MX2012000709A - Inhibidores de pirrolopiridina de cinasas. - Google Patents
Inhibidores de pirrolopiridina de cinasas.Info
- Publication number
- MX2012000709A MX2012000709A MX2012000709A MX2012000709A MX2012000709A MX 2012000709 A MX2012000709 A MX 2012000709A MX 2012000709 A MX2012000709 A MX 2012000709A MX 2012000709 A MX2012000709 A MX 2012000709A MX 2012000709 A MX2012000709 A MX 2012000709A
- Authority
- MX
- Mexico
- Prior art keywords
- kinases
- pyrrolopyridine
- inhibitors
- compounds
- formula
- Prior art date
Links
- 108091000080 Phosphotransferase Proteins 0.000 title abstract 2
- 102000020233 phosphotransferase Human genes 0.000 title abstract 2
- XWIYUCRMWCHYJR-UHFFFAOYSA-N 1h-pyrrolo[3,2-b]pyridine Chemical compound C1=CC=C2NC=CC2=N1 XWIYUCRMWCHYJR-UHFFFAOYSA-N 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
La presente invención se refiere a compuestos de fórmula (I) o sales farmacéuticas aceptables (ver fórmula (I)) en donde R1a, R1b, R1c, X, e Y se definen en la descripción. La presente invención se refiere también a composiciones que contiene los compuestos los cuales son útiles para inhibir las cinasas tal como Cdc7 y métodos para tratar enfermedades tal como el cáncer.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US22574209P | 2009-07-15 | 2009-07-15 | |
| PCT/US2010/042067 WO2011008915A1 (en) | 2009-07-15 | 2010-07-15 | Pyrrolopyridine inhibitors of kinases |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2012000709A true MX2012000709A (es) | 2012-03-16 |
Family
ID=42813135
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2012000709A MX2012000709A (es) | 2009-07-15 | 2010-07-15 | Inhibidores de pirrolopiridina de cinasas. |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8435980B2 (es) |
| EP (1) | EP2454257B1 (es) |
| JP (1) | JP2012533553A (es) |
| CN (1) | CN102471339A (es) |
| CA (1) | CA2767089A1 (es) |
| ES (1) | ES2432029T3 (es) |
| MX (1) | MX2012000709A (es) |
| WO (1) | WO2011008915A1 (es) |
Families Citing this family (43)
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|---|---|---|---|---|
| GEAP202213376A (en) | 2009-06-17 | 2022-02-25 | Vertex Pharmaceuticals Incorporated Us | Inhibitors of influenza viruses replication |
| ES2483594T3 (es) * | 2009-07-15 | 2014-08-06 | Abbott Laboratories | Pirrolopirazinas inhibidoras de quinasas |
| CN102933584A (zh) | 2010-04-16 | 2013-02-13 | Abbvie公司 | 激酶的吡咯并吡嗪酮抑制剂 |
| EP2560971B1 (en) * | 2010-04-19 | 2014-04-09 | Abbvie Inc. | Pyrrolopyridines as inhibitors of kinases |
| GB201017345D0 (en) * | 2010-10-14 | 2010-11-24 | Proximagen Ltd | Receptor antagonists |
| CN103492381A (zh) | 2010-12-16 | 2014-01-01 | 沃泰克斯药物股份有限公司 | 流感病毒复制的抑制剂 |
| JP2013545818A (ja) * | 2010-12-16 | 2013-12-26 | バーテックス ファーマシューティカルズ インコーポレイテッド | インフルエンザウイルス複製阻害物質 |
| US8742113B2 (en) | 2011-03-31 | 2014-06-03 | Sbi Biotech Co., Ltd. | Furanone derivative |
| UA118010C2 (uk) | 2011-08-01 | 2018-11-12 | Вертекс Фармасьютікалз Інкорпорейтед | Інгібітори реплікації вірусів грипу |
| DE102011119127A1 (de) | 2011-11-22 | 2013-05-23 | Merck Patent Gmbh | 3-Cyanaryl-1H-pyrrolo[2.3-b]pyridin-Derivate |
| EA035349B1 (ru) | 2012-11-21 | 2020-05-29 | ПиТиСи ТЕРАПЬЮТИКС, ИНК. | ЗАМЕЩЕННЫЕ ПИРИМИДИНОВЫЕ ОБРАТНЫЕ ИНГИБИТОРЫ Bmi-1 |
| FR3001219A1 (fr) * | 2013-01-22 | 2014-07-25 | Centre Nat Rech Scient | Inhibiteurs de kinases |
| US9314993B2 (en) * | 2013-03-15 | 2016-04-19 | National Nonwovens Inc. | Composites and articles made from nonwoven structures |
| GB2515785A (en) * | 2013-07-03 | 2015-01-07 | Redx Pharma Ltd | Compounds |
| WO2015030847A1 (en) | 2013-08-30 | 2015-03-05 | Ptc Therapeutics, Inc. | Substituted pyrimidine bmi-1 inhibitors |
| HUE052178T2 (hu) | 2013-11-13 | 2021-04-28 | Vertex Pharma | Eljárások influenzavírus-replikáció inhibitorainak elõállítására |
| LT3068776T (lt) | 2013-11-13 | 2019-08-12 | Vertex Pharmaceuticals Incorporated | Gripo virusų replikacijos inhibitoriai |
| WO2015076800A1 (en) | 2013-11-21 | 2015-05-28 | Ptc Therapeutics, Inc. | Substituted pyridine and pyrazine bmi-1 inhibitors |
| EP3094326A4 (en) * | 2014-01-14 | 2017-07-26 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| TN2016000270A1 (en) | 2014-01-14 | 2017-10-06 | Millennium Pharm Inc | Heteroaryls and uses thereof. |
| JP6569908B2 (ja) | 2014-01-31 | 2019-09-04 | カルナバイオサイエンス株式会社 | 抗がん剤組成物 |
| WO2016058544A1 (en) * | 2014-10-16 | 2016-04-21 | Syros Pharmaceuticals, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
| EA037555B1 (ru) | 2015-04-02 | 2021-04-13 | Проксимэйджен, Элэлси | Применение 6-{4-[1-(пропан-2-ил)пиперидин-4-ил]-1,4-диазепан-1-ил}-n-(пиридин-4-ил)пиридин-2-карбоксамида для лечения раковых заболеваний цнс |
| EP3090710B1 (de) * | 2015-05-07 | 2017-07-12 | Mondi AG | Elastische windelkomponente |
| JP6857617B2 (ja) | 2015-05-13 | 2021-04-14 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | インフルエンザウイルスの複製の阻害剤 |
| WO2016183116A1 (en) | 2015-05-13 | 2016-11-17 | Vertex Pharmaceuticals Incorporated | Methods of preparing inhibitors of influenza viruses replication |
| CA2998493A1 (en) | 2015-09-16 | 2017-03-23 | Metacrine, Inc. | Farnesoid x receptor agonists and uses thereof |
| KR101954369B1 (ko) * | 2017-01-26 | 2019-03-05 | 한미약품 주식회사 | 피리미딘 화합물 및 그의 의약 용도 |
| JP7174709B2 (ja) | 2017-03-15 | 2022-11-17 | メタクリン,インク. | ファルネソイドx受容体アゴニストおよびその使用 |
| EP4596041A3 (en) | 2017-03-15 | 2025-12-10 | Eli Lilly and Company | Farnesoid x receptor agonists and uses thereof |
| GB201807147D0 (en) | 2018-05-01 | 2018-06-13 | Oncologica Uk Ltd | Therapeutic combination |
| AU2019203034B1 (en) | 2018-07-25 | 2019-09-26 | Hanmi Pharm. Co., Ltd. | Pyrimidine compounds and pharmaceutical compositions for preventing or treating cancers including the same |
| KR101954370B1 (ko) * | 2018-07-25 | 2019-03-05 | 한미약품 주식회사 | 피리미딘 화합물 및 이를 포함하는 암의 예방 또는 치료용 약학 조성물 |
| AU2019340402B2 (en) | 2018-08-17 | 2025-04-03 | Ptc Therapeutics, Inc. | Method for treating pancreatic cancer |
| KR20250073553A (ko) | 2018-09-18 | 2025-05-27 | 일라이 릴리 앤드 캄파니 | 파르네소이드 x 수용체 효능제 및 그의 용도 |
| US12533353B2 (en) | 2018-09-24 | 2026-01-27 | Carna Biosciences, Inc. | Methods of treatment of cancer comprising CDC7 inhibitors |
| PH12021551985A1 (en) | 2019-02-22 | 2022-08-22 | Hanmi Pharmaceutical Co Ltd | Pharmaceutical composition comprising flt3 inhibitor and hypomethylating agent for treating acute myeloid leukemia |
| WO2020171649A1 (ko) * | 2019-02-22 | 2020-08-27 | 한미약품 주식회사 | Flt3 저해제 및 iap 길항제를 포함하는 급성 골수성 백혈병의 치료를 위한 약학적 조합물 |
| KR20210002015A (ko) * | 2019-06-27 | 2021-01-06 | 한미약품 주식회사 | Flt3 저해제 및 화학치료제를 포함하는 급성 골수성 백혈병 치료용 약학적 조성물 |
| WO2021050824A1 (en) * | 2019-09-11 | 2021-03-18 | Prelude Therapeutics Incorporated | Cdk inhibitors and their use as pharmaceuticals |
| CA3171987A1 (en) | 2020-03-18 | 2021-09-23 | Nicholas D. Smith | Crystalline forms of a farnesoid x receptor agonist |
| US12491160B2 (en) | 2020-03-18 | 2025-12-09 | Eli Lilly And Company | Formulations of a farnesoid X receptor agonist |
| CN116323569A (zh) * | 2020-09-15 | 2023-06-23 | 田边三菱制药株式会社 | 三嗪化合物的盐、其晶型及制造方法 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2215242T3 (es) | 1996-11-19 | 2004-10-01 | Amgen Inc. | Agentes antiinflamatorios de pirrol condensado sustituido con arilo y heteroarilo. |
| US7122552B2 (en) * | 2002-05-30 | 2006-10-17 | Vertex Pharmaceuticals Incorporated | Inhibitors of JAK and CDK2 protein kinases |
| DE10228103A1 (de) | 2002-06-24 | 2004-01-15 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| EP2295433A3 (en) | 2003-03-06 | 2011-07-06 | Eisai R&D Management Co., Ltd. | JNK inhibitors |
| US7563748B2 (en) | 2003-06-23 | 2009-07-21 | Cognis Ip Management Gmbh | Alcohol alkoxylate carriers for pesticide active ingredients |
| GB0330042D0 (en) * | 2003-12-24 | 2004-01-28 | Pharmacia Italia Spa | Pyrrolo [2,3-b] pyridine derivatives active as kinase inhibitors process for their preparation and pharmaceutical compositions them |
| NZ584499A (en) | 2004-03-30 | 2011-08-26 | Vertex Pharma | Azaindoles Useful as Inhibitors of Jak and Other Protein Kinases |
| RU2346996C2 (ru) | 2004-06-29 | 2009-02-20 | ЮРОПИЭН НИКЕЛЬ ПиЭлСи | Усовершенствованное выщелачивание основных металлов |
| WO2006050076A1 (en) * | 2004-10-29 | 2006-05-11 | Janssen Pharmaceutica, N.V. | Pyrimidinyl substituted fused-pyrrolyl compounds useful in treating kinase disorders |
| EP1814883A1 (en) | 2004-11-22 | 2007-08-08 | Vertex Pharmaceuticals Incorporated | Bicyclic inhibitors or rho kinase |
| AU2006247322A1 (en) * | 2005-05-16 | 2006-11-23 | Irm Llc | Pyrrolopyridine derivatives as protein kinase inhibitors |
| KR101280096B1 (ko) | 2005-06-29 | 2013-06-28 | 컴퓨메딕스 리미티드 | 전도성 브리지를 포함하는 센서 어셈블리 |
| DE102006012617A1 (de) | 2006-03-20 | 2007-09-27 | Merck Patent Gmbh | 4-(Pyrrolopyridinyl)-pyrimidinyl-2-amin-derivate |
| EP2010521A1 (en) | 2006-04-19 | 2009-01-07 | Novartis Ag | Indazole compounds and methods for inhibition of cdc7 |
| TW200801513A (en) | 2006-06-29 | 2008-01-01 | Fermiscan Australia Pty Ltd | Improved process |
| FR2907120B1 (fr) * | 2006-10-12 | 2013-01-11 | Sanofi Aventis | Nouveaux derives imidazolones,leur preparation a titre de medicaments,compositions pharmaceutiques,utilisation comme inhibiteurs de proteines kinases notamment cdc7 |
| FR2912744B1 (fr) * | 2007-02-16 | 2012-09-07 | Centre Nat Rech Scient | Composes pyrrolo°2,3-b!pyridine,composes azaindoles utiles dans la synthese de ces composes pyrrolo°2,3-b!pyridine, leurs procedes de fabrication et leurs utilisations. |
| EP2070928A1 (en) * | 2007-12-12 | 2009-06-17 | NERVIANO MEDICAL SCIENCES S.r.l. | 7-azaindol-3-ylacrylamides active as kinase inhibitors |
| AU2009266806A1 (en) * | 2008-07-03 | 2010-01-07 | Exelixis Inc. | CDK modulators |
-
2010
- 2010-07-15 CA CA2767089A patent/CA2767089A1/en not_active Abandoned
- 2010-07-15 US US12/836,753 patent/US8435980B2/en active Active
- 2010-07-15 WO PCT/US2010/042067 patent/WO2011008915A1/en not_active Ceased
- 2010-07-15 EP EP10749531.9A patent/EP2454257B1/en not_active Not-in-force
- 2010-07-15 ES ES10749531T patent/ES2432029T3/es active Active
- 2010-07-15 JP JP2012520765A patent/JP2012533553A/ja active Pending
- 2010-07-15 CN CN2010800360295A patent/CN102471339A/zh active Pending
- 2010-07-15 MX MX2012000709A patent/MX2012000709A/es active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| WO2011008915A1 (en) | 2011-01-20 |
| US20110015173A1 (en) | 2011-01-20 |
| CA2767089A1 (en) | 2011-01-20 |
| JP2012533553A (ja) | 2012-12-27 |
| EP2454257B1 (en) | 2013-08-21 |
| CN102471339A (zh) | 2012-05-23 |
| US8435980B2 (en) | 2013-05-07 |
| EP2454257A1 (en) | 2012-05-23 |
| ES2432029T3 (es) | 2013-11-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| GB | Transfer or rights |
Owner name: ABBVIE INC. |
|
| FG | Grant or registration |