CL2017000588A1 - Derivados de piridona como inhibidores de ret (reorganizado durante la transfección)inhibidores de quinasa - Google Patents
Derivados de piridona como inhibidores de ret (reorganizado durante la transfección)inhibidores de quinasaInfo
- Publication number
- CL2017000588A1 CL2017000588A1 CL2017000588A CL2017000588A CL2017000588A1 CL 2017000588 A1 CL2017000588 A1 CL 2017000588A1 CL 2017000588 A CL2017000588 A CL 2017000588A CL 2017000588 A CL2017000588 A CL 2017000588A CL 2017000588 A1 CL2017000588 A1 CL 2017000588A1
- Authority
- CL
- Chile
- Prior art keywords
- cancer
- functional
- ret
- inhibitors
- syndrome
- Prior art date
Links
Classifications
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- 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
- 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
- A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
-
- 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
- A61K31/4418—Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
-
- 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
-
- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
-
- 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/69—Two or more oxygen atoms
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Abstract
<p>ESTA INVENCIÓN SE REFIERE A NUEVOS COMPUESTOS QUA SON INHIBIDORES DE LA CINASA RET (REORGANIZADO DURANTE LA TRANSFECCIÓN), A COMPOSICIONES FARMACÉUTICAS QUE LOS CONTIENEN, A PROCEDIMIENTOS PARA SU PREPARACIÓN, Y A SU USO PARA TRATAMIENTOS, EN MONOTERAPIA O EN POLITERAPIA, PARA LA NORMALIZACIÓN DE LA SENSIBILIDAD, MOVILIDAD Y/O SECRECIÓN GASTROINTESTINAL Y/O TRASTORNOS A ENFERMEDADES ABDOMINALES Y/O EL TRATAMIENTO RELACIONADO CON ENFERMEDADES RELACIONADAS CON LA DISFUNCIÓN DE RET A EN DONDE LA MODULACIÓN DE LA ACTIVIDAD DE RET PUEDE TENER UN BENEFICIO TERAPÉUTICO, QUE INCLUYE, PERO SIN LIMITARSE A ELLOS, TODAS LAS CLASIFICACIONES DEL SÍNDROME DEL COLON IRRITABLE (SCI), ENTRE ELLAS EL PATRÓN DE DEPOSICIONES DONDE PREDOMINAN LAS DIARREAS, DONDE PREDOMINA EL ESTREÑIMIENTO O SU ALTERNANCIA, METEORISMO FUNCIONAL, ESTREÑIMIENTO FUNCIONAL, DIARREA FUNCIONAL, COLON IRRITABLE FUNCIONAL INESPECÍFICO, SÍNDROME DEL DOLOR ABDOMINAL FUNCIONAL, ESTREÑIMIENTO IDIOPÁTICO CRÓNICO, TRASTORNOS ESOFÁGICOS FUNCIONALES, TRASTORNOS GASTRODUODENALES FUNCIONALES, DOLOR ANORRECTAL FUNCIONAL, ENTEROPATÍA INFAMATORIA, ENFERMEDADES PROLIFERATIVAS TALES COMA CÁNCER DE PULMÓN NO MICROCÍTICO, CARCINOMA HEPATOCELULAR, CÁNCER COLORRECTAL, CÁNCER TIROIDEO MODULAR, CÁNCER TIROIDEO FOLICULAR, CÁNCER TIROIDEO ANAPLÁSICO, CÁNCER TIROIDEO PAPILAR, TUMORES ENCEFÁLICOS, CÁNCER DE LA CAVIDAD PERITONEAL, TUMORES SÓLIDOS, OTRO CÁNCER DE PULMÓN, CÁNCER DE CABEZA Y CUELLO, GLIOMAS, NEUROBLASTOMAS, SÍNDROME DE VON HIPPEL-LINDAU Y TUMORES DE RIÑÓN, CÁNCER DE MAMA, CÁNCER DE LAS TROMPAS DE FALOPIO, CÁNCER DE OVARIO, CÁNCER DE LAS CÉLULAS DE TRANSICIÓN, CÁNCER DE PRÓSTATA, CÁNCER DE ESÓFAGO Y DE LA UNIÓN GASTROESOFÁGICA, CÁNCER BILIAR Y ADENOCARCINOMA, Y CUALQUIER NEOPLASIA MALIGNA CON INCREMENTO DE LA ACTIVIDAD DE LA CINASA RET.</p>
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2014086197 | 2014-09-10 | ||
| CN2015086995 | 2015-08-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2017000588A1 true CL2017000588A1 (es) | 2017-10-06 |
Family
ID=54186249
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2017000588A CL2017000588A1 (es) | 2014-09-10 | 2017-03-09 | Derivados de piridona como inhibidores de ret (reorganizado durante la transfección)inhibidores de quinasa |
Country Status (35)
| Country | Link |
|---|---|
| US (4) | US9918974B2 (es) |
| EP (2) | EP3191450B1 (es) |
| JP (2) | JP6538154B2 (es) |
| KR (1) | KR20170045350A (es) |
| CN (1) | CN107074768B (es) |
| AU (1) | AU2015313841B2 (es) |
| BR (1) | BR112017004900A2 (es) |
| CA (1) | CA2960768A1 (es) |
| CL (1) | CL2017000588A1 (es) |
| CO (1) | CO2017002273A2 (es) |
| CR (1) | CR20170093A (es) |
| CY (1) | CY1121661T1 (es) |
| DK (1) | DK3191450T3 (es) |
| DO (1) | DOP2017000059A (es) |
| EA (1) | EA033544B1 (es) |
| ES (2) | ES2725704T3 (es) |
| HR (1) | HRP20190815T1 (es) |
| HU (1) | HUE044604T2 (es) |
| IL (1) | IL250908B (es) |
| LT (1) | LT3191450T (es) |
| MA (1) | MA40581A (es) |
| ME (1) | ME03432B (es) |
| MX (1) | MX2017003114A (es) |
| MY (1) | MY181913A (es) |
| PE (1) | PE20170705A1 (es) |
| PH (1) | PH12017500425B1 (es) |
| PL (1) | PL3191450T3 (es) |
| PT (1) | PT3191450T (es) |
| RS (1) | RS58813B1 (es) |
| SG (1) | SG11201701694QA (es) |
| SI (1) | SI3191450T1 (es) |
| TW (1) | TWI683807B (es) |
| UA (1) | UA122213C2 (es) |
| UY (1) | UY36293A (es) |
| WO (1) | WO2016038552A1 (es) |
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| ES2628418T3 (es) | 2010-05-20 | 2017-08-02 | Array Biopharma, Inc. | Compuestos macrocíclicos como inhibidores de la TRK cinasa |
| SG11201701694QA (en) | 2014-09-10 | 2017-04-27 | Glaxosmithkline Ip Dev Ltd | Pyridone derivatives as rearranged during transfection (ret) kinase inhibitors |
| KR20170046180A (ko) | 2014-09-10 | 2017-04-28 | 글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드 | 형질감염 중 재배열 (ret) 억제제로서의 신규 화합물 |
| WO2016127074A1 (en) | 2015-02-06 | 2016-08-11 | Blueprint Medicines Corporation | 2-(pyridin-3-yl)-pyrimidine derivatives as ret inhibitors |
| SI3322706T1 (sl) | 2015-07-16 | 2021-04-30 | Array Biopharma, Inc. | Substituirane pirazolo(1,5-A)piridinske spojine kot zaviralci ret-kinaze |
| US10030005B2 (en) | 2015-11-02 | 2018-07-24 | Blueprint Medicines Corporation | Inhibitors of RET |
| WO2017161269A1 (en) | 2016-03-17 | 2017-09-21 | Blueprint Medicines Corporation | Inhibitors of ret receptor tyrosine kinases |
| WO2018017983A1 (en) | 2016-07-22 | 2018-01-25 | Blueprint Medicines Corporation | Compounds useful for treating disorders related to ret |
| JP2018052878A (ja) * | 2016-09-29 | 2018-04-05 | 第一三共株式会社 | ピリジン化合物 |
| JOP20190077A1 (ar) | 2016-10-10 | 2019-04-09 | Array Biopharma Inc | مركبات بيرازولو [1، 5-a]بيريدين بها استبدال كمثبطات كيناز ret |
| TWI704148B (zh) | 2016-10-10 | 2020-09-11 | 美商亞雷生物製藥股份有限公司 | 作為ｒｅｔ激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物 |
| WO2018136663A1 (en) | 2017-01-18 | 2018-07-26 | Array Biopharma, Inc. | Ret inhibitors |
| US11168090B2 (en) | 2017-01-18 | 2021-11-09 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyrazines as RET kinase inhibitors |
| JOP20190213A1 (ar) | 2017-03-16 | 2019-09-16 | Array Biopharma Inc | مركبات حلقية ضخمة كمثبطات لكيناز ros1 |
| US20210290620A1 (en) | 2017-05-15 | 2021-09-23 | Blueprint Medicines Corporation | Combinations of RET Inhibitors and mTORC1 Inhibitors and Uses Thereof for the Treatment of Cancer Mediated by Aberrant RET Activity |
| TWI812649B (zh) | 2017-10-10 | 2023-08-21 | 美商絡速藥業公司 | 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之調配物 |
| TWI791053B (zh) | 2017-10-10 | 2023-02-01 | 美商亞雷生物製藥股份有限公司 | 6-(2-羥基-2-甲基丙氧基)-4-(6-(6-((6-甲氧基吡啶-3-基)甲基)-3,6-二氮雜雙環[3.1.1]庚-3-基)吡啶-3-基)吡唑并[1,5-a]吡啶-3-甲腈之結晶形式及其醫藥組合物 |
| CA3087578C (en) | 2018-01-18 | 2023-08-08 | Array Biopharma Inc. | Substituted pyrazolo[3,4-d]pyrimidine compounds as ret kinase inhibitors |
| CN111971286B (zh) | 2018-01-18 | 2023-04-14 | 阿雷生物药品公司 | 作为RET激酶抑制剂的取代的吡咯并[2,3-d]嘧啶化合物 |
| WO2019143994A1 (en) | 2018-01-18 | 2019-07-25 | Array Biopharma Inc. | Substituted pyrazolyl[4,3-c]pyridinecompounds as ret kinase inhibitors |
| WO2019195471A1 (en) | 2018-04-03 | 2019-10-10 | Blueprint Medicines Corporation | Ret inhibitor for use in treating cancer having a ret alteration |
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| JP4403482B2 (ja) | 1997-12-22 | 2010-01-27 | バイエル コーポレイション | 置換複素環尿素合成のための中間体およびその製造方法 |
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| JP6097998B2 (ja) | 2010-12-16 | 2017-03-22 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ロイコトリエン生成のビアリールアミドインヒビター |
| US8937071B2 (en) | 2013-03-15 | 2015-01-20 | Glaxosmithkline Intellectual Property Development Limited | Compounds as rearranged during transfection (RET) inhibitors |
| AU2014229233B2 (en) * | 2013-03-15 | 2016-08-11 | Glaxosmithkline Intellectual Property Development Limited | Pyridine derivatives as rearranged during transfection (RET) kinase inhibitors |
| KR20170046180A (ko) | 2014-09-10 | 2017-04-28 | 글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드 | 형질감염 중 재배열 (ret) 억제제로서의 신규 화합물 |
| SG11201701694QA (en) | 2014-09-10 | 2017-04-27 | Glaxosmithkline Ip Dev Ltd | Pyridone derivatives as rearranged during transfection (ret) kinase inhibitors |
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2015
- 2015-09-09 SG SG11201701694QA patent/SG11201701694QA/en unknown
- 2015-09-09 US US15/509,613 patent/US9918974B2/en not_active Expired - Fee Related
- 2015-09-09 AU AU2015313841A patent/AU2015313841B2/en not_active Ceased
- 2015-09-09 MY MYPI2017700782A patent/MY181913A/en unknown
- 2015-09-09 WO PCT/IB2015/056905 patent/WO2016038552A1/en active Application Filing
- 2015-09-09 CN CN201580058320.5A patent/CN107074768B/zh not_active Expired - Fee Related
- 2015-09-09 JP JP2017513450A patent/JP6538154B2/ja not_active Expired - Fee Related
- 2015-09-09 CR CR20170093A patent/CR20170093A/es unknown
- 2015-09-09 KR KR1020177009237A patent/KR20170045350A/ko not_active Application Discontinuation
- 2015-09-09 EP EP15767599.2A patent/EP3191450B1/en active Active
- 2015-09-09 ES ES15767599T patent/ES2725704T3/es active Active
- 2015-09-09 ES ES19160650T patent/ES2816453T3/es active Active
- 2015-09-09 MA MA040581A patent/MA40581A/fr unknown
- 2015-09-09 MX MX2017003114A patent/MX2017003114A/es active IP Right Grant
- 2015-09-09 CA CA2960768A patent/CA2960768A1/en not_active Abandoned
- 2015-09-09 ME MEP-2019-136A patent/ME03432B/me unknown
- 2015-09-09 PL PL15767599T patent/PL3191450T3/pl unknown
- 2015-09-09 HU HUE15767599 patent/HUE044604T2/hu unknown
- 2015-09-09 EP EP19160650.8A patent/EP3517526B1/en active Active
- 2015-09-09 EA EA201790546A patent/EA033544B1/ru not_active IP Right Cessation
- 2015-09-09 SI SI201530720T patent/SI3191450T1/sl unknown
- 2015-09-09 BR BR112017004900A patent/BR112017004900A2/pt not_active IP Right Cessation
- 2015-09-09 PE PE2017000417A patent/PE20170705A1/es unknown
- 2015-09-09 UA UAA201703478A patent/UA122213C2/uk unknown
- 2015-09-09 LT LTEP15767599.2T patent/LT3191450T/lt unknown
- 2015-09-09 PT PT15767599T patent/PT3191450T/pt unknown
- 2015-09-09 RS RS20190559A patent/RS58813B1/sr unknown
- 2015-09-09 DK DK15767599.2T patent/DK3191450T3/da active
- 2015-09-10 UY UY0001036293A patent/UY36293A/es unknown
- 2015-09-10 TW TW104129876A patent/TWI683807B/zh not_active IP Right Cessation
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2017
- 2017-03-02 IL IL250908A patent/IL250908B/en active IP Right Grant
- 2017-03-07 DO DO2017000059A patent/DOP2017000059A/es unknown
- 2017-03-07 PH PH12017500425A patent/PH12017500425B1/en unknown
- 2017-03-07 CO CONC2017/0002273A patent/CO2017002273A2/es unknown
- 2017-03-09 CL CL2017000588A patent/CL2017000588A1/es unknown
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2018
- 2018-01-23 US US15/877,524 patent/US10111866B2/en not_active Expired - Fee Related
- 2018-09-28 US US16/145,271 patent/US10292975B2/en not_active Expired - Fee Related
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2019
- 2019-04-05 US US16/376,858 patent/US10709695B2/en active Active
- 2019-05-02 HR HRP20190815TT patent/HRP20190815T1/hr unknown
- 2019-05-09 CY CY20191100502T patent/CY1121661T1/el unknown
- 2019-05-31 JP JP2019102776A patent/JP6728447B2/ja not_active Expired - Fee Related
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