MX2015012896A - Inhibidores de pirrolo [2,3-b] piridina cdk9 cinasa. - Google Patents
Inhibidores de pirrolo [2,3-b] piridina cdk9 cinasa.Info
- Publication number
- MX2015012896A MX2015012896A MX2015012896A MX2015012896A MX2015012896A MX 2015012896 A MX2015012896 A MX 2015012896A MX 2015012896 A MX2015012896 A MX 2015012896A MX 2015012896 A MX2015012896 A MX 2015012896A MX 2015012896 A MX2015012896 A MX 2015012896A
- Authority
- MX
- Mexico
- Prior art keywords
- pyrrolo
- pyridine
- kinase inhibitors
- cdk9 kinase
- compounds
- Prior art date
Links
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
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic 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
- A61K31/535—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
Abstract
Se describen compuestos de la Fórmula (lIIa), (ver Fórmula) en donde R1, R2, R3, X1, X2, X3, X4, X5, tienen los valores definidos anteriormente en la especificación, y sales farmacéuticamente aceptables de los mismos. Los compuestos pueden usarse como agentes en el tratamiento de enfermedades, incluyendo el cáncer. También se proporcionan composiciones farmacéuticas que comprende uno o más compuestos de la Fórmula (lIIa).
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN745DE2013 | 2013-03-14 | ||
US201361904842P | 2013-11-15 | 2013-11-15 | |
PCT/US2014/025740 WO2014151444A1 (en) | 2013-03-14 | 2014-03-13 | Pyrrolo[2,3-b]pyridine cdk9 kinase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2015012896A true MX2015012896A (es) | 2016-06-02 |
Family
ID=54249678
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2015012899A MX2015012899A (es) | 2013-03-14 | 2014-03-13 | Pirrolo [2,3-b] piridina como inhibidores de quinasa cdk9. |
MX2015012896A MX2015012896A (es) | 2013-03-14 | 2014-03-13 | Inhibidores de pirrolo [2,3-b] piridina cdk9 cinasa. |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2015012899A MX2015012899A (es) | 2013-03-14 | 2014-03-13 | Pirrolo [2,3-b] piridina como inhibidores de quinasa cdk9. |
Country Status (9)
Country | Link |
---|---|
US (1) | US9796708B2 (es) |
EP (2) | EP2970264A1 (es) |
JP (2) | JP2016514113A (es) |
CN (2) | CN105246890A (es) |
AR (1) | AR101528A1 (es) |
AU (2) | AU2014234077A1 (es) |
BR (2) | BR112015023187A2 (es) |
CA (2) | CA2905935A1 (es) |
MX (2) | MX2015012899A (es) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109843872B (zh) * | 2017-09-20 | 2022-08-30 | 杭州英创医药科技有限公司 | 作为ido抑制剂和/或ido-hdac双重抑制剂的多环化合物 |
CN111328333B (zh) * | 2019-09-29 | 2023-10-03 | 烟台迈百瑞国际生物医药股份有限公司 | 一种酸法制备抗体药物偶联物中间体的方法及其应用 |
JP2023501081A (ja) * | 2019-10-18 | 2023-01-18 | リード ファーマ ホールディング ビー.ブイ. | エストロゲン関連受容体アルファ(ERRα)モジュレーター |
WO2022078309A1 (zh) * | 2020-10-12 | 2022-04-21 | 上海海雁医药科技有限公司 | 取代的二(吡啶-2-基)胺衍生物、其组合物及医药上的用途 |
CN116685588A (zh) * | 2020-12-25 | 2023-09-01 | 南京明德新药研发有限公司 | 吡啶并吡咯类化合物的晶型、制备方法及其应用 |
CN112852874B (zh) * | 2021-02-04 | 2023-05-23 | 中国农业科学院兰州兽医研究所 | Hdac5基因敲除的bhk-21细胞系及其构建方法和应用 |
CN113248496B (zh) * | 2021-05-06 | 2022-02-11 | 东南大学 | 吡咯并吡啶类化合物及其盐及其用途 |
CN113666934B (zh) * | 2021-07-28 | 2023-06-23 | 北京深度制耀科技有限公司 | Cdk9激酶抑制剂 |
Family Cites Families (40)
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MY115155A (en) | 1993-09-09 | 2003-04-30 | Upjohn Co | Substituted oxazine and thiazine oxazolidinone antimicrobials. |
DE69631347T2 (de) | 1995-09-15 | 2004-10-07 | Upjohn Co | Aminoaryl oxazolidinone n-oxide |
US20030220234A1 (en) | 1998-11-02 | 2003-11-27 | Selvaraj Naicker | Deuterated cyclosporine analogs and their use as immunodulating agents |
GB9918037D0 (en) | 1999-07-30 | 1999-09-29 | Biochemie Gmbh | Organic compounds |
GB9930698D0 (en) * | 1999-12-24 | 2000-02-16 | Rhone Poulenc Rorer Ltd | Chemical compounds |
EE05180B1 (et) | 1999-12-24 | 2009-06-15 | Aventis Pharma Limited | Asaindooli sisaldav farmatseutiline kompositsioon raviotstarbeliseks kasutamiseks, asaindoolid ning nende kasutamine ravimite valmistamiseks, mis on ette nhtud proteiinikinaasi kataltilise toime prssimiseks |
GB0115109D0 (en) | 2001-06-21 | 2001-08-15 | Aventis Pharma Ltd | Chemical compounds |
GB0115393D0 (en) | 2001-06-23 | 2001-08-15 | Aventis Pharma Ltd | Chemical compounds |
ES2294494T3 (es) | 2004-04-19 | 2008-04-01 | Symed Labs Limited | Un nuevo procedimiento para la preparacion de linezolid y compuestos relacionados. |
PL1768967T3 (pl) | 2004-07-20 | 2009-09-30 | Symed Labs Ltd | Nowe związki pośrednie do wytwarzania linezolidu oraz związki pokrewne |
AR050365A1 (es) | 2004-08-02 | 2006-10-18 | Osi Pharm Inc | Compuestos inhibidores de multi- quinasa pirrolopirimidina aril- amino sustituidos. |
WO2006039164A2 (en) | 2004-09-29 | 2006-04-13 | Amr Technology, Inc. | Novel cyclosporin analogues and their pharmaceutical uses |
TW200716636A (en) | 2005-05-31 | 2007-05-01 | Speedel Experimenta Ag | Heterocyclic spiro-compounds |
US7514068B2 (en) | 2005-09-14 | 2009-04-07 | Concert Pharmaceuticals Inc. | Biphenyl-pyrazolecarboxamide compounds |
WO2007076348A2 (en) | 2005-12-23 | 2007-07-05 | Smithkline Beecham Corporation | Azaindole inhibitors of aurora kinases |
PE20080925A1 (es) * | 2006-09-22 | 2008-09-04 | Glaxo Group Ltd | DERIVADOS DE PIRROLO[2,3-b]PIRIDINA COMO INHIBIDORES DE QUINASA, EN PARTICULAR INHIBIDORES IKK2 (O IKK BETA) |
US8796267B2 (en) | 2006-10-23 | 2014-08-05 | Concert Pharmaceuticals, Inc. | Oxazolidinone derivatives and methods of use |
US20080188524A1 (en) | 2006-10-25 | 2008-08-07 | Martin Augustin | Methods of treating pain |
CN101568530A (zh) * | 2006-12-22 | 2009-10-28 | 诺瓦提斯公司 | 吲哚-4-基-嘧啶-2-基胺衍生物及其作为细胞周期蛋白依赖性激酶抑制剂的用途 |
WO2008098857A1 (en) | 2007-02-15 | 2008-08-21 | F. Hoffmann-La Roche Ag | 2-aminooxazolines as taar1 ligands |
EP2139869A2 (en) | 2007-04-13 | 2010-01-06 | SuperGen, Inc. | Axl kinase inhibitors useful for the treatment of cancer or hyperproliferative disorders |
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US7531685B2 (en) | 2007-06-01 | 2009-05-12 | Protia, Llc | Deuterium-enriched oxybutynin |
GB0710528D0 (en) * | 2007-06-01 | 2007-07-11 | Glaxo Group Ltd | Novel compounds |
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US20090118238A1 (en) | 2007-09-17 | 2009-05-07 | Protia, Llc | Deuterium-enriched alendronate |
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US20090088416A1 (en) | 2007-09-26 | 2009-04-02 | Protia, Llc | Deuterium-enriched lapaquistat |
EP2209774A1 (en) | 2007-10-02 | 2010-07-28 | Concert Pharmaceuticals Inc. | Pyrimidinedione derivatives |
CA2702008A1 (en) | 2007-10-12 | 2009-04-16 | Ingenium Pharmaceuticals Gmbh | Inhibitors of protein kinases |
US20090105338A1 (en) | 2007-10-18 | 2009-04-23 | Protia, Llc | Deuterium-enriched gabexate mesylate |
EP2212298B1 (en) | 2007-10-18 | 2013-03-27 | Concert Pharmaceuticals Inc. | Deuterated etravirine |
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US20090118276A1 (en) * | 2007-11-02 | 2009-05-07 | Wyeth | Thienopyrimidines, thienopyridines, and pyrrolopyrimidines as b-raf inhibitors |
GB0804592D0 (en) * | 2008-03-12 | 2008-04-16 | Glaxo Group Ltd | Novel compounds |
CN102143746A (zh) * | 2008-07-03 | 2011-08-03 | 埃克塞利希斯股份有限公司 | Cdk 调节剂 |
NZ591176A (en) | 2008-08-22 | 2012-11-30 | Novartis Ag | Pyrrolopyrimidine compounds as cdk inhibitors |
DE102011111400A1 (de) * | 2011-08-23 | 2013-02-28 | Merck Patent Gmbh | Bicyclische heteroaromatische Verbindungen |
IN2012CH01573A (es) * | 2012-04-20 | 2015-07-10 | Advinus Therapeutics Ltd | |
WO2013157021A1 (en) * | 2012-04-20 | 2013-10-24 | Advinus Therapeutics Limited | Bicyclic compounds, compositions and medicinal applications thereof |
-
2014
- 2014-03-13 AU AU2014234077A patent/AU2014234077A1/en not_active Abandoned
- 2014-03-13 JP JP2015561916A patent/JP2016514113A/ja active Pending
- 2014-03-13 MX MX2015012899A patent/MX2015012899A/es unknown
- 2014-03-13 CN CN201480026207.4A patent/CN105246890A/zh active Pending
- 2014-03-13 CA CA2905935A patent/CA2905935A1/en not_active Abandoned
- 2014-03-13 AR ARP140100937A patent/AR101528A1/es unknown
- 2014-03-13 JP JP2016501955A patent/JP2016516713A/ja active Pending
- 2014-03-13 BR BR112015023187A patent/BR112015023187A2/pt not_active IP Right Cessation
- 2014-03-13 EP EP14715513.9A patent/EP2970264A1/en not_active Withdrawn
- 2014-03-13 US US14/780,018 patent/US9796708B2/en active Active
- 2014-03-13 MX MX2015012896A patent/MX2015012896A/es unknown
- 2014-03-13 BR BR112015023356A patent/BR112015023356A2/pt not_active IP Right Cessation
- 2014-03-13 CA CA2905530A patent/CA2905530A1/en not_active Abandoned
- 2014-03-13 CN CN201480026524.6A patent/CN105324380A/zh active Pending
- 2014-03-13 EP EP14765781.1A patent/EP2970278A4/en not_active Withdrawn
- 2014-03-13 AU AU2014231567A patent/AU2014231567A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
CN105324380A (zh) | 2016-02-10 |
CA2905530A1 (en) | 2014-09-18 |
AU2014234077A1 (en) | 2015-10-01 |
AU2014231567A1 (en) | 2015-10-01 |
JP2016514113A (ja) | 2016-05-19 |
MX2015012899A (es) | 2016-06-02 |
BR112015023187A2 (pt) | 2017-07-18 |
US20160060257A1 (en) | 2016-03-03 |
US9796708B2 (en) | 2017-10-24 |
CN105246890A (zh) | 2016-01-13 |
EP2970264A1 (en) | 2016-01-20 |
EP2970278A1 (en) | 2016-01-20 |
CA2905935A1 (en) | 2014-09-25 |
JP2016516713A (ja) | 2016-06-09 |
BR112015023356A2 (pt) | 2017-07-18 |
EP2970278A4 (en) | 2016-12-07 |
AR101528A1 (es) | 2016-12-28 |
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