MX2009009344A - Formas solidas de un inhibidor de cinasa raf. - Google Patents
Formas solidas de un inhibidor de cinasa raf.Info
- Publication number
- MX2009009344A MX2009009344A MX2009009344A MX2009009344A MX2009009344A MX 2009009344 A MX2009009344 A MX 2009009344A MX 2009009344 A MX2009009344 A MX 2009009344A MX 2009009344 A MX2009009344 A MX 2009009344A MX 2009009344 A MX2009009344 A MX 2009009344A
- Authority
- MX
- Mexico
- Prior art keywords
- kinase inhibitor
- solid forms
- raf kinase
- imidazol
- trifluoromethyl
- Prior art date
Links
- 229940123690 Raf kinase inhibitor Drugs 0.000 title abstract 2
- 102000051624 phosphatidylethanolamine binding protein Human genes 0.000 title abstract 2
- 108700021017 phosphatidylethanolamine binding protein Proteins 0.000 title abstract 2
- 239000007787 solid Substances 0.000 title abstract 2
- 239000000203 mixture 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
- C07D401/14—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
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- 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
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Endocrinology (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Pulmonology (AREA)
- Reproductive Health (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
La presente invención se refiere a las formas sólidas del inhibidor de cinasa Raf de 1-metil-5-(2-(5-(trifluoro-metil)-1H-im idazol-2-il)-piridin-4-iloxi)-N-(4-(trifluoro-metil)-fenil)-1 H-benzo-[d]imidazol-2-amina, así como a composiciones de las mismas y a la utilización de las mismas.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US90445507P | 2007-03-02 | 2007-03-02 | |
| PCT/US2008/055227 WO2008140850A1 (en) | 2007-03-02 | 2008-02-28 | Solid forms of a raf kinase inhibitor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2009009344A true MX2009009344A (es) | 2009-09-11 |
Family
ID=39456506
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2009009344A MX2009009344A (es) | 2007-03-02 | 2008-02-28 | Formas solidas de un inhibidor de cinasa raf. |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US8324389B2 (es) |
| EP (1) | EP2132198A1 (es) |
| JP (1) | JP2010520215A (es) |
| KR (1) | KR20090117833A (es) |
| CN (1) | CN101679372A (es) |
| AR (1) | AR065565A1 (es) |
| AU (1) | AU2008251764B2 (es) |
| BR (1) | BRPI0808526A2 (es) |
| CA (1) | CA2678335A1 (es) |
| CL (1) | CL2008000616A1 (es) |
| CO (1) | CO6230987A2 (es) |
| EC (1) | ECSP099673A (es) |
| GT (1) | GT200900237A (es) |
| IL (1) | IL200441A0 (es) |
| MA (1) | MA31259B1 (es) |
| MX (1) | MX2009009344A (es) |
| MY (1) | MY148438A (es) |
| NZ (1) | NZ579084A (es) |
| PE (1) | PE20081801A1 (es) |
| RU (1) | RU2483064C2 (es) |
| SG (1) | SG179423A1 (es) |
| TN (1) | TN2009000356A1 (es) |
| TW (1) | TW200846341A (es) |
| WO (1) | WO2008140850A1 (es) |
| ZA (1) | ZA200905618B (es) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2009147291A (ru) * | 2007-05-23 | 2011-06-27 | Новартис АГ (CH) | Применение ингибиторов raf для лечения рака щитовидной железы |
| US9408885B2 (en) | 2011-12-01 | 2016-08-09 | Vib Vzw | Combinations of therapeutic agents for treating melanoma |
| US10098859B2 (en) | 2012-09-05 | 2018-10-16 | Amri Ssci, Llc | Cocrystals of p-coumaric acid |
| KR20180018800A (ko) * | 2015-06-19 | 2018-02-21 | 신-낫 프로덕츠 엔터프라이즈 엘엘씨 | 카보플라틴 계 공-결정의 약제학적 조성물 및 이의 용도 |
| JP7341060B2 (ja) | 2017-02-10 | 2023-09-08 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | Mapk経路の活性化に関連付けられる癌の処置のための方法及び医薬組成物 |
| JP7416716B2 (ja) | 2017-12-28 | 2024-01-17 | トラクト ファーマシューティカルズ インコーポレイテッド | 円柱上皮幹細胞のための幹細胞培養系およびそれに関連した使用法 |
| RU2693004C1 (ru) * | 2019-03-15 | 2019-07-01 | Лейсан Фаридовна Минигулова | Противоопухолевая композиция цисплатина с ингибитором 6-фосфоглюконатдегидрогеназы |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6627646B2 (en) * | 2001-07-17 | 2003-09-30 | Sepracor Inc. | Norastemizole polymorphs |
| US7071216B2 (en) * | 2002-03-29 | 2006-07-04 | Chiron Corporation | Substituted benz-azoles and methods of their use as inhibitors of Raf kinase |
| TWI387592B (zh) * | 2005-08-30 | 2013-03-01 | Novartis Ag | 經取代之苯并咪唑及其作為與腫瘤形成相關激酶之抑制劑之方法 |
| AU2007275634B2 (en) * | 2006-07-21 | 2011-01-20 | Novartis Ag | Formulations for benzimidazolyl pyridyl ethers |
| PE20130814A1 (es) * | 2006-08-30 | 2013-08-08 | Novartis Ag | Sales de benzimidazolil piridil eteres y formulaciones que las contienen |
-
2008
- 2008-02-28 MX MX2009009344A patent/MX2009009344A/es active IP Right Grant
- 2008-02-28 SG SG2012014676A patent/SG179423A1/en unknown
- 2008-02-28 RU RU2009136308/04A patent/RU2483064C2/ru not_active IP Right Cessation
- 2008-02-28 KR KR1020097020657A patent/KR20090117833A/ko not_active Ceased
- 2008-02-28 CA CA002678335A patent/CA2678335A1/en not_active Abandoned
- 2008-02-28 JP JP2009551840A patent/JP2010520215A/ja active Pending
- 2008-02-28 MY MYPI20093481A patent/MY148438A/en unknown
- 2008-02-28 US US12/529,258 patent/US8324389B2/en not_active Expired - Fee Related
- 2008-02-28 EP EP08795801A patent/EP2132198A1/en not_active Withdrawn
- 2008-02-28 AU AU2008251764A patent/AU2008251764B2/en not_active Ceased
- 2008-02-28 NZ NZ579084A patent/NZ579084A/en not_active IP Right Cessation
- 2008-02-28 BR BRPI0808526-9A patent/BRPI0808526A2/pt not_active IP Right Cessation
- 2008-02-28 CN CN200880014274A patent/CN101679372A/zh active Pending
- 2008-02-28 WO PCT/US2008/055227 patent/WO2008140850A1/en not_active Ceased
- 2008-02-29 TW TW097107217A patent/TW200846341A/zh unknown
- 2008-02-29 AR ARP080100862A patent/AR065565A1/es not_active Application Discontinuation
- 2008-02-29 PE PE2008000420A patent/PE20081801A1/es not_active Application Discontinuation
- 2008-02-29 CL CL200800616A patent/CL2008000616A1/es unknown
-
2009
- 2009-08-13 ZA ZA200905618A patent/ZA200905618B/xx unknown
- 2009-08-17 IL IL200441A patent/IL200441A0/en unknown
- 2009-08-28 TN TNP2009000356A patent/TN2009000356A1/fr unknown
- 2009-08-31 GT GT200900237A patent/GT200900237A/es unknown
- 2009-09-24 MA MA32229A patent/MA31259B1/fr unknown
- 2009-09-29 CO CO09106547A patent/CO6230987A2/es not_active Application Discontinuation
- 2009-10-02 EC EC2009009673A patent/ECSP099673A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MY148438A (en) | 2013-04-30 |
| NZ579084A (en) | 2012-04-27 |
| AR065565A1 (es) | 2009-06-17 |
| ZA200905618B (en) | 2010-05-26 |
| TW200846341A (en) | 2008-12-01 |
| SG179423A1 (en) | 2012-04-27 |
| CO6230987A2 (es) | 2010-12-20 |
| CA2678335A1 (en) | 2008-11-20 |
| AU2008251764B2 (en) | 2012-09-13 |
| PE20081801A1 (es) | 2009-01-08 |
| KR20090117833A (ko) | 2009-11-12 |
| BRPI0808526A2 (pt) | 2014-08-19 |
| CL2008000616A1 (es) | 2008-09-12 |
| AU2008251764A1 (en) | 2008-11-20 |
| ECSP099673A (es) | 2009-11-30 |
| GT200900237A (es) | 2010-06-24 |
| US20100209418A1 (en) | 2010-08-19 |
| JP2010520215A (ja) | 2010-06-10 |
| IL200441A0 (en) | 2010-04-29 |
| RU2009136308A (ru) | 2011-04-10 |
| US8324389B2 (en) | 2012-12-04 |
| EP2132198A1 (en) | 2009-12-16 |
| WO2008140850A1 (en) | 2008-11-20 |
| MA31259B1 (fr) | 2010-03-01 |
| RU2483064C2 (ru) | 2013-05-27 |
| TN2009000356A1 (en) | 2010-12-31 |
| CN101679372A (zh) | 2010-03-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX2009009344A (es) | Formas solidas de un inhibidor de cinasa raf. | |
| ZA201001513B (en) | 5-(4-(Haloalkoxy) phenyl) pyrimidine-2-amine compounds and compositions as kinase inhibitors | |
| MX2010004263A (es) | Inhibidores de quinasa c-fms. | |
| WO2007105058A3 (en) | Pyrazole compounds | |
| ZA200802636B (en) | Amino-5-[4-(difluoromethoxy)phenyl]-5-phenylimidazolone compounds as inhibitors of the beta-secretase (BACE) | |
| MX2010001485A (es) | Derivado de fenoxi-pirrolidina y su uso, y composiciones. | |
| NZ594537A (en) | Compounds, compositions, and methods for preventing metastasis of cancer cells | |
| MX2010009416A (es) | Compuestos heterociclicos como inhibidores de cxcr2. | |
| PH12013500649A1 (en) | Crystalline (r)-(e)-2-(4-(2-(5-(1-(3, 5-dichloropyridin-4-yl)ethoxy)-1h-indazol-3-yl)vinyl)-1h-pyrazol-1-yl)ethanol and its use as fgfr inhibitor | |
| WO2008017361A3 (de) | 2-(heterocyclylbenzyl)-pyridazinonderivate | |
| IL229395A0 (en) | Modified release of4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-n-5-(4-methyl-1h-imidazol-1-yl)-3-(trifluoromethyl)phenyl]benzamide solubilized using organic acids | |
| NZ593969A (en) | Pyrazine derivatives useful as inhibitors of atr kinase | |
| WO2008059029A3 (en) | New polymorphs of ethyl 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1h-benzimidazole-5-carbonyl)-pyridin-2-yl-amino]-propionate | |
| SI2632921T1 (sl) | Polimorfi in soli 6-(1H- indol-4-il)-4-(5-((4-(1-metiletil)-1-piperazinil)metil)-1,3-oksazol-2- il)-1H-indazola kot inhibitorji PI3K za uporabo pri zdravljenju npr. respiratornih motenj | |
| WO2006047503A3 (en) | Inhibitors of c-fms kinase | |
| PE20080038A1 (es) | Derivados de tiazolidinadiona como inhibidores de la pi3 quinasa | |
| NZ596607A (en) | Anthelmintic agents and their use | |
| WO2008019030A3 (en) | Modified azole compounds as antiinfective agents | |
| WO2007019191A3 (en) | Thiazolopyrimidine kinase inhibitors | |
| MD4215B1 (en) | Inhibitor of human myeloid leukemia based on N-(4-(5-(pyridin-2-yl)-4,5-dihydro-1H-pyrazol-3-yl)phenyl)-2-(pyridin-2-ylmethylen)-hydrazinecarbothioamide | |
| WO2006134499A3 (en) | 2-(1h-indolylsulfanyl)-aryl amine derivatives | |
| NZ600782A (en) | New secondary 8-hydroxyquinoline-7-carboxamide derivatives. | |
| WO2011084652A3 (en) | Crystalline salts of a factor xa inhibitor | |
| WO2013120852A4 (en) | Intermediates for a novel process of preparing imatinib and related tyrosine kinase inhibitors | |
| TW200612944A (en) | 4-(2,4-dichloro-5-methoxyphenyl)amino-6-methoxy-7-{[5-(substituted-amino)methyl]-3-furyl}-3-quinolinecarbonitriles as kinase inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant or registration |