Synthesis, Table of Contents PAPER© Georg Thieme Verlag Stuttgart · New YorkNew Photoactivatable Analogues of Glutathione DisulfideDan Bernardi, Amadou Dicko, Gilbert Kirsch*Laboratoire d’Ingénierie Moléculaire et Biochimie Pharmacologique, Université Paul Verlaine-Metz, 1 Boulevard Arago, 57078 METZ Cedex 3, FranceFax: +33(38)7315801; e-Mail: kirsch@sciences.univ-metz.fr; Recommend Article Abstract Buy Article All articles of this category Abstract New photoactivatable analogues of glutathione disulfide (GSSG) bearing new benzophenone-like photophores were synthesized by using an improved coupling reaction. Key words glutathione disulfide - photoaffinity labeling - benzophenone - heterocycles Full Text References References <A NAME="RZ13505SS-1A">1a</A> Lyon RP. Hill JJ. Atkins WM. Biochemistry 2003, 42: 10418 <A NAME="RZ13505SS-1B">1b</A> Lim MLR. Lum M. Hansen TM. Roucou X. Nagley P. J. Biomed. Sci. 2002, 9: 488 <A NAME="RZ13505SS-1C">1c</A> Hanigan MH. Chemico-Biol. Interact. 1998, 111-112: 333 <A NAME="RZ13505SS-1D">1d</A> Keppler D. Leier I. Jedlitischky G. König J. Chemico-Biol. Interact. 1998, 111-112: 153 <A NAME="RZ13505SS-1E">1e</A> Kauvar LS. Sanderson PE. Henner WD. Chemico-Biol. Interact. 1998, 111-112: 225 <A NAME="RZ13505SS-2A">2a</A> Quian Y. Grant CE. Westlake CJ. Zhang D. Lander PA. Shepard RL. Dantzig AH. Cole SPC. Deeley RG. J. Biol. Chem. 2002, 277: 35225 <A NAME="RZ13505SS-2B">2b</A> Furuta K. Tomokiyo K. Kuo MT. Ishikawa T. Suzuki M. Tetrahedron 1999, 55: 7529 <A NAME="RZ13505SS-2C">2c</A> Furuta K. Hosoya T. Tomokiyo K. Okuda S. Kuniyasu A. Nakayama H. Ishikawa T. Suzuki M. Bioorg. Med. Chem. Lett. 1999, 9: 2661 <A NAME="RZ13505SS-3">3</A> Hall AG. Eur. J. Clin. Invest. 1999, 29: 238 <A NAME="RZ13505SS-4">4</A> Filomeni G. Rotilio G. Ciriolo MR. FASEB J. 2003, 17: 64 <A NAME="RZ13505SS-5">5</A> D’Silva C. Seddon AP. Douglas KT. J. Chem. Soc., Perkin Trans. 1 1981, 3029 <A NAME="RZ13505SS-6">6</A> Douglas KT. Seddon AP. D’Silva C. Bunni M. Biochem. Soc. Trans. 1982, 10: 124 <A NAME="RZ13505SS-7">7</A> Brault L. Migianu E. Néguesque A. Battaglia E. Bagrel D. Kirsch G. Eur. J. Med. Chem. 2005, in press <A NAME="RZ13505SS-8">8</A> Dorman G. Prestwich GD. Biochemistry 1994, 33: 5661 <A NAME="RZ13505SS-9A">9a</A> Bosca F. Miranda MA. J. Photochem. Photobiol., B: Biology 1998, 43: 1 <A NAME="RZ13505SS-9B">9b</A> Lahoz A. Hernandez D. Miranda MA. Perz-Prieto J. Morera IM. Castell JV. Chem. Res. Toxicol. 2001, 14: 1486 <A NAME="RZ13505SS-9C">9c</A> Moser J. Hye A. Lovell WW. Earl LK. Castell JV. Miranda MA. Toxicol. in Vitro 2001, 15: 333 <A NAME="RZ13505SS-9D">9d</A> Arnold DR. Birtwell RJ. J. Am. Chem. Soc. 1973, 95: 4599 <A NAME="RZ13505SS-10">10</A> Holland GF. inventors; US Patent, 4282246. ; Chem. Abstr. 1981, 95, 203733a <A NAME="RZ13505SS-11">11</A> Green TW. Wuts PGM. Protective Groups in Organic Synthesis 2nd ed.: Wiley; New York: 1991. <A NAME="RZ13505SS-12">12</A> Gartner CA. Wen B. Wan J. Becker RS. Jones G. Gygi SP. Nelson SD. Biochemistry 2005, 44: 1846 <A NAME="RZ13505SS-13">13</A> Cadamuro S. Degani I. Dughera S. Fochi R. Gatti A. Piscopo L. J. Chem. Soc., Perkin Trans. 1 1993, 273 <A NAME="RZ13505SS-14">14</A> Zu J. Wang X. Chen Y. Jiang X. Chen X. Li Z. J. Org. Chem. 2004, 69: 6221 <A NAME="RZ13505SS-15">15</A> Anderson GW. Zimmerman JE. Callahan FM. J. Am. Chem. Soc. 1964, 86: 1839