HUP9802259A2 - 1,4,5-Helyettesített imidazolszármazékok, e vegyületeket tartalmazó gyógyászati készítmények, eljárás előállításukra és alkalmazásuk - Google Patents
1,4,5-Helyettesített imidazolszármazékok, e vegyületeket tartalmazó gyógyászati készítmények, eljárás előállításukra és alkalmazásukInfo
- Publication number
- HUP9802259A2 HUP9802259A2 HU9802259A HUP9802259A HUP9802259A2 HU P9802259 A2 HUP9802259 A2 HU P9802259A2 HU 9802259 A HU9802259 A HU 9802259A HU P9802259 A HUP9802259 A HU P9802259A HU P9802259 A2 HUP9802259 A2 HU P9802259A2
- Authority
- HU
- Hungary
- Prior art keywords
- cr10r20
- nr13r14
- alkyl
- substituted
- nnr10c
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 150000002460 imidazoles Chemical class 0.000 title 1
- 239000000843 powder Substances 0.000 abstract 5
- -1 4-quinazolinyl Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 241000251468 Actinopterygii Species 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 108090000623 proteins and genes Proteins 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000004173 1-benzimidazolyl group Chemical group [H]C1=NC2=C([H])C([H])=C([H])C([H])=C2N1* 0.000 abstract 1
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 abstract 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 abstract 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- 108090000695 Cytokines Proteins 0.000 abstract 1
- 102000004127 Cytokines Human genes 0.000 abstract 1
- 101100295738 Gallus gallus COR3 gene Proteins 0.000 abstract 1
- 229910017711 NHRa Inorganic materials 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- VMWNQDUVQKEIOC-CYBMUJFWSA-N apomorphine Chemical compound C([C@H]1N(C)CC2)C3=CC=C(O)C(O)=C3C3=C1C2=CC=C3 VMWNQDUVQKEIOC-CYBMUJFWSA-N 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 125000005956 isoquinolyl group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000005493 quinolyl group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Physical Education & Sports Medicine (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Dermatology (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Epoxy Resins (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
A találmány a gyógyászatban citőkin inhibitőrőként felhasználhatóáltalánős képletű vegyületekre és az ezeket tartalmazógyógyszerkészítményekre vőnatkőzik, ahől a képletben R1 4-piridil-, pirimidinil-, kinőlil-, izőkinőlil-, 4-kinazőlinil-, 1-imidazőlil- vagy 1-benzimidazőlilcsőpőrt, ahől a heterőarilgyűrű -NHRaáltalánős képletű csőpőrttal és adőtt esetben tővábbi helyettesítővelszűbsztitűált; R4 fenil-, 1-naftil-, 2-naftil- vagy heterőarilcsőpőrt, amelyekbármelyike adőtt esetben egyszeresen vagy kétszeresen szűbsztitűált,ahől a szűbsztitűensek egymástól függetlenek és egy 4-fenil-, 4-naft-1-il-, 5-naft-2-il- vagy 6-naft-2-il-szűbsztitűens, halőgénatőm,cianő-, nitrőcsőpőrt, -C(Z)NR7R17, -C(Z)OR16, -(CR10R20)vCOR12, -SR5,-SOR5, -OR12, adőtt esetben halőgénatőmmal szűbsztitűált alkilcsőpőrt,-ZC(Z)R12, -NR10C(Z)R16 vagy -(CR10R20)vNR10R20, míg az egyébpőzíciókban lévő szűbsztitűens halőgénatőm, cianőcsőpőrt, -C(Z)NR13R14, -C(Z)OR3, -(CR10R20)m''COR3, -S(O)mR3, -OR3, adőttesetben halőgénatőmmal szűbsztitűált alkilcsőpőrt, -(CR10R20)m''NR10C(Z)R3, -NR10S(O)m'R8, -NR10S(O)m'NR7R17, -ZC(Z)R3vagy -(CR10R20)m''NR13R14; R2 -(CR10R20)n'OR9, heterőciklűsős csőpőrt, adőtt esetbenheterőciklűsős csőpőrttal szűbsztitűált alkilcsőpőrt, halőgén-alkil-,alkenil-, alkinil-, ciklőalkil-, ciklőalkil-alkil-, ciklőalkenil-,ciklőalkenil-alkil-, aril-, aril-alkil-, heterőaril-, heterőaril-alkil-, -(CR10R20)nOR11, -(CR10R20)nS(O)mR18, -(CR10R20)nNHS(O)2R18, -(CR10R20)nNR13R14, -(CR10R20)nNO2, -(CR10R20)nCN, -(CR10R20)n'SO2R18,-(CR10R20)nS(O)m'NR13R14, -(CR10R20)nC(Z)R11, -(CR10R20)nOC(Z)R11, -(CR10R20)nC(Z)OR11, -(CR10R20)nC(z)NR13R14, -(CR10R20)nC(Z)NR11OR9, -(CR10R20)nNR10C(Z)R11, -(CR10R20)nNR10C(Z(NR13R14,-(CR10R20)nN(OR6)C(Z)NR13R14, -(CR10R20)nN(OR6)C(Z)R11, -(CR10R20)nC(=NOR6)R11, -(CR10R20)nNR10C=NR19)NR13R14, -(CR10R21)nOC(Z)NR13R14, -(CR10R20)nNR10C(Z)NR13R14, -(CR10R20)nR10C(Z)OR10, 5-(R18)-1,2,4-őxadiazől-3-il- vagy 4-(R12)-5-(R18R19)-4,5-dihidrő-1,2,4-őxadiazől-3-il-csőpőrt. ŕ
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US47339695A | 1995-06-07 | 1995-06-07 | |
US63677996A | 1996-04-19 | 1996-04-19 |
Publications (2)
Publication Number | Publication Date |
---|---|
HUP9802259A2 true HUP9802259A2 (hu) | 1999-09-28 |
HUP9802259A3 HUP9802259A3 (en) | 2002-02-28 |
Family
ID=27044121
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU9802259A HUP9802259A3 (en) | 1995-06-07 | 1996-06-07 | 1,4,5-substituted imidazole compounds, pharmaceutical compounds containing them, process for producing them and their use |
Country Status (24)
Country | Link |
---|---|
US (2) | US5658903A (hu) |
EP (2) | EP1314728A1 (hu) |
JP (1) | JPH11513017A (hu) |
KR (1) | KR19990022574A (hu) |
CN (1) | CN1130358C (hu) |
AT (1) | ATE233561T1 (hu) |
BR (1) | BR9608591A (hu) |
CA (1) | CA2223533A1 (hu) |
CZ (1) | CZ392597A3 (hu) |
DE (1) | DE69626513T2 (hu) |
DZ (1) | DZ2043A1 (hu) |
ES (1) | ES2194106T3 (hu) |
HU (1) | HUP9802259A3 (hu) |
IL (1) | IL118544A (hu) |
IN (1) | IN186434B (hu) |
MA (1) | MA24242A1 (hu) |
MY (1) | MY114014A (hu) |
NO (1) | NO975716L (hu) |
NZ (1) | NZ311403A (hu) |
PE (1) | PE7798A1 (hu) |
PL (1) | PL185515B1 (hu) |
TR (1) | TR199701574T2 (hu) |
TW (1) | TW442481B (hu) |
WO (1) | WO1996040143A1 (hu) |
Families Citing this family (193)
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US5916891A (en) | 1992-01-13 | 1999-06-29 | Smithkline Beecham Corporation | Pyrimidinyl imidazoles |
NZ302117A (en) * | 1995-01-12 | 1999-10-28 | Smithkline Beecham Corp | 1-cycloalkyl or cycloalkylalkyl 4,5-trisubstituted imidazole derivatives and medicaments |
US5739143A (en) * | 1995-06-07 | 1998-04-14 | Smithkline Beecham Corporation | Imidazole compounds and compositions |
US6369068B1 (en) | 1995-06-07 | 2002-04-09 | Smithkline Beecham Corporation | Amino substituted pyrimidine containing compounds |
US5658903A (en) | 1995-06-07 | 1997-08-19 | Smithkline Beecham Corporation | Imidazole compounds, compositions and use |
ZA9610687B (en) * | 1995-12-22 | 1997-09-29 | Smithkline Beecham Corp | Novel synthesis. |
US5977103A (en) * | 1996-01-11 | 1999-11-02 | Smithkline Beecham Corporation | Substituted imidazole compounds |
ZA97175B (en) * | 1996-01-11 | 1997-11-04 | Smithkline Beecham Corp | Novel substituted imidazole compounds. |
AP9700912A0 (en) * | 1996-01-11 | 1997-01-31 | Smithkline Beecham Corp | Novel cycloalkyl substituted imidazoles |
US6046208A (en) * | 1996-01-11 | 2000-04-04 | Smithkline Beecham Corporation | Substituted imidazole compounds |
EP1005343A4 (en) * | 1996-03-08 | 2000-06-07 | Smithkline Beecham Corp | USE OF CSAIDS AS ANGIOGENESIS INHIBITORS |
EP0889887A4 (en) * | 1996-03-25 | 2003-06-11 | Smithkline Beecham Corp | TREATMENT OF CENTRAL NERVOUS SYSTEM INJURIES |
WO1997035856A1 (en) * | 1996-03-25 | 1997-10-02 | Smithkline Beecham Corporation | Novel treatment for cns injuries |
WO1998007425A1 (en) | 1996-08-21 | 1998-02-26 | Smithkline Beecham Corporation | Imidazole compounds, compositions and use |
WO1998016230A1 (en) * | 1996-10-17 | 1998-04-23 | Smithkline Beecham Corporation | Methods for reversibly inhibiting myelopoiesis in mammalian tissue |
ZA9711092B (en) * | 1996-12-11 | 1999-07-22 | Smithkline Beecham Corp | Novel compounds. |
US6020357A (en) * | 1996-12-23 | 2000-02-01 | Dupont Pharmaceuticals Company | Nitrogen containing heteroaromatics as factor Xa inhibitors |
US6548512B1 (en) | 1996-12-23 | 2003-04-15 | Bristol-Myers Squibb Pharma Company | Nitrogen containing heteroaromatics as factor Xa inhibitors |
US5929076A (en) * | 1997-01-10 | 1999-07-27 | Smithkline Beecham Corporation | Cycloalkyl substituted imidazoles |
EP1019394A1 (en) * | 1997-05-22 | 2000-07-19 | G.D. Searle & Co. | PYRAZOLE DERIVATIVES AS p38 KINASE INHIBITORS |
US6514977B1 (en) | 1997-05-22 | 2003-02-04 | G.D. Searle & Company | Substituted pyrazoles as p38 kinase inhibitors |
US6979686B1 (en) | 2001-12-07 | 2005-12-27 | Pharmacia Corporation | Substituted pyrazoles as p38 kinase inhibitors |
CA2294057A1 (en) | 1997-06-13 | 1998-12-17 | Smithkline Beecham Corporation | Novel pyrazole and pyrazoline substituted compounds |
AU8154998A (en) | 1997-06-19 | 1999-01-04 | Smithkline Beecham Corporation | Novel aryloxy substituted pyrimidine imidazole compounds |
US6339099B1 (en) | 1997-06-20 | 2002-01-15 | Dupont Pharmaceuticals Company | Guanidine mimics as factor Xa inhibitors |
US6489325B1 (en) | 1998-07-01 | 2002-12-03 | Smithkline Beecham Corporation | Substituted imidazole compounds |
CA2295762A1 (en) | 1997-07-02 | 1999-01-14 | Ravi Shanker Garigipati | Novel cycloalkyl substituted imidazoles |
AR016294A1 (es) * | 1997-07-02 | 2001-07-04 | Smithkline Beecham Corp | Compuesto de imidazol sustituido, composicion farmaceutica que la contiene, su uso en la fabricacion de un medicamento y procedimiento para supreparacion |
US6562832B1 (en) | 1997-07-02 | 2003-05-13 | Smithkline Beecham Corporation | Substituted imidazole compounds |
US7301021B2 (en) | 1997-07-02 | 2007-11-27 | Smithkline Beecham Corporation | Substituted imidazole compounds |
TW517055B (en) | 1997-07-02 | 2003-01-11 | Smithkline Beecham Corp | Novel substituted imidazole compounds |
EP1041989A4 (en) | 1997-10-08 | 2002-11-20 | Smithkline Beecham Corp | NEW SUBSTITUTED CYCLOALCENYL COMPOUNDS |
JP2001519381A (ja) * | 1997-10-10 | 2001-10-23 | インペリアル・カレッジ・イノベイションズ・リミテッド | 子宮収縮管理のためのcsaidtm化合物の使用 |
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WO1999025717A1 (fr) * | 1997-11-14 | 1999-05-27 | Sankyo Company, Limited | Derives de pyridylpyrrole |
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US7517880B2 (en) * | 1997-12-22 | 2009-04-14 | Bayer Pharmaceuticals Corporation | Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas |
US6589954B1 (en) | 1998-05-22 | 2003-07-08 | Scios, Inc. | Compounds and methods to treat cardiac failure and other disorders |
US6867209B1 (en) | 1998-05-22 | 2005-03-15 | Scios, Inc. | Indole-type derivatives as inhibitors of p38 kinase |
US6340685B1 (en) | 1998-05-22 | 2002-01-22 | Scios, Inc. | Compounds and methods to treat cardiac failure and other disorders |
CA2332402A1 (en) | 1998-05-22 | 1999-12-02 | Susan B. Dillon | Novel 2-alkyl substituted imidazole compounds |
US6130235A (en) * | 1998-05-22 | 2000-10-10 | Scios Inc. | Compounds and methods to treat cardiac failure and other disorders |
US6448257B1 (en) | 1998-05-22 | 2002-09-10 | Scios, Inc. | Compounds and methods to treat cardiac failure and other disorders |
US6858617B2 (en) | 1998-05-26 | 2005-02-22 | Smithkline Beecham Corporation | Substituted imidazole compounds |
US6207687B1 (en) * | 1998-07-31 | 2001-03-27 | Merck & Co., Inc. | Substituted imidazoles having cytokine inhibitory activity |
ATE266399T1 (de) * | 1998-08-20 | 2004-05-15 | Smithkline Beecham Corp | Neue substituierte triazolverbindungen |
US6184226B1 (en) | 1998-08-28 | 2001-02-06 | Scios Inc. | Quinazoline derivatives as inhibitors of P-38 α |
CN1261098C (zh) | 1998-08-28 | 2006-06-28 | 西奥斯股份有限公司 | p38-α激酶的抑制剂 |
ES2274634T3 (es) | 1998-08-29 | 2007-05-16 | Astrazeneca Ab | Compuestos de pirimidina. |
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ES2262137T3 (es) * | 1993-10-01 | 2006-11-16 | Novartis Ag | Derivados de pirimidinamina farmacologicamente activos y procedimientos para su preparacion. |
ATE208772T1 (de) * | 1993-10-01 | 2001-11-15 | Novartis Erfind Verwalt Gmbh | Pharmacologisch wirksame pyridinderivate und verfahren zu deren herstellung |
US5612340A (en) * | 1993-10-01 | 1997-03-18 | Ciba-Geigy Corporation | Pyrimidineamine derivatives and processes for the preparation thereof |
US5543520A (en) * | 1993-10-01 | 1996-08-06 | Ciba-Geigy Corporation | Pyrimidine derivatives |
NZ302117A (en) | 1995-01-12 | 1999-10-28 | Smithkline Beecham Corp | 1-cycloalkyl or cycloalkylalkyl 4,5-trisubstituted imidazole derivatives and medicaments |
US5739143A (en) * | 1995-06-07 | 1998-04-14 | Smithkline Beecham Corporation | Imidazole compounds and compositions |
US5658903A (en) | 1995-06-07 | 1997-08-19 | Smithkline Beecham Corporation | Imidazole compounds, compositions and use |
-
1996
- 1996-06-03 US US08/659,102 patent/US5658903A/en not_active Expired - Lifetime
- 1996-06-03 IL IL11854496A patent/IL118544A/en not_active IP Right Cessation
- 1996-06-04 IN IN1210DE1996 patent/IN186434B/en unknown
- 1996-06-05 MY MYPI96002184A patent/MY114014A/en unknown
- 1996-06-05 DZ DZ960087A patent/DZ2043A1/fr active
- 1996-06-06 MA MA24272A patent/MA24242A1/fr unknown
- 1996-06-06 TW TW085106749A patent/TW442481B/zh not_active IP Right Cessation
- 1996-06-07 EP EP02079535A patent/EP1314728A1/en not_active Withdrawn
- 1996-06-07 DE DE69626513T patent/DE69626513T2/de not_active Expired - Fee Related
- 1996-06-07 PL PL96323916A patent/PL185515B1/pl not_active IP Right Cessation
- 1996-06-07 CN CN96195882A patent/CN1130358C/zh not_active Expired - Fee Related
- 1996-06-07 EP EP96921517A patent/EP0831830B1/en not_active Expired - Lifetime
- 1996-06-07 JP JP9502174A patent/JPH11513017A/ja not_active Ceased
- 1996-06-07 HU HU9802259A patent/HUP9802259A3/hu unknown
- 1996-06-07 TR TR97/01574T patent/TR199701574T2/xx unknown
- 1996-06-07 ES ES96921517T patent/ES2194106T3/es not_active Expired - Lifetime
- 1996-06-07 CZ CZ973925A patent/CZ392597A3/cs unknown
- 1996-06-07 AT AT96921517T patent/ATE233561T1/de not_active IP Right Cessation
- 1996-06-07 WO PCT/US1996/010039 patent/WO1996040143A1/en active IP Right Grant
- 1996-06-07 KR KR1019970709055A patent/KR19990022574A/ko active IP Right Grant
- 1996-06-07 PE PE1996000441A patent/PE7798A1/es not_active Application Discontinuation
- 1996-06-07 NZ NZ311403A patent/NZ311403A/xx unknown
- 1996-06-07 CA CA002223533A patent/CA2223533A1/en not_active Abandoned
- 1996-06-07 US US08/973,594 patent/US6218537B1/en not_active Expired - Fee Related
- 1996-06-07 BR BR9608591A patent/BR9608591A/pt not_active Application Discontinuation
-
1997
- 1997-12-05 NO NO975716A patent/NO975716L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
AU699646B2 (en) | 1998-12-10 |
DE69626513D1 (en) | 2003-04-10 |
PL323916A1 (en) | 1998-04-27 |
AU6272696A (en) | 1996-12-30 |
DE69626513T2 (de) | 2003-12-24 |
EP0831830B1 (en) | 2003-03-05 |
PL185515B1 (pl) | 2003-05-30 |
ES2194106T3 (es) | 2003-11-16 |
ATE233561T1 (de) | 2003-03-15 |
IL118544A0 (en) | 1997-03-18 |
CA2223533A1 (en) | 1996-12-19 |
US6218537B1 (en) | 2001-04-17 |
EP0831830A4 (en) | 1998-12-02 |
MA24242A1 (fr) | 1998-07-01 |
BR9608591A (pt) | 1999-01-05 |
TW442481B (en) | 2001-06-23 |
EP1314728A1 (en) | 2003-05-28 |
CN1130358C (zh) | 2003-12-10 |
PE7798A1 (es) | 1998-03-20 |
NZ311403A (en) | 1999-11-29 |
EP0831830A1 (en) | 1998-04-01 |
US5658903A (en) | 1997-08-19 |
IN186434B (hu) | 2001-09-01 |
JPH11513017A (ja) | 1999-11-09 |
WO1996040143A1 (en) | 1996-12-19 |
IL118544A (en) | 2001-08-08 |
NO975716L (no) | 1998-02-04 |
DZ2043A1 (fr) | 2002-10-23 |
CN1192147A (zh) | 1998-09-02 |
CZ392597A3 (cs) | 1998-09-16 |
HUP9802259A3 (en) | 2002-02-28 |
TR199701574T2 (xx) | 1999-09-21 |
NO975716D0 (no) | 1997-12-05 |
MY114014A (en) | 2002-07-31 |
KR19990022574A (ko) | 1999-03-25 |
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