AR075736A1 - Sal de sodio de acido 5- ciclopropil -2-((2-(2,6- difluorofenil ) pirimidin -5-il) amino) benzoico como inhibidor de dhodh (dihidroorotato deshidrogenasa) - Google Patents
Sal de sodio de acido 5- ciclopropil -2-((2-(2,6- difluorofenil ) pirimidin -5-il) amino) benzoico como inhibidor de dhodh (dihidroorotato deshidrogenasa)Info
- Publication number
- AR075736A1 AR075736A1 ARP100100739A ARP100100739A AR075736A1 AR 075736 A1 AR075736 A1 AR 075736A1 AR P100100739 A ARP100100739 A AR P100100739A AR P100100739 A ARP100100739 A AR P100100739A AR 075736 A1 AR075736 A1 AR 075736A1
- Authority
- AR
- Argentina
- Prior art keywords
- difluorophenyl
- amino
- sodium salt
- benzoic
- cyclopropil
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- 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
- 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
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pain & Pain Management (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
La presente se refiere a la sal de sodio cristalina hidrosoluble de ácido 2-{[5-ciclopropil-2-{[2-(2,6'-difluorofenil)pirimidin-5-il]amino}benzoico y a sus solvatos farmacéuticamente aceptables, composiciones farmacéuticas, composiciones utiles para artritis reumatoidea, psoriásica, espondilitis anquilosante, etc.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09382033A EP2239256A1 (en) | 2009-03-13 | 2009-03-13 | Sodium salt of 5-cyclopropyl-2-{[2-(2,6-difluorophenyl)pyrimidin-5-yl]amino}benzoic acid as DHODH inhibitor |
Publications (1)
Publication Number | Publication Date |
---|---|
AR075736A1 true AR075736A1 (es) | 2011-04-20 |
Family
ID=40903239
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP100100739A AR075736A1 (es) | 2009-03-13 | 2010-03-11 | Sal de sodio de acido 5- ciclopropil -2-((2-(2,6- difluorofenil ) pirimidin -5-il) amino) benzoico como inhibidor de dhodh (dihidroorotato deshidrogenasa) |
Country Status (22)
Country | Link |
---|---|
US (1) | US8501943B2 (es) |
EP (2) | EP2239256A1 (es) |
JP (1) | JP2012520250A (es) |
KR (1) | KR20110125653A (es) |
CN (1) | CN102348687B (es) |
AR (1) | AR075736A1 (es) |
AU (1) | AU2010223526A1 (es) |
CA (1) | CA2754801A1 (es) |
CL (1) | CL2011002215A1 (es) |
CO (1) | CO6420336A2 (es) |
EA (1) | EA020218B1 (es) |
EC (1) | ECSP11011383A (es) |
IL (1) | IL214518A0 (es) |
MX (1) | MX2011009148A (es) |
NZ (1) | NZ594492A (es) |
PE (1) | PE20120114A1 (es) |
SG (1) | SG173825A1 (es) |
TW (1) | TW201032811A (es) |
UA (1) | UA105788C2 (es) |
UY (1) | UY32466A (es) |
WO (1) | WO2010102824A2 (es) |
ZA (1) | ZA201105742B (es) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2319596B1 (es) | 2006-12-22 | 2010-02-08 | Laboratorios Almirall S.A. | Nuevos derivados de los acidos amino-nicotinico y amino-isonicotinico. |
UY31272A1 (es) | 2007-08-10 | 2009-01-30 | Almirall Lab | Nuevos derivados de ácido azabifenilaminobenzoico |
EP2135610A1 (en) | 2008-06-20 | 2009-12-23 | Laboratorios Almirall, S.A. | Combination comprising DHODH inhibitors and methotrexate |
EP2376495A4 (en) | 2008-12-08 | 2012-10-31 | Vm Pharma Llc | COMPOSITIONS OF PROTEIN RECEPTOR TYROSINE KINASE INHIBITORS |
EP2314577A1 (en) | 2009-10-16 | 2011-04-27 | Almirall, S.A. | Process for manufacturing 2-[(3,5-difluoro-3'-methoxy-1,1'-biphenyl-4-yl)amino]nicotinic acid |
EP2444088A1 (en) * | 2010-10-22 | 2012-04-25 | Almirall, S.A. | Amino derivatives for the treatment of proliferative skin disorders |
US20120195933A1 (en) * | 2011-01-27 | 2012-08-02 | Ralph Stefan | Pharmaceutical compositions comprising tasocitinib |
US8999992B2 (en) | 2013-03-15 | 2015-04-07 | Vm Pharma Llc | Crystalline forms of tryosine kinase inhibitors and their salts |
MA39286A (fr) | 2014-09-17 | 2016-03-24 | Mundipharma International Corporation Ltd | Formes cristallines d'inhibiteurs de la tyrosine kinase et leurs sels |
WO2018136009A1 (en) | 2017-01-20 | 2018-07-26 | Aslan Pharmaceuticals Pte Ltd | Combination therapy |
CN114957650B (zh) * | 2022-06-11 | 2024-05-10 | 新疆腾域鸿源农业科技有限公司 | 一种聚天冬氨酸钾的制备方法及其在植物生长促进剂中的应用 |
Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2225396C (en) | 1995-06-21 | 2003-03-25 | Asta Medica Aktiengesellschaft | Pharmaceutical powder cartridge with integrated metering device and inhaler for powdered medicaments |
DE19547648A1 (de) | 1995-12-20 | 1997-06-26 | Hoechst Ag | Zubereitung, enthaltend High Density Lipoproteine und Crotonsäureamidderivate |
DE19610955A1 (de) | 1996-03-20 | 1997-09-25 | Hoechst Ag | Kombinationspräparat, enthaltend 5-Methylisoxazol-4-carbonsäure-(4-trifluormethyl)- anilid und N-(4-Trifluormethylphenyl)-2-cyan-3- hydroxycrotonsäureamid |
GB9804343D0 (en) | 1998-02-27 | 1998-04-22 | Univ Cardiff | Chemical compounds |
AP2002002387A0 (en) | 1999-06-10 | 2002-03-31 | Warner Lambert Co | Method of inhibiting amyloid aggregation and imaging amyloid deposits. |
WO2002080897A1 (en) | 2001-04-05 | 2002-10-17 | Aventis Pharmaceuticals Inc. | Use of (z)-2-cyano-3-hydroxy-but-2-enoic acid-(4'-trifluoromethylphenyl)-amide for treating multiple sclerosis |
WO2002102374A1 (en) | 2001-06-19 | 2002-12-27 | Merck & Co., Inc. | Amine salt of an integrin receptor antagonist |
DE10129703A1 (de) | 2001-06-22 | 2003-01-02 | Sofotec Gmbh & Co Kg | Zerstäubungssystem für eine Pulvermischung und Verfahren für Trockenpulverinhalatoren |
WO2003006424A1 (en) | 2001-07-10 | 2003-01-23 | 4Sc Ag | Novel compounds as anti-inflammatory, immunomodulatory and anti-proliferatory agents |
US7258118B2 (en) | 2002-01-24 | 2007-08-21 | Sofotec Gmbh & Co, Kg | Pharmaceutical powder cartridge, and inhaler equipped with same |
DE10202940A1 (de) | 2002-01-24 | 2003-07-31 | Sofotec Gmbh & Co Kg | Patrone für einen Pulverinhalator |
PE20040844A1 (es) | 2002-11-26 | 2004-12-30 | Novartis Ag | Acidos fenilaceticos y derivados como inhibidores de la cox-2 |
US7071355B2 (en) | 2002-12-23 | 2006-07-04 | 4 Sc Ag | Compounds as anti-inflammatory, immunomodulatory and anti-proliferatory agents |
EP1581478A1 (en) | 2002-12-23 | 2005-10-05 | 4Sc Ag | Dhodh-inhibitors and method for their identification |
SE0400234D0 (sv) | 2004-02-06 | 2004-02-06 | Active Biotech Ab | New compounds, methods for their preparation and use thereof |
CN1993125A (zh) | 2004-05-21 | 2007-07-04 | Uab研究基金会 | 涉及嘧啶合成抑制剂的组合物和方法 |
WO2006022442A1 (ja) | 2004-08-24 | 2006-03-02 | Santen Pharmaceutical Co., Ltd. | ジヒドロオロテートデヒドロゲナーゼ阻害活性を有する新規複素環アミド誘導体 |
CN101043883A (zh) | 2004-10-19 | 2007-09-26 | 安万特药物公司 | (z)-2-氰基-3-羟基-丁-2-烯酸-(4'-三氟甲基苯基)-酰胺用于治疗炎症性肠病的用途 |
ES2265276B1 (es) | 2005-05-20 | 2008-02-01 | Laboratorios Almirall S.A. | Derivados de 4-(2-amino-1-hidroxietil)fenol como agonistas del receptor beta2 adrenergico. |
ES2303758B1 (es) | 2006-02-20 | 2009-08-13 | Laboratorios Almirall S.A. | Nuevos derivados de piridin-3-amina. |
ES2301380B1 (es) | 2006-08-09 | 2009-06-08 | Laboratorios Almirall S.A. | Nuevos derivados de 1,7-naftiridina. |
ES2319596B1 (es) | 2006-12-22 | 2010-02-08 | Laboratorios Almirall S.A. | Nuevos derivados de los acidos amino-nicotinico y amino-isonicotinico. |
WO2008097180A1 (en) | 2007-02-06 | 2008-08-14 | Chelsea Therapeutics, Inc. | New compounds, methods for their preparation and use thereof |
UY31272A1 (es) | 2007-08-10 | 2009-01-30 | Almirall Lab | Nuevos derivados de ácido azabifenilaminobenzoico |
EP2135610A1 (en) | 2008-06-20 | 2009-12-23 | Laboratorios Almirall, S.A. | Combination comprising DHODH inhibitors and methotrexate |
EP2210615A1 (en) | 2009-01-21 | 2010-07-28 | Almirall, S.A. | Combinations comprising methotrexate and DHODH inhibitors |
EP2228367A1 (en) | 2009-03-13 | 2010-09-15 | Almirall, S.A. | Addition salts of amines containing hydroxyl and/or carboxylic groups with amino nicotinic acid derivatives as DHODH inhibitors |
EP2230232A1 (en) | 2009-03-13 | 2010-09-22 | Almirall, S.A. | Addition salts of tromethamine with azabiphenylaminobenzoic acid derivatives as DHODH inhibitors |
EP2314577A1 (en) | 2009-10-16 | 2011-04-27 | Almirall, S.A. | Process for manufacturing 2-[(3,5-difluoro-3'-methoxy-1,1'-biphenyl-4-yl)amino]nicotinic acid |
-
2009
- 2009-03-13 EP EP09382033A patent/EP2239256A1/en not_active Withdrawn
-
2010
- 2010-02-24 UY UY0001032466A patent/UY32466A/es unknown
- 2010-03-08 TW TW099106629A patent/TW201032811A/zh unknown
- 2010-03-11 EP EP10708145A patent/EP2406221A2/en not_active Withdrawn
- 2010-03-11 KR KR1020117021316A patent/KR20110125653A/ko not_active Application Discontinuation
- 2010-03-11 MX MX2011009148A patent/MX2011009148A/es active IP Right Grant
- 2010-03-11 AU AU2010223526A patent/AU2010223526A1/en not_active Abandoned
- 2010-03-11 WO PCT/EP2010/001548 patent/WO2010102824A2/en active Application Filing
- 2010-03-11 CA CA2754801A patent/CA2754801A1/en not_active Abandoned
- 2010-03-11 PE PE2011001598A patent/PE20120114A1/es not_active Application Discontinuation
- 2010-03-11 CN CN201080011541.4A patent/CN102348687B/zh not_active Expired - Fee Related
- 2010-03-11 NZ NZ594492A patent/NZ594492A/xx not_active IP Right Cessation
- 2010-03-11 AR ARP100100739A patent/AR075736A1/es not_active Application Discontinuation
- 2010-03-11 JP JP2011553358A patent/JP2012520250A/ja active Pending
- 2010-03-11 US US13/256,127 patent/US8501943B2/en not_active Expired - Fee Related
- 2010-03-11 SG SG2011060837A patent/SG173825A1/en unknown
- 2010-03-11 UA UAA201111805A patent/UA105788C2/uk unknown
- 2010-03-11 EA EA201101301A patent/EA020218B1/ru not_active IP Right Cessation
-
2011
- 2011-08-04 ZA ZA2011/05742A patent/ZA201105742B/en unknown
- 2011-08-08 IL IL214518A patent/IL214518A0/en unknown
- 2011-09-01 CO CO11112334A patent/CO6420336A2/es not_active Application Discontinuation
- 2011-09-08 CL CL2011002215A patent/CL2011002215A1/es unknown
- 2011-10-07 EC EC2011011383A patent/ECSP11011383A/es unknown
Also Published As
Publication number | Publication date |
---|---|
WO2010102824A2 (en) | 2010-09-16 |
IL214518A0 (en) | 2011-09-27 |
AU2010223526A1 (en) | 2011-08-25 |
KR20110125653A (ko) | 2011-11-21 |
CL2011002215A1 (es) | 2012-03-09 |
MX2011009148A (es) | 2011-09-28 |
TW201032811A (en) | 2010-09-16 |
EP2239256A1 (en) | 2010-10-13 |
CO6420336A2 (es) | 2012-04-16 |
WO2010102824A3 (en) | 2010-11-18 |
EA020218B1 (ru) | 2014-09-30 |
NZ594492A (en) | 2013-11-29 |
UY32466A (es) | 2010-09-30 |
CN102348687B (zh) | 2014-04-02 |
UA105788C2 (uk) | 2014-06-25 |
EP2406221A2 (en) | 2012-01-18 |
SG173825A1 (en) | 2011-09-29 |
JP2012520250A (ja) | 2012-09-06 |
EA201101301A1 (ru) | 2012-04-30 |
CA2754801A1 (en) | 2010-09-16 |
US8501943B2 (en) | 2013-08-06 |
ECSP11011383A (es) | 2011-11-30 |
PE20120114A1 (es) | 2012-02-20 |
ZA201105742B (en) | 2012-04-25 |
CN102348687A (zh) | 2012-02-08 |
US20120003184A1 (en) | 2012-01-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR075736A1 (es) | Sal de sodio de acido 5- ciclopropil -2-((2-(2,6- difluorofenil ) pirimidin -5-il) amino) benzoico como inhibidor de dhodh (dihidroorotato deshidrogenasa) | |
PE20090903A1 (es) | Derivados de acido azabifenilaminobenzoico como inhibidores de la dihidroorotato deshidrogenasa | |
MX2013005533A (es) | Derivados de acido amino-bisfenil-pentanoico sustituidos como inhibidores de nep. | |
NZ607845A (en) | Besylate salt of a btk inhibitor | |
MX2012006562A (es) | Formas cristalinas de 3-(2,6-dicloro-3,5-dimetoxi-fenil)-1-{6-[4-( 4-etil-piperazin-1-il)-fenil-amino]-pirimidin-4-il}-1-metil-urea y sales de las mismas. | |
UY33044A (es) | Derivados del acido carbamoil-metil-amino-acetico sustituido como inhibidores de nep novedosos | |
PE20120171A1 (es) | Sales de adicion de aminas que contienen grupos hidroxilo y/o carboxilicos con derivados de acidos aminonicotinico como inhibidores de dhodh | |
CL2011002918A1 (es) | Composicion farmaceutica solida que comprende al inhibidor de quinasa aurora acido 4-{[9-cloro-7-(2-fluoro-6-metoxifenil)-5h-pirimido-[5,4-d][2]benzazepin-2-il]amino}-2-metoxibenzoico, una sal o una forma cristalina del mismo; metodo para prepararla que incluye un proceso de granulacion en humedo. | |
PA8855501A1 (es) | Nuevo procedimiento de sintesis de la ivabradina y de sus sales de adicion a un acido farmaceuticamente aceptable | |
BRPI1012638B8 (pt) | métodos e intermediários para preparar agentes farmacêuticos | |
NI200900155A (es) | COMPUESTOS DE 2-AMINO PIRIMIDINA. Caso: PC 33441A | |
MY152281A (en) | 4-pyrimidinesulfamide derivative | |
PH12014502210A1 (en) | Salts of 5-[(1r)-2-({2-[4-(2,2-difluoro-2-phenylethoxy)phenyl]ethyl}amino)-1-hydroxyethyl]-8-hydroxyquinolin-2(1h)-one | |
PE20080175A1 (es) | Sales de malato, y polimorfos de acido (3s,5s)-7-[3-amino-5-metil-piperidinil]-1-ciclopropil-1,4-dihidro-8-metoxi-4-oxo-3-quinolincarboxilico | |
PT2448933E (pt) | Ácido trans-4-[[(5s)-5-[[[3,5- bis(trifluorometil)fenil]metil] (2-metil-2h-tetrazol-5- il)amino]-2,3,4,5-tetra-hidro-7,9-dimetil-1h-1-benzazepin- 1-il]metil]-ciclo-hexanocarboxílico | |
TN2009000167A1 (en) | Crystalline potassium salt of lipoxin a4 analogs | |
CL2013000929A1 (es) | Forma cristalina c de la sal sodica del acido (4-(4-(5-(6-trifluoro metil piridin-3-il-amino) piridin-2-il-) fenil)-ciclohexil)-acetico; proceso de preparacion; composicion farmaceutica que lo comprende; y su uso para el tratamiento de un trastorno asociado con la actividad del dagt. | |
CL2011002213A1 (es) | Sal de adicion cristalina de (i) trometamina con (ii) un derivado de acido azabifenilaminobenzoico; composicion farmaceutica que comprende a la sal y otros agentes terapeuticos; combinacion farmaceutica; y su uso para el tratamiento de artritis reumatoide, artritis psoriasica, espondilitis anquilosante, esclerosis multiple, entre otras | |
RS53419B (en) | FORMULATIONS OF DEOXYCHOLINIC ACID AND ITS SALTS | |
NZ610765A (en) | Method for the preparation of high-purity pharmaceutical intermediates | |
CL2013000578A1 (es) | Sal cristalina de sodio del acido (e)-3-[2-(1-{[2-(5-bromo-pririmidin-2-il)-3-ciclopentil-1-metil-1h-indol-6-carbonil]-amino}-ciclobutil)-3-metil-3h-bencimidazol-5-il]-acrilico: sal amorfa;compuestos intermediarios; procedimientos de preparacion; composicion farmaceutica. | |
BRPI0808570B8 (pt) | processo para a preparação de inibidores de glyt-1 | |
NZ598693A (en) | Maleic acid salt and crystal thereof | |
FR2984319B1 (fr) | Nouveau procede de synthese de l'ivabradine et de ses sels d'addition a un acide pharmaceutiquement acceptable | |
PA8786301A1 (es) | "un nuevo procedimiento para preparar acido 2-(3-{6-[2(2,4-diclorofenil)-etilamino]-2-metoxipirimidin-4-il}-fenil)-2-metil-propionico" |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |