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Title:
ALICYCLIC PHOSPHOLIPASE A2 INHIBITOR
Document Type and Number:
Japanese Patent JPH0717913
Kind Code:
A
Abstract:

PURPOSE: To provide novel alicyclic compounds exhibiting activities as alicyclic phospholipase A2 inhibitors and useful as anti-inflammatory agents.

CONSTITUTION: The compound of formula I [wherein the bonds between C2 and C3, and/or between C4 and C5 are unsaturated; X represents COOH, H, a halogen, COR'', CONH2, CR''', CHO, CH2OH, OH, OR''', CF3, 1-6C (halo)alkyl, NO2, P(O)(OH)2, SO2H or the like; R represents a substituted or unsubstituted alkyl, aryl, arylalkyl, alkenyl or arylalkenyl (these radicals each has 6 ore more carbons), but R is not a radical of formula II]; R' represents H or a 1-6C alkyl; R'' represents R', C(R3)2OC(O)R4, CH2CH2NR5R6 or the like; R''' represents a 1-6C alkyl; R3 represents H, CH3, C2H5 or the like; R4 represents a 6-12C aryl or 1-7C alkyl; R5 and R6 are each a 1-3C alkyl or 3-6C cycloalkyl by joining together, CH2CH2OCH2CH2], for example (2Z),(4Z)-4-(3- carboxyphenyl)-5-(5,6,7,8-tetrahydro-5,5,8,8-tetra-methyl-2-naphthalenyl)-2,4- pentadienic acid, is provided.


Inventors:
JIYOAN JIEI BURONSON
EFU AIBUII KIYARORU
KIYASARIN EMU GURIIN
ANITA REUIN
MUZAMIRU EMU MANSURI
SUTANRII BUII DANDOREA
Application Number:
JP13153294A
Publication Date:
January 20, 1995
Filing Date:
June 14, 1994
Export Citation:
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Assignee:
BRISTOL MYERS SQUIBB CO
International Classes:
A61K31/19; A61K31/192; A61K31/215; A61P29/00; C07C57/30; C07C57/48; C07C59/64; C07C63/66; C07C65/28; C07C69/00; C07C69/612; C07C69/618; C07C69/65; A61K31/165; C07C69/734; C07C69/76; C07C69/94; C07C205/56; C07C219/10; C07C233/65; C07C309/57; C07C313/04; C07F9/38; (IPC1-7): C07C69/618; A61K31/165; A61K31/19; A61K31/215; C07C57/30; C07C57/48; C07C69/612; C07C205/56; C07C219/10; C07C233/65; C07C309/57; C07C313/04; C07F9/38
Attorney, Agent or Firm:
Minoru Nakamura (7 outside)