SE510650C2 - Ny förening - Google Patents
Ny föreningInfo
- Publication number
- SE510650C2 SE510650C2 SE9702065A SE9702065A SE510650C2 SE 510650 C2 SE510650 C2 SE 510650C2 SE 9702065 A SE9702065 A SE 9702065A SE 9702065 A SE9702065 A SE 9702065A SE 510650 C2 SE510650 C2 SE 510650C2
- Authority
- SE
- Sweden
- Prior art keywords
- omeprazole
- magnesium salt
- salt
- magnesium
- trihydrate
- Prior art date
Links
- 229960000381 omeprazole Drugs 0.000 claims abstract description 57
- 159000000003 magnesium salts Chemical class 0.000 claims abstract description 47
- 238000000034 method Methods 0.000 claims abstract description 22
- 238000004519 manufacturing process Methods 0.000 claims abstract description 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 43
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 15
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 12
- 238000002360 preparation method Methods 0.000 claims description 11
- 238000011282 treatment Methods 0.000 claims description 11
- 210000004211 gastric acid Anatomy 0.000 claims description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 5
- 239000011777 magnesium Substances 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 239000003960 organic solvent Substances 0.000 claims description 5
- 230000001225 therapeutic effect Effects 0.000 claims description 5
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 239000004615 ingredient Substances 0.000 claims description 3
- 239000011591 potassium Substances 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 238000000634 powder X-ray diffraction Methods 0.000 claims description 3
- XURCIPRUUASYLR-UHFFFAOYSA-N Omeprazole sulfide Chemical compound N=1C2=CC(OC)=CC=C2NC=1SCC1=NC=C(C)C(OC)=C1C XURCIPRUUASYLR-UHFFFAOYSA-N 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 claims description 2
- 235000019341 magnesium sulphate Nutrition 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 239000000825 pharmaceutical preparation Substances 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims 2
- 238000001035 drying Methods 0.000 claims 1
- 230000001376 precipitating effect Effects 0.000 claims 1
- -1 4-methoxy-3,5-dimethyl-2-pyridinyl Chemical group 0.000 abstract description 6
- 239000000543 intermediate Substances 0.000 abstract description 3
- 150000004684 trihydrates Chemical class 0.000 abstract description 2
- 150000001875 compounds Chemical class 0.000 description 22
- 239000000203 mixture Substances 0.000 description 18
- 239000013078 crystal Substances 0.000 description 10
- 239000000843 powder Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 3
- 208000007107 Stomach Ulcer Diseases 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- SUBDBMMJDZJVOS-UHFFFAOYSA-N 5-methoxy-2-{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl}-1H-benzimidazole Chemical compound N=1C2=CC(OC)=CC=C2NC=1S(=O)CC1=NC=C(C)C(OC)=C1C SUBDBMMJDZJVOS-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical class CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 206010019375 Helicobacter infections Diseases 0.000 description 2
- 208000028861 Helicobacter pylori infectious disease Diseases 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 150000004683 dihydrates Chemical class 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 201000005917 gastric ulcer Diseases 0.000 description 2
- 239000012452 mother liquor Substances 0.000 description 2
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 description 2
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 2
- SUBDBMMJDZJVOS-XMMPIXPASA-N (R)-omeprazole Chemical class C([S@@](=O)C=1NC2=CC=C(C=C2N=1)OC)C1=NC=C(C)C(OC)=C1C SUBDBMMJDZJVOS-XMMPIXPASA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical class [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 244000304337 Cuminum cyminum Species 0.000 description 1
- 235000007129 Cuminum cyminum Nutrition 0.000 description 1
- 206010017943 Gastrointestinal conditions Diseases 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 201000004681 Psoriasis Diseases 0.000 description 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical group O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 206010046274 Upper gastrointestinal haemorrhage Diseases 0.000 description 1
- 201000008629 Zollinger-Ellison syndrome Diseases 0.000 description 1
- 239000000159 acid neutralizing agent Substances 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229940069428 antacid Drugs 0.000 description 1
- 239000003159 antacid agent Substances 0.000 description 1
- 230000001458 anti-acid effect Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 238000001479 atomic absorption spectroscopy Methods 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000011284 combination treatment Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000002050 diffraction method Methods 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 208000000718 duodenal ulcer Diseases 0.000 description 1
- 206010013864 duodenitis Diseases 0.000 description 1
- 201000006549 dyspepsia Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 230000027119 gastric acid secretion Effects 0.000 description 1
- 201000000052 gastrinoma Diseases 0.000 description 1
- 208000021302 gastroesophageal reflux disease Diseases 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 230000004968 inflammatory condition Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 208000019423 liver disease Diseases 0.000 description 1
- 238000011866 long-term treatment Methods 0.000 description 1
- TZNULHNPXDZANP-UHFFFAOYSA-N magnesium;methanol Chemical compound [Mg].OC TZNULHNPXDZANP-UHFFFAOYSA-N 0.000 description 1
- CRGZYKWWYNQGEC-UHFFFAOYSA-N magnesium;methanolate Chemical compound [Mg+2].[O-]C.[O-]C CRGZYKWWYNQGEC-UHFFFAOYSA-N 0.000 description 1
- YYINWHOQKIUBNL-UHFFFAOYSA-N magnesium;trihydrate Chemical compound O.O.O.[Mg] YYINWHOQKIUBNL-UHFFFAOYSA-N 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- BKBMACKZOSMMGT-UHFFFAOYSA-N methanol;toluene Chemical compound OC.CC1=CC=CC=C1 BKBMACKZOSMMGT-UHFFFAOYSA-N 0.000 description 1
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000006186 oral dosage form Substances 0.000 description 1
- 229940071462 oralone Drugs 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 208000000689 peptic esophagitis Diseases 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002325 prokinetic agent Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000002730 succinyl group Chemical group C(CCC(=O)*)(=O)* 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 238000011287 therapeutic dose Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 238000002424 x-ray crystallography Methods 0.000 description 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Dermatology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Glass Compositions (AREA)
Priority Applications (73)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9702065A SE510650C2 (sv) | 1997-05-30 | 1997-05-30 | Ny förening |
| US09/077,719 US6369085B1 (en) | 1997-05-30 | 1998-05-05 | Form of S-omeprazole |
| HR980263A HRP980263B1 (en) | 1997-05-30 | 1998-05-15 | Novel form of s-omeprazole |
| ZA984179A ZA984179B (en) | 1997-05-30 | 1998-05-18 | Novel form of s-omeprazole |
| TW087107675A TW538040B (en) | 1997-05-30 | 1998-05-18 | Novel form of S-omeprazole |
| ARP980102299A AR012717A1 (es) | 1997-05-30 | 1998-05-18 | Trihidrato de la sal de magnesio de s-omeprazol, proceso para su preparacion, composicion farmaceutica, y uso de dicho trihidrato para la fabricacion de medicamentos. |
| DZ980105A DZ2495A1 (fr) | 1997-05-30 | 1998-05-18 | Formule nouvelle de l'oméprazole-s. |
| MA25085A MA26500A1 (fr) | 1997-05-30 | 1998-05-21 | Forme nouvelle de s-omerprazole |
| UA99116288A UA60334C2 (uk) | 1997-05-30 | 1998-05-25 | Тригідрат магнієвої солі (s)-омепразолу, спосіб отримання тригідрату магнієвої солі (s)-омепразолу (варіанти), спосіб отримання калієвої солі (s)-омепразолу, калієва сіль (s)-омепразолу, фармацевтична композиція та спосіб лікування стану, пов'язаного з порушенням шлункової секреції |
| MEP-180/08A MEP18008A (en) | 1997-05-30 | 1998-05-25 | New process for the preparation of tryhidrate of magnesium salt of s-omeprasole |
| CNB98805521XA CN1161351C (zh) | 1997-05-30 | 1998-05-25 | 新型s-奥美拉唑 |
| EP02019642A EP1273581B1 (en) | 1997-05-30 | 1998-05-25 | New process for the preparation of the trihydrate of the magnesium salt of S-omeprazole |
| ES02019642T ES2236407T3 (es) | 1997-05-30 | 1998-05-25 | Nuevo procedimiento para la preparacion del trihidrato de la sal magnesica de s-omeprazol. |
| DK02019642T DK1273581T3 (da) | 1997-05-30 | 1998-05-25 | Ny fremgangsmåde til fremstilling af trihydratet af magnesiumsaltet af S-omeprazol |
| HU0001849A HU225987B1 (en) | 1997-05-30 | 1998-05-25 | Novel form of s-omeprazole |
| DE69829511T DE69829511T2 (de) | 1997-05-30 | 1998-05-25 | Neuer Prozess zur Herstellung von S-Omeprazol-Magnesiumsalz-Trihydrat |
| RSP-2007/0459A RS50067B (sr) | 1997-05-30 | 1998-05-25 | Novi postupak dobijanja trihidrata soli magnezijum-s- omeprazola |
| TR1999/02934T TR199902934T2 (xx) | 1997-05-30 | 1998-05-25 | S-Omeprazol�n yeni yap�s�. |
| SI9830761T SI1273581T1 (cs) | 1997-05-30 | 1998-05-25 | |
| AT02019642T ATE291574T1 (de) | 1997-05-30 | 1998-05-25 | Neuer prozess zur herstellung von s-omeprazol- magnesiumsalz-trihydrat |
| EEP199900550A EE03875B1 (et) | 1997-05-30 | 1998-05-25 | S-omeprasooli uus vorm |
| YUP-609/99A RS50005B (sr) | 1997-05-30 | 1998-05-25 | Novi oblik s-omeprazola |
| SK76-2005A SK285137B6 (sk) | 1997-05-30 | 1998-05-25 | Spôsob prípravy trihydrátu horečnatej soli S-omeprazolu, draselná soľ S-omeprazolu a spôsob jej prípravy |
| AU77935/98A AU722839B2 (en) | 1997-05-30 | 1998-05-25 | Novel form of S-omeprazole |
| CA002290963A CA2290963C (en) | 1997-05-30 | 1998-05-25 | S-omeprazole magnesium trihydrate |
| MEP-249/08A MEP24908A (en) | 1997-05-30 | 1998-05-25 | Novel form of s-omeprazole |
| PT02019642T PT1273581E (pt) | 1997-05-30 | 1998-05-25 | Novo processo para a preparacao do sal de magnesio de s-omeprazole tri-hidratado |
| BR9809509-9A BR9809509A (pt) | 1997-05-30 | 1998-05-25 | Composto, processo para preparação e uso do sal de magnésio de s-omeprazol triidratado, composição farmacêutica, e, processo para tratamento de uma condição relacionada com acidez gástrica |
| ES98926005.4T ES2195345T7 (es) | 1997-05-30 | 1998-05-25 | Nueva forma de S-omeprazol |
| DK98926005T DK0984957T3 (da) | 1997-05-30 | 1998-05-25 | Hidtil ukendt form af S-omeprazol |
| IDW991449A ID29306A (id) | 1997-05-30 | 1998-05-25 | Bentuk baru s-omeprazola |
| KR1019997011106A KR100540720B1 (ko) | 1997-05-30 | 1998-05-25 | 신규형의 ｓ-오메프라졸 |
| EP98926005.4A EP0984957B3 (en) | 1997-05-30 | 1998-05-25 | Novel form of s-omeprazole |
| NZ500991A NZ500991A (en) | 1997-05-30 | 1998-05-25 | Magnesium salt of S-omeprazole |
| JP50057899A JP4002303B2 (ja) | 1997-05-30 | 1998-05-25 | Ｓ−オメプラゾールの新規な形態 |
| SK1625-99A SK284837B6 (sk) | 1997-05-30 | 1998-05-25 | Trihydrát horečnatej soli S-omeprazolu, spôsob jeho prípravy, farmaceutická kompozícia s jeho obsahom a jeho použitie |
| HK00105176.5A HK1025962B (en) | 1997-05-30 | 1998-05-25 | Novel form of s-omeprazole |
| CA002521391A CA2521391C (en) | 1997-05-30 | 1998-05-25 | Potassium salt of s-omeprazole as intermediate in the preparation of the magnesium salt of s-omeprazole trihydrate |
| KR10-2005-7006896A KR100527804B1 (ko) | 1997-05-30 | 1998-05-25 | Ｓ-오메프라졸의 칼륨염 |
| PL98337180A PL193546B1 (pl) | 1997-05-30 | 1998-05-25 | Trihydrat soli magnezowej S-omeprazolu, sposób wytwarzania trihydratu soli magnezowej S-omeprazolu,sól potasowa S-omeprazolu, sposób wytwarzania soli potasowej S-omeprazolu, środek farmaceutyczny i zastosowanie trihydratu soli magnezowej S-omeprazolu |
| CZ20041090A CZ297585B6 (cs) | 1997-05-30 | 1998-05-25 | Nový způsob přípravy trihydrátu hořečnatésoli S-omeprazolu |
| DE69814069.9T DE69814069T3 (de) | 1997-05-30 | 1998-05-25 | Neuartige form von s-omeprazol |
| SI9830424T SI0984957T1 (en) | 1997-05-30 | 1998-05-25 | Novel form of s-omeprazole |
| IL13294798A IL132947A0 (en) | 1997-05-30 | 1998-05-25 | Novel form of s-omeprazole |
| PT98926005T PT984957E (pt) | 1997-05-30 | 1998-05-25 | Novas formas de s-omeprazole |
| MEP-2008-249A ME00198B (me) | 1997-05-30 | 1998-05-25 | Novi oblik s-omeprazola |
| AT98926005T ATE239011T1 (de) | 1997-05-30 | 1998-05-25 | Neuartige form von s-omeprazol |
| PCT/SE1998/000974 WO1998054171A1 (en) | 1997-05-30 | 1998-05-25 | Novel form of s-omeprazole |
| RU99128072/04A RU2184115C2 (ru) | 1997-05-30 | 1998-05-25 | Тригидрат магниевой соли s-омепразола, способы его получения, промежуточный продукт для его получения, содержащая его фармацевтическая композиция и способ лечения |
| EG58098A EG24291A (en) | 1997-05-30 | 1998-05-27 | Novel form of s-omeprazole |
| MYPI98002399A MY120745A (en) | 1997-05-30 | 1998-05-29 | Novel form of s-omeprazole |
| TNTNSN98074A TNSN98074A1 (fr) | 1997-05-30 | 1998-05-29 | Forme nouvelle de l'omeprazoles |
| MYPI20032997A MY127793A (en) | 1997-05-30 | 1998-05-29 | Novel form of s-omeprazole. |
| SA98190280A SA98190280B1 (ar) | 1997-05-30 | 1998-07-12 | صيغة جديدة لـ -s إس أومبرازول s-omeprazole |
| SA5260296A SA05260296B1 (ar) | 1997-05-30 | 1998-07-12 | عملية جديدة لتحضير تراي هيدرات ملح الماغنسيوم trihydrate of the magnesium salt من أوميبرازول S-omeprazole |
| IS5272A IS2142B (is) | 1997-05-30 | 1999-11-25 | Nýtt form S-ómeprasóls |
| NO19995852A NO317518B1 (no) | 1997-05-30 | 1999-11-29 | Ny form av S-omeprazol, farmasoytisk preparat som inneholder denne, fremgangmsate for dens fremstilling, anvendelse derav samt mellomprodukt og dets fremstilling |
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| US10/076,711 US6677455B2 (en) | 1997-05-30 | 2002-02-14 | Potassium salt of S-omeprazole |
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| US10/672,936 US7411070B2 (en) | 1997-05-30 | 2003-09-25 | Form of S-omeprazole |
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| US11/853,323 US7745466B2 (en) | 1997-05-30 | 2007-09-11 | Form of S-omeprazole |
| US12/784,881 US8076361B2 (en) | 1997-05-30 | 2010-05-21 | Form of S-omeprazole |
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| US13/298,373 US8466175B2 (en) | 1997-05-30 | 2011-11-17 | Form of S-omeprazole |
| DE201212000017 DE122012000017I1 (de) | 1997-05-30 | 2012-03-26 | Neuartige form von s-omeprazol. |
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| FR2722191B1 (fr) * | 1994-07-08 | 1996-08-23 | Rhone Poulenc Rorer Sa | Procede de preparation du trihydrate du (2r,3s)-3-tertbutoxycarbonylamino-2-hydroxy-3-phenylpropionate de 4-acetoxy2alpha-benzoyloxy-5beta,20epoxy-1,7beta,10beta trihydroxy-9-oxo-tax-11-en-13alpha-yle |
| SE504459C2 (sv) | 1994-07-15 | 1997-02-17 | Astra Ab | Förfarande för framställning av substituerade sulfoxider |
| PT792879E (pt) * | 1994-11-14 | 2001-08-30 | Daiichi Seiyaku Co | Processo para a preparacao de dicloridrato-3,5-hidrato do 3-¬2-¬4-(3-cloro-2-metilfenil)-1-piperazinil|-etil|-5,6-dimetoxi-1-(4-imidazolilmetil)-1h-indazol |
| GB9423970D0 (en) * | 1994-11-28 | 1995-01-11 | Astra Ab | Oxidation |
| SE9500422D0 (sv) | 1995-02-06 | 1995-02-06 | Astra Ab | New oral pharmaceutical dosage forms |
| CN1042423C (zh) | 1995-05-25 | 1999-03-10 | 常州市第四制药厂 | 奥美拉唑盐水合物及其制备方法 |
| SE9600072D0 (sv) | 1996-01-08 | 1996-01-08 | Astra Ab | New oral formulation of two active ingredients II |
| SE9600070D0 (sv) | 1996-01-08 | 1996-01-08 | Astra Ab | New oral pharmaceutical dosage forms |
| SE9600071D0 (sv) | 1996-01-08 | 1996-01-08 | Astra Ab | New oral formulation of two active ingredients I |
| SE510650C2 (sv) * | 1997-05-30 | 1999-06-14 | Astra Ab | Ny förening |
| US6747155B2 (en) * | 1997-05-30 | 2004-06-08 | Astrazeneca Ab | Process |
| AR057181A1 (es) | 2005-11-30 | 2007-11-21 | Astra Ab | Nueva forma de dosificacion de combinacion |
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1997
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