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Title:
抗炎症剤
Document Type and Number:
Japanese Patent JP2008543822
Kind Code:
A
Abstract:
The invention relates inter alia to a compound of general formula (I) or (I'): wherein z is 1,2 or 4; X is -CO-Y k -(R 1 ) n or SO 2 -Y k -(R 1 ) n ; k is 0 or 1; Y is a cycloalkyl or polycyloalkyl group (such as an adamantyl, adamantanemethyl, bicyclooctyl, cyclohexyl, cyclopropyl group); or is a cycloalkenyl or polycycloalkenyl group; each R 1 is independently selected from hydrogen or an alkyl, haloalkyl, alkoxy, haloalkoxy, alkenyl, alkynyl or alkylamino radical of 1 to 20 carbon atoms (for example of 5 to 20 carbon atoms, of 8 to 20 carbon atoms, of 9 to 20 carbon atoms, of 10 to 18 carbon atoms, of 12 to 18 carbon atoms, of 13 to 18 carbon atoms, of 14 to 18 carbon atoms, of 13 to 17 carbon atoms); or each R 1 is independently selected from fluoro, chloro, bromo, iodo, hydroxy, oxyalkyl, amino, aminoalkyl or aminodialkyl radical; and n is any integer from 1 to m, where m is the maximum number of substitutions permissible on the cyclo-group Y (such that n=1 if k=0, such that the R 1 group is bonded directly to the carbonyl or sulfonyl group); provided that simultaneously X cannot be an undec-10-en-1-oyl group and z be equal to 1 or 2; or alternatively R 1 is selected from a peptido radical having from 1 to 4 peptidic moieties linked together by peptide bonds.

Inventors:
Granger, David John
Fox, david john
Application Number:
JP2008516414A
Publication Date:
December 04, 2008
Filing Date:
June 14, 2006
Export Citation:
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Assignee:
Cambridge Enterprise Limited
International Classes:
C07D207/273; A61K31/395; A61K31/4015; A61K31/45; A61P9/00; A61P11/06; A61P17/02; A61P17/06; A61P19/02; A61P19/10; A61P25/00; A61P25/28; A61P29/00; A61P31/12; A61P33/00; A61P35/00; A61P37/02; A61P37/06; A61P37/08; A61P41/00; A61P43/00; C07D207/267; C07D211/76; C07D225/02; C07D207/26
Domestic Patent References:
JP2002536411A2002-10-29
JP2000507950A2000-06-27
Foreign References:
EP0519877A11992-12-23
Other References:
JPN6012027204; Chemistry Letters No.12, 1981, p.1691-1694
JPN6012027205; Journal of the American Chemical Society Vol.86, No.12, 1964, p.2441-2445
JPN6012027206; Tetrahedron Letters No.15, 1975, p.1309-1312
JPN6012027207; Journal of Chromatography Vol.357, 1986, p.335-339
JPN6012027208; Chemical Abstracts Vol.63, No.9, 1965, 11691f-11693a
JPN6012027209; Journal of Medicinal Chemistry Vol.31, No.7, 1988, p.1430-1436
JPN6012027210; European Journal of Biochemistry Vol.163, No.2, 1987, 297-302
JPN6012027211; Journal of the American Chemical Society Vol.115, No.23, 1993, p.10492-10496
JPN6012027212; Journal of the American Chemical Society Vol.77, 1955, p.6690-6691
JPN6012027213; Journal of the American Chemical Society Vol.102, No.15, 1980, p.4855-4863
JPN6012027214; Journal of the Chemical Society C:Organic No.22, 1971, p.3743-3748
JPN6012027215; IL FARMACO Vol.59, No.4, 2004, 271-277
JPN6012027216; Journal of Medicinal Chemistry Vol.48, No.3, 2005, 867-874
Attorney, Agent or Firm:
Atsushi Aoki
Takashi Ishida
Fukumoto product
Tetsuji Koga
Kazuhiro Nakamura
Yoichi Watanabe
Kazumi Nakamura