CL2012003048A1 - Compuestos derivados de n-fenil-3-(1h-pirazol-4-il)quinoxalin-6-amina, inhibidores de tirosino quinasa fgfr; proceso de preparación; composición farmacéutica; y su uso en la prevención o tratamiento de cáncer. - Google Patents
Compuestos derivados de n-fenil-3-(1h-pirazol-4-il)quinoxalin-6-amina, inhibidores de tirosino quinasa fgfr; proceso de preparación; composición farmacéutica; y su uso en la prevención o tratamiento de cáncer.Info
- Publication number
- CL2012003048A1 CL2012003048A1 CL2012003048A CL2012003048A CL2012003048A1 CL 2012003048 A1 CL2012003048 A1 CL 2012003048A1 CL 2012003048 A CL2012003048 A CL 2012003048A CL 2012003048 A CL2012003048 A CL 2012003048A CL 2012003048 A1 CL2012003048 A1 CL 2012003048A1
- Authority
- CL
- Chile
- Prior art keywords
- quinoxalin
- pyrazol
- cancer
- amine
- phenyl
- Prior art date
Links
- IDFGZOWBIHLRPV-UHFFFAOYSA-N N-phenyl-3-(1H-pyrazol-4-yl)quinoxalin-6-amine Chemical compound N1N=CC(=C1)C=1C=NC2=CC=C(C=C2N=1)NC1=CC=CC=C1 IDFGZOWBIHLRPV-UHFFFAOYSA-N 0.000 title abstract 2
- 206010028980 Neoplasm Diseases 0.000 title abstract 2
- 201000011510 cancer Diseases 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 238000002360 preparation method Methods 0.000 title abstract 2
- 230000002265 prevention Effects 0.000 title abstract 2
- 229940121358 tyrosine kinase inhibitor Drugs 0.000 title 1
- 239000005483 tyrosine kinase inhibitor Substances 0.000 title 1
- 229940043355 kinase inhibitor Drugs 0.000 abstract 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
Classifications
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- C07—ORGANIC CHEMISTRY
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- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- 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
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
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Abstract
Compuestos derivados de n-fenil-3-(1h-pirazol-4-il)quinoxalin-6-amina, inhibidores de pirazolil quinazolina quinasa; proceso de preparación; composición farmacéutica; y su uso en la prevención o tratamiento de cáncer.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US32988410P | 2010-04-30 | 2010-04-30 | |
GB201007286A GB201007286D0 (en) | 2010-04-30 | 2010-04-30 | New compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
CL2012003048A1 true CL2012003048A1 (es) | 2013-04-19 |
Family
ID=42289929
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CL2012003048A CL2012003048A1 (es) | 2010-04-30 | 2012-10-30 | Compuestos derivados de n-fenil-3-(1h-pirazol-4-il)quinoxalin-6-amina, inhibidores de tirosino quinasa fgfr; proceso de preparación; composición farmacéutica; y su uso en la prevención o tratamiento de cáncer. |
Country Status (35)
Country | Link |
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US (6) | US8895601B2 (es) |
EP (3) | EP3178818B1 (es) |
JP (1) | JP5639261B2 (es) |
KR (2) | KR101889565B1 (es) |
CN (2) | CN102858765B (es) |
AP (1) | AP3210A (es) |
AR (1) | AR080982A1 (es) |
AU (2) | AU2011247047B2 (es) |
BR (1) | BR112012027509B1 (es) |
CA (1) | CA2796204C (es) |
CL (1) | CL2012003048A1 (es) |
CR (2) | CR20180339A (es) |
CY (2) | CY1121882T1 (es) |
DK (3) | DK3178818T3 (es) |
EA (2) | EA023222B8 (es) |
EC (1) | ECSP12012318A (es) |
ES (3) | ES2742409T3 (es) |
GB (1) | GB201007286D0 (es) |
HR (1) | HRP20211675T1 (es) |
HU (3) | HUE033702T2 (es) |
IL (1) | IL222600A (es) |
IN (1) | IN2012MN02591A (es) |
JO (1) | JO3366B1 (es) |
LT (3) | LT3178818T (es) |
ME (1) | ME01825B (es) |
MX (2) | MX365702B (es) |
MY (2) | MY189427A (es) |
NZ (1) | NZ602726A (es) |
PL (3) | PL2563775T3 (es) |
PT (3) | PT3590934T (es) |
RS (3) | RS62570B1 (es) |
SG (2) | SG10201708578QA (es) |
SI (3) | SI3178818T1 (es) |
TW (1) | TWI545122B (es) |
WO (1) | WO2011135376A1 (es) |
Families Citing this family (92)
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US8053440B2 (en) | 2007-02-01 | 2011-11-08 | Resverlogix Corporation | Compounds for the prevention and treatment of cardiovascular diseases |
NZ708314A (en) | 2009-03-18 | 2017-08-25 | Resverlogix Corp | Quinazolinones for use as anticancer agents |
PL2421533T3 (pl) | 2009-04-22 | 2019-05-31 | Resverlogix Corp | Nowe środki przeciwzapalne |
GB201007286D0 (en) | 2010-04-30 | 2010-06-16 | Astex Therapeutics Ltd | New compounds |
GB201020179D0 (en) | 2010-11-29 | 2011-01-12 | Astex Therapeutics Ltd | New compounds |
US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
GB201118675D0 (en) | 2011-10-28 | 2011-12-14 | Astex Therapeutics Ltd | New compounds |
GB201118654D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201118652D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201118656D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201209613D0 (en) * | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
GB201209609D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
US9611267B2 (en) | 2012-06-13 | 2017-04-04 | Incyte Holdings Corporation | Substituted tricyclic compounds as FGFR inhibitors |
JP6104377B2 (ja) | 2012-07-11 | 2017-03-29 | ブループリント メディシンズ コーポレイション | 線維芽細胞成長因子受容体の阻害剤 |
WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
US8884046B2 (en) * | 2012-10-15 | 2014-11-11 | Resverlogix Corp. | Compounds useful in the synthesis of benzamide compounds |
EP2914621B1 (en) | 2012-11-05 | 2023-06-07 | Foundation Medicine, Inc. | Novel ntrk1 fusion molecules and uses thereof |
US9719970B2 (en) | 2012-11-30 | 2017-08-01 | Waters Technologies Corporation | Methods and apparatus for the analysis of vitamin D metabolites |
US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
AR094812A1 (es) | 2013-02-20 | 2015-08-26 | Eisai R&D Man Co Ltd | Derivado de piridina monocíclico como inhibidor del fgfr |
US9321786B2 (en) | 2013-03-15 | 2016-04-26 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
CN105307657B (zh) * | 2013-03-15 | 2020-07-10 | 西建卡尔有限责任公司 | 杂芳基化合物和其用途 |
CA2907243C (en) | 2013-03-15 | 2021-12-28 | Celgene Avilomics Research, Inc. | Substituted dihydropyrimidopyrimidinone compounds and pharmaceutical compositions thereof use fgfr4 inhibitor |
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