MX2012014386A - Formas cristalinas de inhibidores de cinasa. - Google Patents
Formas cristalinas de inhibidores de cinasa.Info
- Publication number
- MX2012014386A MX2012014386A MX2012014386A MX2012014386A MX2012014386A MX 2012014386 A MX2012014386 A MX 2012014386A MX 2012014386 A MX2012014386 A MX 2012014386A MX 2012014386 A MX2012014386 A MX 2012014386A MX 2012014386 A MX2012014386 A MX 2012014386A
- Authority
- MX
- Mexico
- Prior art keywords
- crystalline forms
- kinase inhibitors
- thieno
- pyrazol
- pyridin
- Prior art date
Links
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
- WPHKIQPVPYJNAX-UHFFFAOYSA-N 1-[4-[4-amino-7-[1-(2-hydroxyethyl)pyrazol-4-yl]thieno[3,2-c]pyridin-3-yl]phenyl]-3-(3-fluorophenyl)urea Chemical class C1=2SC=C(C=3C=CC(NC(=O)NC=4C=C(F)C=CC=4)=CC=3)C=2C(N)=NC=C1C=1C=NN(CCO)C=1 WPHKIQPVPYJNAX-UHFFFAOYSA-N 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- 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
- 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)
- 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)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Las sales de N-(4-{4-amino-7-[1-(2-hidroxietil)-1H-pirazol-4-il]ti eno[3, 2-c]piridin-3-iI}fenil)N'-(3-fluorofenil) urea y las formas cristalinas de la misma, son ingredientes farmacéuticos adecuados para composiciones farmacéuticas útiles en el tratamiento de una enfermedad, por ejemplo cáncer.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35317010P | 2010-06-09 | 2010-06-09 | |
| PCT/US2011/039603 WO2011156473A1 (en) | 2010-06-09 | 2011-06-08 | Crystalline forms of kinase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2012014386A true MX2012014386A (es) | 2013-05-01 |
Family
ID=44454074
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2012014386A MX2012014386A (es) | 2010-06-09 | 2011-06-08 | Formas cristalinas de inhibidores de cinasa. |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8633317B2 (es) |
| EP (1) | EP2580221B1 (es) |
| JP (1) | JP5727599B2 (es) |
| CN (1) | CN103003283A (es) |
| CA (1) | CA2802042A1 (es) |
| ES (1) | ES2559212T3 (es) |
| MX (1) | MX2012014386A (es) |
| WO (1) | WO2011156473A1 (es) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG10201911668VA (en) * | 2014-02-07 | 2020-01-30 | Global Blood Therapeutics Inc | Crystalline polymorphs of the free base of 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde |
| WO2015200635A1 (en) * | 2014-06-25 | 2015-12-30 | Abbvie Inc. | N-(4-{4-AMINO-7-[1-(2-HYDROXYETHYL)-1H-PYRAZOL-4-yl]THIENO[3,2-c]PYRIDIN-3-YL}PHENYL)-N'-(3-FLUOROPHENYL)UREA DOCUSATE |
| CN106854197B (zh) * | 2015-12-08 | 2020-09-01 | 浙江亚太药业股份有限公司 | 一种吡啶衍生物的多晶型及其制备方法、用途 |
| JP7038675B2 (ja) | 2016-03-11 | 2022-03-18 | ステルス バイオセラピューティクス インコーポレイテッド | 結晶塩形態 |
| CN110914287A (zh) | 2017-04-05 | 2020-03-24 | 隐形生物治疗公司 | Boc-d-arg-dmt-lys-(boc)-phe-nh2的结晶盐形式 |
| US10676506B2 (en) | 2018-01-26 | 2020-06-09 | Stealth Biotherapeutics Corp. | Crystalline bis- and tris-hydrochloride salt of elamipretide |
| CA3178415A1 (en) * | 2020-05-11 | 2021-11-18 | Mark R. Bray | Salt and crystal forms of 4-amino-5-(6-(4-methylpiperazin-1-yl)-1h-benzo[d]imidazol-2-yl)thieno[2,3-b]pyridin-6(7h)-one |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050020619A1 (en) * | 2003-07-24 | 2005-01-27 | Patrick Betschmann | Thienopyridine kinase inhibitors |
| US20050026944A1 (en) * | 2003-07-24 | 2005-02-03 | Patrick Betschmann | Thienopyridine and furopyridine kinase inhibitors |
| GB0402518D0 (en) * | 2004-02-05 | 2004-03-10 | Astrazeneca Ab | Therapeutic agents |
| EP1968979A2 (en) * | 2005-12-08 | 2008-09-17 | Abbott Laboratories | 9-membered heterobicyclic compounds as inhibitors of protein kinases |
| AR070539A1 (es) * | 2008-03-05 | 2010-04-14 | Methylgene Inc | Inhibidores de la actividad de proteina tirosina quinasa |
| UY32291A (es) * | 2008-12-05 | 2010-07-30 | Abbott Lab | Inhibidores de quinasa con perfiles de seguridad cyp mejorados |
-
2011
- 2011-06-08 MX MX2012014386A patent/MX2012014386A/es active IP Right Grant
- 2011-06-08 CN CN2011800375187A patent/CN103003283A/zh active Pending
- 2011-06-08 EP EP11726598.3A patent/EP2580221B1/en not_active Not-in-force
- 2011-06-08 US US13/156,070 patent/US8633317B2/en not_active Expired - Fee Related
- 2011-06-08 CA CA2802042A patent/CA2802042A1/en not_active Abandoned
- 2011-06-08 WO PCT/US2011/039603 patent/WO2011156473A1/en not_active Ceased
- 2011-06-08 ES ES11726598.3T patent/ES2559212T3/es active Active
- 2011-06-08 JP JP2013514335A patent/JP5727599B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP2580221A1 (en) | 2013-04-17 |
| JP5727599B2 (ja) | 2015-06-03 |
| HK1182383A1 (zh) | 2013-11-29 |
| WO2011156473A1 (en) | 2011-12-15 |
| CN103003283A (zh) | 2013-03-27 |
| US20120203002A1 (en) | 2012-08-09 |
| ES2559212T3 (es) | 2016-02-11 |
| JP2013528222A (ja) | 2013-07-08 |
| US8633317B2 (en) | 2014-01-21 |
| EP2580221B1 (en) | 2015-10-21 |
| CA2802042A1 (en) | 2011-12-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant or registration |