AR089550A1 - Compuestos quimicos - Google Patents
Compuestos quimicosInfo
- Publication number
- AR089550A1 AR089550A1 ARP110102793A ARP110102793A AR089550A1 AR 089550 A1 AR089550 A1 AR 089550A1 AR P110102793 A ARP110102793 A AR P110102793A AR P110102793 A ARP110102793 A AR P110102793A AR 089550 A1 AR089550 A1 AR 089550A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- halo
- optionally substituted
- heterocyclic ring
- membered
- Prior art date
Links
Classifications
-
- 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
- C07D401/14—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 three or more hetero rings
-
- 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
- A61K31/495—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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6568—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms
- C07F9/65685—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms the ring phosphorus atom being part of a phosphine oxide or thioxide
Abstract
Compuestos, composiciones farmacéuticas y métodos para su preparación. Estos compuestos inhiben la actividad cinasa de ALK y, por lo tanto, se pueden utilizar para tratar el cáncer. Reivindicación 1: Un compuesto de fórmula (1) caracterizado porque, o una sal farmacéuticamente aceptable de este, donde: X¹ se selecciona entre los restos de fórmula (2) y (3); X² se selecciona entre -NH- y -N(alquilo C₁₋₄)-; R¹ se selecciona entre H y alquilo C₁₋₄, donde dicho alquilo C₁₋₄ está opcionalmente sustituido con uno o más hidroxi; R² se selecciona entre H, alquilo C₁₋₄, cicloalquilo C₃₋₆ y heterociclilo de 4 a 7 miembros, donde dicho alquilo C₁₋₄ está opcionalmente sustituido con uno o más hidroxi; o R¹ y R² junto con el átomo de nitrógeno al cual están enlazados forman un anillo heterocíclico de 4 a 7 miembros, donde dicho anillo heterocíclico de 4 a 7 miembros está opcionalmente sustituido en carbono con uno o más R²⁰ y donde, si dicho anillo heterocíclico de 4 a 7 miembros contiene un resto -NH-, ese nitrógeno está opcionalmente sustituido con R²⁰*; R³ se selecciona entre H, halo y metilo; R⁴ se selecciona entre halo, -CN, metilo y trifluorometilo; R⁵ se selecciona entre H, halo y alquilo C₁₋₄; R²⁰ en cada caso se selecciona entre halo y alquilo C₁₋₆; R²⁰* se selecciona entre alquilo C₁₋₆, carbociclilo de 3 a 6 miembros, -S(O)R²⁰ᵇ y -S(O)₂R²⁰ᵇ; y R²⁰ᵇ en cada caso se selecciona independientemente entre alquilo C₁₋₆ y carbociclilo de 3 a 6 miembros.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US36991710P | 2010-08-02 | 2010-08-02 | |
US37205510P | 2010-08-09 | 2010-08-09 | |
US39094410P | 2010-10-07 | 2010-10-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR089550A1 true AR089550A1 (es) | 2014-09-03 |
Family
ID=45527326
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP110102793A AR089550A1 (es) | 2010-08-02 | 2011-08-02 | Compuestos quimicos |
Country Status (14)
Country | Link |
---|---|
US (1) | US8461170B2 (es) |
EP (1) | EP2601186A2 (es) |
JP (1) | JP2013534221A (es) |
KR (1) | KR20130096241A (es) |
CN (1) | CN103153982A (es) |
AR (1) | AR089550A1 (es) |
AU (1) | AU2011287386A1 (es) |
BR (1) | BR112013002587A2 (es) |
CA (1) | CA2805827A1 (es) |
MX (1) | MX2013001361A (es) |
RU (1) | RU2013109132A (es) |
TW (1) | TW201219383A (es) |
UY (1) | UY33539A (es) |
WO (1) | WO2012017239A2 (es) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103702990B (zh) | 2011-07-27 | 2015-09-09 | 阿斯利康(瑞典)有限公司 | 2-(2,4,5-取代苯胺)嘧啶衍生物作为egfr调谐子用于治疗癌症 |
CN102899882B (zh) * | 2012-11-07 | 2014-08-06 | 西南大学 | 超亲水涤纶织物的磷酸制备方法 |
CN104876914B (zh) * | 2014-02-28 | 2017-04-19 | 山东轩竹医药科技有限公司 | 嘧啶衍生物类间变性淋巴瘤激酶抑制剂 |
CN105085550B (zh) * | 2014-05-21 | 2017-05-24 | 海门慧聚药业有限公司 | 一类alk激酶抑制剂及其制备方法 |
MA40240B1 (fr) * | 2014-06-19 | 2019-03-29 | Ariad Pharma Inc | Composés hétéroaryle d'inhibition de la kinase |
AU2015407300B2 (en) * | 2015-08-31 | 2019-06-20 | Wuxi Shuangliang Biotechnology Co., Ltd. | 2-Arylamino pyridine, pyridine or triazine derivative, preparation method and use thereof |
CN106810553B (zh) * | 2015-11-30 | 2020-03-17 | 江苏正大丰海制药有限公司 | 3-(4,5-取代氨基嘧啶)苯基衍生物及其应用 |
BR112018074232A2 (pt) | 2016-05-26 | 2019-03-06 | Zeno Royalties & Milestones, LLC | compostos inibidores de egfr |
MX2019008808A (es) * | 2017-01-26 | 2019-09-16 | Hanmi Pharma Co Ltd | Compuesto de pirimidina y su uso farmaceutico. |
WO2019019043A1 (zh) * | 2017-07-26 | 2019-01-31 | 鼎科医疗技术(苏州)有限公司 | 一种表面液化药物涂层球囊 |
CA3096790C (en) * | 2018-04-09 | 2024-03-19 | Shanghaitech University | Target protein degradation compounds, their anti-tumor use, their intermediates and use of intermediates |
KR101954370B1 (ko) * | 2018-07-25 | 2019-03-05 | 한미약품 주식회사 | 피리미딘 화합물 및 이를 포함하는 암의 예방 또는 치료용 약학 조성물 |
CA3129665A1 (en) | 2019-03-21 | 2020-09-24 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
WO2021089791A1 (en) | 2019-11-08 | 2021-05-14 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
CN113387935B (zh) * | 2021-07-23 | 2022-06-10 | 苏州雅深智慧科技有限公司 | 抑制三突变表皮生长因子受体酪氨酸激酶的化合物及用途 |
CN116763792B (zh) * | 2023-06-19 | 2024-03-12 | 西安国际医学中心医院 | Hg-14-10-04在制备治疗食管鳞癌的药物中的应用 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
HUP9901155A3 (en) | 1996-02-13 | 2003-04-28 | Astrazeneca Ab | Quinazoline derivatives as vegf inhibitors |
KR100489174B1 (ko) | 1996-03-05 | 2005-09-30 | 제네카-파마 소시에떼아노님 | 4-아닐리노퀴나졸린유도체 |
GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
CA2406979A1 (en) | 2000-05-31 | 2001-12-06 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
EE200300015A (et) | 2000-07-07 | 2004-10-15 | Angiogene Pharmaceuticals Limited | Kolhinooli derivaadid kui angiogeneesi inhibiitorid |
IL153484A0 (en) | 2000-07-07 | 2003-07-06 | Angiogene Pharm Ltd | Colchinol derivatives as angiogenesis inhibitors |
US20080312211A1 (en) | 2005-12-23 | 2008-12-18 | Astrazeneca Ab | Antibacterial Pyrrolopyridines, Pyrrolopyrimidines and Pyrroloazepines-154 |
CA2659582A1 (en) * | 2006-06-22 | 2007-12-27 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
CN101932580B (zh) | 2007-06-01 | 2013-05-22 | 葛兰素史密丝克莱恩有限责任公司 | 咪唑并吡啶激酶抑制剂 |
EA201000341A1 (ru) | 2007-08-23 | 2010-10-29 | Астразенека Аб | 2-анилинопурин-8-оны в качестве ингибиторов ttk/mps1 для лечения пролиферативных нарушений |
TW201022262A (en) * | 2008-10-29 | 2010-06-16 | Astrazeneca Ab | Novel compounds 515 |
-
2011
- 2011-08-01 UY UY0001033539A patent/UY33539A/es not_active Application Discontinuation
- 2011-08-01 TW TW100127241A patent/TW201219383A/zh unknown
- 2011-08-02 KR KR1020137003860A patent/KR20130096241A/ko not_active Application Discontinuation
- 2011-08-02 WO PCT/GB2011/051465 patent/WO2012017239A2/en active Application Filing
- 2011-08-02 RU RU2013109132/04A patent/RU2013109132A/ru not_active Application Discontinuation
- 2011-08-02 BR BR112013002587A patent/BR112013002587A2/pt not_active IP Right Cessation
- 2011-08-02 CN CN201180047702XA patent/CN103153982A/zh active Pending
- 2011-08-02 CA CA2805827A patent/CA2805827A1/en not_active Abandoned
- 2011-08-02 AU AU2011287386A patent/AU2011287386A1/en not_active Abandoned
- 2011-08-02 JP JP2013522307A patent/JP2013534221A/ja not_active Withdrawn
- 2011-08-02 MX MX2013001361A patent/MX2013001361A/es not_active Application Discontinuation
- 2011-08-02 AR ARP110102793A patent/AR089550A1/es not_active Application Discontinuation
- 2011-08-02 US US13/196,189 patent/US8461170B2/en not_active Expired - Fee Related
- 2011-08-02 EP EP11746007.1A patent/EP2601186A2/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
KR20130096241A (ko) | 2013-08-29 |
WO2012017239A2 (en) | 2012-02-09 |
RU2013109132A (ru) | 2014-09-10 |
US8461170B2 (en) | 2013-06-11 |
MX2013001361A (es) | 2013-05-17 |
UY33539A (es) | 2012-02-29 |
CA2805827A1 (en) | 2012-02-09 |
AU2011287386A1 (en) | 2013-03-07 |
BR112013002587A2 (pt) | 2019-09-24 |
JP2013534221A (ja) | 2013-09-02 |
EP2601186A2 (en) | 2013-06-12 |
WO2012017239A3 (en) | 2012-04-05 |
TW201219383A (en) | 2012-05-16 |
US20120028924A1 (en) | 2012-02-02 |
CN103153982A (zh) | 2013-06-12 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |