BR0009952A - Composto, pró-droga, processo para produzir um composto, composição farmacêutica, método para antagonizar um receptor de adenosina a3, para inibir a p38 map quinase e a produção de tnf-alfa e para prevenir ou tratar doenças, e uso de um composto - Google Patents
Composto, pró-droga, processo para produzir um composto, composição farmacêutica, método para antagonizar um receptor de adenosina a3, para inibir a p38 map quinase e a produção de tnf-alfa e para prevenir ou tratar doenças, e uso de um compostoInfo
- Publication number
- BR0009952A BR0009952A BR0009952-0A BR0009952A BR0009952A BR 0009952 A BR0009952 A BR 0009952A BR 0009952 A BR0009952 A BR 0009952A BR 0009952 A BR0009952 A BR 0009952A
- Authority
- BR
- Brazil
- Prior art keywords
- compound
- tnf
- adenosine receptor
- antagonizing
- inhibit
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
-
- 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
- A61P11/06—Antiasthmatics
-
- 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
- A61P17/06—Antipsoriatics
-
- 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
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- 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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- 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
- A61P37/08—Antiallergic agents
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- 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
-
- 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
- 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
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Endocrinology (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Virology (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
Abstract
"COMPOSTO, PRó-DROGA PROCESSO PARA PRODUZIR UM COMPOSTO, COMPOSIçãO FARMACêUTICA MéTODO PARA ANTAGONIZAR UM RECEPTOR DE ADENOSINA A3, PARA INIBIR A P38 MAP QUINASE E A PRODUçãO DE TNF-ALFA E PARA PREVENIR OU TRATAR DOENçAS, E USO DE UM COMPOSTO". Os compostos opcionalmente oxidados em N representados pela fórmula geral (I) seus sais que são usáveis como preventivos ou remédios para doenças em associação com o receptor de adenosina A3 porque têm excelente antagonismo ao receptor de adenosina A3 em que R^ 1^ representa hidrogênio, hidrocarbila, um heterociclo, amino ou acila; R^ 2^ representa um grupo aromático; R^ 3^ representa hidrogênio, piridila ou hidrocarbila aromática; X representa oxigênio ou enxofre opcionalmente oxidado; Y representa uma ligação, oxigênio, enxofre opcionalmente oxidado ou NR^ 4^ (em que R^ 4^ representa hidrogênio, hidrocarbila, ou acila); e Z representa uma ligação ou um hidrocarbila de cadeia bivalente. Além disso, os compostos (1) ou seus sais exibem excelentes efeitos de inibir p38MAP quinase e inibir a TNF-<244> e, portanto, também são usáveis como preventivos ou remédios para doenças em associação com a p38MAP quinase ou TNF-<244>.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11668699 | 1999-04-23 | ||
JP22465099 | 1999-08-06 | ||
PCT/JP2000/002575 WO2000064894A1 (fr) | 1999-04-23 | 2000-04-20 | Composes 5-pyridyle-1,3-azole, leur procede de fabrication et leur utilisation |
Publications (1)
Publication Number | Publication Date |
---|---|
BR0009952A true BR0009952A (pt) | 2002-03-26 |
Family
ID=26454974
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR0009952-0A BR0009952A (pt) | 1999-04-23 | 2000-04-20 | Composto, pró-droga, processo para produzir um composto, composição farmacêutica, método para antagonizar um receptor de adenosina a3, para inibir a p38 map quinase e a produção de tnf-alfa e para prevenir ou tratar doenças, e uso de um composto |
Country Status (24)
Country | Link |
---|---|
US (3) | US7101899B1 (pt) |
EP (1) | EP1180518B1 (pt) |
KR (2) | KR100449215B1 (pt) |
CN (1) | CN1156471C (pt) |
AU (1) | AU765473B2 (pt) |
BR (1) | BR0009952A (pt) |
CA (1) | CA2370264A1 (pt) |
CZ (1) | CZ300709B6 (pt) |
DE (1) | DE60033028T2 (pt) |
DK (1) | DK1180518T3 (pt) |
ES (1) | ES2275500T3 (pt) |
HK (1) | HK1044338B (pt) |
HU (1) | HUP0203766A3 (pt) |
IL (1) | IL146105A (pt) |
MX (1) | MXPA01010675A (pt) |
MY (1) | MY126736A (pt) |
NO (1) | NO320588B1 (pt) |
NZ (1) | NZ515215A (pt) |
PL (1) | PL351148A1 (pt) |
PT (1) | PT1180518E (pt) |
RU (1) | RU2237062C2 (pt) |
SI (1) | SI1180518T1 (pt) |
SK (1) | SK286666B6 (pt) |
WO (1) | WO2000064894A1 (pt) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
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AU765473B2 (en) | 1999-04-23 | 2003-09-18 | Takeda Pharmaceutical Company Limited | 5-pyridyl-1,3-azole compounds, process for producing the same and use thereof |
US7122666B2 (en) | 1999-07-21 | 2006-10-17 | Sankyo Company, Limited | Heteroaryl-substituted pyrrole derivatives, their preparation and their therapeutic uses |
ES2254238T3 (es) * | 1999-10-27 | 2006-06-16 | Novartis Ag | Compuestos de tiazol e imidazo(4,5-b)piridina y su uso farmaceutico. |
WO2001074811A2 (en) * | 2000-03-30 | 2001-10-11 | Takeda Chemical Industries, Ltd. | Substituted 1,3-thiazole compounds, their production and use |
ATE440096T1 (de) | 2000-12-08 | 2009-09-15 | Takeda Pharmaceutical | Substituierte thiazolderivate mit 3- pyridylgruppen, verfahren zu deren herstellung und deren verwendung |
WO2002051442A1 (fr) * | 2000-12-26 | 2002-07-04 | Takeda Chemical Industries, Ltd. | Co-prescriptions |
WO2002062792A1 (fr) * | 2001-02-02 | 2002-08-15 | Takeda Chemical Industries, Ltd. | Inhibiteur de jnk |
DE60212836T2 (de) * | 2001-05-16 | 2007-01-25 | Gpc Biotech Ag | Pyridylpyrimidin-derivate als wirksame verbindungen gegen prionen-krankheiten |
RS95003A (en) * | 2001-05-31 | 2007-02-05 | Sanofi-Aventis, | Aminoquinoline and aminopyridine derivatives and their use as adenosine a3 ligands |
WO2002100433A1 (en) * | 2001-06-11 | 2002-12-19 | Takeda Chemical Industries, Ltd. | Medicinal compositions |
MXPA04003729A (es) * | 2001-10-22 | 2004-07-23 | Tanabe Seiyaku Co | Compuestos de 4-imidazolin-2-ona. |
US7473695B2 (en) | 2001-10-22 | 2009-01-06 | Mitsubishi Tanabe Pharma Corporation | 4-imidazolin-2-one compounds |
US7064139B2 (en) * | 2001-10-29 | 2006-06-20 | Uniroyal Chemical Company, Inc. | Method for treating retroviral infections |
WO2004004720A1 (en) * | 2002-07-03 | 2004-01-15 | Astex Technology Limited | 3-`(hetero) arylmethoxy ! pyridines and their analogues as p38 map kinase inhibitors |
EP1554269A1 (en) | 2002-07-09 | 2005-07-20 | Vertex Pharmaceuticals Incorporated | Imidazoles, oxazoles and thiazoles with protein kinase inhibiting activities |
NZ537980A (en) * | 2002-08-23 | 2007-08-31 | Rigel Pharmaceuticals Inc | Pyridyl substituted heterocycles useful for treating or preventing HCV infection |
AR044519A1 (es) * | 2003-05-02 | 2005-09-14 | Novartis Ag | Derivados de piridin-tiazol amina y de pirimidin-tiazol amina |
US7326790B2 (en) | 2003-05-02 | 2008-02-05 | Rigel Pharmaceuticals, Inc. | Diphenylisoxazole compounds and hydro isomers thereof |
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DK1700856T3 (en) * | 2003-12-26 | 2015-12-14 | Kyowa Hakko Kirin Co Ltd | thiazole |
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JP2007223903A (ja) * | 2004-07-09 | 2007-09-06 | Takeda Chem Ind Ltd | 新規な固体分散体およびその製造方法 |
US7713998B2 (en) | 2004-11-10 | 2010-05-11 | Ono Pharmaceutical Co., Ltd. | Nitrogenous heterocyclic compound and pharmaceutical use thereof |
CN101203498A (zh) | 2005-05-02 | 2008-06-18 | 里格尔药品股份有限公司 | 包括可代谢部分的杂环抗病毒化合物及其用途 |
WO2006137658A1 (en) * | 2005-06-20 | 2006-12-28 | Dongbu Hitek Co., Ltd. | New substituted 1,3-thiazole derivatives or pharmaceutically acceptable salts thereof having immunosuppression and inflammation inhibitory acitivity, intermediate compounds or pharmaceutically acceptable salts thereof, a process for the preparation thereof, and pharmaceutical composition comprising the same |
US7494519B2 (en) * | 2005-07-28 | 2009-02-24 | 3M Innovative Properties Company | Abrasive agglomerate polishing method |
PT1921077T (pt) * | 2005-08-02 | 2017-10-26 | Kyowa Hakko Kirin Co Ltd | Agente para tratar e/ou prevenir distúrbio do sono |
WO2007022415A2 (en) * | 2005-08-18 | 2007-02-22 | Pharmacopeia, Inc. | Substituted 2-aminothiazoles for treating neurodegenerative diseases |
US7968572B2 (en) | 2005-10-03 | 2011-06-28 | Ono Pharmaceuticals Co., Ltd. | Nitrogen-containing heterocyclic compound and pharmaceutical application thereof |
JP5324785B2 (ja) | 2005-10-28 | 2013-10-23 | 武田薬品工業株式会社 | 複素環アミド化合物及びその用途 |
JPWO2007083522A1 (ja) * | 2006-01-18 | 2009-06-11 | 株式会社ネクスト21 | 医療用ゲル形成組成物,その組成物の投与デバイス及び薬剤放出制御担体 |
EP2044957A4 (en) | 2006-06-28 | 2011-01-05 | Aska Pharm Co Ltd | TREATMENT AGENT FOR INFLAMMATORY BOWEL DISEASE |
EP2055268A4 (en) | 2006-08-21 | 2012-05-30 | Next21 Kk | BONE MODEL, BONE FILLER AND METHOD FOR PRODUCING THE BONE FILLER |
EP2123255B1 (en) * | 2007-02-16 | 2013-05-15 | ASKA Pharmaceutical Co., Ltd. | Pharmaceutical composition containing fine particle oil-based suspension |
WO2008133102A1 (ja) | 2007-04-20 | 2008-11-06 | Daido Chemical Corporation | 新規乾式固体分散体用基剤、該基剤を含有する固体分散体及び該分散体を含有する組成物 |
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EP2540286A4 (en) | 2010-02-26 | 2015-05-27 | Nisshin Kasei Co Ltd | HARD CAPSULE AND METHOD OF PRODUCING THE SAME |
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CN103288817A (zh) * | 2013-07-02 | 2013-09-11 | 天津理工大学 | 一种基于1,3,4-噻二唑和1,3,4-噁二唑的希夫碱衍生物及其制备方法和应用 |
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KR101851972B1 (ko) | 2015-10-21 | 2018-06-11 | 주식회사 제이아이바이오팜 | 청호, 구절초, 애엽, 인진호, 괴각, 대계, 및 목향을 포함하는 한약 추출물이 함유된 탈모개선 및 탈모방지용 복합조성물 및 그 제조방법 |
WO2017151409A1 (en) | 2016-02-29 | 2017-09-08 | University Of Florida Research Foundation, Incorporated | Chemotherapeutic methods |
EP3238711B1 (en) | 2016-04-26 | 2023-07-12 | Mitsubishi Chemical Corporation | Base for solid dispersion, production method for solid dispersion using same, and solid dispersion |
ES2676535B1 (es) | 2017-01-20 | 2019-04-29 | Palobiofarma Sl | Moduladores de los receptores a3 de adenosina |
CN108017584B (zh) * | 2017-06-20 | 2021-03-23 | 南开大学 | A3腺苷受体的小分子拮抗剂 |
CN109293652B (zh) * | 2017-07-24 | 2021-10-22 | 四川科伦博泰生物医药股份有限公司 | 一种取代的噻唑衍生物及其用途 |
US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
WO2019071147A1 (en) | 2017-10-05 | 2019-04-11 | Fulcrum Therapeutics, Inc. | INHIBITORS OF KINASE P38 REDUCING EXPRESSION OF DUX4 GENE AND DOWNSTREAM GENES FOR THE TREATMENT OF FSHD |
TW202112368A (zh) | 2019-06-13 | 2021-04-01 | 荷蘭商法西歐知識產權股份有限公司 | 用於治療有關dux4表現之疾病的抑制劑組合 |
Family Cites Families (9)
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EP0149884B1 (en) | 1983-09-09 | 1992-12-16 | Takeda Chemical Industries, Ltd. | 5-pyridyl-1,3-thiazole derivatives, their production and use |
JPH0570446A (ja) | 1991-09-13 | 1993-03-23 | Taisho Pharmaceut Co Ltd | N−チアゾリルスルホンアミド誘導体 |
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AU765473B2 (en) * | 1999-04-23 | 2003-09-18 | Takeda Pharmaceutical Company Limited | 5-pyridyl-1,3-azole compounds, process for producing the same and use thereof |
US20040097555A1 (en) * | 2000-12-26 | 2004-05-20 | Shinegori Ohkawa | Concomitant drugs |
WO2002100433A1 (en) * | 2001-06-11 | 2002-12-19 | Takeda Chemical Industries, Ltd. | Medicinal compositions |
-
2000
- 2000-04-20 AU AU38401/00A patent/AU765473B2/en not_active Ceased
- 2000-04-20 DK DK00917375T patent/DK1180518T3/da active
- 2000-04-20 IL IL14610500A patent/IL146105A/xx unknown
- 2000-04-20 ES ES00917375T patent/ES2275500T3/es not_active Expired - Lifetime
- 2000-04-20 NZ NZ515215A patent/NZ515215A/en unknown
- 2000-04-20 KR KR10-2001-7013493A patent/KR100449215B1/ko not_active IP Right Cessation
- 2000-04-20 EP EP00917375A patent/EP1180518B1/en not_active Expired - Lifetime
- 2000-04-20 SK SK1495-2001A patent/SK286666B6/sk not_active IP Right Cessation
- 2000-04-20 PT PT00917375T patent/PT1180518E/pt unknown
- 2000-04-20 CA CA002370264A patent/CA2370264A1/en not_active Abandoned
- 2000-04-20 HU HU0203766A patent/HUP0203766A3/hu unknown
- 2000-04-20 US US09/959,356 patent/US7101899B1/en not_active Expired - Fee Related
- 2000-04-20 KR KR1020027008313A patent/KR100558123B1/ko not_active IP Right Cessation
- 2000-04-20 PL PL00351148A patent/PL351148A1/xx not_active Application Discontinuation
- 2000-04-20 CN CNB008085498A patent/CN1156471C/zh not_active Expired - Fee Related
- 2000-04-20 MX MXPA01010675A patent/MXPA01010675A/es active IP Right Grant
- 2000-04-20 RU RU2001131556/04A patent/RU2237062C2/ru active
- 2000-04-20 WO PCT/JP2000/002575 patent/WO2000064894A1/ja active IP Right Grant
- 2000-04-20 DE DE60033028T patent/DE60033028T2/de not_active Expired - Fee Related
- 2000-04-20 CZ CZ20013805A patent/CZ300709B6/cs not_active IP Right Cessation
- 2000-04-20 SI SI200030940T patent/SI1180518T1/sl unknown
- 2000-04-20 BR BR0009952-0A patent/BR0009952A/pt not_active Application Discontinuation
- 2000-10-20 MY MYPI20004966A patent/MY126736A/en unknown
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2001
- 2001-10-22 NO NO20015156A patent/NO320588B1/no not_active IP Right Cessation
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2002
- 2002-08-13 HK HK02105924.8A patent/HK1044338B/zh not_active IP Right Cessation
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2006
- 2006-02-16 US US11/354,897 patent/US7276527B2/en not_active Expired - Fee Related
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2007
- 2007-08-29 US US11/896,072 patent/US20090048307A1/en not_active Abandoned
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