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Title:
NOVEL FUSED IMIDAZOLE DERIVATIVE
Document Type and Number:
WIPO Patent Application WO/2003/104229
Kind Code:
A1
Abstract:
A compound represented by the general formula (I) [wherein T1 means an optionally substituted, monocyclic or bicyclic, 4- to 12-membered, heterocyclic group containing one or two nitrogen atoms in the ring; X means optionally substituted C1-6 alkyl, etc.; Z1 and Z2 each independently means nitrogen or a group represented by the formula -CR2-; and R1 and R2 each independently means hydrogen, optionally substituted C1-6 alkyl, optionally substituted C1-6 alkoxy, etc.], a salt of the compound, or a hydrate of either. These are novel compounds having excellent DPPIV inhibitory activity.

Inventors:
YOSHIKAWA SEIJI (JP)
EMORI EITA (JP)
MATSUURA FUMIYOSHI (JP)
RICHARD CLARK (JP)
IKUTA HIRONORI (JP)
KIRA KAZUNOBU (JP)
YASUDA NOBUYUKI (JP)
NAGAKURA TADASHI (JP)
YAMAZAKI KAZUTO (JP)
Application Number:
PCT/JP2003/007010
Publication Date:
December 18, 2003
Filing Date:
June 03, 2003
Export Citation:
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Assignee:
EISAI CO LTD (JP)
YOSHIKAWA SEIJI (JP)
EMORI EITA (JP)
MATSUURA FUMIYOSHI (JP)
RICHARD CLARK (JP)
IKUTA HIRONORI (JP)
KIRA KAZUNOBU (JP)
YASUDA NOBUYUKI (JP)
NAGAKURA TADASHI (JP)
YAMAZAKI KAZUTO (JP)
International Classes:
A61K31/496; A61K31/5025; A61K31/522; A61K31/5377; A61K31/541; A61P1/00; A61P3/04; A61P3/06; A61P3/10; A61P9/00; A61P15/00; A61P15/08; A61P19/02; A61P19/10; A61P29/00; A61P31/18; A61P35/00; A61P37/00; A61P37/02; A61P37/08; A61P43/00; C07D473/04; C07D473/06; C07D471/04; C07D473/18; C07D473/22; C07D473/24; C07D473/30; C07D473/36; C07D473/40; C07D487/04; C07D491/14; (IPC1-7): C07D471/04; C07D473/06; C07D473/18; C07D473/22; C07D473/30; C07D473/40; C07D487/04; C07D498/14; A61K31/5025; A61K31/522; A61K31/5365; A61K31/519; A61P1/00; A61P3/04; A61P3/06; A61P3/10; A61P15/00; A61P19/10; A61P29/00; A61P35/00; A61P37/02; A61P37/08; A61P43/00
Domestic Patent References:
WO2002002560A22002-01-10
WO2002068420A12002-09-06
WO2003004496A12003-01-16
WO2000056296A22000-09-28
WO2002002560A22002-01-10
WO2003004496A12003-01-16
Foreign References:
EP0206415A21986-12-30
US20020161001A12002-10-31
US20020198205A12002-12-26
Other References:
BELJEAN-LEYMARIE M.: "Heterocyclic hydrazines and hydrazones. IV. Synthesis of hydrazine derivatives in the (4,5-d)imidazo-4-pyridazinone series", CANADIAN JOURNAL OF CHEMISTRY, vol. 61, no. 11, 1983, pages 2563 - 2566, XP002970248
BERRY D.A.: "Synthesis of 8-amino-3-deatahuanine via imidazole precursors. Antitumor activity and inhibition of purine nucleoside phosphorylase", JOURNAL OF MEDICINAL CHEMISTRY, vol. 29, no. 10, 1986, pages 2034 - 2037, XP002970249
CLINICAL CHEMISTRY, vol. 34, 1988, pages 2499 - 2501
"preventive and therapeutic agents for intestinal disorders", ENDOCRINOLOGY, vol. 141, 2000, pages 4013 - 4020
"preventive and therapeutic agents for diabetes mellitus, obesity, and hyperlipidemia", DIABETES, vol. 47, 1998, pages 1663 - 1670
LIFE SCI, vol. 66, no. 2, 2000, pages 91 - 103
"preventive and therapeutic agents for angiogenesis", AGENTS AND ACTIONS, vol. 32, 1991, pages 125 - 127
"preventive and therapeutic agents for inflammatory diseases, autoimmune diseases, and chronic rheumatoid arthritis", THE JOURNAL OF IMMUNOLOGY, vol. 166, 2001, pages 2041 - 2048
"preventive and therapeutic agents for cancer", BR J CANCER, vol. 7.9, no. 7-8, March 1999 (1999-03-01), pages 1042 - 8
J ANDROL, vol. 21, no. 2, March 2000 (2000-03-01), pages 220 - 6
See also references of EP 1514552A4
Attorney, Agent or Firm:
Shimizu, Hatsushi (1-1-1 Oroshi-mach, Tsuchiura-shi Ibaraki, JP)
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