YU35102A - Derivati heterociklo-alkilsulfonil pirazola kao anti- inflamatorni/analgetički agensi - Google Patents
Derivati heterociklo-alkilsulfonil pirazola kao anti- inflamatorni/analgetički agensiInfo
- Publication number
- YU35102A YU35102A YU35102A YUP35102A YU35102A YU 35102 A YU35102 A YU 35102A YU 35102 A YU35102 A YU 35102A YU P35102 A YUP35102 A YU P35102A YU 35102 A YU35102 A YU 35102A
- Authority
- YU
- Yugoslavia
- Prior art keywords
- heterocyclo
- inflammatory
- pyrazole derivatives
- analgesic agents
- alkylsulfonyl
- Prior art date
Links
- 239000000730 antalgic agent Substances 0.000 title 1
- 239000002260 anti-inflammatory agent Substances 0.000 title 1
- 230000003110 anti-inflammatory effect Effects 0.000 title 1
- 206010061218 Inflammation Diseases 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 230000004054 inflammatory process Effects 0.000 abstract 2
- 208000024827 Alzheimer disease Diseases 0.000 abstract 1
- 241000282472 Canis lupus familiaris Species 0.000 abstract 1
- 206010009944 Colon cancer Diseases 0.000 abstract 1
- 241000282326 Felis catus Species 0.000 abstract 1
- 241000282412 Homo Species 0.000 abstract 1
- 208000029742 colonic neoplasm Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 244000144972 livestock Species 0.000 abstract 1
- 201000008482 osteoarthritis Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 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
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- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- 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
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Endocrinology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Reproductive Health (AREA)
- Oncology (AREA)
- Hospice & Palliative Care (AREA)
- Gynecology & Obstetrics (AREA)
- Psychology (AREA)
- Dermatology (AREA)
- Psychiatry (AREA)
- Pregnancy & Childbirth (AREA)
- Communicable Diseases (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
Abstract
Ovaj pronalazak se odnosi na jedinjenja formule (I) gde su R2, R3, R6 i A definisani u opisu, na farmaceutske preparate koji ih sadrže i na njihovu upotrebu u medicini. Jedinjenja iz ovog pronalaska su korisna pri tretmanu ili ublažavanju inflamacije i drugih poremećaja povezanih sa inflamacijom, kao što su osteoartritis, reumatoidni artritis, kancer debelog creva i Alzheimer-ova bolest, kod sisara (poželjno humanih bića, pasa, mačaka i stoke).[The present invention relates to compounds of formula (I) wherein R2, R3, R6 and A are defined as in the specification, to pharmaceutical compositions containing them and to their medicinal use. The compounds of the invention are useful in the treatment or alleviation of inflammation and other inflammation associated disorders, such as osteoarthritis, rheumatoid arthritis, colon cancer and Alzheimer's disease, in mammais (preferably humans, dogs, cats and livestock).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16870199P | 1999-12-03 | 1999-12-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| YU35102A true YU35102A (sh) | 2005-03-15 |
Family
ID=22612589
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| YU35102A YU35102A (sh) | 1999-12-03 | 2000-11-24 | Derivati heterociklo-alkilsulfonil pirazola kao anti- inflamatorni/analgetički agensi |
Country Status (34)
| Country | Link |
|---|---|
| US (2) | US6531492B1 (sh) |
| EP (1) | EP1233959B1 (sh) |
| JP (1) | JP2003517475A (sh) |
| KR (1) | KR20020058074A (sh) |
| CN (1) | CN1423646A (sh) |
| AP (1) | AP2002002532A0 (sh) |
| AR (1) | AR026711A1 (sh) |
| AT (1) | ATE291019T1 (sh) |
| AU (1) | AU783359B2 (sh) |
| BG (1) | BG106694A (sh) |
| BR (1) | BR0016031A (sh) |
| CA (1) | CA2392931A1 (sh) |
| CO (1) | CO5261496A1 (sh) |
| DE (1) | DE60018792T2 (sh) |
| DZ (1) | DZ3246A1 (sh) |
| EA (1) | EA200200520A1 (sh) |
| ES (1) | ES2238324T3 (sh) |
| GT (1) | GT200000204A (sh) |
| HK (1) | HK1052701A1 (sh) |
| HU (1) | HUP0300157A3 (sh) |
| IL (1) | IL149581A0 (sh) |
| IS (1) | IS6376A (sh) |
| MA (1) | MA26848A1 (sh) |
| MX (1) | MXPA02005539A (sh) |
| NO (1) | NO20022624L (sh) |
| OA (1) | OA12100A (sh) |
| PA (1) | PA8508201A1 (sh) |
| PE (1) | PE20010962A1 (sh) |
| PL (1) | PL356669A1 (sh) |
| SK (1) | SK7412002A3 (sh) |
| TN (1) | TNSN00235A1 (sh) |
| WO (1) | WO2001040216A1 (sh) |
| YU (1) | YU35102A (sh) |
| ZA (1) | ZA200204285B (sh) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6833373B1 (en) | 1998-12-23 | 2004-12-21 | G.D. Searle & Co. | Method of using an integrin antagonist and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia |
| US20040248945A1 (en) * | 1999-04-23 | 2004-12-09 | Smithkline Beecham P.L.C. | Thiazolidinedione derivative and its use as antidiabetic |
| WO2001040216A1 (en) * | 1999-12-03 | 2001-06-07 | Pfizer Products Inc. | Heterocyclo-alkylsulfonyl pyrazole derivatives as anti-inflammatory/analgesic agents |
| WO2003018008A1 (fr) * | 2000-02-25 | 2003-03-06 | Shionogi & Co., Ltd. | Agent d'accélération de l'expression de apo ai |
| EP1273582B1 (en) * | 2001-07-05 | 2005-06-29 | Pfizer Products Inc. | Heterocyclo-alkylsulfonyl pyrazoles as anti-inflammatory/analgesic agents |
| DE10135027A1 (de) * | 2001-07-18 | 2003-02-06 | Solvay Pharm Gmbh | Verwendung Trifluoracetylalkyl-substituierter Phenyl-, Phenol- und Benzoylderivate in der Behandlung und/oder Prophylaxe von Obestias und deren Begleit- und/oder Folgeerkrankungen |
| GT200200183A (es) * | 2001-09-28 | 2003-05-23 | Procedimiento para preparar derivados de heterocicloalquilsulfonil pirazol | |
| YU67702A (sh) * | 2001-09-28 | 2004-12-31 | Pfizer Products Inc. | Postupak za dobijanje alkansulfonil piridina |
| KR100954625B1 (ko) * | 2001-10-25 | 2010-04-27 | 노파르티스 아게 | 선택적 사이클로옥시게나제-2 억제제를 포함하는 조합물 |
| WO2003037351A1 (en) | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | Heterocyclo-alkylsulfonyl pyrazoles and their use as cox-2 inhibitors |
| WO2003037352A1 (en) * | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | 1-phenyl-5-n-heterocyclyl-pyrazoles as cyclooxygenase inhibitors for the treatment of inflammation associated disorders |
| WO2003037330A1 (en) * | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | Sulfonyl-and sulfonylheteroaryl-pyrazoles with a hydrazinyl or nitrogen oxide substituent at the 5-position for use as cyclooxygenase inhibitors |
| WO2003037874A1 (en) | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | An efficient synthesis of 5-heteroatom-containing-pyrazoles |
| WO2003037335A1 (en) | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | 5-heteroatom-substituted pyrazoles |
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| PH27357A (en) * | 1989-09-22 | 1993-06-21 | Fujisawa Pharmaceutical Co | Pyrazole derivatives and pharmaceutical compositions comprising the same |
| IL104311A (en) | 1992-02-05 | 1997-07-13 | Fujisawa Pharmaceutical Co | Pyrazole derivatives, processes for the preparation thereof and pharmaceutical compositions containing the same |
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| US5475018A (en) | 1993-11-30 | 1995-12-12 | G. D. Searle & Co. | 1,5-diphenyl pyrazole compounds for treatment of inflammation |
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| JPH10504542A (ja) | 1994-07-27 | 1998-05-06 | ジー．ディー．サール アンド カンパニー | 炎症処置用の置換チアゾール化合物 |
| US5620999A (en) | 1994-07-28 | 1997-04-15 | Weier; Richard M. | Benzenesulfonamide subtituted imidazolyl compounds for the treatment of inflammation |
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| DE69529690T2 (de) | 1994-12-21 | 2003-11-13 | Merck Frosst Canada Inc | Diaryl-2(5h)-fuaranone als cox-2-inhibitoren |
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| GB9520584D0 (en) | 1995-10-09 | 1995-12-13 | Fujisawa Pharmaceutical Co | Pyrazole derivatives,processes for preparation thereof and pharmaceutical composition comprising the same |
| UA57002C2 (uk) | 1995-10-13 | 2003-06-16 | Мерк Фросст Кенада Енд Ко./Мерк Фросст Кенада Енд Сі. | Похідне (метилсульфоніл)феніл-2-(5н)-фуранону, фармацевтична композиція та спосіб лікування |
| JP3337477B2 (ja) | 1995-10-30 | 2002-10-21 | メルク フロスト カナダ アンド カンパニー | Ｃｏｘ−２阻害剤のプロドラッグとしての３，４−ジアリール−２−ヒドロキシ−２，５−ジヒドロフラン |
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