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
- group
- stands
- manufacture
- derivatives
- alkoxy
- 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
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 |
---|---|---|---|
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. |
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. |
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 |
---|---|---|---|
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. |
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. |
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) | DE3789536T3 (es) |
DK (2) | DK171024B1 (es) |
ES (3) | ES2118457T3 (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 |
EG19302A (en) * | 1988-12-22 | 1994-11-30 | Haessle Ab | Compound with gastric acid inhibitory effect and process for its preparation |
SE8804629D0 (sv) * | 1988-12-22 | 1988-12-22 | Ab Haessle | New therapeutically active compounds |
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. |
NZ244301A (en) * | 1991-09-20 | 1994-08-26 | Merck & Co Inc | Preparation of 2-pyridylmethylsulphinylbenzimidazole and pyridoimidazole derivatives from the corresponding sulphenyl compounds |
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 |
EP0683776B1 (de) * | 1993-02-17 | 1999-04-07 | Byk Gulden Lomberg Chemische Fabrik GmbH | Substituierte heteroarylalkylthiopyridine zur bekämpfung von helicobacter bakterien |
CA2166327A1 (en) * | 1993-06-29 | 1995-01-12 | Bernhard Kohl | Substituted arylthioalkylthiopyridines |
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 |
US6051570A (en) * | 1997-05-30 | 2000-04-18 | Dr. Reddy's Research Foundation | Benzimidazole derivatives as antiulcer agents, process for their preparation and pharmaceutical compositions containing them |
DE69827392T2 (de) | 1997-07-25 | 2005-10-27 | Altana Pharma Ag | Protonenpumpenhemmer als kombinationstherapeutika mit antibakteriell wirkenden substanzen |
US7230014B1 (en) * | 1997-10-14 | 2007-06-12 | Eisai Co., Ltd. | Pharmaceutical formulation comprising glycine as a stabilizer |
EP1039905B1 (en) * | 1997-10-14 | 2006-07-05 | Eisai Co., Ltd. | Pharmaceutical formulation comprising glycine as a stabilizer |
ATE271555T1 (de) | 1998-01-14 | 2004-08-15 | Uab Research Foundation | Verfahren zur herstellung und screening von inhibitoren des bakteriellen nad synthetase enzyms, verbindungen daraus und methoden zur behandlung bakterieller und mikrobieller infektionen mit diesen inhibitoren |
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 |
AU3967399A (en) * | 1998-04-30 | 1999-11-16 | Sepracor, Inc. | S-rabeprazole compositions and methods |
EP1073332A4 (en) * | 1998-04-30 | 2005-06-15 | Sepracor Inc | R-RABEPRAZOL COMPOSITIONS AND METHODS |
AU4387799A (en) * | 1998-06-26 | 2000-01-17 | 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 |
CN100396675C (zh) | 1998-08-10 | 2008-06-25 | 加利福尼亚州大学董事会 | 质子泵抑制剂的前药 |
AU772726B2 (en) | 1998-08-12 | 2004-05-06 | Takeda Gmbh | Oral administration form for pyridin-2-ylmethylsulfinyl-1H-benzimidazoles |
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 |
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 |
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 |
US6174902B1 (en) | 1999-04-28 | 2001-01-16 | Sepracor Inc. | R-rabeprazole compositions and methods |
ATE300285T1 (de) | 1999-06-07 | 2005-08-15 | Altana Pharma Ag | Neue zubereitung und darreichungsform enthaltend einen säurelabilen protonenpumpeninhibitor |
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 |
US20020064555A1 (en) * | 2000-09-29 | 2002-05-30 | Dan Cullen | Proton pump inhibitor formulation |
BR0115989A (pt) | 2000-12-07 | 2004-01-13 | Altana Pharma Ag | Preparação farmacêutica na forma de uma suspensão compreendendo um ingrediente ativo instável a ácido |
CA2430816C (en) | 2000-12-07 | 2012-05-15 | Altana Pharma Ag | Pharmaceutical preparation in the form of a paste comprising an acid-labile active ingredient |
SI1341528T1 (sl) | 2000-12-07 | 2012-05-31 | Nycomed Gmbh | Hitro razpadljiva tableta ki obsega kislinsko labilno aktivno sestavino |
NL1018295C2 (nl) * | 2001-06-15 | 2002-12-17 | Dsm Nv | Werkwijze voor de bereiding van 4-chloor-pyridine-n-oxiden. |
EP1428825A4 (en) | 2001-09-18 | 2005-03-23 | Zeria Pharm 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 |
AU2003224781A1 (en) * | 2002-03-26 | 2003-10-13 | Dr. Reddy's Laboratories Limited | Crystalline forms of rabeprazole sodium |
WO2003097011A1 (en) * | 2002-05-17 | 2003-11-27 | 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 |
JP4634144B2 (ja) * | 2002-08-01 | 2011-02-16 | ニコックス エスエー | ニトロソ化プロトンポンプ阻害剤、組成物および使用方法 |
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 |
BRPI0310118B1 (pt) | 2002-12-06 | 2015-10-20 | Altana Pharma Ag | processo para a preparação de inibidores de bomba de próton (ppi) opticamente puro possuindo uma estrutura de sulfinila |
US7301030B2 (en) | 2002-12-06 | 2007-11-27 | Nycomed Gmbh | Process for preparing (S)-pantoprazole |
WO2004055001A2 (en) * | 2002-12-16 | 2004-07-01 | Ranbaxy Laboratories Limited | Rabeprazole calcium |
WO2004056804A2 (en) * | 2002-12-19 | 2004-07-08 | Teva Pharmaceutical Industries Ltd. | Solid states of pantoprazole sodium, processes for preparing them and processes for preparing known pantoprazole sodium hydrates |
CN1723208A (zh) * | 2003-01-07 | 2006-01-18 | 兰贝克赛实验室有限公司 | 咪唑衍生物的镁盐 |
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 |
WO2004080487A1 (ja) * | 2003-03-13 | 2004-09-23 | Eisai Co. Ltd. | 歯ぎしりの予防剤または治療剤 |
ATE508124T1 (de) | 2003-03-24 | 2011-05-15 | Eisai R&D Man Co Ltd | Verfahren zur herstellung von amorphem rabeprazole-natrium-salz |
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 |
PE20050150A1 (es) | 2003-05-08 | 2005-03-22 | Altana Pharma Ag | Una forma de dosificacion que contiene (s)-pantoprazol como ingrediente activo |
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 |
CA2528993A1 (en) * | 2003-06-10 | 2004-12-23 | Teva Pharmaceutical Industries Ltd. | Process for preparing 2-[(pyridinyl)methyl]sulfinyl-substituted benzimidazoles and novel chlorinated derivatives of pantoprazole |
CA2529984C (en) | 2003-06-26 | 2012-09-25 | Isa Odidi | Oral multi-functional pharmaceutical capsule preparations of proton pump inhibitors |
NZ544173A (en) * | 2003-07-15 | 2009-04-30 | Alevium Pharmaceuticals Inc | Process for preparing isomerically pure prodrugs of benzimidazole derivative proton pump inhibitors |
US8993599B2 (en) | 2003-07-18 | 2015-03-31 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
EP1660052A2 (en) * | 2003-09-03 | 2006-05-31 | 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 |
WO2005077936A1 (en) | 2004-02-11 | 2005-08-25 | Ulkar Kimya Sanayii Ve Ticaret A.S. | Pyridine benzimidazole sulfoxides with high purity |
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 |
US20070060621A1 (en) * | 2004-02-18 | 2007-03-15 | Hughes Patrick M | Methods and compositions for the administration of prodrugs of proton pump inhibitors |
JP2007532677A (ja) * | 2004-04-16 | 2007-11-15 | サンタラス インコーポレイティッド | プロトンポンプ阻害剤、緩衝剤、および運動促進薬の組み合わせ |
RS52233B (en) * | 2004-05-07 | 2012-10-31 | Nycomed Gmbh | THE PHARMACEUTICAL DOSAGE FORM CONTAINING GRANULES AND ITS PRODUCTION PROCEDURE |
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 |
JP3921497B2 (ja) * | 2004-08-06 | 2007-05-30 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | ベンズイミダゾール誘導体とアミンとの塩およびその製造方法 |
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 |
CA2603290A1 (en) * | 2004-09-30 | 2006-04-06 | Jiangsu Hansen Pharmaceutical Co., Ltd. | Prazole derivatives and salts thereof and use of same |
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 |
US20090169566A1 (en) | 2004-11-22 | 2009-07-02 | 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 |
AU2006245298A1 (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 |
ES2374730T3 (es) | 2006-03-10 | 2012-02-21 | Arigen Pharmaceuticals, Inc. | Nuevo derivado de piridina que tiene actividad contra helicobacter pylori. |
JP5457830B2 (ja) | 2006-04-03 | 2014-04-02 | オディディ,イサ | オルガノゾル被膜を含む制御放出送達デバイス |
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 |
EP2068841B1 (en) | 2006-10-05 | 2018-09-26 | Santarus, Inc. | Novel formulations of proton pump inhibitors and methods of using these formulations |
JP5492417B2 (ja) * | 2006-10-13 | 2014-05-14 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 胃酸分泌抑制作用を有するベンズイミダゾール化合物 |
US20080103169A1 (en) | 2006-10-27 | 2008-05-01 | The Curators Of The University Of Missouri | Compositions comprising acid labile proton pump inhibiting agents, at least one other pharmaceutically active agent and methods of using same |
PL2103608T3 (pl) | 2006-12-18 | 2013-02-28 | Link Genomics Inc | Środek do eradykacji Helicobacter pylori mający działanie hamujące na sekrecję kwasu żołądkowego |
ITMI20062449A1 (it) | 2006-12-19 | 2008-06-20 | Dipharma Spa | Forma cristallina di rabeprazolo sodico |
RU2491075C2 (ru) | 2006-12-22 | 2013-08-27 | Айронвуд Фармасьютикалз, Инк. | Способы и композиции для лечения расстройств пищевода |
US20100145057A1 (en) * | 2007-03-15 | 2010-06-10 | Sun Pharma Advanced Research Company Ltd. | Novel prodrugs |
US20100204478A1 (en) * | 2007-05-25 | 2010-08-12 | Hetero Drugs Limited | Improved process for amophous rabeprazole sodium |
US8247568B2 (en) * | 2007-06-21 | 2012-08-21 | Matrix Laboratories Ltd | Process for the preparation of pure rabeprazole |
WO2009010937A1 (en) * | 2007-07-17 | 2009-01-22 | Ranbaxy Laboratories Limited | Process for the preparation op pantoprazole sodium and pantoprazole sodium sesquihydrate |
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 |
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 |
SI22806A (sl) * | 2008-06-23 | 2009-12-31 | Krka, Tovarna Zdravil, D.D., Novo Mesto | Nove kristalinične oblike natrijevega rabeprazola |
RU2484089C1 (ru) * | 2009-04-09 | 2013-06-10 | Ариджен Фармасьютикалз, Инк. | Тиопроизводное пиридина и фармацевтическая композиция, которая его содержит и имеет способность действовать против helicobacter pylori |
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 |
WO2013108068A1 (en) | 2012-01-21 | 2013-07-25 | Jubilant Life Sciences Limited | Process for the preparation of 2-pyridinylmethylsulfinyl benzimidazoles, their analogs and optically active enantiomers |
WO2014091450A1 (en) | 2012-12-12 | 2014-06-19 | Ranbaxy Laboratories Limited | Process for the preparation of rabeprazole |
AU2014207680B2 (en) | 2013-01-15 | 2018-09-06 | Ironwood Pharmaceuticals, Inc. | Gastro-retentive sustained-release oral dosage form of a bile acid sequestrant |
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 |
US20180015118A1 (en) | 2015-02-03 | 2018-01-18 | Ironwood Pharmaceuticals, Inc. | Methods of treating upper gastrointestinal disorders in ppi refractory gerd |
EP3288556A4 (en) | 2015-04-29 | 2018-09-19 | 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 |
JP7044789B2 (ja) | 2016-09-24 | 2022-03-30 | ワシントン・ユニバーシティ | Sarm1 nadアーゼ活性の阻害剤およびその使用 |
MX2022002949A (es) | 2019-09-24 | 2022-04-06 | Prolacta Bioscience Inc | Composiciones y metodos para el tratamiento de enfermedades inflamatorias e inmunes. |
WO2024075017A1 (en) | 2022-10-04 | 2024-04-11 | Zabirnyk Arsenii | Inhibition of aortic valve calcification |
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 EP EP91117132A patent/EP0475456B1/en not_active Expired - Lifetime
- 1987-11-13 CN CN87107777A patent/CN1018923B/zh not_active Expired
- 1987-11-13 ES ES95102165T patent/ES2118457T3/es not_active Expired - Lifetime
- 1987-11-13 ES ES91117132T patent/ES2112260T3/es not_active Expired - Lifetime
- 1987-11-13 DE DE3789536T patent/DE3789536T3/de not_active Expired - Lifetime
- 1987-11-13 DE DE1999175035 patent/DE19975035I2/de active Active
- 1987-11-13 ES ES87116797T patent/ES2061471T5/es not_active Expired - Lifetime
- 1987-11-13 EP EP95102165A patent/EP0654471B1/en not_active Expired - Lifetime
- 1987-11-13 AT AT95102165T patent/ATE168111T1/de not_active IP Right Cessation
- 1987-11-13 AT AT91117132T patent/ATE163011T1/de not_active IP Right Cessation
- 1987-11-13 DE DE3752167T patent/DE3752167T2/de not_active Expired - Lifetime
- 1987-11-13 DE DE3752201T patent/DE3752201T2/de not_active Expired - Lifetime
- 1987-11-13 KR KR1019870012813A patent/KR910003330B1/ko not_active IP Right Cessation
- 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 DK131893A patent/DK131893A/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/xx 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. | |
EP0097323A3 (en) | 2-(4-pyridyl)-thiazole derivatives | |
HUT43843A (en) | Process for production of derivatives of benzimidasole and medical compounds containing thereof | |
DK256890A (da) | Benzo-piperidin-, -piperidyliden- og piperazinforbindelser, kompositioner indeholdende forbindelserne og fremgangsmaader til forbindelsernes fremstilling og anvendelse | |
FI894693A (fi) | Menetelmä valmistaa farmaseuttisesti arvokasta imidatsoliinijohdannaista | |
NO885655D0 (no) | Analogifremgangsmaate for fremstilling av terapeutisk aktive n-methylpyrrolidin- og fucitolderivater. | |
NO923983L (no) | Bisfenyletanderivater, fremgangsmaate for deres fremstilling og farmasoeytiske preparater derav | |
GR3026762T3 (en) | Pyridine derivatives, pharmaceutical compositions comprising the same, the use of the same for the manufacture of medicaments having therapeutic or preventative value, and a process for preparing the same | |
SE8300865D0 (sv) | Mjoldrygealkaloider, forfarande for framstellning derav och dessa foreningar innehallande farmaceutiska kompositioner | |
DE3884878T2 (de) | Uricosuretische Zusammensetzung. | |
IT7926945A0 (it) | Derivati eterociclici azotati adattivita'terapeutica ,processi per la loro preparazione e composizioni farmaceutiche contenenti detti derivati | |
RU92004439A (ru) | Азотсодержащие тетрациклические соединения, способ их получения, применение и фармацевтическая композиция | |
NO881798L (no) | Fremgangsmaate for fremstilling av et antiastmapreparat. |
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 |