IL145996A0 - Benzimidazole compound crystal - Google Patents
Benzimidazole compound crystalInfo
- Publication number
- IL145996A0 IL145996A0 IL14599600A IL14599600A IL145996A0 IL 145996 A0 IL145996 A0 IL 145996A0 IL 14599600 A IL14599600 A IL 14599600A IL 14599600 A IL14599600 A IL 14599600A IL 145996 A0 IL145996 A0 IL 145996A0
- Authority
- IL
- Israel
- Prior art keywords
- compound crystal
- benzimidazole compound
- benzimidazole
- crystal
- compound
- Prior art date
Links
Classifications
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- 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
- 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
- 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
-
- 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
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17150999 | 1999-06-17 | ||
PCT/JP2000/003880 WO2000078745A2 (en) | 1999-06-17 | 2000-06-15 | Crystalline form of (r)-2-[[[3-methyl- 4- (2,2,2,- trifluoroethoxy) -2- pyridinyl] methyl] sulfinyl] -1h-benzimidazole |
Publications (1)
Publication Number | Publication Date |
---|---|
IL145996A0 true IL145996A0 (en) | 2002-07-25 |
Family
ID=15924444
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL14599600A IL145996A0 (en) | 1999-06-17 | 2000-06-15 | Benzimidazole compound crystal |
IL145996A IL145996A (en) | 1999-06-17 | 2001-10-17 | Crystal of benzimidazole compounds |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL145996A IL145996A (en) | 1999-06-17 | 2001-10-17 | Crystal of benzimidazole compounds |
Country Status (27)
Country | Link |
---|---|
US (11) | US6462058B1 (sr) |
EP (3) | EP2343289A1 (sr) |
KR (3) | KR100407847B1 (sr) |
CN (1) | CN1150186C (sr) |
AR (5) | AR031069A1 (sr) |
AT (1) | ATE391126T1 (sr) |
AU (1) | AU778820B2 (sr) |
BE (1) | BE2014C017I2 (sr) |
BR (1) | BRPI0011674B8 (sr) |
CA (1) | CA2375201C (sr) |
CY (2) | CY1110384T1 (sr) |
DE (1) | DE60038481T2 (sr) |
DK (2) | DK1129088T3 (sr) |
ES (2) | ES2426985T3 (sr) |
HK (2) | HK1038227A1 (sr) |
HU (1) | HU229067B1 (sr) |
IL (2) | IL145996A0 (sr) |
MX (1) | MXPA01012642A (sr) |
MY (1) | MY125399A (sr) |
NO (1) | NO321168B1 (sr) |
NZ (1) | NZ515702A (sr) |
PL (1) | PL201068B1 (sr) |
PT (2) | PT1129088E (sr) |
SI (1) | SI1129088T1 (sr) |
TW (2) | TWI289557B (sr) |
WO (2) | WO2000078745A2 (sr) |
ZA (1) | ZA200108331B (sr) |
Families Citing this family (95)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6489346B1 (en) * | 1996-01-04 | 2002-12-03 | The 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 |
US20040224989A1 (en) * | 1999-01-29 | 2004-11-11 | Barberich Timothy J. | S-lansoprazole compositions and methods |
TWI289557B (en) * | 1999-06-17 | 2007-11-11 | Takeda Chemical Industries Ltd | A crystal of a hydrate of (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]-1H-benzimidazole |
CA2375091A1 (en) * | 1999-06-30 | 2001-01-11 | Takeda Chemical Industries, Ltd. | Crystals of benzimidazole compounds |
CN1193024C (zh) | 2000-04-28 | 2005-03-16 | 武田药品工业株式会社 | 生产旋光的亚砜衍生物的方法 |
US7169799B2 (en) * | 2000-05-15 | 2007-01-30 | Takeda Pharmaceutical Company Limited | Process for producing crystal |
EP1306375B1 (en) | 2000-08-04 | 2006-10-11 | Takeda Pharmaceutical Company Limited | Salts of benzimidazole compound and application thereof |
KR100887912B1 (ko) * | 2000-12-01 | 2009-03-12 | 다케다 야쿠힌 고교 가부시키가이샤 | (r)- 또는 (s)-란소프라졸의 결정화 방법 |
DK2258351T3 (da) | 2001-10-17 | 2013-08-26 | Takeda Pharmaceutical | Granula indeholdende lansoprazol i stor mængde |
KR100467100B1 (ko) * | 2002-03-20 | 2005-01-24 | 일양약품주식회사 | 2-[(4-메톡시-3-메틸)-2-피리디닐]메틸설피닐-5-(1H-피롤-1-릴)-1H-벤즈이미다졸 또는 이의 Nа염을 함유하는주사제의 제조방법 |
EP1476442A2 (en) * | 2002-03-27 | 2004-11-17 | Teva Pharmaceutical Industries Ltd. | Lansoprazole polymorphs and processes for preparation thereof |
EP1552833B1 (en) | 2002-10-16 | 2016-12-28 | Takeda Pharmaceutical Company Limited | Process for producing an amorphous optically active isomer of lansoprazole |
MY148805A (en) | 2002-10-16 | 2013-05-31 | Takeda Pharmaceutical | Controlled release preparation |
US20050220870A1 (en) * | 2003-02-20 | 2005-10-06 | Bonnie Hepburn | Novel formulation, omeprazole antacid complex-immediate release for rapid and sustained suppression of gastric acid |
KR100714375B1 (ko) * | 2003-03-24 | 2007-05-02 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 술폭시드 유도체 또는 그 염의 아몰퍼스의 제조방법 |
CA2529255A1 (en) * | 2003-06-20 | 2004-12-29 | Ch Chemicals (Pty) Ltd | Polyurethane-based cementitious liner |
US8993599B2 (en) | 2003-07-18 | 2015-03-31 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
AU2004257864A1 (en) * | 2003-07-18 | 2005-01-27 | Santarus, Inc. | Pharmaceutical formulation and method for treating acid-caused gastrointestinal disorders |
WO2005007115A2 (en) * | 2003-07-18 | 2005-01-27 | Santarus, Inc. | Pharmaceutical composition for inhibiting acid secretion |
US20070292498A1 (en) * | 2003-11-05 | 2007-12-20 | Warren Hall | Combinations of proton pump inhibitors, sleep aids, buffers and pain relievers |
AU2005213472A1 (en) * | 2004-02-10 | 2005-08-25 | Santarus, Inc. | Combination of proton pump inhibitor, buffering agent, and nonsteroidal anti-inflammatory agent |
AU2005249367A1 (en) * | 2004-04-16 | 2005-12-15 | Santarus, Inc. | Combination of proton pump inhibitor, buffering agent, and prokinetic agent |
US8906940B2 (en) | 2004-05-25 | 2014-12-09 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
US8815916B2 (en) | 2004-05-25 | 2014-08-26 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
JP5563735B2 (ja) | 2004-06-16 | 2014-07-30 | タケダ ファーマシューティカルズ ユー.エス.エー. インコーポレイティド | Ppi多回剤形 |
WO2006030936A1 (ja) | 2004-09-13 | 2006-03-23 | Takeda Pharmaceutical Company Limited | 酸化化合物の製造方法及び製造装置 |
WO2006090845A1 (ja) | 2005-02-25 | 2006-08-31 | Takeda Pharmaceutical Company Limited | 顆粒の製造方法 |
ES2259269B1 (es) | 2005-03-03 | 2007-11-01 | Esteve Quimica, S.A. | Procedimiento para la preparacion de derivados de 2-(2-piridilmetilsulfinil)-bencimidazol opticamente activos. |
JP2009511481A (ja) * | 2005-10-06 | 2009-03-19 | オースペックス・ファーマシューティカルズ・インコーポレイテッド | 増強された治療特性を持つ、胃H+,K+−ATPaseの重水素化阻害剤 |
SG184754A1 (en) | 2005-12-28 | 2012-10-30 | Takeda Pharmaceutical | Controlled release solid preparation |
KR100758600B1 (ko) | 2006-01-05 | 2007-09-13 | 주식회사 대웅제약 | 란소프라졸 결정형 a의 제조방법 |
US20090092658A1 (en) * | 2007-10-05 | 2009-04-09 | Santarus, Inc. | Novel formulations of proton pump inhibitors and methods of using these formulations |
WO2008068767A2 (en) * | 2006-12-07 | 2008-06-12 | Hetero Drugs Limited | A novel crystalline form of lansoprazole |
WO2008081891A1 (ja) | 2006-12-28 | 2008-07-10 | Takeda Pharmaceutical Company Limited | 口腔内崩壊性固形製剤 |
WO2009049160A1 (en) * | 2007-10-12 | 2009-04-16 | Takeda Pharmaceuticals North America | Methods of treating gastrointestinal disorders independent of the intake of food |
BRPI0821386A2 (pt) * | 2007-12-18 | 2015-06-16 | Watson Pharma Private Ltd | Processo para a preparação de r-lansoprazol amorfo estável |
EP2573082A1 (en) * | 2007-12-31 | 2013-03-27 | Takeda Pharmaceutical Company Limited | Crystalline solvated forms of (r)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridinyl]methyl]sulfinyl]-1h-benzimidazole |
CL2009000547A1 (es) * | 2008-03-10 | 2010-05-07 | Takeda Pharmaceuticals Co | Forma cristalina de (r)-2[[[3-metil-4-(2,2,2-trifluoroetoxi)-2-piridinil]metil]sulfinil]-1h-bencimidazol, metodo de preparacion; composicion farmaceutica y su uso para la profilaxis o tratamiento de ulcera peptica, gastritis, esofagitis erosiva, esofago de barret,dispepsia funcional, cancer gastrico. |
UY31698A (es) | 2008-03-11 | 2009-11-10 | Takeda Pharmaceutical | Preparacion solida de desintegracion oral |
EP2265605A4 (en) * | 2008-03-18 | 2011-08-03 | Reddys Lab Ltd Dr | METHOD OF MANUFACTURING DEXLANSOPRAZOLE AND POLYMORPHIDE THEREOF |
US20090263475A1 (en) * | 2008-04-21 | 2009-10-22 | Nagaraju Manne | Dexlansoprazole compositions |
AU2009336561A1 (en) | 2008-05-14 | 2010-07-15 | Watson Pharma Private Limited | Stable R-(+)-lansoprazole amine salt and a process for preparing the same |
GEP20146122B (en) * | 2008-07-28 | 2014-07-25 | Takeda Pharmaceuticals Co | Pharmaceutical composition |
US20100113527A1 (en) * | 2008-09-30 | 2010-05-06 | Teva Pharmaceutical Industries Ltd. | Crystalline forms of dexlansoprazole |
IT1391758B1 (it) * | 2008-11-11 | 2012-01-27 | Dipharma Francis Srl | Procedimento per la preparazione di dexlansoprazolo amorfo |
WO2010056059A2 (en) * | 2008-11-14 | 2010-05-20 | Hanmi Pharm. Co., Ltd. | Novel crystalline dexlansoprazole and pharmaceutical composition comprising same |
IT1391776B1 (it) * | 2008-11-18 | 2012-01-27 | Dipharma Francis Srl | Procedimento per la preparazione di dexlansoprazolo |
IT1392813B1 (it) | 2009-02-06 | 2012-03-23 | Dipharma Francis Srl | Forme cristalline di dexlansoprazolo |
US20110009637A1 (en) * | 2009-02-10 | 2011-01-13 | Dario Braga | Crystals of Dexlansoprazole |
WO2011004387A2 (en) * | 2009-06-18 | 2011-01-13 | Matrix Laboratories Ltd | Process for the preparation of dexlansoprazole polymorphic forms |
IT1395118B1 (it) * | 2009-07-29 | 2012-09-05 | Dipharma Francis Srl | Procedimento per la preparazione di dexlansoprazolo cristallino |
US10273219B2 (en) | 2009-11-12 | 2019-04-30 | Pharmatrophix, Inc. | Crystalline forms of neurotrophin mimetic compounds and their salts |
WO2011060262A1 (en) | 2009-11-12 | 2011-05-19 | Pharmatrophix, Inc. | Crystalline forms of neurotrophin mimetic compounds and their salts |
CN102108076B (zh) * | 2009-12-23 | 2014-07-23 | 江苏豪森医药集团有限公司 | 制备无定形右兰索拉唑的方法 |
US20130197232A1 (en) | 2010-01-29 | 2013-08-01 | Ranbaxy Laboratories Limited | Process for the preparation of crystalline forms of dexlansoprazole |
US20110189271A1 (en) * | 2010-02-02 | 2011-08-04 | Vishal Lad | Pharmaceutical formulations of acid-labile drugs |
EP2552904A1 (en) * | 2010-03-31 | 2013-02-06 | Ranbaxy Laboratories Limited | Process for the preparation of dexlansoprazole |
CA2795056C (en) | 2010-03-31 | 2015-03-24 | Ranbaxy Laboratories Limited | Salts of dexlansoprazole and their preparation |
EP2384745A3 (en) | 2010-05-05 | 2012-01-18 | Sanovel Ilac Sanayi ve Ticaret A.S. | Modified release pharmaceutical compositions of dexlansoprazole |
EP2384747A3 (en) | 2010-05-05 | 2012-01-18 | Sanovel Ilac Sanayi ve Ticaret A.S. | Oral Tablet Compositions Of Dexlansoprazole |
EP2384746A3 (en) | 2010-05-05 | 2012-03-07 | Sanovel Ilac Sanayi ve Ticaret A.S. | Dual release oral tablet compositions of dexlansoprazole |
US20130216617A1 (en) | 2010-06-29 | 2013-08-22 | Cadila Healthcare Limited | Pharmaceutical compositions of (r)-lansoprazole |
JP6037840B2 (ja) | 2010-12-03 | 2016-12-07 | 武田薬品工業株式会社 | 口腔内崩壊錠 |
CA2823166C (en) | 2010-12-27 | 2019-04-09 | Takeda Pharmaceutical Company Limited | Orally disintegrating tablet |
EP2663306A4 (en) * | 2011-01-12 | 2014-01-01 | Hetero Research Foundation | POLYMORPHS OF DEXLANSOPRAZOLE SALTS |
WO2012104805A1 (en) | 2011-02-01 | 2012-08-09 | Ranbaxy Laboratories Limited | Process for the preparation of dexlansoprazole |
WO2012111024A1 (en) | 2011-02-18 | 2012-08-23 | Suven Nishtaa Pharma Pvt Ltd | Pharmaceutical compositions of dexlansoprazole |
CA2840309A1 (en) * | 2011-06-21 | 2012-12-27 | Ranbaxy Laboratories Limited | Process for the preparation of dexlansoprazole |
CN102875531B (zh) * | 2011-07-15 | 2015-08-19 | 上海睿智化学研究有限公司 | 一种(r)-兰索拉唑无水晶型及其制备方法 |
CN102875530A (zh) * | 2011-07-15 | 2013-01-16 | 上海睿智化学研究有限公司 | 一种(r)-兰索拉唑叔丁胺盐及其晶型和制备方法 |
CN102875532B (zh) * | 2011-07-15 | 2015-05-13 | 上海睿智化学研究有限公司 | 一种(r)-兰索拉唑异丙胺盐及其晶型和制备方法 |
CN102234265B (zh) * | 2011-08-08 | 2013-11-20 | 天津市汉康医药生物技术有限公司 | 兰索拉唑化合物 |
US9433632B2 (en) | 2011-11-30 | 2016-09-06 | Takeda Pharmaceutical Company Limited | Dry coated tablet |
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 |
WO2013140120A1 (en) | 2012-03-22 | 2013-09-26 | Cipla Limited | Glycerol solvate forms of (r) - 2 - [ [ [3 -methyl -4 (2,2, 2 - trifluoroethoxy) pyridin- 2 - yl] methyl] sulphinyl] - 1h - ben zimidazole |
WO2013179194A1 (en) | 2012-05-31 | 2013-12-05 | Ranbaxy Laboratories Limited | Process for the preparation of crystalline dexlansoprazole |
CN103709139B (zh) * | 2012-10-09 | 2016-12-21 | 上海汇伦生命科技有限公司 | 无水右兰索拉唑的制备方法 |
CN104177333A (zh) * | 2013-05-24 | 2014-12-03 | 四川海思科制药有限公司 | 一种理化性质稳定的(r)-2-[[[3-甲基-4-(2,2,2-三氟乙氧基)-2-吡啶基]甲基]亚磺酰基]-1h-苯并咪唑 |
CN104650035A (zh) * | 2013-11-25 | 2015-05-27 | 天津市汉康医药生物技术有限公司 | 右兰索拉唑倍半水合物化合物 |
CN103664889B (zh) * | 2013-12-19 | 2014-11-19 | 悦康药业集团有限公司 | 一种兰索拉唑化合物 |
EP2933002A1 (en) | 2014-04-11 | 2015-10-21 | Sanovel Ilac Sanayi ve Ticaret A.S. | Pharmaceutical combinations of dabigatran and proton pump inhibitors |
WO2015155307A1 (en) | 2014-04-11 | 2015-10-15 | Sanovel Ilac Sanayi Ve Ticaret A.S. | Pharmaceutical combinations of rivaroxaban and proton pump inhibitors |
CN104844576B (zh) * | 2015-04-28 | 2017-03-08 | 山东罗欣药业集团股份有限公司 | 一种兰索拉唑或右旋兰索拉唑晶型化合物及其制备方法 |
CN104829594A (zh) * | 2015-05-15 | 2015-08-12 | 苗怡文 | 一种治疗胃溃疡的药物兰索拉唑化合物 |
CN105017218A (zh) * | 2015-07-01 | 2015-11-04 | 合肥安德生制药有限公司 | 一种右兰索拉唑晶型及其制备方法 |
CN104958276A (zh) * | 2015-07-30 | 2015-10-07 | 青岛蓝盛洋医药生物科技有限责任公司 | 一种治疗胃溃疡的药物兰索拉唑组合物胶囊 |
CN104997738A (zh) * | 2015-08-10 | 2015-10-28 | 青岛蓝盛洋医药生物科技有限责任公司 | 一种治疗胃病的药物兰索拉唑组合物干混悬剂 |
CN105399728B (zh) * | 2015-12-20 | 2017-11-28 | 寿光富康制药有限公司 | 一种适用于工业化生产的右兰索拉唑的处理方法 |
CN108164507A (zh) * | 2016-12-07 | 2018-06-15 | 天津药物研究院有限公司 | 一种右兰索拉唑单晶及其制备方法和用途 |
TR201701461A2 (tr) | 2017-01-31 | 2018-08-27 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | Dekslansoprazolün Enterik Kaplı Farmasötik Kompozisyonları |
CN106866630B (zh) * | 2017-04-01 | 2018-08-07 | 上海华源医药科技发展有限公司 | 一种右兰索拉唑的制备方法 |
CN107011329A (zh) * | 2017-05-05 | 2017-08-04 | 广州大光制药有限公司 | 兰索拉唑一水合物晶型及其结晶制备方法 |
CN108794450B (zh) * | 2018-07-24 | 2022-08-19 | 浙江恒康药业股份有限公司 | 制备无定型右旋兰索拉唑的方法 |
WO2024075017A1 (en) | 2022-10-04 | 2024-04-11 | Zabirnyk Arsenii | Inhibition of aortic valve calcification |
Family Cites Families (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6150978A (ja) | 1984-08-16 | 1986-03-13 | Takeda Chem Ind Ltd | ピリジン誘導体およびその製造法 |
DK171989B1 (da) | 1987-08-04 | 1997-09-08 | Takeda Chemical Industries Ltd | Fremgangsmåde til fremstilling af 2-(2-pyridylmethylsulfinyl)-benzimidazoler |
DE4035455A1 (de) | 1990-11-08 | 1992-05-14 | Byk Gulden Lomberg Chem Fab | Enantiomerentrennung |
SE504459C2 (sv) | 1994-07-15 | 1997-02-17 | Astra Ab | Förfarande för framställning av substituerade sulfoxider |
GB9423968D0 (en) * | 1994-11-28 | 1995-01-11 | Astra Ab | Resolution |
HRP960232A2 (en) | 1995-07-03 | 1998-02-28 | Astra Ab | A process for the optical purification of compounds |
US5840737A (en) * | 1996-01-04 | 1998-11-24 | The Curators Of The University Of Missouri | Omeprazole solution and method for using same |
EP0941226A1 (de) | 1996-11-12 | 1999-09-15 | Byk Gulden Lomberg Chemische Fabrik GmbH | (2,3-dihydrobenzofuranyl)-thiazole als phosphodiesterasehemmer |
TW385306B (en) * | 1996-11-14 | 2000-03-21 | Takeda Chemical Industries Ltd | Method for producing crystals of benzimidazole derivatives |
WO1998022118A1 (en) * | 1996-11-22 | 1998-05-28 | The Procter & Gamble Company | Compositions for the treatment of gastrointestinal disorders containing bismuth and nsaid |
SE510666C2 (sv) | 1996-12-20 | 1999-06-14 | Astra Ab | Nya Kristallmodifikationer |
WO1999038513A1 (en) | 1998-01-30 | 1999-08-05 | Sepracor Inc. | R-lansoprazole compositions and methods |
JP2002501896A (ja) | 1998-01-30 | 2002-01-22 | セプラコール, インク. | S−ランソプラゾール組成物及び方法 |
AU3596199A (en) * | 1998-05-06 | 1999-11-23 | Kobenhavns Universitet | Treatment of celiac disease |
JP3283252B2 (ja) * | 1999-06-17 | 2002-05-20 | 武田薬品工業株式会社 | ベンズイミダゾール化合物の結晶 |
TWI289557B (en) * | 1999-06-17 | 2007-11-11 | Takeda Chemical Industries Ltd | A crystal of a hydrate of (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]-1H-benzimidazole |
CA2375091A1 (en) * | 1999-06-30 | 2001-01-11 | Takeda Chemical Industries, Ltd. | Crystals of benzimidazole compounds |
CN1117747C (zh) * | 2000-06-19 | 2003-08-13 | 中国科学院成都有机化学研究所 | 光学纯兰索拉唑的制备方法 |
EP1552833B1 (en) * | 2002-10-16 | 2016-12-28 | Takeda Pharmaceutical Company Limited | Process for producing an amorphous optically active isomer of lansoprazole |
KR100714375B1 (ko) * | 2003-03-24 | 2007-05-02 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 술폭시드 유도체 또는 그 염의 아몰퍼스의 제조방법 |
CA2591983A1 (en) * | 2004-12-20 | 2006-06-29 | Dr. Reddy's Laboratories Ltd. | Pharmaceutical compositions comprising amorphous benzimidazole compounds |
CN101111233A (zh) * | 2004-12-23 | 2008-01-23 | 兰贝克赛实验室有限公司 | 稳定的口服苯并咪唑组合物及其制备方法 |
US20060210637A1 (en) * | 2005-03-17 | 2006-09-21 | Qpharma, Llc | Stable tablet dosage forms of proton pump inhibitors |
BRPI0821386A2 (pt) * | 2007-12-18 | 2015-06-16 | Watson Pharma Private Ltd | Processo para a preparação de r-lansoprazol amorfo estável |
-
2000
- 2000-05-30 TW TW090111098A patent/TWI289557B/zh not_active IP Right Cessation
- 2000-05-30 TW TW089110444A patent/TWI275587B/zh not_active IP Right Cessation
- 2000-06-02 MY MYPI20002497 patent/MY125399A/en unknown
- 2000-06-14 AR ARP000102917A patent/AR031069A1/es not_active Application Discontinuation
- 2000-06-15 BR BRPI0011674A patent/BRPI0011674B8/pt not_active IP Right Cessation
- 2000-06-15 IL IL14599600A patent/IL145996A0/xx unknown
- 2000-06-15 AU AU52478/00A patent/AU778820B2/en not_active Expired
- 2000-06-15 EP EP20100177981 patent/EP2343289A1/en not_active Withdrawn
- 2000-06-15 WO PCT/JP2000/003880 patent/WO2000078745A2/en active Application Filing
- 2000-06-15 CN CNB008090637A patent/CN1150186C/zh not_active Expired - Lifetime
- 2000-06-15 WO PCT/JP2000/003881 patent/WO2004083200A1/en active Application Filing
- 2000-06-15 AT AT00937235T patent/ATE391126T1/de active
- 2000-06-15 NZ NZ515702A patent/NZ515702A/en not_active IP Right Cessation
- 2000-06-15 ES ES08151945T patent/ES2426985T3/es not_active Expired - Lifetime
- 2000-06-15 DK DK00937235T patent/DK1129088T3/da active
- 2000-06-15 PL PL352193A patent/PL201068B1/pl unknown
- 2000-06-15 DK DK08151945.6T patent/DK1977751T3/da active
- 2000-06-15 US US09/674,624 patent/US6462058B1/en not_active Expired - Lifetime
- 2000-06-15 DE DE60038481T patent/DE60038481T2/de not_active Expired - Lifetime
- 2000-06-15 EP EP08151945.6A patent/EP1977751B1/en not_active Expired - Lifetime
- 2000-06-15 KR KR10-2000-7013512A patent/KR100407847B1/ko active IP Right Grant
- 2000-06-15 ES ES00937235T patent/ES2300265T3/es not_active Expired - Lifetime
- 2000-06-15 PT PT00937235T patent/PT1129088E/pt unknown
- 2000-06-15 CA CA2375201A patent/CA2375201C/en not_active Expired - Lifetime
- 2000-06-15 MX MXPA01012642A patent/MXPA01012642A/es active IP Right Grant
- 2000-06-15 HU HU0201659A patent/HU229067B1/hu active Protection Beyond IP Right Term
- 2000-06-15 KR KR10-2003-7009783A patent/KR100514204B1/ko active IP Right Grant
- 2000-06-15 PT PT81519456T patent/PT1977751E/pt unknown
- 2000-06-15 SI SI200030990T patent/SI1129088T1/sl unknown
- 2000-06-15 KR KR10-2000-7013530A patent/KR100537029B1/ko active IP Right Grant
- 2000-06-15 EP EP00937235A patent/EP1129088B1/en not_active Expired - Lifetime
-
2001
- 2001-09-29 HK HK01106916A patent/HK1038227A1/xx not_active IP Right Cessation
- 2001-10-10 ZA ZA200108331A patent/ZA200108331B/en unknown
- 2001-10-17 IL IL145996A patent/IL145996A/en not_active IP Right Cessation
- 2001-12-13 NO NO20016087A patent/NO321168B1/no not_active IP Right Cessation
-
2002
- 2002-09-13 US US10/243,329 patent/US6664276B2/en not_active Expired - Lifetime
-
2003
- 2003-09-04 US US10/655,114 patent/US6939971B2/en not_active Expired - Lifetime
-
2005
- 2005-06-10 US US11/149,903 patent/US7339064B2/en not_active Expired - Lifetime
-
2008
- 2008-01-07 US US12/006,845 patent/US7569697B2/en not_active Expired - Fee Related
- 2008-06-26 CY CY20081100671T patent/CY1110384T1/el unknown
-
2009
- 2009-02-26 US US12/393,409 patent/US7737282B2/en not_active Expired - Fee Related
- 2009-04-01 HK HK09103096.8A patent/HK1123985A1/xx not_active IP Right Cessation
-
2010
- 2010-04-30 US US12/771,486 patent/US8030333B2/en not_active Expired - Fee Related
- 2010-12-15 AR ARP100104648A patent/AR079473A2/es not_active Application Discontinuation
-
2011
- 2011-09-01 US US13/223,988 patent/US20110319450A1/en not_active Abandoned
-
2012
- 2012-08-22 US US13/591,992 patent/US8552198B2/en not_active Expired - Fee Related
-
2013
- 2013-09-06 US US14/020,286 patent/US8884019B2/en not_active Expired - Fee Related
- 2013-10-09 CY CY20131100882T patent/CY1114485T1/el unknown
- 2013-11-26 AR ARP130104346A patent/AR093609A2/es unknown
-
2014
- 2014-03-04 BE BE2014C017C patent/BE2014C017I2/fr unknown
- 2014-10-07 US US14/508,651 patent/US9145389B2/en not_active Expired - Fee Related
- 2014-11-12 AR ARP140104252A patent/AR100473A2/es not_active Application Discontinuation
-
2015
- 2015-12-28 AR ARP150104310A patent/AR103295A2/es not_active Application Discontinuation
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
IL145996A0 (en) | Benzimidazole compound crystal | |
HUP0202028A2 (en) | Substituted benzimidazole | |
GB2357761B (en) | Compounds | |
GB9904933D0 (en) | Compounds | |
GB9924797D0 (en) | Compound | |
GB9920919D0 (en) | Novel compound | |
GB9908828D0 (en) | Compounds | |
GB9902399D0 (en) | Compounds | |
GB9904930D0 (en) | Thiazoloindolinone compounds | |
GB9921928D0 (en) | Compound | |
GB9905771D0 (en) | Compounds | |
GB9914342D0 (en) | Compound | |
GB0031563D0 (en) | Compound | |
GB0031557D0 (en) | Compound | |
GB9929255D0 (en) | Compound | |
GB9921929D0 (en) | Compound | |
EP1209240A4 (en) | CONNECTION F-15078 | |
GB9924965D0 (en) | Compound | |
GB9915436D0 (en) | Compound | |
GB9929445D0 (en) | Compound | |
GB9917377D0 (en) | Compound | |
GB9905415D0 (en) | Novel compound | |
GB9902935D0 (en) | Novel compound | |
GB9906278D0 (en) | Compounds | |
GB9905238D0 (en) | Compounds |