Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Ketone doai
Reexamination Certificate
2007-05-01
2007-05-01
Aulakh, Charanjit S. (Department: 1625)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Ketone doai
C568S308000, C568S077000, C568S075000, C568S008000, C514S706000
Reexamination Certificate
active
11238231
ABSTRACT:
The invention provides novel tetradentate enediyne ligands that are themselves thermally stable, yet react at about room temperature or slightly higher upon addition of metal ions or under photothermal conditions. In another aspect of the invention, a method of treating a disorder in a mammal comprising administering a therapeutically effective amount of a compound or composition is provided. In addition, the free ligand can be delivered to the mammal prior to complexation to metals, such that the ligand is exposed to a metal in the body and forms a metal complex in vivo. Furthermore, a metal complex of the invention can be administered to the mammal such that the complex exchanges the first metal center with another endogenous metal in order to form a second metal complex in vivo. The second metal complex is capable of forming a benzenoid diradical under physiological conditions and/or under photothermal conditions.
REFERENCES:
patent: 5371199 (1994-12-01), Therien et al.
patent: 5986090 (1999-11-01), Therien et al.
patent: 6043237 (2000-03-01), Meadows et al.
patent: 6514995 (2003-02-01), Zaleski et al.
patent: 6828439 (2004-12-01), Zaleski et al.
patent: 6987132 (2006-01-01), Zaleski et al.
Chemin, D. et al.: Palladium-catalyzed reaction of (E) and (Z)-dichloroethenes with 1-alkynes. An efficient stereospecific synthesis of (E) and (Z)-enediynes. Tetrahedron, vol. 50, pp. 5335-5344, 1994.
Carpita, A et al.: Synthesis of stereochemically pure (E)-1,5-diyn-3-enes and (E)-1-bromo-3-YN-1-enes by diastereoselective palladium-catalyzed cross-coupling reaction of 1-alkynylzinc chlorides with a stereoisomeric mixture of 1,2-dibromoethylene. Tetrahedron Lett. vol. 27, pp. 4351-4354, 1986.
U.S. Appl. No. 10/268,172, filed Oct. 10, 2002, Zaleski et al.
Ali et al.,Chem Rev., 99, 2379-2450 (1999).
Basak et al.,Chem. Commun., 749-750 (1996).
Bergman,Accounts of Chemical Research, 6, 25-31 (1973).
Bonadies et al.,J. Am. Chem. Soc., 108, 4088-4095 (1986).
Bonnett,Chem. Soc. Reviews, 24, 19-33 (1995).
Boyle et al.,Photochemistry and Photobiology, 64 (3), 469-485 (1996).
Branca et al.,Inorg. Chem., 29, 1586-1589 (1990).
Chapman et al.,J. Am. Chem. Soc., 98 (18), 5703-5705 (1976).
Christner et al.,J. Am. Chem. Soc., 114, 8763-8767 (1992).
Churcher et al.,J. Am. Chem. Soc., 120, 3518-3519 (1998).
Cummings et al.,Inorg. Chem., 34, 2007-2014 (1995).
Cummings et al.,J. Am. Chem. Soc., 118, 1949-1960 (1996).
Dai et al,.J. Org. Chem., 64, 682-683 (1999).
Evenzahav et al.,J. Am. Chem. Soc., 120, 1835-1841 (1998).
Funk et al.,J. Am. Chem. Soc., 118, 3291-3292 (1996).
Golik et al.,J. Am. Chem. Soc., 109, 3461-3462 (1987).
Golik et al.,J. Am. Chem. Soc., 109, 3462-3464 (1987).
Hangeland et al.,J. Am. Chem Soc., 114, 9200-9202 (1992).
Holmes et al.,Inorg. Chem., 30, 1231-1235 (1991).
Kaneko et al.,Angew. Chem. Int. Ed., 38 (9), 1267-1268 (1999).
Kim et al.,J. Org. Chem., 63, 8229-8234 (1998).
Konig et al.,Angew. Chem. Int. Ed. Engl., 34 (22), 2538-2540 (1995).
Konig et al.,J. Org. Chem., 61, 4258-4261 (1996).
Kusakabe et al.,Biochemistry, 32, 11669-11675 (1993).
Lee et al.,J. Am. Chem. Soc., 114, 985-997 (1992).
Leet et al.,J. Am. Chem. Soc., 115, 8432-8443 (1993).
Li et al.,Inogr. Chem., 27, 4657-4664 (1988).
Lockhart et al.,J. Am. Chem. Soc., 103, 4091-4096 (1981).
Magnus et al.,J. Am. Chem. Soc., 112, 4986-4987 (1990).
Maier,Synlett, 13-26 (1995).
Marthur et al.,Biochemistry, 36, 14868-14873 (1997).
Minami et al.,Tetrahedron Letters, 34(16), 2633-2636 (1993).
Myers et al.,J. Am. Chem. Soc., 114, 5859-5860 (1992).
Myers et al.,J. Am. Chem. Soc., 120, 5319-5320 (1998).
Kappen et al.,Biochemistry, 38, 235-242 (1999).
Nicolaou et al.,Chem. Abst., 117, Abstract 233658v and 233659w, 835 (1992).
Nicolaou et al.,Angew. Chem. Int. Ed. Engl., 30 (8), 1032-1036 (1991).
Nicolaou et al.,J. Am. Chem. Soc., 110, 4866-4868 (1988).
Nicolaou et al.,J. Am. Chem. Soc., 113, 3106-3114 (1991).
Nicolaou et al.,J. Am. Chem. Soc., 114, 7360-7371 (1992).
Nicolaou et al.,J. Am. Chem. Soc., 114, 9279-9282 (1992).
Nicolaou et al.,Proc. Natl. Acad. Sci. USA, 90, 5881-5888 (1993).
O'Brien et al.,Photochemistry and Photobiology, 54 (5), 851-854 (1991).
Oseroff et al.,Photochemistry and Photobiology, 46 (1), 83-96 (1987).
Pandey et al.,J. Med. Chem., 33, 2032-2038 (1990).
Pandey et al.,J. Med. Chem., 40, 2770-2779 (1997).
Ramkumar et al.,J. Org. Chem., 61, 2247-2250 (1996).
Rawat et al.,J. Am. Chem. Soc., 123, 9675-9676 (2001).
Ressler et al.,Chemtech, 28 (3), 39-45 (1998).
Schreiner,Chem. Commun., 483-484 (1998).
Schreiner,J. Am. Chem. Soc., 120, 4184-4190 (1998).
Sessler et al.,Acc. Chem. Res., 27, 43-50 (1994).
Shain et al.,Tetrahedron Letters, 38 (34), 6067-6070 (1997).
Shair et al.,J. Am. Chem. Soc., 118, 9509-9525 (1996).
Shiraki et al.,Biochemistry, 29, 9795-9798 (1990).
Smith et al.,Journal of Medicinal Chemistry, 39 (11), 2103-2117 (1996).
Sugiura et al. ,Proc. Natl. Acad. Sci. USA, 87, 3831-3835 (1990).
Turro et al.,Tetrahedron Letters, 35 (44), 8089-8092 (1994).
Warner et al.,Science, 269, 814-816 (1995).
Wells,Chemistry&Biology, 4 (10), 775-776 (1997).
Wender et al.,J. Org. Chem., 58 (22), 5867-5869 (1993).
Wisniewski Grissom et al.,J. Org. Chem., 59, 5833-5835 (1994).
Xi et al.,Biochemistry, 38, 4342-4354 (1999).
Xu et al.,Biochemistry, 36, 14975-14984 (1997).
Xu et al.,Biochemistry, 37, 1890-1897 (1998).
Zein et al.,J. Am. Chem. Soc., 111, 6888-6890 (1989).
Zein et al.,Science, 240, 1198-1201 (1988).
Zein et al.,Science, 244, 697-699 (1989).
Rawat Diwan Singh
Zaleski Jeffrey M.
Aulakh Charanjit S.
Indiana University Research and Technology Corporation
Leydig , Voit & Mayer, Ltd.
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