ATE361748T1 - 1-(4-sulfamylphenyl)-3-trifluormethyl-5-aryl-2- pyrazoline als cyclooxygenase-2 inhibitoren - Google Patents
1-(4-sulfamylphenyl)-3-trifluormethyl-5-aryl-2- pyrazoline als cyclooxygenase-2 inhibitorenInfo
- Publication number
- ATE361748T1 ATE361748T1 AT00939946T AT00939946T ATE361748T1 AT E361748 T1 ATE361748 T1 AT E361748T1 AT 00939946 T AT00939946 T AT 00939946T AT 00939946 T AT00939946 T AT 00939946T AT E361748 T1 ATE361748 T1 AT E361748T1
- Authority
- AT
- Austria
- Prior art keywords
- sub
- cyclooxygenase
- group
- inhibitors
- aryl
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/06—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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-
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- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A—HUMAN NECESSITIES
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- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Virology (AREA)
- Oncology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Dermatology (AREA)
- Communicable Diseases (AREA)
- Ophthalmology & Optometry (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Vascular Medicine (AREA)
- Obesity (AREA)
- Transplantation (AREA)
- Emergency Medicine (AREA)
- Molecular Biology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13941699P | 1999-06-16 | 1999-06-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE361748T1 true ATE361748T1 (de) | 2007-06-15 |
Family
ID=22486543
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT00939946T ATE361748T1 (de) | 1999-06-16 | 2000-06-16 | 1-(4-sulfamylphenyl)-3-trifluormethyl-5-aryl-2- pyrazoline als cyclooxygenase-2 inhibitoren |
Country Status (11)
Country | Link |
---|---|
US (2) | US6376519B1 (de) |
EP (1) | EP1191931B1 (de) |
JP (1) | JP2003501464A (de) |
KR (1) | KR100796851B1 (de) |
AT (1) | ATE361748T1 (de) |
AU (1) | AU771668C (de) |
CA (1) | CA2377153A1 (de) |
DE (1) | DE60034785D1 (de) |
IL (2) | IL146851A0 (de) |
NZ (1) | NZ516553A (de) |
WO (1) | WO2000076503A1 (de) |
Families Citing this family (34)
Publication number | Priority date | Publication date | Assignee | Title |
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US6716991B1 (en) * | 1993-11-30 | 2004-04-06 | G. D. Searle & Co. | Process for preparing a substituted pyrazolyl benzenesulfonamide for the treatment of inflammation |
US20040072889A1 (en) * | 1997-04-21 | 2004-04-15 | Pharmacia Corporation | Method of using a COX-2 inhibitor and an alkylating-type antineoplastic agent as a combination therapy in the treatment of neoplasia |
US20040122011A1 (en) * | 1998-12-23 | 2004-06-24 | Pharmacia Corporation | Method of using a COX-2 inhibitor and a TACE inhibitors as a combination therapy |
US20030096854A1 (en) * | 2002-06-12 | 2003-05-22 | Ho-Shen Lin | Substituted tricyclics |
ES2174757B1 (es) * | 2001-04-06 | 2003-11-01 | Esteve Labor Dr | Empleo de derivados de firazolinas en la elaboracion de un medicamentopara la prevencion y/o el tratamiento de enfermedades proliferativas celulares. |
US6878729B2 (en) | 2001-05-04 | 2005-04-12 | The Procter & Gamble Company | Medicinal uses of dihydropyrazoles |
ES2183720B1 (es) * | 2001-06-18 | 2004-01-16 | Esteve Labor Dr | Procedimiento para la preparacion de derivados de 1,5-diaril-3-trifluorometil-delta2-pirazolinas racemicas y enantiomericamente puras. |
WO2003024958A2 (en) * | 2001-09-18 | 2003-03-27 | Onconova Therapeutics, Inc. | Processes for the preparation of 1,5-diaryl-3-substituted-pyrazoles |
AU2002330042A1 (en) | 2001-09-18 | 2003-04-01 | Onconova Therapeutics, Inc. | Process for the preparation of 1,5-diarylpyrazoles |
EP1578721A2 (de) | 2001-10-12 | 2005-09-28 | Onconova Therapeutics, Inc. | Verfahren zur herstellung von substituierten isoxazolen und 2-isoxazolinen |
US20030220374A1 (en) * | 2002-01-14 | 2003-11-27 | Pharmacia Corporation | Compositions and methods of treatment involving peroxisome proliferator-activated receptor-gamma agonists and cyclooxygenase-2 selective inhibitors |
US20030212138A1 (en) * | 2002-01-14 | 2003-11-13 | Pharmacia Corporation | Combinations of peroxisome proliferator-activated receptor-alpha agonists and cyclooxygenase-2 selective inhibitors and therapeutic uses therefor |
US7745639B2 (en) | 2002-03-08 | 2010-06-29 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
AU2003270049A1 (en) * | 2002-08-29 | 2004-03-19 | University Of Florida Research Foundation Incorporated | Cox-2 mediated altered prostaglandin balance in diabetes complications |
US20040147581A1 (en) * | 2002-11-18 | 2004-07-29 | Pharmacia Corporation | Method of using a Cox-2 inhibitor and a 5-HT1A receptor modulator as a combination therapy |
ATE465725T1 (de) | 2002-12-13 | 2010-05-15 | Warner Lambert Co | Alpha-2-delta-ligand zur behandlung vonsymptomen der unteren harnwege |
US20040220155A1 (en) * | 2003-03-28 | 2004-11-04 | Pharmacia Corporation | Method of providing a steroid-sparing benefit with a cyclooxygenase-2 inhibitor and compositions therewith |
WO2004093829A2 (en) * | 2003-03-31 | 2004-11-04 | Temple University-Of The Commonwealth System Of Higher Education | (-)1-(4-sulfamylaryl)-3-substituted-5-heteroaryl-2 pyrazolines as inhibitors of cyclooxygenase-2 |
WO2005009342A2 (en) * | 2003-07-16 | 2005-02-03 | Pharmacia Corporation | Method for the treatment or prevention of dermatological disorders with a cyclooxygenase-2 inhibitor alone and in combination with a dermatological treatment agent and compositions therewith |
US20050119262A1 (en) * | 2003-08-21 | 2005-06-02 | Pharmacia Corporation | Method for preventing or treating an optic neuropathy with a cox-2 inhibitor and an intraocular pressure reducing agent |
US20050107350A1 (en) * | 2003-08-22 | 2005-05-19 | Pharmacia Corporation | Method for the treatment or prevention of bone disorders with a cyclooxygenase-2 inhibitor alone and in combination with a bone disorder treatment agent and compositions therewith |
US20050187278A1 (en) * | 2003-08-28 | 2005-08-25 | Pharmacia Corporation | Treatment or prevention of vascular disorders with Cox-2 inhibitors in combination with cyclic AMP-specific phosphodiesterase inhibitors |
US20050113409A1 (en) * | 2003-09-03 | 2005-05-26 | Pharmacia Corporation | Method for the prevention or treatment of pain, inflammation and inflammation-related disorders with a Cox-2 selective inhibitor in combination with a nitric oxide-donating agent and compositions therewith |
WO2005079808A1 (en) | 2004-01-22 | 2005-09-01 | Pfizer Limited | Triazole derivatives which inhibit vasopressin antagonistic activity |
ES2238923B1 (es) * | 2004-02-16 | 2006-11-01 | Laboratorios Del Dr. Esteve, S.A. | Nuevos derivados pirazolinicos sustituidos. |
KR20070044799A (ko) * | 2004-02-16 | 2007-04-30 | 라보라토리오스 델 드라. 에스테브.에스.에이. | 암 치료에 유용한 피라졸린 유도체 |
TW200533657A (en) | 2004-02-17 | 2005-10-16 | Esteve Labor Dr | Substituted pyrazoline compounds, their preparation and use as medicaments |
EA012980B1 (ru) | 2004-03-16 | 2010-02-26 | Темпл Юниверсити Оф Дзе Коммонвелт Систем Оф Хайер Эдьюкейшн | Замещённые фенокси- и фенилтиопроизводные для лечения пролиферативных нарушений |
BRPI0510340A (pt) * | 2004-04-28 | 2007-10-30 | Pfizer | derivados de 3-heterociclil-4-feniltriazol como inibidores do receptor via da vasopressina |
ES2257929B1 (es) | 2004-07-16 | 2007-05-01 | Laboratorios Del Dr. Esteve, S.A. | Derivados de pirazolina, procedimiento para su obtencion y utilizacion de los mismos como agentes terapeuticos. |
EP1743892A1 (de) | 2005-07-15 | 2007-01-17 | Laboratorios del Dr. Esteve S.A. | Substituierte Pyrazolin Verbindungen, deren Herstellung und Verwendung als Medikament |
US7897589B2 (en) | 2005-07-15 | 2011-03-01 | Laboratorios Del Dr. Esteve, S.A. | Substituted pyrazoline compounds, their preparation and use as medicaments |
EP1743890A1 (de) | 2005-07-15 | 2007-01-17 | Laboratorios Del Dr. Esteve, S.A. | 4,5-Dihydro-1H-Pyrazol-Derivative, Verfahren zur Herstellung und ihre Verwendung als Medikamente. |
CN101600458A (zh) | 2006-12-22 | 2009-12-09 | 瑞蔻达蒂爱尔兰有限公司 | 采用α2δ配体和NSAID的下泌尿道疾病的联合治疗 |
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US2740793A (en) | 1956-04-03 | Pyrazolines | ||
US2640056A (en) | 1949-06-03 | 1953-05-26 | Ilford Ltd | Pyrazoline sulphonic acids |
BE788658R (fr) | 1971-09-09 | 1973-03-12 | Hoechst Ag | Derives de 3-(3', 4'-dichloro-6'-alkylphenyl) -delta2-pyrazolines, leurpreparation et leur utilisation comme agents d'azurage |
US3836523A (en) | 1972-11-03 | 1974-09-17 | Sun Research Development | One-step synthesis of caprolactam |
US4045571A (en) | 1973-04-17 | 1977-08-30 | Bayer Aktiengesellschaft | Pyrazol-5-ones |
DE2452946A1 (de) | 1974-11-08 | 1976-05-13 | Merck Patent Gmbh | Pyrazolidinone und verfahren zu ihrer herstellung |
US4448973A (en) | 1981-07-13 | 1984-05-15 | American Cyanamid Company | Therapeutically active 3-substituted amino-1-phenyl and substituted phenyl-2-pyrazolines |
US4447442A (en) | 1981-07-13 | 1984-05-08 | American Cyanamid Company | 3-Trifluoroacetylamino-1-aryl-2-pyrazolines |
US4407803A (en) | 1981-08-17 | 1983-10-04 | Abbott Laboratories | Antiinflammatory 1-(quinolinyl)-2-pyrazoline derivatives |
AU626881B2 (en) | 1988-07-14 | 1992-08-13 | F. Hoffmann-La Roche Ag | Benzofused heterocyclics used as pharmaceuticals |
DE3831430A1 (de) | 1988-09-15 | 1990-03-22 | Bayer Ag | Substituierte 4-heterocyclyloximino-pyrazolin-5-one, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel |
US5134148A (en) | 1989-02-28 | 1992-07-28 | Imperial Chemical Industries Plc | Heterocycles for use as inhibitors of leukotrienes |
DE4126994A1 (de) | 1991-08-16 | 1993-02-18 | Basf Ag | (alpha)-arylacrylsaeurederivate, ihre herstellung und verwendung zur bekaempfung von schaedlingen und pilzen |
US5334719A (en) | 1992-06-17 | 1994-08-02 | Merck Frosst Canada, Inc. | Bicyclic(azaaromatic)indoles as inhibitors of leukotriene bisynthesis |
US5434178A (en) | 1993-11-30 | 1995-07-18 | G.D. Searle & Co. | 1,3,5 trisubstituted pyrazole compounds for treatment of inflammation |
US5908852A (en) | 1994-11-14 | 1999-06-01 | G. D. Searle & Co. | 1,3,5 trisubstituted pyrazole compounds for treatment of inflammation |
US5700816A (en) | 1995-06-12 | 1997-12-23 | Isakson; Peter C. | Treatment of inflammation and inflammation-related disorders with a combination of a cyclooxygenase-2 inhibitor and a leukotriene A4 hydrolase inhibitor |
US5756529A (en) | 1995-09-29 | 1998-05-26 | G.D. Searle & Co. | Substituted pyrazolyl benzenesulfonamides for use in veterinary therapies |
JP2002504909A (ja) * | 1997-06-13 | 2002-02-12 | スミスクライン・ビーチャム・コーポレイション | 新規な置換ピラゾールおよびピラゾリン化合物 |
US5972986A (en) | 1997-10-14 | 1999-10-26 | G.D. Searle & Co. | Method of using cyclooxygenase-2 inhibitors in the treatment and prevention of neoplasia |
US6025353A (en) | 1997-11-19 | 2000-02-15 | G.D. Searle & Co. | Method of using cyclooxygenase-2 inhibitors as anti-angiogenic agents |
AUPP103497A0 (en) | 1997-12-19 | 1998-01-15 | Panbio Pty Ltd | Assay apparatus |
ES2137138B1 (es) * | 1998-05-29 | 2000-09-16 | Esteve Labor Dr | Derivados de pirazolinas, su preparacion y su aplicacion como medicamentos. |
-
2000
- 2000-06-16 KR KR1020017016170A patent/KR100796851B1/ko not_active IP Right Cessation
- 2000-06-16 EP EP00939946A patent/EP1191931B1/de not_active Expired - Lifetime
- 2000-06-16 NZ NZ516553A patent/NZ516553A/xx not_active IP Right Cessation
- 2000-06-16 US US09/595,760 patent/US6376519B1/en not_active Ceased
- 2000-06-16 AU AU54951/00A patent/AU771668C/en not_active Ceased
- 2000-06-16 AT AT00939946T patent/ATE361748T1/de not_active IP Right Cessation
- 2000-06-16 IL IL14685100A patent/IL146851A0/xx active IP Right Grant
- 2000-06-16 CA CA002377153A patent/CA2377153A1/en not_active Abandoned
- 2000-06-16 JP JP2001502836A patent/JP2003501464A/ja active Pending
- 2000-06-16 DE DE60034785T patent/DE60034785D1/de not_active Expired - Lifetime
- 2000-06-16 WO PCT/US2000/016656 patent/WO2000076503A1/en active IP Right Grant
-
2001
- 2001-11-30 IL IL146851A patent/IL146851A/en not_active IP Right Cessation
-
2003
- 2003-07-29 US US10/630,397 patent/USRE39681E1/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JP2003501464A (ja) | 2003-01-14 |
AU5495100A (en) | 2001-01-02 |
CA2377153A1 (en) | 2000-12-21 |
EP1191931A1 (de) | 2002-04-03 |
AU771668B2 (en) | 2004-04-01 |
USRE39681E1 (en) | 2007-06-05 |
KR100796851B1 (ko) | 2008-01-22 |
EP1191931A4 (de) | 2002-11-27 |
NZ516553A (en) | 2004-01-30 |
KR20020015350A (ko) | 2002-02-27 |
IL146851A (en) | 2008-03-20 |
IL146851A0 (en) | 2002-07-25 |
US6376519B1 (en) | 2002-04-23 |
WO2000076503A1 (en) | 2000-12-21 |
AU771668C (en) | 2005-08-11 |
EP1191931B1 (de) | 2007-05-09 |
DE60034785D1 (en) | 2007-06-21 |
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