 (2003). (http://dx.doi.org/10.1039/b211778a)
22. C. Schweitzer, R. Schmidt. Chem. Rev. 103, 1685 (2003). (http://dx.doi.org/10.1021/cr010371d)
23. A. H. Thomas, C. Lorente, A. L. Capparelli, C. G. Martínez, A. M. Braun, E. Oliveros. Photochem. Photobiol. Sci. 2, 245 (2003) and refs. therein. (http://dx.doi.org/10.1039/b209993d)
24. F. M. Cabrerizo, A. H. Thomas, C. Lorente, M. L. Dántola, G. Petroselli, R. Erra-Balsells, A. L. Capparelli. Helv. Chim. Acta 87, 349 (2004). (http://dx.doi.org/10.1002/hlca.200490032)
25. F. M. Cabrerizo, C. Lorente, M. Vignoni, R. Cabrerizo, A. H. Thomas, A. L. Capparelli. Photochem. Photobiol. 81, 793 (2005). (http://dx.doi.org/10.1562/2004-11-29-RA-383R.1)
26. M. L. Dántola, A. H. Thomas, A. M. Braun, E. Oliveros, C. Lorente. J. Phys. Chem. A 111, 4280 (2007). (http://dx.doi.org/10.1021/jp071278h)
27. A. M. Braun, E. Oliveros. Pure Appl. Chem. 62, 1467 (1990). (http://dx.doi.org/10.1351/pac199062081467)
28. F. M. Cabrerizo, M. L. Dántola, G. Petroselli, A. L. Capparelli, A. H. Thomas, A. M. Braun, C. Lorente, E. Oliveros. Photochem. Photobiol. 83, 526 (2007) and refs. therein. (http://dx.doi.org/10.1562/2006-09-15-RA-1041)
29. F. Wilkinson, H. P. Helman, A. B. Ross. J. Phys. Chem. Ref. Data 24, 663 (1995). (http://dx.doi.org/10.1063/1.555965)
30. F. M. Cabrerizo, G. Petroselli, A. H. Thomas, C. Lorente, A. L. Capparelli, A. M. Braun, E. Oliveros. Photochem. Photobiol. 81, 1234 (2005). (http://dx.doi.org/10.1562/2005-05-10-RA-522)
31. W. Pfleiderer. In Biochemical and Clinical Aspects of Pteridines, Vol. 5, W. Pfleiderer, H. Wachter, J. A. Blair (Eds.), pp. 3–21, Walter de Gruyter, Berlin (1987).
32. F. M. Cabrerizo, M. L. Dántola, A. H. Thomas, C. Lorente, A. M. Braun, E. Oliveros, A. L. Capparelli. Chem. Biodiv. 1, 1800 (2004). (http://dx.doi.org/10.1002/cbdv.200490135)
33. E. L. Clennan, A. Pace. Tetrahedron 61, 6665 (2005). (http://dx.doi.org/10.1016/j.tet.2005.04.017)
34. B. M. Monroe. J. Phys. Chem. 81, 1861 (1977). (http://dx.doi.org/10.1021/j100534a016)
35a. A. P. Darmanyan, W. S. Jenks, P. Jardon. J. Phys. Chem. A 102, 7420 (1998). (http://dx.doi.org/10.1021/jp982326o)
35b. Erratum: A. P. Darmanyan, W. S. Jenks, P. Jardon. J. Phys. Chem. A 102, 9308 (1998). (http://dx.doi.org/10.1021/jp983710o)
36. K. Gollnick, J. H. E. Lindner. Tetrahedron Lett. 14, 1903 (1973). (http://dx.doi.org/10.1016/S0040-4039(01)96272-0)
37. M. Valko, D. Leibfritz, J. Moncol, M. T. D. Cronin, M. Mazur, J. Telser. Int. J. Biochem. Cell Biol. 39, 44 (2007). (http://dx.doi.org/10.1016/j.biocel.2006.07.001)
38. M. L. Dántola, M. Vignoni, C. González, C. Lorente, P. Vicendo, E. Oliveros, A. H. Thomas. Free Rad. Biol. Med. 49 1014 (2010). (http://dx.doi.org/10.1016/j.freeradbiomed.2010.06.011)
39. M. Vignoni, F. M. Cabrerizo, C. Lorente, A. H. Thomas. Photochem. Photobiol. 85, 365 (2009). (http://dx.doi.org/10.1111/j.1751-1097.2008.00450.x)
40. M. Vignoni, M. L. Salum, R. Erra-Balsells, A. H. Thomas, F. M. Cabrerizo. Chem. Phys. Lett. 484, 330 (2010). (http://dx.doi.org/10.1016/j.cplett.2009.12.008)
41. H. Rokos, W. D. Beazley, K. U. Schallreuter. Biochem. Biophys. Res. Commun. 292, 805 (2002). (http://dx.doi.org/10.1006/bbrc.2002.6727)
42. M. L. Dántola, T. M. Schuler, M. P. Denofrio, M. Vignoni, A. L. Capparelli, C. Lorente, A. H. Thomas. Tetrahedron 64, 8692 (2008). (http://dx.doi.org/10.1016/j.tet.2008.07.005)
43. M. L. Dántola, M. Vignoni, A. L. Capparelli, C. Lorente, A. H. Thomas. Helv. Chim. Acta 91, 411 (2008). (http://dx.doi.org/10.1002/hlca.200890046)
44. K. Hirakawa, H. Suzuki, S. Oikawa, S. Kawanishi. Arch. Biochem. Biophys. 410, 261 (2003). (http://dx.doi.org/10.1016/S0003-9861(02)00722-1)
45. G. Petroselli, R. Erra-Balsells, F. M. Cabrerizo, C. Lorente, A. L. Capparelli, A. M. Braun, E. Oliveros, A. H. Thomas. Org. Biomol. Chem. 5, 2792 (2007). (http://dx.doi.org/10.1039/b707312g)
46. G. Petroselli, M. L. Dántola, F. M. Cabrerizo, A. L. Capparelli, C. Lorente, E. Oliveros, A. H. Thomas. J. Am. Chem. Soc. 130, 3001 (2008). (http://dx.doi.org/10.1021/ja075367j)

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Production and quenching of reactive oxygen species by pterin derivatives, an intriguing class of biomolecules

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