ES2061471T3 - Derivados de la piridina, compuestos farmaceuticos que comprenden la misma, su utilizacion para la fabricacion de medicamentos con valor terapeutico o preventivo y procedimiento para su fabricacion. - Google Patents
Derivados de la piridina, compuestos farmaceuticos que comprenden la misma, su utilizacion para la fabricacion de medicamentos con valor terapeutico o preventivo y procedimiento para su fabricacion.Info
- Publication number
- ES2061471T3 ES2061471T3 ES87116797T ES87116797T ES2061471T3 ES 2061471 T3 ES2061471 T3 ES 2061471T3 ES 87116797 T ES87116797 T ES 87116797T ES 87116797 T ES87116797 T ES 87116797T ES 2061471 T3 ES2061471 T3 ES 2061471T3
- Authority
- ES
- Spain
- Prior art keywords
- aloil
- aloyl
- manufacture
- same
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000003814 drug Substances 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 230000003449 preventive effect Effects 0.000 title abstract 2
- 230000001225 therapeutic effect Effects 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 2
- 150000001875 compounds Chemical class 0.000 title 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 abstract 1
- 208000008469 Peptic Ulcer Diseases 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- 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
-
- 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
-
- 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
-
- 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
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D417/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
LA PRESENTE INVENCION PROPORCIONA DERIVADOS DE PIRIDINA Y SALES FARMACEUTICAMENTE ACEPTABLES DE ELLOS DE FORMULA GENERAL (I) EN LA QUE R1 Y R2 QUE PUEDEN SER IGUALES O DIFERENTES REPRESENTAN UN ATOMO DE HIDROGENO O DE HALOGENO O UN GRUPO ALQUILO, ALCOXI, ALQUILO HALOGENADO, ALCOXICARBONILO O CARBOXILO; X REPRESENTA UN GRUPO DE FORMULA (II) ( EN EL QUE R3 ES H O UN GRUPO ALQUILO, FENILO, BENCILO O ALCOXICARBONILO); Z ES UN GRUPO DE UNA SERIE DE ELLOS ESPECIFICADOS EN LA INVENCION; J Y K QUE PUEDEN SER IGUALES O DIFERENTES REPRESENTAN CADA UNO UN ATOMO DE HIDROGENO O UN GRUPO ALQUILO DE CADENA CORTA. TAMBIEN SE REFIERE LA INVENCION A COMPOSICIONES FARMACEUTICAS QUE CONTIENEN LOS INDICADOS DERIVADOS, A SU EMPLEO EN LA PREPARACION DE MEDICAMENTOS DE VALOR TERAPEUTICO O PREVENTIVO PARA EL TRATAMIENTO DE ULCERAS PEPTICAS Y A PROCESOS PARA SU PREPARACION.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27053686 | 1986-11-13 | ||
| JP2198987 | 1987-02-02 | ||
| JP7778487 | 1987-03-31 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| ES2061471T3 true ES2061471T3 (es) | 1994-12-16 |
| ES2061471T5 ES2061471T5 (es) | 1998-07-16 |
Family
ID=27283658
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES91117132T Expired - Lifetime ES2112260T3 (es) | 1986-11-13 | 1987-11-13 | Derivados de piridina, composiciones farmaceuticas que comprenden los mismos, su utilizacion en la fabricacion de medicamentos que tienen valor terapeutico o preventivo y procedimiento para su fabricacion. |
| ES95102165T Expired - Lifetime ES2118457T3 (es) | 1986-11-13 | 1987-11-13 | Derivados de piridina, composiciones farmaceuticas que comprenden los mismos, el uso de los mismos para la fabricacion de medicamentos que tienen valor terapeutico o preventivo, y un proceso para preparar los mismos. |
| ES87116797T Expired - Lifetime ES2061471T5 (es) | 1986-11-13 | 1987-11-13 | Derivados de la piridina, compuestos farmaceuticos que comprenden la misma, su utilizacion para la fabricacion de medicamentos con valor terapeutico o preventivo y procedimiento para su fabricacion. |
Family Applications Before (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES91117132T Expired - Lifetime ES2112260T3 (es) | 1986-11-13 | 1987-11-13 | Derivados de piridina, composiciones farmaceuticas que comprenden los mismos, su utilizacion en la fabricacion de medicamentos que tienen valor terapeutico o preventivo y procedimiento para su fabricacion. |
| ES95102165T Expired - Lifetime ES2118457T3 (es) | 1986-11-13 | 1987-11-13 | Derivados de piridina, composiciones farmaceuticas que comprenden los mismos, el uso de los mismos para la fabricacion de medicamentos que tienen valor terapeutico o preventivo, y un proceso para preparar los mismos. |
Country Status (18)
| Country | Link |
|---|---|
| US (3) | US5045552A (es) |
| EP (3) | EP0475456B1 (es) |
| JP (1) | JP2544567B2 (es) |
| KR (1) | KR910003330B1 (es) |
| CN (1) | CN1018923B (es) |
| AT (2) | ATE168111T1 (es) |
| AU (1) | AU594836B2 (es) |
| CA (1) | CA1265138A (es) |
| DE (4) | DE3752201T2 (es) |
| DK (2) | DK171024B1 (es) |
| ES (3) | ES2112260T3 (es) |
| FI (1) | FI90544C (es) |
| HK (1) | HK194296A (es) |
| HU (1) | HU198475B (es) |
| LU (1) | LU90396I2 (es) |
| NL (1) | NL990015I2 (es) |
| NO (2) | NO170932C (es) |
| NZ (1) | NZ222488A (es) |
Families Citing this family (152)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62201884A (ja) * | 1986-02-28 | 1987-09-05 | Tokyo Tanabe Co Ltd | ベンズイミダゾール誘導体及びその製造法 |
| JPH0768125B2 (ja) * | 1988-05-18 | 1995-07-26 | エーザイ株式会社 | 酸不安定化合物の内服用製剤 |
| AT391693B (de) * | 1988-11-15 | 1990-11-12 | Cl Pharma | Verfahren zur herstellung von 3-5-dimethyl-4methoxypyridinderivaten sowie neues zwischenprodukt hierfuer |
| US5294629A (en) * | 1988-11-22 | 1994-03-15 | Meiji Seika Kaisha, Ltd. | Benzothiazole and benzimidazole derivatives and antiulcer agent containing the same |
| SE8804629D0 (sv) * | 1988-12-22 | 1988-12-22 | Ab Haessle | New therapeutically active compounds |
| IE64199B1 (en) * | 1988-12-22 | 1995-07-12 | Haessle Ab | Compound with gastric acid inhibitory effect and process for its preparation |
| US4965269A (en) * | 1989-12-20 | 1990-10-23 | Ab Hassle | Therapeutically active chloro substituted benzimidazoles |
| US5049674A (en) * | 1989-12-20 | 1991-09-17 | Aktiebolaget Hassle | Therapeutically active fluoro substituted benzimidazoles |
| ES2024357A6 (es) * | 1990-12-05 | 1992-02-16 | Genesis Para La Investigacion | Procedimiento de obtencion de halohidrato de 2-halometil-3,5-dimetil-4-metoxipiri-dina. |
| WO1993006097A1 (en) * | 1991-09-20 | 1993-04-01 | Merck & Co., Inc. | Novel process for the preparation of anti-ulcer agents |
| US5504082A (en) * | 1992-06-01 | 1996-04-02 | Yoshitomi Pharmaceutical Industries, Ltd. | Pyridine compound and pharmaceutical compostions |
| DE69302646T2 (de) * | 1992-08-21 | 1996-10-31 | Eisai Co Ltd | Benzimidazolverbindungen als Antibiotika gegen Campylobacter pylon |
| AU674058B2 (en) * | 1993-02-17 | 1996-12-05 | Altana Pharma Ag | Substituted heteroarylalkylthiopyridines for controlling helicobacter bacteria |
| UA32583C2 (uk) * | 1993-06-29 | 2001-02-15 | Бік Гульден Ломберг Хеміше Фабрік Гмбх | Похідні арилтіоалкілтіопіридину |
| TW280770B (es) | 1993-10-15 | 1996-07-11 | Takeda Pharm Industry Co Ltd | |
| CA2175235A1 (en) * | 1993-10-29 | 1995-05-04 | Takeshi Kawakita | Pyridine compound and medicinal use thereof |
| KR0142815B1 (ko) * | 1994-12-02 | 1998-07-15 | 정도언 | 신규한 5-피롤릴-6-할로게노-2피리딜메틸설피닐벤즈이미다졸 유도체 |
| KR0179401B1 (ko) * | 1994-02-28 | 1999-03-20 | 송택선 | 신규한 5-피롤릴-2-피리딜메틸설피닐벤즈이미다졸 유도체 |
| HRP960232A2 (en) * | 1995-07-03 | 1998-02-28 | Astra Ab | A process for the optical purification of compounds |
| US5824339A (en) * | 1995-09-08 | 1998-10-20 | Takeda Chemical Industries, Ltd | Effervescent composition and its production |
| KR970032861A (ko) * | 1995-12-29 | 1997-07-22 | 김준웅 | 헬리코박터 피로리 제거용 약제 투여방법 |
| US6489346B1 (en) | 1996-01-04 | 2002-12-03 | The Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and method of using same |
| US6645988B2 (en) | 1996-01-04 | 2003-11-11 | Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and method of using same |
| US5840737A (en) | 1996-01-04 | 1998-11-24 | The Curators Of The University Of Missouri | Omeprazole solution and method for using same |
| EP0983263A1 (en) * | 1997-05-30 | 2000-03-08 | Dr. Reddy's Research Foundation | Novel benzimidazole derivatives as antiulcer agents, process for their preparation and pharmaceutical compositions containing them |
| US6303644B1 (en) | 1997-07-25 | 2001-10-16 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Proton pump inhibitor in therapeutic combination with antibacterial substances |
| AU1361399A (en) * | 1997-10-14 | 1999-05-03 | Eisai Co. Ltd. | Pharmaceutical formulation comprising glycine as a stabilizer |
| US7230014B1 (en) | 1997-10-14 | 2007-06-12 | Eisai Co., Ltd. | Pharmaceutical formulation comprising glycine as a stabilizer |
| WO1999036422A1 (en) | 1998-01-14 | 1999-07-22 | The Uab Research Foundation | Methods of synthesizing and screening inhibitors of bacterial nad synthetase enzyme, compounds thereof, and methods of treating bacterial and microbial infections with inhibitors of bacterial nad synthetase enzyme |
| US6861448B2 (en) | 1998-01-14 | 2005-03-01 | Virtual Drug Development, Inc. | NAD synthetase inhibitors and uses thereof |
| DE19815634A1 (de) * | 1998-04-07 | 1999-10-14 | Bayer Ag | Verfahren zur Herstellung von 3-Methoxy-1-propanol |
| WO1999055158A1 (en) * | 1998-04-30 | 1999-11-04 | Sepracor Inc. | S-rabeprazole compositions and methods |
| WO1999055157A1 (en) * | 1998-04-30 | 1999-11-04 | Sepracor Inc. | R-rabeprazole compositions and methods |
| WO2000000474A1 (en) * | 1998-06-26 | 2000-01-06 | Russinsky Limited | Pyridine building blocks as intermediates in the synthesis of pharmaceutically active compounds |
| US6093734A (en) * | 1998-08-10 | 2000-07-25 | Partnership Of Michael E. Garst, George Sachs, And Jai Moo Shin | Prodrugs of proton pump inhibitors |
| NZ510180A (en) | 1998-08-10 | 2002-11-26 | Univ California | Prodrugs of the pyridyl-methylsulphonyl-benzimidazole type proton pump inhibitors |
| JP4988088B2 (ja) | 1998-08-12 | 2012-08-01 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | ピリジン−2−イルメチルスルフィニル−1h−ベンズイミダゾール、もしくはピリジン−2−イルメチルスルフィニル−1h−ベンズイミダゾールの骨格を有する化合物、またはその薬学的に許容される塩の経口投与形組成物を固定的に組み合わせた組成物 |
| DE19843413C1 (de) * | 1998-08-18 | 2000-03-30 | Byk Gulden Lomberg Chem Fab | Neue Salzform von Pantoprazol |
| JP3926936B2 (ja) | 1998-11-16 | 2007-06-06 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | スルホキシド誘導体・アセトン錯体およびその製造法 |
| US6852739B1 (en) | 1999-02-26 | 2005-02-08 | Nitromed Inc. | Methods using proton pump inhibitors and nitric oxide donors |
| US6353005B1 (en) | 1999-03-02 | 2002-03-05 | Sepracor, Inc. | Method and compositions using (+) norcisapride in combination with proton pump inhibitors or H2 receptor antagonist |
| US6362202B1 (en) | 1999-03-02 | 2002-03-26 | Sepracor Inc. | Methods and compositions using (−) norcisapride in combination with proton pump inhibitors or H2 receptor antagonists |
| US6174902B1 (en) | 1999-04-28 | 2001-01-16 | Sepracor Inc. | R-rabeprazole compositions and methods |
| CA2376202C (en) | 1999-06-07 | 2008-11-18 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Novel preparation and administration form comprising an acid-labile active compound |
| US6555139B2 (en) | 1999-06-28 | 2003-04-29 | Wockhardt Europe Limited | Preparation of micron-size pharmaceutical particles by microfluidization |
| US6245913B1 (en) | 1999-06-30 | 2001-06-12 | Wockhardt Europe Limited | Synthetic procedure for 5-methoxy-2-[(4-methoxy-3,5-dimethyl-2-pyridinyl)-methylthio]-IH-benzimidazole hydrochloride and its conversion to omeprazole |
| WO2001074810A2 (en) * | 2000-03-31 | 2001-10-11 | Ortho Mcneil Pharmaceutical, Inc. | Method for using 2-aryloxyalkylaminobenzoxazoles and 2-aryloxyalkylaminobenzothiazoles as h3 antagonists |
| WO2001097753A2 (en) | 2000-06-19 | 2001-12-27 | Eisai Co. Ltd. | Novel methods using pyridine derivatives |
| US6544556B1 (en) * | 2000-09-11 | 2003-04-08 | Andrx Corporation | Pharmaceutical formulations containing a non-steroidal antiinflammatory drug and a proton pump inhibitor |
| WO2002026210A2 (en) * | 2000-09-29 | 2002-04-04 | Geneva Pharmaceuticals Inc. | Proton pump inhibitor formulation |
| KR20030059318A (ko) | 2000-12-07 | 2003-07-07 | 알타나 파마 아게 | 산 불안정성 활성 성분을 포함하는 현탁액 형태의 약학 제제 |
| KR20030072555A (ko) | 2000-12-07 | 2003-09-15 | 알타나 파마 아게 | 산 불안정성 활성 성분을 포함하는 신속 붕해 정제 |
| CN100536844C (zh) | 2000-12-07 | 2009-09-09 | 尼科梅德有限责任公司 | 包含酸不稳定活性成分的糊剂形式的药物制剂 |
| NL1018295C2 (nl) * | 2001-06-15 | 2002-12-17 | Dsm Nv | Werkwijze voor de bereiding van 4-chloor-pyridine-n-oxiden. |
| US6884810B2 (en) | 2001-09-18 | 2005-04-26 | Zeria Pharmaceutical Co., Ltd. | Benzimidazole derivatives |
| WO2003063927A2 (en) * | 2001-11-16 | 2003-08-07 | Eisai Co. Ltd | Compositions and methods to treat gastrointestinal disorders |
| SE0104295D0 (sv) * | 2001-12-18 | 2001-12-18 | Astrazeneca Ab | New process |
| CA2480358A1 (en) * | 2002-03-26 | 2003-10-09 | Dr. Reddy's Laboratories Limited | Crystalline forms of rabeprazole sodium |
| AU2003241464A1 (en) * | 2002-05-17 | 2003-12-02 | Eisai Co., Ltd. | Compositions and methods using proton pump inhibitors |
| US20030228363A1 (en) * | 2002-06-07 | 2003-12-11 | Patel Mahendra R. | Stabilized pharmaceutical compositons containing benzimidazole compounds |
| TW200410955A (en) | 2002-07-29 | 2004-07-01 | Altana Pharma Ag | Novel salt of (S)-PANTOPRAZOLE |
| WO2004012659A2 (en) * | 2002-08-01 | 2004-02-12 | Nitromed, Inc. | Nitrosated proton pump inhibitors, compositions and methods of use |
| AT413538B (de) * | 2002-10-01 | 2006-03-15 | Dsm Fine Chem Austria Gmbh | Verfahren zur herstellung von substituierten pyridin-n-oxid-verbindungen |
| DE10254167A1 (de) | 2002-11-20 | 2004-06-09 | Icon Genetics Ag | Verfahren zur Kontrolle von zellulären Prozessen in Pflanzen |
| ES2397380T3 (es) | 2002-12-06 | 2013-03-06 | Takeda Gmbh | Procedimiento para preparar compuestos activos ópticamente puros |
| ES2383679T3 (es) | 2002-12-06 | 2012-06-25 | Nycomed Gmbh | Procedimiento para la preparación de (S)-pantoprazol |
| AU2003288576A1 (en) * | 2002-12-16 | 2004-07-09 | Ranbaxy Laboratories Limited | Rabeprazole calcium |
| US7507829B2 (en) * | 2002-12-19 | 2009-03-24 | Teva Pharmaceuticals Industries, Ltd | Solid states of pantoprazole sodium, processes for preparing them and processes for preparing known pantoprazole sodium hydrates |
| WO2004060263A2 (en) * | 2003-01-07 | 2004-07-22 | Ranbaxy Laboratories Limited | Magnesium salt of imidazole derivative |
| US20040180935A1 (en) * | 2003-02-28 | 2004-09-16 | Dr. Reddy's Laboratories Limited Dr. Reddy's Laboratories Inc. | Crystalline form Z of rabeprazole sodium and process for preparation thereof |
| WO2004080961A2 (en) * | 2003-03-12 | 2004-09-23 | Teva Pharmaceutical Industries Ltd. | Crystalline and amorphous solids of pantoprazole and processes for their preparation |
| JP4355703B2 (ja) * | 2003-03-13 | 2009-11-04 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 歯ぎしりの予防剤または治療剤 |
| DE602004032524D1 (de) | 2003-03-24 | 2011-06-16 | Eisai R&D Man Co Ltd | Verfahren zur herstellung von amorphem rabeprazole-natrium-salz |
| PE20050150A1 (es) | 2003-05-08 | 2005-03-22 | Altana Pharma Ag | Una forma de dosificacion que contiene (s)-pantoprazol como ingrediente activo |
| CL2004000983A1 (es) | 2003-05-08 | 2005-03-04 | Altana Pharma Ag | Composicion farmaceutica oral en forma de tableta que comprende a pantoprazol magnetico dihidratado, en donde la forma de tableta esta compuesto por un nucleo, una capa intermedia y una capa exterior; y uso de la composicion farmaceutica en ulceras y |
| WO2004101533A1 (en) * | 2003-05-12 | 2004-11-25 | Janssen Pharmaceutica, N.V. | 1, 3, 4-benzotriazepin-2-one salts and their use as cck receptor ligands |
| US7683177B2 (en) * | 2003-06-10 | 2010-03-23 | Teva Pharmaceutical Industries Ltd | Process for preparing 2-[(pyridinyl)methyl]sulfinyl-substituted benzimidazoles and novel chlorinated derivatives of pantoprazole |
| WO2004112756A1 (en) * | 2003-06-26 | 2004-12-29 | Isa Odidi | Proton pump-inhibitor-containing capsules which comprise subunits differently structured for a delayed release of the active ingredient |
| BRPI0412590A (pt) * | 2003-07-15 | 2006-09-19 | Allergan Inc | processo para preparação de pró-drogas isomericamente puras de inibidores de bomba de próton |
| US8993599B2 (en) | 2003-07-18 | 2015-03-31 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| WO2005020954A2 (en) * | 2003-09-03 | 2005-03-10 | Agi Therapeutics Limited | Proton pump inhibitor formulations, and methods of preparing and using such formulations |
| TWI372066B (en) | 2003-10-01 | 2012-09-11 | Wyeth Corp | Pantoprazole multiparticulate formulations |
| US20050075371A1 (en) * | 2003-10-03 | 2005-04-07 | Allergan, Inc. | Methods and compositions for the oral administration of prodrugs of proton pump inhibitors |
| WO2005039640A1 (en) * | 2003-10-03 | 2005-05-06 | Allergan Inc. | Compositions comprising trefoil factor family peptides and/or mucoadhesives and proton pump inhibitor prodrugs |
| EP1716136A1 (en) | 2004-02-11 | 2006-11-02 | Ulkar Kimya Sanayii Ve Ticaret A.S. | Pyridine benzimidazole sulfoxides of high purity |
| BRPI0507784A (pt) * | 2004-02-18 | 2007-07-17 | Allergan Inc | métodos e composições para a administração de pró-fármacos de inibidores da bomba de prótons |
| JP2007523164A (ja) * | 2004-02-18 | 2007-08-16 | アラーガン、インコーポレイテッド | プロトンポンプインヒビターに関連する化合物の静脈内投与のための方法および組成物 |
| CA2561700A1 (en) * | 2004-04-16 | 2005-12-15 | Santarus, Inc. | Combination of proton pump inhibitor, buffering agent, and prokinetic agent |
| PT1746980E (pt) * | 2004-05-07 | 2012-01-25 | Nycomed Gmbh | Forma de dosagem farmacêutica compreendendo granulados assim como o seu processo de fabrico |
| US8815916B2 (en) | 2004-05-25 | 2014-08-26 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| US8906940B2 (en) | 2004-05-25 | 2014-12-09 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| WO2006003946A1 (ja) * | 2004-06-30 | 2006-01-12 | Eisai R & D Management Co., Ltd. | ベンズイミダゾール誘導体塩沈殿物の製造方法 |
| US8394409B2 (en) | 2004-07-01 | 2013-03-12 | Intellipharmaceutics Corp. | Controlled extended drug release technology |
| US20060024362A1 (en) | 2004-07-29 | 2006-02-02 | Pawan Seth | Composition comprising a benzimidazole and process for its manufacture |
| AU2005268056B2 (en) * | 2004-08-06 | 2008-07-31 | Eisai R&D Management Co., Ltd. | Salts of benzimidazole derivative with amines and process for production thereof |
| US10624858B2 (en) | 2004-08-23 | 2020-04-21 | Intellipharmaceutics Corp | Controlled release composition using transition coating, and method of preparing same |
| WO2006024890A1 (en) * | 2004-08-30 | 2006-03-09 | Apollo International Limited | Improved process for rabeprazole sodium in amorphous form |
| JP2008514653A (ja) * | 2004-09-30 | 2008-05-08 | 江▲蘇▼豪森▲薬▼▲業▼股▲分▼有限公司 | プラゾール類誘導体及びその塩と用途 |
| CN100364989C (zh) * | 2004-09-30 | 2008-01-30 | 江苏豪森药业股份有限公司 | 拉唑类衍生物及其盐和用途 |
| WO2006053383A1 (en) | 2004-11-22 | 2006-05-26 | Anadis Ltd | Bioactive compositions |
| NZ561008A (en) * | 2005-02-21 | 2009-09-25 | Cipla Ltd | New process for synthesis of proton pump inhibitors, namely Rabeprazole sodium |
| WO2006120701A1 (en) * | 2005-03-30 | 2006-11-16 | Lupin Limited | An improved process for the manufacture of rabeprazole sodium |
| US7601737B2 (en) | 2005-07-26 | 2009-10-13 | Nycomed Gmbh | Isotopically substituted proton pump inhibitors |
| GB0525710D0 (en) * | 2005-12-17 | 2006-01-25 | Pliva Hrvatska D O O | An improved process for preparing of substituted 2-benzimidazolesulfoxide compounds |
| US10064828B1 (en) | 2005-12-23 | 2018-09-04 | Intellipharmaceutics Corp. | Pulsed extended-pulsed and extended-pulsed pulsed drug delivery systems |
| EP1818331A1 (en) | 2006-02-14 | 2007-08-15 | EOS Eczacibasi Ozgun Kimyasal Urunler Sanayi Ve Ti Caret A.S. | Process for the preparation of 2-[{4-(3-methoxypropoxy)-3-methylpyridin-2-yl}methylsulfinyl]-1H-benzimidazole substantially free of sulfone impurity |
| ATE533757T1 (de) | 2006-03-10 | 2011-12-15 | Arigen Pharmaceuticals Inc | Neues pyridinderivat mit wirkung gegen helicobacter pylori |
| CA2648280C (en) | 2006-04-03 | 2014-03-11 | Isa Odidi | Controlled release delivery device comprising an organosol coat |
| KR100771655B1 (ko) * | 2006-04-24 | 2007-10-30 | 주식회사 카이로제닉스 | 라베프라졸 및 그 중간체의 제조방법 |
| US10960077B2 (en) | 2006-05-12 | 2021-03-30 | Intellipharmaceutics Corp. | Abuse and alcohol resistant drug composition |
| US7786309B2 (en) * | 2006-06-09 | 2010-08-31 | Apotex Pharmachem Inc. | Process for the preparation of esomeprazole and salts thereof |
| US7863330B2 (en) | 2006-06-14 | 2011-01-04 | Rottapharm S.P.A. | Deloxiglumide and proton pump inhibitor combination in the treatment of gastrointestinal disorders |
| WO2008017020A2 (en) * | 2006-08-03 | 2008-02-07 | Dr. Reddy's Laboratories Limited | Process for preparing proton pump inhibitors |
| US20100317689A1 (en) * | 2006-09-19 | 2010-12-16 | Garst Michael E | Prodrugs of proton pump inhibitors including the 1h-imidazo[4,5-b] pyridine moiety |
| WO2008067037A2 (en) | 2006-10-05 | 2008-06-05 | Santarus, Inc. | Novel formulations of proton pump inhibitors and methods of using these formulations |
| WO2008047681A1 (en) * | 2006-10-13 | 2008-04-24 | Eisai R & D Management Co., Ltd. | Benzimidazole compound having gastric acid secretion inhibitory activity |
| EP2086543A2 (en) | 2006-10-27 | 2009-08-12 | The Curators of the University of Missouri | Compositions comprising at least one acid labile proton pump inhibiting agents, optionally other pharmaceutically active agents and methods of using same |
| CA2671949C (en) | 2006-12-18 | 2011-11-01 | Arigen Pharmaceuticals, Inc. | Helicobacter pylori eradicating agent having inhibitory activity on gastric acid secretion |
| ITMI20062449A1 (it) | 2006-12-19 | 2008-06-20 | Dipharma Spa | Forma cristallina di rabeprazolo sodico |
| TR201910825T4 (tr) | 2006-12-22 | 2019-08-21 | Ironwood Pharmaceuticals Inc | Yemek borusu rahatsizliklarini tedavi̇ etmek i̇çi̇n yöntemler ve bi̇leşi̇mler |
| CA2679741A1 (en) * | 2007-03-15 | 2008-09-18 | Sun Pharma Advanced Research Company Ltd. | Novel prodrugs |
| WO2008146297A2 (en) * | 2007-05-25 | 2008-12-04 | Hetero Drugs Limited | Improved process for amorphous rabeprazole sodium |
| US8247568B2 (en) * | 2007-06-21 | 2012-08-21 | Matrix Laboratories Ltd | Process for the preparation of pure rabeprazole |
| EP2181106A1 (en) * | 2007-07-17 | 2010-05-05 | Ranbaxy Laboratories Limited | Process for the preparation op pantoprazole sodium and pantoprazole sodium sesquihydrate |
| CN101497603B (zh) * | 2008-01-30 | 2012-11-07 | 山东轩竹医药科技有限公司 | 含有被烷氧烷胺氧基取代的吡啶的苯并咪唑衍生物 |
| CN101497604B (zh) * | 2008-01-30 | 2012-09-26 | 山东轩竹医药科技有限公司 | 含有被烷氧乙酰胺基氧基取代的吡啶的苯并咪唑衍生物 |
| SI22806A (sl) * | 2008-06-23 | 2009-12-31 | Krka, Tovarna Zdravil, D.D., Novo Mesto | Nove kristalinične oblike natrijevega rabeprazola |
| CA2756104C (en) | 2009-04-09 | 2013-01-22 | Arigen Pharmaceuticals, Inc. | Pyridine thio derivative, and pharmaceutical composition which contains same and has anti-helicobacter pylori action |
| WO2010134099A1 (en) | 2009-05-21 | 2010-11-25 | Cadila Healthcare Limited | One pot process for preparing omeprazole and related compounds |
| WO2011004281A1 (en) | 2009-07-09 | 2011-01-13 | Alembic Limited | A process for the preparation of amorphous form of rabeprazole sodium |
| CN102140099A (zh) | 2010-02-02 | 2011-08-03 | 山东轩竹医药科技有限公司 | 新的吡啶衍生物 |
| CA2795056C (en) | 2010-03-31 | 2015-03-24 | Ranbaxy Laboratories Limited | Salts of dexlansoprazole and their preparation |
| CN102219777B (zh) * | 2010-04-19 | 2013-06-05 | 江苏豪森药业股份有限公司 | 制备雷贝拉唑钠的方法 |
| CN101805327B (zh) * | 2010-04-29 | 2012-11-21 | 郝志艳 | 一种雷贝拉唑钠化合物及其制法 |
| US20130156720A1 (en) | 2010-08-27 | 2013-06-20 | Ironwood Pharmaceuticals, Inc. | Compositions and methods for treating or preventing metabolic syndrome and related diseases and disorders |
| EP2790696A1 (en) | 2011-12-16 | 2014-10-22 | Atopix Therapeutics Limited | Combination of crth2 antagonist and a proton pump inhibitor for the treatment of eosinophilic esophagitis |
| CN104203938A (zh) | 2012-01-21 | 2014-12-10 | 朱比兰特生命科学有限公司 | 用于制备2-吡啶基甲基亚硫酰基苯并咪唑、它们的类似物和光学活性对映体的方法 |
| WO2014091450A1 (en) | 2012-12-12 | 2014-06-19 | Ranbaxy Laboratories Limited | Process for the preparation of rabeprazole |
| JP6716255B2 (ja) | 2013-01-15 | 2020-07-01 | アイロンウッド ファーマシューティカルズ,インコーポレーテッドIronwood Pharmaceuticals, Inc. | 胆汁酸捕捉剤の胃内滞留型徐放性経口剤形 |
| CN103073536B (zh) * | 2013-01-17 | 2015-06-24 | 丽珠医药集团股份有限公司 | 一种艾普拉唑的制备方法 |
| CN103709141A (zh) * | 2013-10-14 | 2014-04-09 | 寿光富康制药有限公司 | 雷贝拉唑钠的晶型及无定形形式 |
| CN104119315B (zh) * | 2014-05-21 | 2016-03-02 | 丽珠医药集团股份有限公司 | 一种雷贝拉唑钠的制备方法 |
| RU2554735C1 (ru) * | 2014-08-20 | 2015-06-27 | Открытое Акционерное Общество "Татхимфармпрепараты" | Фармацевтическая композиция, содержащая рабепразол натрия, и способ ее получения |
| WO2016126625A1 (en) | 2015-02-03 | 2016-08-11 | Ironwood Pharmaceuticals, Inc. | Methods of treating upper gastrointestinal disorders in ppi refractory gerd |
| WO2016174664A1 (en) | 2015-04-29 | 2016-11-03 | Dexcel Pharma Technologies Ltd. | Orally disintegrating compositions |
| WO2017145146A1 (en) | 2016-02-25 | 2017-08-31 | Dexcel Pharma Technologies Ltd. | Compositions comprising proton pump inhibitors |
| CN106083705A (zh) * | 2016-06-14 | 2016-11-09 | 上药康丽(常州)药业有限公司 | 2‑羟甲基‑4‑(甲氧基丙氧基)‑3‑甲基吡啶盐酸盐的制备方法 |
| US10076494B2 (en) | 2016-06-16 | 2018-09-18 | Dexcel Pharma Technologies Ltd. | Stable orally disintegrating pharmaceutical compositions |
| CN106349220A (zh) * | 2016-08-25 | 2017-01-25 | 岳阳正昊化学科技有限公司 | 一种右旋雷贝拉唑钠的纯化方法 |
| WO2018057989A1 (en) | 2016-09-24 | 2018-03-29 | Washington University | INHIBITORS OF SARM1 NADase ACTIVITY AND USES THEREOF |
| TW202126317A (zh) | 2019-09-24 | 2021-07-16 | 美商普拉塔生技公司 | 用於治療發炎和免疫疾病之組成物和方法 |
| JP2025532389A (ja) | 2022-10-04 | 2025-09-29 | ザビリュク,アルセニー | 大動脈弁の石灰化の抑制 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE7804231L (sv) * | 1978-04-14 | 1979-10-15 | Haessle Ab | Magsyrasekretionsmedel |
| IL66340A (en) * | 1981-08-13 | 1986-08-31 | Haessle Ab | Pharmaceutical compositions comprising pyridylmethyl-thiobenzimidazole derivatives,certain such novel derivatives and their preparation |
| SE8300736D0 (sv) * | 1983-02-11 | 1983-02-11 | Haessle Ab | Novel pharmacologically active compounds |
| GB8417171D0 (en) * | 1984-07-05 | 1984-08-08 | Beecham Group Plc | Compounds |
| SE8404065D0 (sv) * | 1984-08-10 | 1984-08-10 | Haessle Ab | Novel biologically active compounds |
| DE3509333A1 (de) * | 1985-03-15 | 1986-09-18 | Hoechst Ag, 6230 Frankfurt | Substituierte benzimidazolderivate, verfahren zu ihrer herstellung, sie enthaltende pharmazeutische zubereitungen und ihre verwendung als magensaeuresekretionshemmer |
| JPH0674272B2 (ja) * | 1986-11-13 | 1994-09-21 | エーザイ株式会社 | ピリジン誘導体及びそれを含有する潰瘍治療剤 |
| DE4036908A1 (de) * | 1990-11-20 | 1992-05-21 | Ruetgers Pagid Ag | Nutausbildung |
-
1987
- 1987-10-26 FI FI874709A patent/FI90544C/fi not_active IP Right Cessation
- 1987-10-27 NO NO874477A patent/NO170932C/no not_active IP Right Cessation
- 1987-11-03 DK DK575887A patent/DK171024B1/da not_active IP Right Cessation
- 1987-11-09 NZ NZ222488A patent/NZ222488A/en unknown
- 1987-11-12 HU HU875044A patent/HU198475B/hu unknown
- 1987-11-12 CA CA000551684A patent/CA1265138A/en not_active Expired - Lifetime
- 1987-11-12 AU AU81138/87A patent/AU594836B2/en not_active Expired
- 1987-11-13 DE DE3752201T patent/DE3752201T2/de not_active Expired - Lifetime
- 1987-11-13 ES ES91117132T patent/ES2112260T3/es not_active Expired - Lifetime
- 1987-11-13 EP EP91117132A patent/EP0475456B1/en not_active Expired - Lifetime
- 1987-11-13 DE DE1999175035 patent/DE19975035I2/de active Active
- 1987-11-13 ES ES95102165T patent/ES2118457T3/es not_active Expired - Lifetime
- 1987-11-13 AT AT95102165T patent/ATE168111T1/de not_active IP Right Cessation
- 1987-11-13 KR KR1019870012813A patent/KR910003330B1/ko not_active Expired
- 1987-11-13 DE DE3789536T patent/DE3789536T3/de not_active Expired - Lifetime
- 1987-11-13 DE DE3752167T patent/DE3752167T2/de not_active Expired - Lifetime
- 1987-11-13 ES ES87116797T patent/ES2061471T5/es not_active Expired - Lifetime
- 1987-11-13 AT AT91117132T patent/ATE163011T1/de not_active IP Right Cessation
- 1987-11-13 CN CN87107777A patent/CN1018923B/zh not_active Expired
- 1987-11-13 EP EP95102165A patent/EP0654471B1/en not_active Expired - Lifetime
- 1987-11-13 EP EP87116797A patent/EP0268956B2/en not_active Expired - Lifetime
-
1989
- 1989-12-28 US US07/462,328 patent/US5045552A/en not_active Expired - Lifetime
-
1993
- 1993-01-07 JP JP5001119A patent/JP2544567B2/ja not_active Expired - Lifetime
- 1993-11-24 DK DK931318A patent/DK131893D0/da not_active Application Discontinuation
-
1994
- 1994-12-06 US US08/354,726 patent/US5840910A/en not_active Expired - Lifetime
-
1996
- 1996-07-09 US US08/679,473 patent/US5998445A/en not_active Expired - Fee Related
- 1996-10-24 HK HK194296A patent/HK194296A/en not_active IP Right Cessation
-
1999
- 1999-05-07 LU LU90396C patent/LU90396I2/fr unknown
- 1999-05-26 NL NL990015C patent/NL990015I2/nl unknown
-
2000
- 2000-08-18 NO NO2000006C patent/NO2000006I1/no unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2061471T3 (es) | Derivados de la piridina, compuestos farmaceuticos que comprenden la misma, su utilizacion para la fabricacion de medicamentos con valor terapeutico o preventivo y procedimiento para su fabricacion. | |
| ES2056190T3 (es) | Derivados de 4(4-fenil-1-piperazinil)fenoles, inhibidores de 5-lipoxigenasa. | |
| IS1564B (is) | Aðferð við framleiðslu á N1-súbstitúeruðum bensimidasólafleiðum til að nota við lækningar | |
| ES2058527T3 (es) | Derivados de pirimidina condensados procedimiento y compuestos intermedios para su preparacion y composiciones farmaceuticas que los contienen. | |
| CU22305A3 (es) | Procedimiento para la preparacion de un derivado de aminoacidos | |
| MX9303145A (es) | 7-(2-aminoetil)benzotiazolonas. | |
| ES2054860T3 (es) | Nuevos derivados de 9-halogeno-(z)-prostaglandinas, procedimiento para su preparacion, asi como a su utilizacion como medicamentos. | |
| AR012593A1 (es) | Pirrolopiridinas sustituidas, composicion farmaceutica que las contiene, procedimiento para su preparacion y el uso de las mismas en la manufacturade un medicamento | |
| GB1069343A (en) | Propanolamine derivatives | |
| MX9300031A (es) | Derivados de piperazina, procedimiento para su preparacion y composicion farmaucetica que los contiene. | |
| IS3284A7 (is) | Aðferð við framleiðslu á N1-súbstitúeruðum bensimidasólafleiðum til að nota við lækningar | |
| NO166938C (no) | Analogifremgangsmaate for fremstilling av terapeutisk aktive fenoxyeddiksyrederivater. | |
| NO810485L (no) | Nye derivater av 3,4,5-trihydroksypiperdin, fremgangsmaate til deres fremstilling, og deres anvendelse som legemiddel, samt i dyreernaering | |
| AR035465A1 (es) | Compuestos de imidazopiridina, procesos para su preparacion,formulacion farmaceutica, usos de estos compuestos para la fabricacion de medicamentos e intermediarios | |
| ES2046193T3 (es) | Un procedimiento para la preparacion de un compuesto de imidazolidinona. | |
| NO168243C (no) | Analogifremgangsmaate for fremstilling av terapeutisk aktive alkansulfonanilid-derivater. | |
| ES2055717T3 (es) | Derivados de benzo- y tieno-3,4-dihidro-piridina, procedimientos para su preparacion y medicamentos que contienen estos compuestos. | |
| ATE38982T1 (de) | Guanidinmethylcyclohexancarbonsaeure-derivate, verfahren zur herstellung und pharmazeutische mittel. | |
| ES2063771T3 (es) | Nuevos derivados de amida del acido 4-oxo-4h-pirido (1,2-a) pirimidin-3-carboxilicos, su preparacion y elaboracion de medicamentos que contienen estos compuestos, asi como la preparacion de los mismos. | |
| ATE75399T1 (de) | Therapeutikum zur behandlung von magengeschwueren. | |
| ATE18761T1 (de) | Carbamoyloxybenzhydrol-derivate, ihre herstellung und ihre pharmazeutische zusammensetzungen. | |
| ES2122982T3 (es) | Derivados de tetrahidrocarbazol para la fabricacion de un medicamento para el tratamiento de una enfermedad en la que esta indicado un agonista similar a 5-ht1. | |
| ES2031889T3 (es) | Un procedimiento para preparar un derivado de pirido (1,2-a)pirimidina. | |
| MX9204220A (es) | Bencimidazoles. | |
| ES2192827T3 (es) | Derivados de 8h-(2,3-b)-pirrolicin-8-ona, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
Ref document number: 268956 Country of ref document: ES |
|
| SPCF | Request for supplementary protection certificate filed |
Free format text: RABEPRAZOL (PARIET) Spc suppl protection certif: C9900039 Filing date: 19991021 |
|
| SPCG | Supplementary protection certificate granted |
Free format text: RABEPRAZOL (PARIET) Spc suppl protection certif: C9900039 Filing date: 19991021 Expiry date: 20121113 Effective date: 20030220 |