GT200600496A - SALTS, PROFARMS AND FORMULATIONS OF 1- [5- (4-AMINO-7-ISOPROPIL-7H-PIRROLO [2,3-D] PIIRIMIDIN-5-CARBONIL) -2-METOXI-FEIL] -3- (2,4 -DICLORO-PHENIL) -UREA. - Google Patents
SALTS, PROFARMS AND FORMULATIONS OF 1- [5- (4-AMINO-7-ISOPROPIL-7H-PIRROLO [2,3-D] PIIRIMIDIN-5-CARBONIL) -2-METOXI-FEIL] -3- (2,4 -DICLORO-PHENIL) -UREA.Info
- Publication number
- GT200600496A GT200600496A GT200600496A GT200600496A GT200600496A GT 200600496 A GT200600496 A GT 200600496A GT 200600496 A GT200600496 A GT 200600496A GT 200600496 A GT200600496 A GT 200600496A GT 200600496 A GT200600496 A GT 200600496A
- Authority
- GT
- Guatemala
- Prior art keywords
- profarms
- piirimidin
- isopropil
- carbonil
- phenil
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title abstract 2
- 239000004202 carbamide Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 230000003463 hyperproliferative effect Effects 0.000 abstract 1
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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
LA PRESENTE INVENCIÓN SE REFIERE A COMPUESTOS DE LA FÓRMULA 1, O UNA SAL FARMACÉUTICAMENTE ACEPTABLE, PROFÁRMACO O HIDRATOS DE LOS MISMOS. LA INVENCIÓN TAMBIÉN SE REFIERE A COMPOISICONES FARMACÉUTICAS QUE CONTIENEN LOS COMPUESTOS DE FÓRMULA 1, Y A MÉTODOS PARA TRATAR TRASTORONOS HIPERPROLIFERATIVOS EN UN MAMÍFERO POR MEDIO DE LA ADMINISTRACIÓN DE LOS COMPUESTOS DE FÓRMULA 1. T2006THE PRESENT INVENTION REFERS TO COMPOUNDS OF FORMULA 1, OR A PHARMACEUTICALLY ACCEPTABLE, PROPHARM OR HYDRAPHY SALT OF THE SAME. THE INVENTION ALSO REFERS TO PHARMACEUTICAL COMPOUNDS CONTAINING FORMULA 1 COMPOUNDS, AND METHODS TO TREAT HYPERPROLIFERATIVE DISORDERS IN A MAMMER THROUGH THE ADMINISTRATION OF FORMULA COMPOUNDS 1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US74907005P | 2005-12-09 | 2005-12-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GT200600496A true GT200600496A (en) | 2007-07-17 |
Family
ID=38123252
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GT200600496A GT200600496A (en) | 2005-12-09 | 2006-12-07 | SALTS, PROFARMS AND FORMULATIONS OF 1- [5- (4-AMINO-7-ISOPROPIL-7H-PIRROLO [2,3-D] PIIRIMIDIN-5-CARBONIL) -2-METOXI-FEIL] -3- (2,4 -DICLORO-PHENIL) -UREA. |
Country Status (8)
| Country | Link |
|---|---|
| AR (1) | AR058293A1 (en) |
| DO (1) | DOP2006000271A (en) |
| GT (1) | GT200600496A (en) |
| NL (1) | NL2000337A1 (en) |
| PE (1) | PE20071037A1 (en) |
| TW (1) | TW200733965A (en) |
| UY (1) | UY29991A1 (en) |
| WO (1) | WO2007066189A2 (en) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR068916A1 (en) * | 2007-10-19 | 2009-12-16 | Abbott Gmbh & Co Kg | SOLID DISPERSION PRODUCT CONTAINING A N-ARIL UREA-BASED COMPOUND |
| JP2011500649A (en) * | 2007-10-19 | 2011-01-06 | アボット ゲーエムベーハー ウント カンパニー カーゲー | Solid dispersion products of N-arylureas |
| DK2358720T3 (en) * | 2008-10-16 | 2016-06-06 | Univ California | Heteroarylkinaseinhibitorer fused-ring |
| CN102892768A (en) | 2009-12-30 | 2013-01-23 | 艾科尔公司 | Substituted pyrrolo-aminopyrimidine compounds |
| ES2676209T3 (en) * | 2010-06-23 | 2018-07-17 | Metabolex Inc. | Compositions of 5-ethyl-2- {4- [4- (4-tetrazol-1-yl-phenoxymethyl) -thiazol-2-yl] -piperidin-1-yl} -pyrimidine |
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
| WO2013077921A2 (en) | 2011-09-02 | 2013-05-30 | The Regents Of The University Of California | Substituted pyrazolo[3,4-d]pyrimidines and uses thereof |
| US20140004192A1 (en) * | 2012-04-13 | 2014-01-02 | Ziopharm Oncology, Inc. | Pharmaceutical formulations of indibulin and uses thereof |
| CN107652289B (en) | 2012-06-13 | 2020-07-21 | 因塞特控股公司 | Substituted tricyclic compounds as FGFR inhibitors |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| RU2015115631A (en) | 2012-09-26 | 2016-11-20 | Дзе Риджентс Оф Дзе Юниверсити Оф Калифорния | MODULATION IRE1 |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| KR102269032B1 (en) | 2013-04-19 | 2021-06-24 | 인사이트 홀딩스 코포레이션 | Bicyclic heterocycles as fgfr inhibitors |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
| PE20171514A1 (en) | 2015-02-20 | 2017-10-20 | Incyte Corp | BICYCLE HETEROCYCLES AS FGFR INHIBITORS |
| MA41551A (en) | 2015-02-20 | 2017-12-26 | Incyte Corp | BICYCLIC HETEROCYCLES USED AS FGFR4 INHIBITORS |
| CN107722012B (en) * | 2016-08-11 | 2020-05-29 | 斯福瑞(南通)制药有限公司 | Process for preparing 4-chloro-7H-pyrrolo [2,3-d ] pyrimidines |
| AR111960A1 (en) | 2017-05-26 | 2019-09-04 | Incyte Corp | CRYSTALLINE FORMS OF A FGFR INHIBITOR AND PROCESSES FOR ITS PREPARATION |
| SG11202010636VA (en) | 2018-05-04 | 2020-11-27 | Incyte Corp | Solid forms of an fgfr inhibitor and processes for preparing the same |
| BR112020022373A2 (en) | 2018-05-04 | 2021-02-02 | Incyte Corporation | salts of a fgfr inhibitor |
| WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
| WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021076602A1 (en) | 2019-10-14 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| JP7720840B2 (en) | 2019-12-04 | 2025-08-08 | インサイト・コーポレイション | Tricyclic heterocycles as FGFR inhibitors |
| CN115151539A (en) | 2019-12-04 | 2022-10-04 | 因赛特公司 | Derivatives of FGFR Inhibitors |
| WO2021146424A1 (en) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| US12065494B2 (en) | 2021-04-12 | 2024-08-20 | Incyte Corporation | Combination therapy comprising an FGFR inhibitor and a Nectin-4 targeting agent |
| AR126102A1 (en) | 2021-06-09 | 2023-09-13 | Incyte Corp | TRICYCLIC HETEROCYCLES AS FGFR INHIBITORS |
| CA3220155A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| JP2025015449A (en) * | 2023-07-18 | 2025-01-30 | 信越化学工業株式会社 | Composition for solid dispersion, solid dispersion, and method of manufacturing solid dispersion |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT901786E (en) * | 1997-08-11 | 2007-08-07 | Pfizer Prod Inc | Solid pharmaceutical dispersions with enhanced bioavailability |
| UA80171C2 (en) * | 2002-12-19 | 2007-08-27 | Pfizer Prod Inc | Pyrrolopyrimidine derivatives |
-
2006
- 2006-11-24 WO PCT/IB2006/003416 patent/WO2007066189A2/en not_active Ceased
- 2006-11-27 NL NL2000337A patent/NL2000337A1/en active Search and Examination
- 2006-12-05 DO DO2006000271A patent/DOP2006000271A/en unknown
- 2006-12-06 PE PE2006001565A patent/PE20071037A1/en not_active Application Discontinuation
- 2006-12-06 UY UY29991A patent/UY29991A1/en not_active Application Discontinuation
- 2006-12-07 AR ARP060105422A patent/AR058293A1/en unknown
- 2006-12-07 GT GT200600496A patent/GT200600496A/en unknown
- 2006-12-08 TW TW095145947A patent/TW200733965A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| UY29991A1 (en) | 2007-07-31 |
| NL2000337A1 (en) | 2007-06-12 |
| DOP2006000271A (en) | 2007-08-15 |
| TW200733965A (en) | 2007-09-16 |
| AR058293A1 (en) | 2008-01-30 |
| PE20071037A1 (en) | 2007-11-19 |
| WO2007066189A3 (en) | 2008-08-14 |
| WO2007066189A2 (en) | 2007-06-14 |
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