US2003060494A1PendingUtilityA1
Pharmaceutical use of N-carbamoylazole derivatives
Priority: May 18, 2001Filed: May 15, 2002Published: Mar 27, 2003
Est. expiryMay 18, 2021(expired)· nominal 20-yr term from priority
Inventors:Nobuyuki YasudaTadashi NagakuraKazuto YamazakiSeiji YoshikawaToshimi OkadaHironori IkutaMika Koyanagi
C07D 405/12A61P 3/00C07D 471/04C07D 401/12C07D 249/12C07D 403/12C07D 413/12C07D 451/02
42
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Claims
Abstract
The present invention relates to use of 1-carbamoylazole derivatives as medicaments and pharmaceutical compositions containing 1-carbamoylazole derivatives as the active ingredient, based on their DPPIV inhibiting effects. The present invention provides a dipeptidyl peptidase IV inhibiting agent comprising a compound represented by the general formula (I):
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A dipeptidyl peptidase IV inhibiting agent comprising a compound represented by following general formula (I):
wherein R 1a represents a C 1-6 alkyl group, a C 3-8 cycloalkyl group, a 5- to 10-membered aromatic heterocyclic group, a C 6-10 aromatic hydrocarbon-cyclic group, a 4- to 10-membered heterocyclic group, or a C 4-13 polycycloalkyl group;
n means an integer of 0 to 2;
W represents a single bond, a C 1-6 alkylene group, or a group represented by following formula W-1:
wherein W 2 represents a nitrogen atom or methine group, m means an integer of 0 to 3, and R 1b represents a C 1-6 alkyl group, a C 3-8 cycloalkyl group, a 5- to 10-membered aromatic heterocyclic group, a C 6-10 aromatic hydrocarbon-cyclic group, a 4- to 10-membered heterocyclic group, or a C 4-13 polycycloalkyl group;
each of X 1 and X 2 independently represents a nitrogen atom or a methine group;
Z represents a group represented by following formula Z-1 or Z-2:
wherein each of R 2a and R 2b independently represents a C 1-6 alkyl group, a C 2-6 alkenyl group, or a phenyl group, and Z 2 represents a sulfur atom or a methylene group; and
wherein R 1a and R 1b may be substituted with one to three substituents selected from the group consisting of (1) halogen atoms, (2) a hydroxyl group, (3) C 2-6 alkenyl groups, (4) C 2-6 alkynyl groups, (5) a phenyl group, (6) a cyano group, (7) C 1-6 alkoxy groups which may be substituted with one to three halogen atoms or C 1-6 alkoxy groups, and (8) C 1-6 alkyl groups which may be substituted with one to three halogen atoms or C 1-6 alkoxy groups.
2 . The dipeptidyl peptidase IV inhibiting agent according to claim 1 , wherein Z is a group represented by following formula Z-3:
wherein R 2b represents a C 1-6 alkyl group, a C 2-6 alkenyl group, or a phenyl group.
3 . The dipeptidyl peptidase IV inhibiting agent according to claim 1 , wherein R 1a is a phenyl group or a 4-pyrazolyl group.
4 . The dipeptidyl peptidase IV inhibiting agent according to claim 1 , wherein X 1 is a nitrogen atom, and X 2 is a methine group.
5 . The dipeptidyl peptidase IV inhibiting agent according to claim 1 , wherein X 1 and X 2 are methine group.
6 . The dipeptidyl peptidase IV inhibiting agent according to claim 1 , wherein n is 1 or 2.
7 . The dipeptidyl peptidase IV inhibiting agent according to claim 1 , wherein the inhibiting agent is an agent for the treatment and prophylaxis of diabetic diseases.
8 . The dipeptidyl peptidase IV inhibiting agent according to claim 1 , wherein the inhibiting agent is an agent for the treatment and prophylaxis of obesity.
9 . The dipeptidyl peptidase IV inhibiting agent according to claim 1 , wherein the inhibiting agent is a hyperlipemia treating agent, an AIDS treating agent, an osteoporosis treating agent, an agent for treating intestinal disorders, a neovascularization treating agent, an infertility treating agent, an anti-inflammatory agent, an anti-allergic agent, an immune-modulating agent, a hormone-modulating agent, an antirheumatic agent, or an agent for treating cancers.Join the waitlist — get patent alerts
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