HUP0001547A2 - Az S-omeprazol új formája - Google Patents
Az S-omeprazol új formájaInfo
- Publication number
- HUP0001547A2 HUP0001547A2 HU0001547A HUP0001547A HUP0001547A2 HU P0001547 A2 HUP0001547 A2 HU P0001547A2 HU 0001547 A HU0001547 A HU 0001547A HU P0001547 A HUP0001547 A HU P0001547A HU P0001547 A2 HUP0001547 A2 HU P0001547A2
- Authority
- HU
- Hungary
- Prior art keywords
- omeprazole
- neutral
- organic solvents
- solution
- solid
- Prior art date
Links
- 229960000381 omeprazole Drugs 0.000 title 1
- SUBDBMMJDZJVOS-DEOSSOPVSA-N esomeprazole Chemical compound C([S@](=O)C1=NC2=CC=C(C=C2N1)OC)C1=NC=C(C)C(OC)=C1C SUBDBMMJDZJVOS-DEOSSOPVSA-N 0.000 abstract 6
- 229960004770 esomeprazole Drugs 0.000 abstract 6
- 230000007935 neutral effect Effects 0.000 abstract 3
- 239000003960 organic solvent Substances 0.000 abstract 3
- 239000007787 solid Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- 230000008020 evaporation Effects 0.000 abstract 1
- 238000001704 evaporation Methods 0.000 abstract 1
- 159000000011 group IA salts Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000002904 solvent Substances 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
-
- 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
Abstract
A találmány tárgyát az (S)-omeprazol neutrális alakjának új, szilárdhalmazállapotú, legalább részben kristályos formája, eljárás ennekelőállítására és ezt a formát tartalmazó gyógyszerkészítményekképezik. A találmány szerint úgy járnak el, hogy a) neutrális (S)-omeprazol egy vagy több szerves oldószerrel készített oldatát nagyontöményre bepárolják, további oldószert adva hozzá folytatják abepárlást mindaddig, amíg szilárd, amorf, neutrális (S)-omeprazolkeletkezik; vagy b) az (S)-omeprazolt egy vagy több szervesoldószerrel és adott esetben vízzel készített oldatábólkristályosítják; vagy c) az (S)-omeprazol alkalikus sójának vízzel ésadott esetben egy vagy több szerves oldószerrel készített oldatából az(S)-omeprazolt megfelelő savval kicsapják. Ó
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE9604793A SE510666C2 (sv) | 1996-12-20 | 1996-12-20 | Nya Kristallmodifikationer |
PCT/SE1997/002125 WO1998028294A1 (en) | 1996-12-20 | 1997-12-16 | A novel compound form |
Publications (4)
Publication Number | Publication Date |
---|---|
HUP0001547A2 true HUP0001547A2 (hu) | 2002-05-29 |
HU0001547D0 HU0001547D0 (hu) | 2002-05-29 |
HUP0001547A3 HUP0001547A3 (en) | 2002-06-28 |
HU227589B1 HU227589B1 (en) | 2011-09-28 |
Family
ID=20405146
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0001547A HU227589B1 (en) | 1996-12-20 | 1997-12-16 | Crystal form of (s)-omeprazole |
Country Status (37)
Country | Link |
---|---|
US (1) | US6162816A (hu) |
EP (1) | EP0946547B1 (hu) |
JP (1) | JP4402174B2 (hu) |
KR (1) | KR20000069595A (hu) |
CN (1) | CN1109684C (hu) |
AR (1) | AR010361A1 (hu) |
AT (1) | ATE236898T1 (hu) |
AU (1) | AU730129B2 (hu) |
BR (1) | BR9714059A (hu) |
CA (1) | CA2274076C (hu) |
CZ (1) | CZ294784B6 (hu) |
DE (1) | DE69720774T2 (hu) |
DK (1) | DK0946547T3 (hu) |
EE (1) | EE03923B1 (hu) |
EG (1) | EG24414A (hu) |
ES (1) | ES2194231T3 (hu) |
HK (1) | HK1022909A1 (hu) |
HU (1) | HU227589B1 (hu) |
ID (1) | ID21850A (hu) |
IL (1) | IL130450A0 (hu) |
IS (1) | IS1981B (hu) |
MY (1) | MY117032A (hu) |
NO (1) | NO317191B1 (hu) |
NZ (1) | NZ336024A (hu) |
PL (1) | PL190377B1 (hu) |
PT (1) | PT946547E (hu) |
RS (1) | RS49685B (hu) |
RU (1) | RU2184734C2 (hu) |
SA (1) | SA97180739B1 (hu) |
SE (1) | SE510666C2 (hu) |
SI (1) | SI0946547T1 (hu) |
SK (1) | SK285151B6 (hu) |
TR (1) | TR199901410T2 (hu) |
TW (1) | TW538039B (hu) |
UA (1) | UA55436C2 (hu) |
WO (1) | WO1998028294A1 (hu) |
ZA (1) | ZA9711046B (hu) |
Families Citing this family (60)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6699885B2 (en) | 1996-01-04 | 2004-03-02 | The Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and methods of using same |
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 |
US6645988B2 (en) | 1996-01-04 | 2003-11-11 | Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and method of using same |
SI20019A (sl) * | 1998-07-13 | 2000-02-29 | LEK, tovarna farmacevtskih in kemi�nih izdelkov, d.d. | Izboljšan postopek sinteze 5-metoksi -2-/(4-metoksi-3,5-dimetil-2-piridil)metil/ sulfinil-1H-benzimidazola |
IL142703A (en) | 1998-11-10 | 2006-04-10 | Astrazeneca Ab | Crystalline form of omeprazole |
UA72748C2 (en) * | 1998-11-10 | 2005-04-15 | Astrazeneca Ab | A novel crystalline form of omeprazole |
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 |
SE9804003D0 (sv) | 1998-11-23 | 1998-11-23 | Astra Ab | A method of producing drug particles |
SE9900274D0 (sv) * | 1999-01-28 | 1999-01-28 | Astra Ab | New compound |
JP2000344739A (ja) * | 1999-06-01 | 2000-12-12 | Sumitomo Chem Co Ltd | N−保護−アゼチジン−2−カルボン酸の製造方法 |
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 |
SE0000773D0 (sv) * | 2000-03-08 | 2000-03-08 | Astrazeneca Ab | New formulation |
SE0000774D0 (sv) | 2000-03-08 | 2000-03-08 | Astrazeneca Ab | New formulation |
KR101035534B1 (ko) * | 2000-05-15 | 2011-05-23 | 다케다 야쿠힌 고교 가부시키가이샤 | 결정의 제조방법 |
GB0016040D0 (en) * | 2000-06-29 | 2000-08-23 | Glaxo Group Ltd | Novel process for preparing crystalline particles |
CA2417311C (en) | 2000-08-04 | 2012-07-10 | Takeda Chemical Industries, Ltd. | Crystalline alkali metal salts of lansoprazole and their production and use |
SI20875A (sl) * | 2001-04-25 | 2002-10-31 | LEK, tovarna farmacevtskih in kemi�nih izdelkov, d.d. | Kristalna oblika omeprazola |
US8206741B2 (en) | 2001-06-01 | 2012-06-26 | Pozen Inc. | Pharmaceutical compositions for the coordinated delivery of NSAIDs |
EP2163241A1 (en) | 2001-06-01 | 2010-03-17 | Pozen, Inc. | Pharmaceutical compositions for the coordinated delivery of NSAIDs |
GB2376231A (en) | 2001-06-06 | 2002-12-11 | Cipla Ltd | Benzimidazole-cyclodextrin inclusion complex |
SE0102993D0 (sv) | 2001-09-07 | 2001-09-07 | Astrazeneca Ab | New self emulsifying drug delivery system |
EP1515963B1 (en) | 2002-06-27 | 2007-02-14 | Dr. Reddy's Laboratories Ltd. | A process for preparation of optically pure or optically enriched sulfoxide compounds, including amorphous esomeprazole and salts thereof |
AU2003247729B2 (en) * | 2002-06-27 | 2009-10-08 | Dr. Reddy's Laboratories Limited | A process for preparation of optically pure or optically enriched sulfoxide compounds, including amorphous esomeprazole and salts thereof |
US7612098B2 (en) * | 2002-08-30 | 2009-11-03 | Dr. Reddy's Laboratories Limited | Amorphous hydrous esomeprazole magnesium |
EP2596792A1 (en) | 2002-10-16 | 2013-05-29 | Takeda Pharmaceutical Company Limited | Stable solid preparations |
US20040235903A1 (en) * | 2002-10-22 | 2004-11-25 | Khanna Mahavir Singh | Amorphous form of esomeprazole salts |
WO2004046134A2 (en) * | 2002-11-18 | 2004-06-03 | Dr. Reddy's Laboratories Limited | Crystalline form ii of esomeprazole magnesium trihydrate and process for its preparation |
CA2517714A1 (en) * | 2003-02-28 | 2004-09-10 | Ranbaxy Laboratories Limited | Polymorphs of s-omeprazole |
CN100364987C (zh) * | 2003-03-24 | 2008-01-30 | 卫材R&D管理有限公司 | 亚砜衍生物或其盐的非定形态的制备方法 |
US20070060556A1 (en) * | 2003-05-05 | 2007-03-15 | Yatendra Kumar | Barium salt of benzimidazole derivative |
US8993599B2 (en) | 2003-07-18 | 2015-03-31 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
SE0400410D0 (sv) | 2004-02-20 | 2004-02-20 | Astrazeneca Ab | New compounds |
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 |
AU2005264864B2 (en) | 2004-06-16 | 2011-08-11 | Takeda Pharmaceutical Company Limited | Multiple PPI dosage form |
NZ551970A (en) * | 2004-06-24 | 2010-01-29 | Astrazeneca Ab | New process for the preparation of crystal modifications for use in the preparation of esomeprazole sodium salt |
ES2246149B1 (es) * | 2004-07-02 | 2007-06-01 | Esteve Quimica, S.A. | Formas solidas de la sal magnesica de s-omeprazol y procedimientos para su preparacion. |
WO2006120520A1 (en) * | 2005-05-06 | 2006-11-16 | Glenmark Pharmaceuticals Limited | Esomeprazole strontium salt, process for its preparation and pharmaceutical compositions containing same |
EP1907375B1 (en) * | 2005-06-08 | 2013-07-24 | LEK Pharmaceuticals d.d. | Crystalline solvate of omeprazole sodium |
US7563812B2 (en) | 2005-06-15 | 2009-07-21 | Hetero Drugs Limited | Amorphous esomeprazole hydrate |
NL2000126C2 (nl) * | 2005-07-15 | 2008-01-29 | Solvay | Werkwijze voor de vervaardiging van eptifibatide. |
US20070043085A1 (en) * | 2005-08-19 | 2007-02-22 | Glenmark Pharmaceuticals Limited | Process for the preparation of amorphous form of neutral esomeprazole |
US7576219B2 (en) | 2005-10-26 | 2009-08-18 | Hanmi Pharm. Co., Ltd | Crystalline S-omeprazole strontium hydrate, method for preparing same, and pharmaceutical composition containing same |
EP1948637A4 (en) * | 2005-11-14 | 2010-09-08 | Hetero Drugs Ltd | PROCESS FOR AMORPHES ESOMEPRAZOLE |
JP2009518394A (ja) * | 2005-12-05 | 2009-05-07 | アストラゼネカ・アクチエボラーグ | エソメプラゾールの非塩形態の新規の製造方法 |
EP1801110A1 (en) | 2005-12-22 | 2007-06-27 | KRKA, tovarna zdravil, d.d., Novo mesto | Esomeprazole arginine salt |
US7799925B2 (en) | 2005-12-28 | 2010-09-21 | Unión Químico Farmacéutica, S.A. | Process for the preparation of the (S)-enantiomer of omeprazole |
EP2000468A1 (en) * | 2007-05-09 | 2008-12-10 | Dr. Reddy's Laboratories Ltd. | Esomeprazole salts and processes for preparation thereof |
WO2009047775A2 (en) * | 2007-10-08 | 2009-04-16 | Hetero Drugs Limited | Polymorphs of esomeprazole salts |
NZ588379A (en) | 2008-03-10 | 2012-07-27 | Takeda Pharmaceutical | Crystal of benzimidazole compound |
EP2143722A1 (en) | 2008-07-09 | 2010-01-13 | Lek Pharmaceuticals D.D. | Process for preparation of esomeprazole sodium of high chemical purity and new forms of esomeprazole sodium |
AU2009290712A1 (en) * | 2008-09-09 | 2010-03-18 | Astrazeneca Ab | Method for delivering a pharmaceutical composition to patient in need thereof |
SG176724A1 (en) | 2009-06-25 | 2012-01-30 | Astrazeneca Ab | Method for treating a patient at risk for developing an nsaid-associated ulcer |
SG181535A1 (en) | 2009-12-08 | 2012-07-30 | Codexis Inc | Synthesis of prazole compounds |
EP2649187B1 (en) | 2010-12-08 | 2017-11-22 | Codexis, Inc. | Biocatalysts and methods for the synthesis of armodafinil |
EA028049B1 (ru) | 2011-12-28 | 2017-10-31 | Поузен Инк. | Улучшенные композиции и способы доставки омепразола и ацетилсалициловой кислоты |
RU2501549C1 (ru) | 2012-08-30 | 2013-12-20 | Авва Девелопмент Лтд | Фармацевтическая композиция для лечения гастроэзофагеальной рефлюксной болезни |
CN107043367A (zh) * | 2017-05-26 | 2017-08-15 | 重庆莱美隆宇药业有限公司 | 一种中性s‑奥美拉唑的干燥工艺 |
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 |
SE8301182D0 (sv) * | 1983-03-04 | 1983-03-04 | Haessle Ab | Novel compounds |
GB2189698A (en) * | 1986-04-30 | 1987-11-04 | Haessle Ab | Coated omeprazole tablets |
DE4035455A1 (de) * | 1990-11-08 | 1992-05-14 | Byk Gulden Lomberg Chem Fab | Enantiomerentrennung |
US5877192A (en) * | 1993-05-28 | 1999-03-02 | Astra Aktiebolag | Method for the treatment of gastric acid-related diseases and production of medication using (-) enantiomer of omeprazole |
SE9301830D0 (sv) * | 1993-05-28 | 1993-05-28 | Ab Astra | New compounds |
SE9302396D0 (sv) * | 1993-07-09 | 1993-07-09 | Ab Astra | A novel compound form |
HUT75775A (en) * | 1994-07-08 | 1997-05-28 | Astra Ab | Medicament with multiple unit tablated dosage form containing omeprazole |
-
1996
- 1996-12-20 SE SE9604793A patent/SE510666C2/sv unknown
-
1997
- 1997-12-08 TW TW086118449A patent/TW538039B/zh not_active IP Right Cessation
- 1997-12-09 ZA ZA9711046A patent/ZA9711046B/xx unknown
- 1997-12-16 TR TR1999/01410T patent/TR199901410T2/xx unknown
- 1997-12-16 ID IDW990483A patent/ID21850A/id unknown
- 1997-12-16 HU HU0001547A patent/HU227589B1/hu not_active IP Right Cessation
- 1997-12-16 WO PCT/SE1997/002125 patent/WO1998028294A1/en not_active Application Discontinuation
- 1997-12-16 PT PT97951367T patent/PT946547E/pt unknown
- 1997-12-16 IL IL13045097A patent/IL130450A0/xx not_active IP Right Cessation
- 1997-12-16 EE EEP199900259A patent/EE03923B1/xx not_active IP Right Cessation
- 1997-12-16 US US09/000,154 patent/US6162816A/en not_active Expired - Lifetime
- 1997-12-16 NZ NZ336024A patent/NZ336024A/en not_active IP Right Cessation
- 1997-12-16 DK DK97951367T patent/DK0946547T3/da active
- 1997-12-16 BR BR9714059-7A patent/BR9714059A/pt not_active Application Discontinuation
- 1997-12-16 KR KR1019997005574A patent/KR20000069595A/ko active Search and Examination
- 1997-12-16 RU RU99116303/04A patent/RU2184734C2/ru not_active IP Right Cessation
- 1997-12-16 SK SK765-99A patent/SK285151B6/sk not_active IP Right Cessation
- 1997-12-16 CA CA002274076A patent/CA2274076C/en not_active Expired - Fee Related
- 1997-12-16 CZ CZ19992202A patent/CZ294784B6/cs not_active IP Right Cessation
- 1997-12-16 PL PL97334297A patent/PL190377B1/pl not_active IP Right Cessation
- 1997-12-16 ES ES97951367T patent/ES2194231T3/es not_active Expired - Lifetime
- 1997-12-16 UA UA99073869A patent/UA55436C2/uk unknown
- 1997-12-16 AT AT97951367T patent/ATE236898T1/de active
- 1997-12-16 EP EP97951367A patent/EP0946547B1/en not_active Expired - Lifetime
- 1997-12-16 RS YUP-281/99A patent/RS49685B/sr unknown
- 1997-12-16 CN CN97180849A patent/CN1109684C/zh not_active Expired - Fee Related
- 1997-12-16 AR ARP970105920A patent/AR010361A1/es active IP Right Grant
- 1997-12-16 DE DE69720774T patent/DE69720774T2/de not_active Expired - Lifetime
- 1997-12-16 JP JP52868598A patent/JP4402174B2/ja not_active Expired - Fee Related
- 1997-12-16 SI SI9730528T patent/SI0946547T1/xx unknown
- 1997-12-16 AU AU55026/98A patent/AU730129B2/en not_active Ceased
- 1997-12-19 MY MYPI97006176A patent/MY117032A/en unknown
- 1997-12-20 EG EG136097A patent/EG24414A/xx active
- 1997-12-27 SA SA97180739A patent/SA97180739B1/ar unknown
-
1999
- 1999-06-07 IS IS5070A patent/IS1981B/is unknown
- 1999-06-21 NO NO19993068A patent/NO317191B1/no not_active IP Right Cessation
-
2000
- 2000-03-31 HK HK00101986A patent/HK1022909A1/xx not_active IP Right Cessation
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HUP0001547A2 (hu) | Az S-omeprazol új formája | |
NO2005025I1 (no) | Krystalinsk ceftiofurfri syre, fremgangsmate for fremstilling av denne, og farmasoytisk preparat | |
RU99116303A (ru) | Новая форма соединения | |
RU94031126A (ru) | Циклические мочевины и их аналоги, пригодные в качестве ингибиторов протеазы ретровирусов, способ лечения вирусных инфекций, фармацевтическая композиция | |
BR9903984A (pt) | Composição aquosa que contém peptìdio farmaceuticamente efetivo, utilização dessa composição, processo para a produção de uma composição farmacêutica para aplicação local e processo para aumentar a atividade de um polipeptìdio | |
DK0948527T3 (da) | Cylosporinderivater, fremstilling af disse og farmaceutiske præparater indeholdende disse | |
ES2178268T3 (es) | Formulaciones de liberacion controlada. | |
IT1254619B (it) | Procedimento per la purificazione di acido ftalimmido-perossicaproico (pap) da impurezze di solventi clorurati | |
FI940806A (fi) | Sykliset johdokset, näitä yhdisteitä sisältävät lääkeaineet ja menetelmä niiden valmistamiseksi | |
AU5669398A (en) | Novel cyclosporin derivatives, method of preparation and pharmaceutical compositions containing them | |
HUP0400781A2 (hu) | Eljárás (R)- vagy (S)-lansoprazol kristályosítására, az előállított kristályok, azokat tartalmazó gyógyszerkészítmények és alkalmazásuk | |
FI883249A (fi) | Menetelmä terapeuttisesti käyttökelpoisten 3-desmetyylimevalonihappojohdannaisten valmistamiseksi | |
NO20012514D0 (no) | Fremgangsmåte for fremstilling av partikler med en omdannet amorf og/eller meta-stabil krystallinsk region til krystallinsktilstand | |
RU94028888A (ru) | Производные 1,3-замещенного циклоалкана и циклоалкена, смесь их изомеров или индивидуальные изомеры, их гидраты и соли, способ их получения и фармацевтическая композиция | |
HUP0302099A2 (hu) | Az azithromicin monohidrátja, eljárás az előállítására és a monohidrátot tartalmazó gyógyszerkészítmény | |
MY126071A (en) | Crystalline form ii of cabergoline. | |
HUP9901713A2 (hu) | Eljárás enantiomer-tiszta 2-azetidinkarbonsav előállítására | |
CA2460970A1 (en) | Processes for preparing crystalline and amorphous mupirocin calcium | |
ATE274513T1 (de) | Verbindungen und verfahren zur behandlung von schmerz | |
Pincock et al. | Spontaneous and induced generation of optical activity in racemic 1, 1′-Binaphthyl | |
ES2272198B1 (es) | Procedimiento para la obtencion de hidrato de calcipotriol. | |
FI20001655A (fi) | Kiteytysmenetelmõ | |
NO305658B1 (no) | Termodynamisk stabil krystallform av 4"-deoksy-4"-epi-metylaminoavermektin-B1a/B1b-benzosyresalt og fremgangsmÕte for fremstilling av dette | |
HUP0004916A2 (hu) | Eljárás 1,2,3,4-tetrahidroizokinolin-2,3-dikarbonsavanhidrid és felhasználásával (S)-N-terc-butil-1,2,3,4-tetrahidroizokinolin-3-karboxamid előállítására | |
Cuthbert et al. | Cyclic sulphamidite analogues of penicillanic acid |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Lapse of definitive patent protection due to non-payment of fees |