BR0212822A - Formas cristalinas de n-(2-hidroxiacetil)-5-(4-piperdil)-4-(4-pirimidinil)-3-(4-clo rofenil)pirazol e composições farmacêuticas contendo as mesmas - Google Patents
Formas cristalinas de n-(2-hidroxiacetil)-5-(4-piperdil)-4-(4-pirimidinil)-3-(4-clo rofenil)pirazol e composições farmacêuticas contendo as mesmasInfo
- Publication number
- BR0212822A BR0212822A BR0212822-5A BR0212822A BR0212822A BR 0212822 A BR0212822 A BR 0212822A BR 0212822 A BR0212822 A BR 0212822A BR 0212822 A BR0212822 A BR 0212822A
- Authority
- BR
- Brazil
- Prior art keywords
- crystalline forms
- forms
- crystalline
- compound
- hydroxyacetyl
- Prior art date
Links
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
- C07D401/14—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 three or more hetero rings
-
- 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
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
"FORMAS CRISTALINAS DE N-(2-HIDROXIACETIL)5-(4-PIPERIDIL)-4-(4-PIRIMIDINIL)-3-(4-CLO ROFENIL)PIRAZOL E COMPOSIçõES FARMACêUTICAS CONTENDO AS MESMAS". A presente invenção refere-se a formas cristalinas do inibidor de p38 quinase N-(2-hidroxiacetil)-5-(4-piperidil)-4-(4-pirimidinil)-3-(4-clorofenil) pirazol. Estas formas cristalinas incluem: (a) uma primeira forma cristalina anidra possuindo estabilidade física melhorada com relação a outras formas de estado sólido do Composto; (b) uma segunda forma cristalina anidra possuindo propriedades únicas com relação a outras formas de estado sólido do Composto; (c) uma terceira forma cristalina anidra possuindo propriedades únicas com relação a outras formas de estado sólido do Composto; e (d) formas cristalinas solvatadas, formas cristalinas hidratadas, e formas cristalinas salinas do Composto que são úteis, por exemplo, como formas de estado sólido intermediárias na preparação de outras formas cristalinas do Composto. São também fornecidas combinações e composições farmacêuticas compreendendo pelo menos uma destas formas cristalinas, processos para o preparo destas formas cristalinas e para preparo das composições compreendendo estas formas cristalinas, e métodos para profilaxia e/ou tratamento de uma condição mediada por p38 quinase compreendendo a administração a um paciente de um montante terapeuticamente eficaz de pelo menos uma destas formas cristalinas.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US32498701P | 2001-09-25 | 2001-09-25 | |
PCT/US2002/030538 WO2003026662A1 (en) | 2001-09-25 | 2002-09-25 | Solid-state forms of n-(2-hydroxyacetyl)-5-(4-piperidyl)-4-(4-pyrimidinyl)-3-(4-chlorophenyl)pyrazole |
Publications (1)
Publication Number | Publication Date |
---|---|
BR0212822A true BR0212822A (pt) | 2005-08-30 |
Family
ID=23265959
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR0212822-5A BR0212822A (pt) | 2001-09-25 | 2002-09-25 | Formas cristalinas de n-(2-hidroxiacetil)-5-(4-piperdil)-4-(4-pirimidinil)-3-(4-clo rofenil)pirazol e composições farmacêuticas contendo as mesmas |
Country Status (8)
Country | Link |
---|---|
US (1) | US6872725B2 (pt) |
EP (1) | EP1429772A1 (pt) |
JP (1) | JP2005529060A (pt) |
BR (1) | BR0212822A (pt) |
CA (1) | CA2461080A1 (pt) |
MX (1) | MXPA04002762A (pt) |
WO (1) | WO2003026662A1 (pt) |
ZA (1) | ZA200402323B (pt) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CL2004000366A1 (es) * | 2003-02-26 | 2005-01-07 | Pharmacia Corp Sa Organizada B | USO DE UNA COMBINACION DE UN COMPUESTO DERIVADO DE PIRAZOL INHIBIDOR DE QUINASA p38, Y UN INHIBIDOR DE ACE PARA TRATAR DISFUNCION RENAL, ENFERMEDAD CARDIOVASCULAR Y VASCULAR, RETINOPATIA, NEUROPATIA, EDEMA, DISFUNCION ENDOTELIAL O INSULINOPATIA. |
PE20100742A1 (es) * | 2005-11-15 | 2010-11-25 | Glaxo Group Ltd | Nuevos procedimientos y formulaciones |
RS53150B (en) * | 2008-11-14 | 2014-06-30 | E. I. Du Pont De Nemours And Company | PROCEDURE FOR PREPARING A NON-HYDRATABLE CRYSTAL FORM |
Family Cites Families (36)
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US4826689A (en) | 1984-05-21 | 1989-05-02 | University Of Rochester | Method for making uniformly sized particles from water-insoluble organic compounds |
FR2634376B1 (fr) | 1988-07-21 | 1992-04-17 | Farmalyoc | Nouvelle forme unitaire, solide et poreuse comprenant des microparticules et/ou des nanoparticules, ainsi que sa preparation |
IT1227626B (it) | 1988-11-28 | 1991-04-23 | Vectorpharma Int | Farmaci supportati aventi velocita' di dissoluzione aumentata e procedimento per la loro preparazione |
IT1243390B (it) | 1990-11-22 | 1994-06-10 | Vectorpharma Int | Composizioni farmaceutiche in forma di particelle atte al rilascio controllato di sostanze farmacologicamente attive e procedimento per la loro preparazione. |
US5145684A (en) | 1991-01-25 | 1992-09-08 | Sterling Drug Inc. | Surface modified drug nanoparticles |
US5552160A (en) | 1991-01-25 | 1996-09-03 | Nanosystems L.L.C. | Surface modified NSAID nanoparticles |
CA2118517C (en) | 1992-06-10 | 2003-10-14 | Gary G. Liversidge | Surface modified nsaid nanoparticles |
NZ248813A (en) | 1992-11-25 | 1995-06-27 | Eastman Kodak Co | Polymeric grinding media used in grinding pharmaceutical substances |
US5346702A (en) | 1992-12-04 | 1994-09-13 | Sterling Winthrop Inc. | Use of non-ionic cloud point modifiers to minimize nanoparticle aggregation during sterilization |
US5298262A (en) | 1992-12-04 | 1994-03-29 | Sterling Winthrop Inc. | Use of ionic cloud point modifiers to prevent particle aggregation during sterilization |
US5302401A (en) | 1992-12-09 | 1994-04-12 | Sterling Winthrop Inc. | Method to reduce particle size growth during lyophilization |
US5340564A (en) | 1992-12-10 | 1994-08-23 | Sterling Winthrop Inc. | Formulations comprising olin 10-G to prevent particle aggregation and increase stability |
US5336507A (en) | 1992-12-11 | 1994-08-09 | Sterling Winthrop Inc. | Use of charged phospholipids to reduce nanoparticle aggregation |
US5429824A (en) | 1992-12-15 | 1995-07-04 | Eastman Kodak Company | Use of tyloxapole as a nanoparticle stabilizer and dispersant |
US5352459A (en) | 1992-12-16 | 1994-10-04 | Sterling Winthrop Inc. | Use of purified surface modifiers to prevent particle aggregation during sterilization |
US5587143A (en) | 1994-06-28 | 1996-12-24 | Nanosystems L.L.C. | Butylene oxide-ethylene oxide block copolymer surfactants as stabilizer coatings for nanoparticle compositions |
US5585108A (en) | 1994-12-30 | 1996-12-17 | Nanosystems L.L.C. | Formulations of oral gastrointestinal therapeutic agents in combination with pharmaceutically acceptable clays |
US5665331A (en) | 1995-01-10 | 1997-09-09 | Nanosystems L.L.C. | Co-microprecipitation of nanoparticulate pharmaceutical agents with crystal growth modifiers |
US5560932A (en) | 1995-01-10 | 1996-10-01 | Nano Systems L.L.C. | Microprecipitation of nanoparticulate pharmaceutical agents |
US5662883A (en) | 1995-01-10 | 1997-09-02 | Nanosystems L.L.C. | Microprecipitation of micro-nanoparticulate pharmaceutical agents |
US5569448A (en) | 1995-01-24 | 1996-10-29 | Nano Systems L.L.C. | Sulfated nonionic block copolymer surfactants as stabilizer coatings for nanoparticle compositions |
US5571536A (en) | 1995-02-06 | 1996-11-05 | Nano Systems L.L.C. | Formulations of compounds as nanoparticulate dispersions in digestible oils or fatty acids |
US5560931A (en) | 1995-02-14 | 1996-10-01 | Nawosystems L.L.C. | Formulations of compounds as nanoparticulate dispersions in digestible oils or fatty acids |
US5503723A (en) | 1995-02-08 | 1996-04-02 | Eastman Kodak Company | Isolation of ultra small particles |
US5534270A (en) | 1995-02-09 | 1996-07-09 | Nanosystems Llc | Method of preparing stable drug nanoparticles |
US5518738A (en) | 1995-02-09 | 1996-05-21 | Nanosystem L.L.C. | Nanoparticulate nsaid compositions |
US5622938A (en) | 1995-02-09 | 1997-04-22 | Nano Systems L.L.C. | Sugar base surfactant for nanocrystals |
US5591456A (en) | 1995-02-10 | 1997-01-07 | Nanosystems L.L.C. | Milled naproxen with hydroxypropyl cellulose as a dispersion stabilizer |
US5573783A (en) | 1995-02-13 | 1996-11-12 | Nano Systems L.L.C. | Redispersible nanoparticulate film matrices with protective overcoats |
US5510118A (en) | 1995-02-14 | 1996-04-23 | Nanosystems Llc | Process for preparing therapeutic compositions containing nanoparticles |
US5580579A (en) | 1995-02-15 | 1996-12-03 | Nano Systems L.L.C. | Site-specific adhesion within the GI tract using nanoparticles stabilized by high molecular weight, linear poly (ethylene oxide) polymers |
US5718919A (en) | 1995-02-24 | 1998-02-17 | Nanosystems L.L.C. | Nanoparticles containing the R(-)enantiomer of ibuprofen |
US5747001A (en) | 1995-02-24 | 1998-05-05 | Nanosystems, L.L.C. | Aerosols containing beclomethazone nanoparticle dispersions |
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US6514977B1 (en) * | 1997-05-22 | 2003-02-04 | G.D. Searle & Company | Substituted pyrazoles as p38 kinase inhibitors |
-
2002
- 2002-09-25 BR BR0212822-5A patent/BR0212822A/pt not_active IP Right Cessation
- 2002-09-25 US US10/254,697 patent/US6872725B2/en not_active Expired - Fee Related
- 2002-09-25 CA CA002461080A patent/CA2461080A1/en not_active Abandoned
- 2002-09-25 WO PCT/US2002/030538 patent/WO2003026662A1/en active Application Filing
- 2002-09-25 JP JP2003530297A patent/JP2005529060A/ja not_active Ceased
- 2002-09-25 EP EP02778346A patent/EP1429772A1/en not_active Withdrawn
- 2002-09-25 MX MXPA04002762A patent/MXPA04002762A/es active IP Right Grant
-
2004
- 2004-03-24 ZA ZA200402323A patent/ZA200402323B/en unknown
Also Published As
Publication number | Publication date |
---|---|
CA2461080A1 (en) | 2003-04-03 |
WO2003026662A1 (en) | 2003-04-03 |
MXPA04002762A (es) | 2004-06-29 |
ZA200402323B (en) | 2005-04-29 |
US6872725B2 (en) | 2005-03-29 |
EP1429772A1 (en) | 2004-06-23 |
JP2005529060A (ja) | 2005-09-29 |
US20030153583A1 (en) | 2003-08-14 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 8A ANUIDADE(S). |
|
B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 2108 DE 31/05/2011. |