BRPI0513396A - produtos de degradação oxidativa de atorvastatina de cálcio - Google Patents
produtos de degradação oxidativa de atorvastatina de cálcioInfo
- Publication number
- BRPI0513396A BRPI0513396A BRPI0513396-3A BRPI0513396A BRPI0513396A BR PI0513396 A BRPI0513396 A BR PI0513396A BR PI0513396 A BRPI0513396 A BR PI0513396A BR PI0513396 A BRPI0513396 A BR PI0513396A
- Authority
- BR
- Brazil
- Prior art keywords
- degradation products
- oxidative degradation
- atorvastatin calcium
- atorvastatin
- calcium
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/14—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/36—Oxygen or sulfur atoms
- C07D207/40—2,5-Pyrrolidine-diones
- C07D207/416—2,5-Pyrrolidine-diones with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/48—Compounds containing oxirane rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Epoxy Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
PRODUTOS DE DEGRADAçãO OXIDATIVA DE ATORVASTATINA DE CáLCIO. A presente invenção refere-se aos produtos de degradação oxidativa de atorvastatina de cálcio e o processo da preparação. A presente invenção da mesma forma refere-se a atorvastatina de cálcio substancialmente livre de produtos de degradação oxidativos e as composições farmacêuticas contendo tal atorvastatina de cálcio.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SI200400209 | 2004-07-16 | ||
SI200400348 | 2004-12-24 | ||
PCT/EP2005/007739 WO2006008091A2 (en) | 2004-07-16 | 2005-07-15 | Oxidative degradation products of atorvastatin calcium |
Publications (1)
Publication Number | Publication Date |
---|---|
BRPI0513396A true BRPI0513396A (pt) | 2008-05-06 |
Family
ID=35457712
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BRPI0513396-3A BRPI0513396A (pt) | 2004-07-16 | 2005-07-15 | produtos de degradação oxidativa de atorvastatina de cálcio |
Country Status (14)
Country | Link |
---|---|
US (4) | US8044086B2 (pt) |
EP (1) | EP1771455B1 (pt) |
JP (1) | JP5000502B2 (pt) |
CN (1) | CN1997651B (pt) |
AU (1) | AU2005263550C1 (pt) |
BR (1) | BRPI0513396A (pt) |
CA (2) | CA2833770A1 (pt) |
ES (1) | ES2586561T3 (pt) |
HU (1) | HUE029911T2 (pt) |
MX (1) | MX2007000582A (pt) |
PL (1) | PL1771455T3 (pt) |
RU (1) | RU2412191C2 (pt) |
SI (1) | SI1771455T1 (pt) |
WO (1) | WO2006008091A2 (pt) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI321132B (en) | 2004-09-28 | 2010-03-01 | Teva Pharma | Process for preparing forms of atorvastatin calcium substantially free of impurities |
ES2304335T3 (es) | 2005-11-21 | 2010-05-19 | Warner-Lambert Company Llc | Formas nuevas del acido (r-(r*,r*))-2-(4-fluorofenil)-b,b-dihidroxi-5-(1-metiletil)-3-fenil-4-((fenilamino)carbonil)1h-pirrol-1-heptanoico, de magnesio. |
US20070265456A1 (en) * | 2006-05-09 | 2007-11-15 | Judith Aronhime | Novel crystal forms of atorvastatin hemi-calcium and processes for their preparation as well as novel processes for preparing other forms |
IS8607A (is) * | 2007-02-09 | 2008-08-10 | Actavis Group Hf. | Stöðugar atorvastatin samsetningar |
WO2011077843A1 (ja) | 2009-12-25 | 2011-06-30 | 沢井製薬株式会社 | アトルバスタチン含有被覆製剤 |
CN110646550B (zh) * | 2018-06-26 | 2022-12-02 | 北京伟林恒昌医药科技有限公司 | 一种阿托伐他汀钙中有关物质的检测方法 |
CN115754025A (zh) * | 2021-09-02 | 2023-03-07 | 上虞京新药业有限公司 | 一种匹伐他汀钙中基因毒性杂质gt1的检测方法 |
Family Cites Families (47)
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US3114497A (en) * | 1962-05-18 | 1963-12-17 | Kugler Emanuel | Drawstring bag |
US5245047A (en) * | 1988-02-22 | 1993-09-14 | Warner-Lambert Company | Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
US5097045A (en) * | 1989-02-01 | 1992-03-17 | Warner-Lambert Company | Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
US5216174A (en) * | 1988-02-22 | 1993-06-01 | Warner-Lambert Co. | Process for trans-6-[12-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
US5149837A (en) * | 1988-02-22 | 1992-09-22 | Warner-Lambert Company | Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
US5124482A (en) * | 1988-02-22 | 1992-06-23 | Warner-Lambert Company | Process for trans-6-(2-substituted-pyrrol-1-yl)alkyl)pyran-2-one inhibitors of cholesterol synthesis |
US5003080A (en) * | 1988-02-22 | 1991-03-26 | Warner-Lambert Company | Process for trans-6-(2-(substituted-pyrrol-1-yl)alkyl)pryan-2-one inhibitors of cholesterol synthesis |
FI94339C (fi) * | 1989-07-21 | 1995-08-25 | Warner Lambert Co | Menetelmä farmaseuttisesti käyttökelpoisen /R-(R*,R*)/-2-(4-fluorifenyyli)- , -dihydroksi-5-(1-metyylietyyli)-3-fenyyli-4-/(fenyyliamino)karbonyyli/-1H-pyrroli-1-heptaanihapon ja sen farmaseuttisesti hyväksyttävien suolojen valmistamiseksi |
US5103024A (en) * | 1990-10-17 | 1992-04-07 | Warner-Lambert Company | Process for the synthesis of (4r-cis)-1,1-dimethylethyl 6-cyanomethyl-2,2-dimethyl-1,3-dioxane-4-acetate |
US5248793A (en) * | 1990-10-17 | 1993-09-28 | Warner-Lambert Company | Process for the synthesis of (4R-cis)-1,1-dimethylethyl 6-iodomethyl or 6-(phenyl-substituted)sulfonyloxymethyl-2,2-dimethyl-1,3-dioxane-4-acetate |
US5155251A (en) * | 1991-10-11 | 1992-10-13 | Warner-Lambert Company | Process for the synthesis of (5R)-1,1-dimethylethyl-6-cyano-5-hydroxy-3-oxo-hexanoate |
ES2133158T3 (es) * | 1993-01-19 | 1999-09-01 | Warner Lambert Co | Formulacion ci-981 oral, estable y proceso de preparacion del mismo. |
US5298627A (en) * | 1993-03-03 | 1994-03-29 | Warner-Lambert Company | Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
HRP960313B1 (en) * | 1995-07-17 | 2002-08-31 | Warner Lambert Co | Form iii crystalline (r- (r*, r*)-2- (4-fluorophenyl) -beta-delta-hydroxy-5-(1-methylethyl) -3-phenyl-4- ((phenylamino) carbonyl -1h-pyrrole-1-heptanoic acid calcium salt (2:1) |
CZ294108B6 (cs) * | 1995-07-17 | 2004-10-13 | Warner@Lambertácompany | Krystalická forma I hydrátu atorvastatinuŹ tj@ semivápenaté soli kyseliny [R@}RgŹRgB]@}@fluorfenylB@betaŹdelta@dihydroxy@Q@}�@methylethylB@fenyl[}fenylaminoBkarbonyl]@�H@pyrrol@�@heptanové |
HRP960312B1 (en) * | 1995-07-17 | 2001-10-31 | Warner Lambert Co | NOVEL PROCESS FOR THE PRODUCTION OF AMORPHOUS /R-(R*, R*)/-2-(4-FLUOROPHENYL)-"beta", "delta"-DIHYDROXY-5-PHENYL-4-/(PHENYLAMINO)CARBONYL/-1H-PYRROLE -1-HEPTANOIC ACID CALCIUM SALT (2 : 1) |
KR100668575B1 (ko) * | 1997-12-19 | 2007-01-17 | 워너-램버트 익스포트 리미티드 | 1,3-디올의 합성방법 |
IN191236B (pt) * | 1999-05-25 | 2003-10-11 | Ranbaxy Lab Ltd | |
US6646133B1 (en) * | 2000-10-17 | 2003-11-11 | Egis Gyogyszergyar Rt. | Process for the preparation of amorphous atorvastatin calcium |
AU780624B2 (en) | 1999-11-04 | 2005-04-07 | Andrx Corporation | Method of treating amyloid beta precursor disorders |
WO2001037876A2 (en) | 1999-11-24 | 2001-05-31 | Bayer Aktiengesellschaft | Methods of ameliorating abnormal bone states |
SI20425A (sl) * | 1999-12-10 | 2001-06-30 | LEK tovarna farmacevtskih in kemi�nih izdelkov d.d. | Priprava amorfnega atorvastatina |
EP1584616A1 (en) * | 1999-12-17 | 2005-10-12 | Pfizer Science and Technology Ireland Limited | Industrial process for the production of crystalline atorvastatin trihydrate hemi calcium salt |
IL149088A0 (en) * | 1999-12-17 | 2002-11-10 | Warner Lambert Res & Dev Ie | A process for producing crystalline atorvastatin calcium |
JP2003518038A (ja) * | 1999-12-20 | 2003-06-03 | ニコラス, ジェイ カークホフ, | 流動床噴霧乾燥によるナノ粒子製造方法 |
CA2399396A1 (en) | 2000-02-10 | 2001-08-16 | Yasuo Sugiyama | Tnf- .alpha. inhibitors |
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KR100877165B1 (ko) * | 2000-11-16 | 2009-01-07 | 테바 파마슈티컬 인더스트리즈 리미티드 | 수산화 칼슘을 이용한[R(R*,R*)]-2-(4-플루오로페닐)-β,δ-디하이드록시-5-(1-메틸에틸)-3-페닐-4-[(페닐아미노)카보닐]-1H-피롤-1-헵탄산 에스테르의 가수분해 |
US7501450B2 (en) * | 2000-11-30 | 2009-03-10 | Teva Pharaceutical Industries Ltd. | Crystal forms of atorvastatin hemi-calcium and processes for their preparation as well as novel processes for preparing other forms |
IL156055A0 (en) * | 2000-11-30 | 2003-12-23 | Teva Pharma | Novel crystal forms of atorvastatin hemi calcium and processes for their preparation as well as novel processes for preparing other forms |
CA2622697A1 (en) * | 2000-12-27 | 2002-07-04 | Teva Pharmaceutical Industries Ltd. | Crystalline forms of atorvastatin |
US6476235B2 (en) * | 2001-01-09 | 2002-11-05 | Warner-Lambert Company | Process for the synthesis of 5-(4-fluorophenyl)-1-[2-((2R,4R)-4-hydroxy-6-oxo-tetrahydro-pyran-2-yl)-ethyl]-2-isopropyl-4-phenyl-1H-pyrrole-3-carboxylic acid phenylamide |
WO2002057229A1 (en) * | 2001-01-19 | 2002-07-25 | Biocon India Limited | FORM V CRYSTALLINE [R-(R*,R*)]-2-(4-FLUOROPHENYL)-ß,$G(D)-DIHYDROXY-5-(1-METHYLETHYL)-3-PHENYL-4-[(PHENYLAMINO)CARBONYL]-1H-PYRROLE-1- HEPTANOIC ACID HEMI CALCIUM SALT. (ATORVASTATIN) |
SI20814A (sl) * | 2001-01-23 | 2002-08-31 | LEK, tovarna farmacevtskih in kemi�nih izdelkov, d.d. | Priprava amorfnega atorvastatina |
PL368647A1 (en) | 2001-07-30 | 2005-04-04 | Dr.Reddy's Laboratories Ltd. | Crystalline forms vi and vii of atorvastatin calcium |
US7074818B2 (en) * | 2001-07-30 | 2006-07-11 | Dr. Reddy's Laboratories Limited | Crystalline forms VI and VII of Atorvastatin calcium |
PE20030324A1 (es) * | 2001-07-31 | 2003-04-03 | Warner Lambert Co | Composiciones farmaceuticas de amlodipina y atorvastatina |
AU2001284385A1 (en) * | 2001-08-31 | 2003-03-10 | Morepen Laboratories Ltd. | An improved process for the preparation of amorphous atorvastatin calcium salt (2:1) |
UA77990C2 (en) * | 2001-12-12 | 2007-02-15 | Crystalline calcium salt of (2:1) [r-(r*,r*)]-2-(4-fluorophenyl)-?,?-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1h-pyrroleheptanic acid | |
CZ296967B6 (cs) * | 2002-02-01 | 2006-08-16 | Zentiva, A.S. | Zpusob výroby amorfní formy hemivápenaté soli (3R,5R) 7-[3-fenyl-4-fenylkarbamoyl-2-(4-fluorfenyl)-5-isopropylpyrrol-1-yl]-3,5-dihydroxyheptanové kyseliny (atorvastatinu) |
PL372241A1 (en) * | 2002-02-19 | 2005-07-11 | Teva Pharmaceutical Industries Ltd. | Processes for desolvating solvates of atorvastatin hemi-calcium and atorvastatin hemi-calcium essentially free of organic solvent |
ITMI20020907A1 (it) * | 2002-04-29 | 2003-10-29 | Chemi Spa | Processo di preparazione della forma amorfa del sale di calcio della atorvastatina |
JP2006503024A (ja) * | 2002-09-03 | 2006-01-26 | モレペン、ラボラトリーズ、リミテッド | Vi型アトルバスタチンカルシウムまたはその水和物 |
SI21302A (sl) | 2002-10-11 | 2004-04-30 | LEK farmacevtska dru�ba d.d. | Stabiliziran farmacevtski izdelek z amorfno aktivno učinkovino |
CA2508871C (en) * | 2002-11-28 | 2008-09-09 | Teva Pharmaceutical Industries Ltd. | Crystalline form f of atorvastatin hemi-calcium salt |
HU227041B1 (en) * | 2003-03-24 | 2010-05-28 | Richter Gedeon Nyrt | Process for the synthesis of amorphous atorvastatin calcium |
ES2381473T3 (es) * | 2004-03-17 | 2012-05-28 | Ranbaxy Laboratories Limited | Procedimiento para la preparación de atorvastatina cálcica en forma amorfa |
-
2005
- 2005-07-15 SI SI200532085A patent/SI1771455T1/sl unknown
- 2005-07-15 CA CA 2833770 patent/CA2833770A1/en not_active Abandoned
- 2005-07-15 BR BRPI0513396-3A patent/BRPI0513396A/pt not_active Application Discontinuation
- 2005-07-15 WO PCT/EP2005/007739 patent/WO2006008091A2/en active Application Filing
- 2005-07-15 JP JP2007520774A patent/JP5000502B2/ja not_active Expired - Fee Related
- 2005-07-15 EP EP05760907.5A patent/EP1771455B1/en not_active Revoked
- 2005-07-15 MX MX2007000582A patent/MX2007000582A/es active IP Right Grant
- 2005-07-15 RU RU2007105689A patent/RU2412191C2/ru active
- 2005-07-15 HU HUE05760907A patent/HUE029911T2/en unknown
- 2005-07-15 US US11/632,608 patent/US8044086B2/en not_active Expired - Fee Related
- 2005-07-15 PL PL05760907.5T patent/PL1771455T3/pl unknown
- 2005-07-15 ES ES05760907.5T patent/ES2586561T3/es active Active
- 2005-07-15 CA CA2573969A patent/CA2573969C/en not_active Expired - Fee Related
- 2005-07-15 CN CN2005800240856A patent/CN1997651B/zh active Active
- 2005-07-15 AU AU2005263550A patent/AU2005263550C1/en not_active Ceased
-
2009
- 2009-11-06 US US12/613,787 patent/US20100056605A1/en not_active Abandoned
-
2010
- 2010-04-30 US US12/771,726 patent/US20100219063A1/en not_active Abandoned
-
2014
- 2014-12-18 US US14/575,339 patent/US9453030B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
CA2573969C (en) | 2014-02-04 |
US8044086B2 (en) | 2011-10-25 |
US20070208071A1 (en) | 2007-09-06 |
RU2412191C2 (ru) | 2011-02-20 |
RU2007105689A (ru) | 2008-08-27 |
US20100219063A1 (en) | 2010-09-02 |
JP2008506655A (ja) | 2008-03-06 |
CA2573969A1 (en) | 2006-01-26 |
PL1771455T3 (pl) | 2016-11-30 |
CA2833770A1 (en) | 2006-01-26 |
ES2586561T3 (es) | 2016-10-17 |
AU2005263550B2 (en) | 2011-11-03 |
JP5000502B2 (ja) | 2012-08-15 |
EP1771455B1 (en) | 2016-05-11 |
US9453030B2 (en) | 2016-09-27 |
MX2007000582A (es) | 2007-03-30 |
CN1997651A (zh) | 2007-07-11 |
CN1997651B (zh) | 2012-06-06 |
HUE029911T2 (en) | 2017-04-28 |
AU2005263550C1 (en) | 2013-01-17 |
WO2006008091A2 (en) | 2006-01-26 |
WO2006008091A3 (en) | 2006-09-08 |
US20100056605A1 (en) | 2010-03-04 |
EP1771455A2 (en) | 2007-04-11 |
AU2005263550A1 (en) | 2006-01-26 |
US20150105551A1 (en) | 2015-04-16 |
SI1771455T1 (sl) | 2016-09-30 |
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