PL386051A1 - Stable, oral compound pharmaceutical containing pharmaceutically permissible content of [(E)-7-[4-(4-fluorphenyl)-6-isopropyl-2-[methyl(methylsulfonyl)amino]pyrimidine-5-yl] (3R,5S)-3,5-dihydroxy-hept-6-enoate acid salt - Google Patents
Stable, oral compound pharmaceutical containing pharmaceutically permissible content of [(E)-7-[4-(4-fluorphenyl)-6-isopropyl-2-[methyl(methylsulfonyl)amino]pyrimidine-5-yl] (3R,5S)-3,5-dihydroxy-hept-6-enoate acid saltInfo
- Publication number
- PL386051A1 PL386051A1 PL386051A PL38605108A PL386051A1 PL 386051 A1 PL386051 A1 PL 386051A1 PL 386051 A PL386051 A PL 386051A PL 38605108 A PL38605108 A PL 38605108A PL 386051 A1 PL386051 A1 PL 386051A1
- Authority
- PL
- Poland
- Prior art keywords
- fluorphenyl
- enoate
- hept
- methylsulfonyl
- dihydroxy
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2009—Inorganic compounds
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Inorganic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL386051A PL386051A1 (en) | 2008-09-09 | 2008-09-09 | Stable, oral compound pharmaceutical containing pharmaceutically permissible content of [(E)-7-[4-(4-fluorphenyl)-6-isopropyl-2-[methyl(methylsulfonyl)amino]pyrimidine-5-yl] (3R,5S)-3,5-dihydroxy-hept-6-enoate acid salt |
PCT/PL2009/000084 WO2010030201A2 (en) | 2008-09-09 | 2009-09-02 | Stable oral pharmaceutical composition containing a pharmaceutically acceptable salt of [(e)-7-[4-(4-fluorophenyl)-6-isopropyl-2- [methyl(methylsulfonyl)amino]pyrimidine-5-yl] (3r, 5s) - 3,5 dihydroxyhept-6- enoic acid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL386051A PL386051A1 (en) | 2008-09-09 | 2008-09-09 | Stable, oral compound pharmaceutical containing pharmaceutically permissible content of [(E)-7-[4-(4-fluorphenyl)-6-isopropyl-2-[methyl(methylsulfonyl)amino]pyrimidine-5-yl] (3R,5S)-3,5-dihydroxy-hept-6-enoate acid salt |
Publications (1)
Publication Number | Publication Date |
---|---|
PL386051A1 true PL386051A1 (en) | 2010-03-15 |
Family
ID=42005665
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL386051A PL386051A1 (en) | 2008-09-09 | 2008-09-09 | Stable, oral compound pharmaceutical containing pharmaceutically permissible content of [(E)-7-[4-(4-fluorphenyl)-6-isopropyl-2-[methyl(methylsulfonyl)amino]pyrimidine-5-yl] (3R,5S)-3,5-dihydroxy-hept-6-enoate acid salt |
Country Status (2)
Country | Link |
---|---|
PL (1) | PL386051A1 (en) |
WO (1) | WO2010030201A2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TR200904341A2 (en) * | 2009-06-03 | 2010-12-21 | Bi̇lgi̇ç Mahmut | Stable pharmaceutical compositions containing rosuvastatin calcium. |
TR201009399A2 (en) * | 2010-11-11 | 2012-05-21 | Bi̇lgi̇ç Mahmut | Rapidly soluble effervescent rosuvastatin formulations. |
US20140179712A1 (en) * | 2012-12-21 | 2014-06-26 | Astrazeneca Ab | Pharmaceutical formulation of n-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2h-pyrazol-3-yl]-4-[(3r,5s)-3,5-dimethylpiperazin-1-yl]benzamide |
WO2016076280A1 (en) | 2014-11-11 | 2016-05-19 | 塩野義製薬株式会社 | Multi-layered tablet containing drug unstable with respect to light |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5180589A (en) * | 1988-03-31 | 1993-01-19 | E. R. Squibb & Sons, Inc. | Pravastatin pharmaceuatical compositions having good stability |
GB0001621D0 (en) * | 2000-01-26 | 2000-03-15 | Astrazeneca Ab | Pharmaceutical compositions |
EA015682B1 (en) * | 2005-12-20 | 2011-10-31 | Лек Фармасьютиклз Д.Д. | Pharmaceutical composition |
HU227610B1 (en) * | 2006-09-18 | 2011-09-28 | Richter Gedeon Nyrt | Pharmaceutical compositions containing rosuvastatin potassium |
WO2009112870A1 (en) * | 2008-03-11 | 2009-09-17 | Belupo-Lijekovi I Kozmetika D.D. | Pharmaceutical composition comprising rosuvastatin calcium and magnesium carbonate hydroxide pentahydrate as a stabilizer |
-
2008
- 2008-09-09 PL PL386051A patent/PL386051A1/en not_active Application Discontinuation
-
2009
- 2009-09-02 WO PCT/PL2009/000084 patent/WO2010030201A2/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
WO2010030201A2 (en) | 2010-03-18 |
WO2010030201A3 (en) | 2010-07-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
TWI341310B (en) | Improved production of (e)-7-[4-(4-fluorophenyl)-6-isopropyl-2-[methyl(methylsulfonyl)amino]pyrimidin-5-yl](3r,5s)-3,5-dihydroxyhept-6-enoic acid calcium salt | |
IS8385A (en) | Crystalline form bis [(E) -7- [4- (4-fluorophenyl) -6-isopropyl-2- [methyl (methylsulfonyl) amino] pyrimidin-5-yl] (3R, 5S) -3,5-dihydroxyheptin 6-enoic acid] calcium salt | |
IS8478A (en) | Process for the preparation of the calcium salt of rosuvatatin (E) -7- [4- (4-fluorophenyl) -6-isopropyl-2- [methyl (methylsulfonyl) amino] pyrimidin-5-yl] (3R, 5S) -3,5- dihydroxyhept-6-enoic acid and its crystalline intermediates | |
WO2009157014A3 (en) | A process for preparing hmg-coa reductase inhibitors and intermediates | |
WO2012147107A3 (en) | Novel & improved processes for preparing indoline derivatives and its pharmaceutical composition | |
SI1873148T1 (en) | Pharmaceutical compositions containing crystalline salts of 7-?á4-(4-fluorophenyl)-6-isopropyl-2-?ámethyl(methylsulfonyl)amino?åpyrimidin-5-yl?å-(3R,5S)-3,5-dihydroxyhept-6-enoic acid | |
MX2011012344A (en) | Disaccharin, difumaric acid, di-l-hydroxy-2-naphthoic acid and mono-benzoic acid salts of 4- (dimethylamin0)butyl 2- (4- ( (2-amino-4-methyl-6- (pentylamino) pyrimidin- 5 -yl) methyl) phenyl)acetate. | |
FR16C1023I1 (en) | 4-[[4-[[4-(2-Cyanoethenyl)-2,6-dimethylphenyl]amino]-2-Pyrimidinyl]amino]benzonitrile salt | |
IL202363A0 (en) | Crystalline form of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]amino]benzonitrile | |
EP3255043A3 (en) | N-(6-((2r,3s)-3,4-dihydroxybutan-2-yloxy)-2-(4-fluorobenzylthio)pyrimidin-4-yl)-3- methylazetidine-1-sulfonamide as chemokine receptor modulator | |
ZA200807158B (en) | Malate salts, and polymorphs of (3S,5S)-7-[3-amino-5-methyl-piperidinyl]-1-cyclopropyl-1, 4-dihydro-8-methoxy-4-oxo-3-quinolinecaroxylic acid | |
EA201270099A1 (en) | TRANS-4 - [[(5S) -5 - [[[3,5-BIS (TRIFTOROMETYL) PHENYL] METHYL] (2-METHYL-2H-TETRAZOL-5-IL) AMINO] -2,3,4,5 -TETRAHYDRO-7,9-DIMETHYL-1H-1-BENZAZEPIN-1-IL] METHYL] CYCLOHEXANKARBONIC ACID | |
PL386051A1 (en) | Stable, oral compound pharmaceutical containing pharmaceutically permissible content of [(E)-7-[4-(4-fluorphenyl)-6-isopropyl-2-[methyl(methylsulfonyl)amino]pyrimidine-5-yl] (3R,5S)-3,5-dihydroxy-hept-6-enoate acid salt | |
EA200801447A1 (en) | PHARMACEUTICAL COMPOSITION | |
EA201390771A1 (en) | METHOD OF OBTAINING PHARMACEUTICAL INTERMEDIATE COMPOUNDS OF HIGH PURITY | |
PL1704144T3 (en) | A method of preparation of the hemi-calcium salt of (e)-7- [4-(4-fluorophenyl)-6-isopropyl-2- [me thyl(methylsulfonyl)amino]pyrimidin-5-yl](3r,5s)-3,5-dihydroxy-6-heptenoic acid | |
WO2012011129A3 (en) | Novel polymorph of bis[(e)-7-[4-(4-fluorophenyl)-6-iso-propyl-2-[methyl (methylsulfonyl)amino]pyrimidin-5-yl](3r,5s)-3,5-dihydroxyhept-6-enoic acid] calcium salt | |
MX2011013149A (en) | (s) -2-benzyl-3- ( (3r, 4r) -4- (3 -carbamo ylphenyl) -3, 4-dimethylpiperidinyl) propanoic acid and salt therof as antagonists of the opioid receptors. | |
UA92467C2 (en) | Hydrochloride of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl] amino]benzonitrile | |
WO2009091346A3 (en) | Stable pharmaceutical formulation and preparation methods | |
ZA200705514B (en) | Preparation of pharmaceutical salts of piperazine compounds | |
UY30336A1 (en) | PHARMACEUTICAL COMPOSITIONS CONTAINING ACID (E) -7- (4- (4-FLUOROPHENYL) -6-ISOPROPIL-2- (METHYL (METILSULFONIL) AMINO) PIRIMIDIN-5-IL) - (3R, 5S) -3,5-DIHYDROXIHEPT -6-ENOICO AND PHARMACEUTICALLY ACCEPTABLE SALTS OF THE SAME | |
TH133899A (en) | Acid sodium salt 5-cyclo-propyl-2 - {[2- (2,6-difluorophenyl) pyrimidin -5-il] amino} benzoic As a DHODH inhibitor |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
REFS | Decisions on refusal to grant patents (taken after the publication of the particulars of the applications) |