PE20081490A1 - N-(4-(2-amino-3-cloropiridin-4-iloxi)-3-fluorofenil)-4-etoxi-1-(4-fluorofenil)-2-oxo-1,2-dihidropiridina-3-carboxamida y una composicion farmaceutica - Google Patents
N-(4-(2-amino-3-cloropiridin-4-iloxi)-3-fluorofenil)-4-etoxi-1-(4-fluorofenil)-2-oxo-1,2-dihidropiridina-3-carboxamida y una composicion farmaceuticaInfo
- Publication number
- PE20081490A1 PE20081490A1 PE2007001538A PE2007001538A PE20081490A1 PE 20081490 A1 PE20081490 A1 PE 20081490A1 PE 2007001538 A PE2007001538 A PE 2007001538A PE 2007001538 A PE2007001538 A PE 2007001538A PE 20081490 A1 PE20081490 A1 PE 20081490A1
- Authority
- PE
- Peru
- Prior art keywords
- fluorophenyl
- iloxi
- etoxy
- chloropyridin
- dihydropyridine
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- 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
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- 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)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Medicinal Preparation (AREA)
Abstract
SE REFIERE A UNA COMPOSICION FARMACEUTICA QUE COMPRENDE UNA CANTIDAD EFECTIVA DEL COMPUESTO N-(4-(2-AMINO-3-CLOROPIRIDIN-4-ILOXI)-3-FLUOROFENIL)-4-ETOXI-1-(4-FLUOROFENIL)-2-OXO-1,2-DIHIDROPIRIDINA-3-CARBOXAMIDA, EN UN PORTADOR QUE COMPRENDE CELULOSA MICROCRISTALINA Y MANITOL O LACTOSA Y ADEMAS COMPRENDE UN AGENTE LUBRICANTE Y DESINTEGRANTE, SIENDO UTIL EN EL TRATAMIENTO DEL CANCER DEPENDIENTE DE LA ACTIVACION DE Met REGULADA POR LA AMPLIFICACION DEL GEN, UNA MUTACION Met ACTIVADA Y/O ESTIMULACION HGF
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US85754006P | 2006-11-08 | 2006-11-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20081490A1 true PE20081490A1 (es) | 2008-10-30 |
Family
ID=39048786
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2007001538A PE20081490A1 (es) | 2006-11-08 | 2007-11-08 | N-(4-(2-amino-3-cloropiridin-4-iloxi)-3-fluorofenil)-4-etoxi-1-(4-fluorofenil)-2-oxo-1,2-dihidropiridina-3-carboxamida y una composicion farmaceutica |
Country Status (21)
Country | Link |
---|---|
US (2) | US7851489B2 (es) |
EP (1) | EP2089364B1 (es) |
JP (1) | JP5276005B2 (es) |
KR (1) | KR101390076B1 (es) |
CN (1) | CN101535264B (es) |
AR (1) | AR063628A1 (es) |
AU (1) | AU2007317296B2 (es) |
CA (1) | CA2669266C (es) |
CL (1) | CL2007003226A1 (es) |
DK (1) | DK2089364T3 (es) |
ES (1) | ES2424851T3 (es) |
HK (1) | HK1131608A1 (es) |
HR (1) | HRP20130626T1 (es) |
MX (1) | MX2009004699A (es) |
NO (1) | NO342395B1 (es) |
PE (1) | PE20081490A1 (es) |
PL (1) | PL2089364T3 (es) |
PT (1) | PT2089364E (es) |
SI (1) | SI2089364T1 (es) |
TW (1) | TWI409259B (es) |
WO (1) | WO2008058229A1 (es) |
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JP5693239B2 (ja) | 2008-01-23 | 2015-04-01 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | 4−ピリジノン化合物および癌についてのその使用 |
US8304413B2 (en) | 2008-06-03 | 2012-11-06 | Intermune, Inc. | Compounds and methods for treating inflammatory and fibrotic disorders |
US8569319B2 (en) | 2010-04-29 | 2013-10-29 | Deciphera Pharmaceuticals, LLS | Pyridone amides and analogs exhibiting anti-cancer and anti-proliferative activities |
EP2563763B1 (en) * | 2010-04-30 | 2014-12-31 | Bristol-Myers Squibb Company | Pharmaceutical compositions comprising n-(4-(2-amino-3-chloropyridin-4-yloxy)-3-fluorophenyl)-4-ethoxy-l-(4-fluorophenyl)-2-oxo- 1,2-dihydropyridine-3 -carboxamide |
CN102241625B (zh) * | 2010-05-13 | 2014-10-29 | 中南大学 | 1-(取代芳基)-5-((取代芳胺基)甲基)吡啶-2(1h)酮化合物、制备方法及其用途 |
CN102070518B (zh) * | 2011-01-24 | 2012-05-02 | 江苏先声药物研究有限公司 | 取代吡啶及氮杂吲哚衍生物的合成 |
EA031153B1 (ru) | 2011-06-10 | 2018-11-30 | Мерк Патент Гмбх | Применение пиримидиновых соединений с btk ингибирующей активностью |
WO2013078295A2 (en) | 2011-11-22 | 2013-05-30 | Deciphera Pharmaceuticals, Llc | Pyridone amides and analogs exhibiting anti-cancer and anti-proliferative activities |
WO2014022116A2 (en) | 2012-07-28 | 2014-02-06 | Calitor Sciences, Llc | Substituted pyrazolone compounds and methods of use |
US8975282B2 (en) | 2012-07-28 | 2015-03-10 | Sunshine Lake Pharma Co., Ltd. | Substituted pyrazolone compounds and methods of use |
AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
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TW201834649A (zh) | 2017-03-02 | 2018-10-01 | 新加坡商亞獅康私人有限公司 | 癌症療法 |
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JP2022504201A (ja) | 2018-10-09 | 2022-01-13 | アスラン ファーマシューティカルズ ピーティーイー リミテッド | バリチニブのマロン酸塩 |
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US20220119425A1 (en) * | 2019-01-15 | 2022-04-21 | The Translational Genomics Research Institute | Phosphonate conjugates and uses thereof |
WO2021025407A1 (ko) | 2019-08-02 | 2021-02-11 | 웰마커바이오 주식회사 | 옥소-피리딘 융합고리 유도체 및 이를 포함하는 약학적 조성물 |
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CA3200844A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Process for making a pd-1/pd-l1 inhibitor and salts and crystalline forms thereof |
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CN117355533A (zh) * | 2021-06-22 | 2024-01-05 | 株式会社Lg化学 | 作为蛋白激酶抑制剂的新型化合物 |
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WO1997017329A1 (fr) | 1995-11-07 | 1997-05-15 | Kirin Beer Kabushiki Kaisha | Derives de quinoline et derives de quinazoline inhibant l'autophosphorylation d'un recepteur de facteur de croissance originaire de plaquettes, et compositions pharmaceutiques les contenant |
WO1999065867A1 (en) * | 1998-06-17 | 1999-12-23 | Du Pont Pharmaceuticals Company | Cyclic hydroxamic acids as metalloproteinase inhibitors |
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US7348325B2 (en) * | 2005-11-30 | 2008-03-25 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
-
2007
- 2007-11-08 CN CN2007800414202A patent/CN101535264B/zh active Active
- 2007-11-08 AR ARP070104987A patent/AR063628A1/es active Pending
- 2007-11-08 US US11/936,984 patent/US7851489B2/en active Active
- 2007-11-08 WO PCT/US2007/084047 patent/WO2008058229A1/en active Application Filing
- 2007-11-08 KR KR1020097009449A patent/KR101390076B1/ko active IP Right Grant
- 2007-11-08 ES ES07844974T patent/ES2424851T3/es active Active
- 2007-11-08 EP EP07844974.1A patent/EP2089364B1/en active Active
- 2007-11-08 PE PE2007001538A patent/PE20081490A1/es active IP Right Grant
- 2007-11-08 CL CL200703226A patent/CL2007003226A1/es unknown
- 2007-11-08 DK DK07844974.1T patent/DK2089364T3/da active
- 2007-11-08 PL PL07844974T patent/PL2089364T3/pl unknown
- 2007-11-08 SI SI200731303T patent/SI2089364T1/sl unknown
- 2007-11-08 AU AU2007317296A patent/AU2007317296B2/en active Active
- 2007-11-08 MX MX2009004699A patent/MX2009004699A/es active IP Right Grant
- 2007-11-08 JP JP2009536476A patent/JP5276005B2/ja active Active
- 2007-11-08 CA CA2669266A patent/CA2669266C/en active Active
- 2007-11-08 TW TW096142253A patent/TWI409259B/zh active
- 2007-11-08 PT PT78449741T patent/PT2089364E/pt unknown
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2009
- 2009-04-22 NO NO20091605A patent/NO342395B1/no unknown
- 2009-11-02 HK HK09110170.2A patent/HK1131608A1/xx unknown
-
2010
- 2010-11-08 US US12/941,419 patent/US8536200B2/en active Active
-
2013
- 2013-07-03 HR HRP20130626TT patent/HRP20130626T1/hr unknown
Also Published As
Publication number | Publication date |
---|---|
CL2007003226A1 (es) | 2008-02-08 |
CA2669266C (en) | 2014-04-29 |
TWI409259B (zh) | 2013-09-21 |
EP2089364A1 (en) | 2009-08-19 |
ES2424851T3 (es) | 2013-10-09 |
HK1131608A1 (en) | 2010-01-29 |
CA2669266A1 (en) | 2008-05-15 |
TW200829564A (en) | 2008-07-16 |
KR101390076B1 (ko) | 2014-04-29 |
AU2007317296A1 (en) | 2008-05-15 |
AR063628A1 (es) | 2009-02-04 |
WO2008058229A1 (en) | 2008-05-15 |
MX2009004699A (es) | 2009-05-15 |
CN101535264B (zh) | 2012-11-28 |
AU2007317296B2 (en) | 2012-07-05 |
CN101535264A (zh) | 2009-09-16 |
DK2089364T3 (da) | 2013-09-02 |
US8536200B2 (en) | 2013-09-17 |
PL2089364T3 (pl) | 2013-11-29 |
NO342395B1 (no) | 2018-05-14 |
JP5276005B2 (ja) | 2013-08-28 |
EP2089364B1 (en) | 2013-06-12 |
US20110052583A1 (en) | 2011-03-03 |
KR20090096423A (ko) | 2009-09-10 |
JP2010509362A (ja) | 2010-03-25 |
PT2089364E (pt) | 2013-08-26 |
NO20091605L (no) | 2009-05-27 |
US20080114033A1 (en) | 2008-05-15 |
HRP20130626T1 (en) | 2013-08-31 |
US7851489B2 (en) | 2010-12-14 |
SI2089364T1 (sl) | 2013-10-30 |
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