TNSN01035A1 - Derives d'ethers de pyrazole nouveaux, et compositions pharmaceutiques les contenant. - Google Patents
Derives d'ethers de pyrazole nouveaux, et compositions pharmaceutiques les contenant.Info
- Publication number
- TNSN01035A1 TNSN01035A1 TNTNSN01035A TNSN01035A TNSN01035A1 TN SN01035 A1 TNSN01035 A1 TN SN01035A1 TN TNSN01035 A TNTNSN01035 A TN TNSN01035A TN SN01035 A TNSN01035 A TN SN01035A TN SN01035 A1 TNSN01035 A1 TN SN01035A1
- Authority
- TN
- Tunisia
- Prior art keywords
- pharmaceutical compositions
- compositions containing
- ether derivatives
- new pyrazole
- pyrazole ether
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- -1 PYRAZOLE ETHER DERIVATIVES Chemical class 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
- 241000124008 Mammalia Species 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 239000000203 mixture Substances 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
- C07D401/02—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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
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- A61P11/08—Bronchodilators
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/14—Antitussive agents
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
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- 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
- 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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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
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- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
- A61P5/16—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4 for decreasing, blocking or antagonising the activity of the thyroid hormones
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
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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
- A61P9/12—Antihypertensives
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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
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
- C07D231/24—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms having sulfone or sulfonic acid radicals in the molecule
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Urology & Nephrology (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Ophthalmology & Optometry (AREA)
- Psychology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Obesity (AREA)
- Immunology (AREA)
Abstract
LA PRESENTE INVENTION CONCERNE DES COMPOSES DE FORMULE : DANS LAQUELLE R1 ET R3 REPRESENTENT DIVERS RADICAUX, R2, R4, R5, R6, R7, ET R8 REPRESENTENT H OU DIVERS RADICAUX. A REPRESENTE O, S, UN GROUPE SO, SO2 OU NR4, X REPRESENTE UN GROUPE CR7 OU N ET Y REPRESENTE UN GROUPE CR8 OU N. ELLE CONCERNE EGALEMENT DES COMPOSITIONS PHARMACEUTIQUES LES CONTENANT. APPLICATION : UTILISATION DE CES COMPOSES ET COMPOSITIONS DANS LE TRAITEMENT OU LE SOULAGEMENT DE L'INFLAMMATION ET D'AUTRES TROUBLES ASSOCIES A L'INFLAMMATION CHEZ LES MAMMIFERES.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18686900P | 2000-03-03 | 2000-03-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TNSN01035A1 true TNSN01035A1 (fr) | 2005-11-10 |
Family
ID=22686598
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TNTNSN01035A TNSN01035A1 (fr) | 2000-03-03 | 2001-03-02 | Derives d'ethers de pyrazole nouveaux, et compositions pharmaceutiques les contenant. |
Country Status (16)
| Country | Link |
|---|---|
| US (3) | US6878726B2 (fr) |
| EP (1) | EP1259504A1 (fr) |
| JP (1) | JP2003525288A (fr) |
| AR (1) | AR027967A1 (fr) |
| AU (2) | AU2001232175B2 (fr) |
| BR (1) | BR0108908A (fr) |
| CA (1) | CA2401697A1 (fr) |
| CO (1) | CO5271651A1 (fr) |
| GT (1) | GT200100036A (fr) |
| HN (1) | HN2001000037A (fr) |
| MX (1) | MXPA02008627A (fr) |
| PA (1) | PA8513101A1 (fr) |
| PE (1) | PE20011164A1 (fr) |
| TN (1) | TNSN01035A1 (fr) |
| WO (1) | WO2001064669A1 (fr) |
| ZA (1) | ZA200207015B (fr) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR0108908A (pt) * | 2000-03-03 | 2002-12-24 | Pfizer Prod Inc | Derivados de éteres de pirazol como agentes antiinflamatórios/analgésicos |
| US20040092552A1 (en) * | 2000-04-25 | 2004-05-13 | Brown David L | 2-Fluorobenzenesulfonyl compounds for the treatment of inflammation |
| CN100506224C (zh) * | 2001-10-25 | 2009-07-01 | 诺瓦提斯公司 | 包含选择性环加氧酶-2抑制剂的组合 |
| JP2005515171A (ja) * | 2001-11-02 | 2005-05-26 | ファイザー・プロダクツ・インク | 5−ヘテロ原子含有ピラゾールの効率的な合成法 |
| WO2003037351A1 (fr) * | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | Heterocyclo-alkylsulfonyle pyrazoles et leur utilisation comme inhibiteurs de cox-2 |
| WO2003037335A1 (fr) | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | Pyrazoles substitues a 5 heteroatomes |
| WO2003037336A1 (fr) * | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | Derives de 1-(5-sulfonyl-pyridin-2-yl)-5-(methylidene-cycloalkylmethoxy)-1h-pyrazole-4-carbonitrile et autres composes utilises en tant qu'inhibiteurs de la cyclooxygenase dans le traitement de l'arthrite, de la neurodegeneration et du cancer du colon |
| WO2003037352A1 (fr) * | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | 1-phenyl-5-n-heterocyclyl-pyrazoles utiles comme inhibiteurs de cyclooxygenase pour le traitement de troubles associes a l'inflammation |
| WO2003037330A1 (fr) | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | Sulfonylpyrazoles et sulfonyl-heteroaryl pyrazoles presentant un substituant hydrazinyle ou oxyde d'azote en position 5, servant d'inhibiteurs de la cyclooxygenase |
| ATE325115T1 (de) * | 2002-08-19 | 2006-06-15 | Glaxo Group Ltd | Pyrimidinderivate als selektive cox-2-inhibitoren |
| AU2004261264A1 (en) | 2003-08-01 | 2005-02-10 | Janssen Pharmaceutica N.V. | Substituted indazole-O-glucosides |
| TW200524951A (en) | 2003-08-01 | 2005-08-01 | Janssen Pharmaceutica Nv | Substituted benzimidazole-, benztriazole-, and benzimidazolone-O-glucosides |
| US8785403B2 (en) | 2003-08-01 | 2014-07-22 | Mitsubishi Tanabe Pharma Corporation | Glucopyranoside compound |
| CA2549015A1 (fr) | 2003-08-01 | 2005-02-10 | Janssen Pharmaceutica N.V. | C-glycosides heterocycliques fusionnes substitues |
| EP2514756B1 (fr) | 2003-08-01 | 2014-12-17 | Mitsubishi Tanabe Pharma Corporation | Nouveaux composés présentant une activité inhibitrice contre le transporteur dépendant du sodium |
| UY30730A1 (es) | 2006-12-04 | 2008-07-03 | Mitsubishi Tanabe Pharma Corp | Forma cristalina del hemihidrato de 1-(b (beta)-d-glucopiranosil) -4-metil-3-[5-(4-fluorofenil) -2-tienilmetil]benceno |
| HUE035130T2 (en) | 2007-09-10 | 2018-05-02 | Janssen Pharmaceutica Nv | A method for preparing compounds useful as SGLT inhibitors |
| CL2008003653A1 (es) | 2008-01-17 | 2010-03-05 | Mitsubishi Tanabe Pharma Corp | Uso de un inhibidor de sglt derivado de glucopiranosilo y un inhibidor de dppiv seleccionado para tratar la diabetes; y composicion farmaceutica. |
| US9056850B2 (en) | 2008-10-17 | 2015-06-16 | Janssen Pharmaceutica N.V. | Process for the preparation of compounds useful as inhibitors of SGLT |
| DE112010001898T5 (de) | 2009-04-27 | 2012-08-02 | Dow Agrosciences Llc | Insektizide Pyridinverbindungen |
| US20110009347A1 (en) | 2009-07-08 | 2011-01-13 | Yin Liang | Combination therapy for the treatment of diabetes |
| EP2488515B1 (fr) | 2009-10-14 | 2017-01-04 | Janssen Pharmaceutica NV | Procédé pour la préparation de composés utiles en tant qu'inhibiteurs de sglt2 |
| TWI599360B (zh) | 2010-05-11 | 2017-09-21 | 健生藥品公司 | 醫藥調配物 |
| RS55056B1 (sr) | 2011-04-13 | 2016-12-30 | Janssen Pharmaceutica Nv | Proces za pripremu jedinjenja koja su korisna kao inhibitori sglt2 |
| TWI542596B (zh) | 2011-05-09 | 2016-07-21 | 健生藥品公司 | (2s,3r,4r,5s,6r)-2-(3-((5-(4-氟苯基)噻吩-2-基)甲基)-4-甲基苯基)-6-(羥甲基)四氫-2h-哌喃-3,4,5-三醇之l-脯胺酸及檸檬酸共晶體 |
| SG11201405761WA (en) | 2012-03-16 | 2014-10-30 | Axikin Pharmaceuticals Inc | 3,5-diaminopyrazole kinase inhibitors |
| JO3215B1 (ar) | 2012-08-09 | 2018-03-08 | Phenex Pharmaceuticals Ag | حلقات غير متجانسة بها 5 ذرات تحتوي على النيتروجين بها استبدال بكربوكساميد أو سلفوناميد كمعدلات لمستقبل نووي غير محمي RORy |
| NZ631142A (en) | 2013-09-18 | 2016-03-31 | Axikin Pharmaceuticals Inc | Pharmaceutically acceptable salts of 3,5-diaminopyrazole kinase inhibitors |
| HUE049801T2 (hu) | 2014-12-23 | 2020-10-28 | Sma Therapeutics Inc | 3,5-diaminopirazol kináz inhibitorok |
| CN104892514A (zh) * | 2015-05-19 | 2015-09-09 | 广州诺威生物技术有限公司 | 一种咪唑类新化合物 |
| US20170071970A1 (en) | 2015-09-15 | 2017-03-16 | Janssen Pharmaceutica Nv | Co-therapy comprising canagliflozin and phentermine for the treatment of obesity and obesity related disorders |
| GB202011068D0 (en) * | 2020-07-17 | 2020-09-02 | Syngenta Crop Protection Ag | Improvements in or relating to organic compounds |
| CN119930520A (zh) * | 2023-11-03 | 2025-05-06 | 中国药科大学 | N-芳基吡唑类化合物及其药物组合物和应用 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE49198T1 (de) * | 1984-05-12 | 1990-01-15 | Fisons Plc | Antiinflammatorische 1,n-diarylpyrazol-3-amine, deren zusammensetzungen und verfahren zu deren herstellung. |
| FI855180A7 (fi) * | 1985-01-18 | 1986-07-19 | Nissan Chemical Ind Ltd | Pyratsolisulfonamidijohdannainen, menetelmä sen valmistamiseksi ja sitä sisältävä rikkaruohomyrkky. |
| US4881985A (en) * | 1988-08-05 | 1989-11-21 | General Motors Corporation | Method for producing anisotropic RE-FE-B type magnetically aligned material |
| PH27357A (en) * | 1989-09-22 | 1993-06-21 | Fujisawa Pharmaceutical Co | Pyrazole derivatives and pharmaceutical compositions comprising the same |
| FR2652352A1 (fr) * | 1989-09-28 | 1991-03-29 | Jouveinal Sa | Benzodiazepines, leur procede et intermediaires de preparation et leurs applications en therapeutique. |
| US5434178A (en) * | 1993-11-30 | 1995-07-18 | G.D. Searle & Co. | 1,3,5 trisubstituted pyrazole compounds for treatment of inflammation |
| US5466823A (en) * | 1993-11-30 | 1995-11-14 | G.D. Searle & Co. | Substituted pyrazolyl benzenesulfonamides |
| FR2725719B1 (fr) * | 1994-10-14 | 1996-12-06 | Jouveinal Inst Rech | Diazepino-indoles inhibiteurs de phosphodiesterases iv |
| 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 |
| FR2746800B1 (fr) * | 1996-03-29 | 1998-06-05 | Jouveinal Inst Rech | Diazepino-indoles inhibiteurs de phosphodiesterases 4 |
| BR9708574A (pt) * | 1996-04-12 | 1999-08-03 | Searle & Co | Derivados benzeno sulfonamida substituídos como pródrogas de inibidores cox-2 |
| FR2762841B1 (fr) * | 1997-04-30 | 1999-07-02 | Jouveinal Inst Rech | Diazepino-indolones inhibitrices de phosphodiesterases iv |
| JP3516658B2 (ja) | 1997-09-24 | 2004-04-05 | メルク エンド カムパニー インコーポレーテッド | Cox−2のインヒビターとして有用な3−アリールオキシ,4−アリールフラン−2−オンの製造方法 |
| EP1028951A1 (fr) | 1997-10-30 | 2000-08-23 | Merck Frosst Canada Inc. | Diaryl-5-alkyl-5-methyl-2(5h)-furanones utilisees en tant qu'inhibiteurs selectifs de cyclo-oxygenase-2 |
| IL139169A0 (en) * | 1998-05-05 | 2001-11-25 | Hoffmann La Roche | Pyrazole derivatives as p-38 map kinase inhibitors |
| JP2000169453A (ja) * | 1998-09-30 | 2000-06-20 | Mitsubishi Chemicals Corp | 1―フェニルピラゾ―ル―3―カルボキサミド誘導体、その中間体およびこれを有効成分とする農薬 |
| BR0108908A (pt) * | 2000-03-03 | 2002-12-24 | Pfizer Prod Inc | Derivados de éteres de pirazol como agentes antiinflamatórios/analgésicos |
-
2001
- 2001-02-22 BR BR0108908-0A patent/BR0108908A/pt not_active IP Right Cessation
- 2001-02-22 WO PCT/IB2001/000237 patent/WO2001064669A1/fr not_active Ceased
- 2001-02-22 AU AU2001232175A patent/AU2001232175B2/en not_active Ceased
- 2001-02-22 AU AU3217501A patent/AU3217501A/xx active Pending
- 2001-02-22 MX MXPA02008627A patent/MXPA02008627A/es unknown
- 2001-02-22 EP EP01904263A patent/EP1259504A1/fr not_active Withdrawn
- 2001-02-22 JP JP2001563509A patent/JP2003525288A/ja active Pending
- 2001-02-22 CA CA002401697A patent/CA2401697A1/fr not_active Abandoned
- 2001-03-01 AR ARP010100978A patent/AR027967A1/es not_active Application Discontinuation
- 2001-03-01 PE PE2001000213A patent/PE20011164A1/es not_active Application Discontinuation
- 2001-03-02 CO CO01016923A patent/CO5271651A1/es not_active Application Discontinuation
- 2001-03-02 GT GT200100036A patent/GT200100036A/es unknown
- 2001-03-02 US US09/798,752 patent/US6878726B2/en not_active Expired - Fee Related
- 2001-03-02 HN HN2001000037A patent/HN2001000037A/es unknown
- 2001-03-02 TN TNTNSN01035A patent/TNSN01035A1/fr unknown
- 2001-03-02 PA PA20018513101A patent/PA8513101A1/es unknown
-
2002
- 2002-09-02 ZA ZA200207015A patent/ZA200207015B/en unknown
-
2004
- 2004-07-16 US US10/893,520 patent/US20040259879A1/en not_active Abandoned
- 2004-07-16 US US10/893,521 patent/US20050004135A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| PE20011164A1 (es) | 2001-11-13 |
| ZA200207015B (en) | 2003-09-02 |
| US6878726B2 (en) | 2005-04-12 |
| AR027967A1 (es) | 2003-04-16 |
| AU2001232175B2 (en) | 2005-07-07 |
| EP1259504A1 (fr) | 2002-11-27 |
| AU3217501A (en) | 2001-09-12 |
| US20020058681A1 (en) | 2002-05-16 |
| BR0108908A (pt) | 2002-12-24 |
| PA8513101A1 (es) | 2003-06-30 |
| JP2003525288A (ja) | 2003-08-26 |
| GT200100036A (es) | 2001-12-18 |
| CA2401697A1 (fr) | 2001-09-07 |
| US20050004135A1 (en) | 2005-01-06 |
| MXPA02008627A (es) | 2003-02-24 |
| HN2001000037A (es) | 2001-06-18 |
| WO2001064669A1 (fr) | 2001-09-07 |
| CO5271651A1 (es) | 2003-04-30 |
| US20040259879A1 (en) | 2004-12-23 |
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