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MX2009005011A - Imidazopirazinas como inhibidores de proteina quinasa. - Google Patents

Imidazopirazinas como inhibidores de proteina quinasa.

Info

Publication number
MX2009005011A
MX2009005011A MX2009005011A MX2009005011A MX2009005011A MX 2009005011 A MX2009005011 A MX 2009005011A MX 2009005011 A MX2009005011 A MX 2009005011A MX 2009005011 A MX2009005011 A MX 2009005011A MX 2009005011 A MX2009005011 A MX 2009005011A
Authority
MX
Mexico
Prior art keywords
compounds
methods
imidazopyrazines
protein kinase
kinase inhibitors
Prior art date
Application number
MX2009005011A
Other languages
English (en)
Inventor
M Arshad Siddiqui
Lianyun Zhao
Timothy J Guzi
David B Belanger
Patrick J Curran
Blake Hamann
Panduranga Adulla P Reddy
Praveen K Tadikonda
Original Assignee
Schering Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39276164&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MX2009005011(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Schering Corp filed Critical Schering Corp
Publication of MX2009005011A publication Critical patent/MX2009005011A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—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)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

En sus muchas modalidades, la presente invención provee una nueva clase de compuestos de imidazopirazina de la siguiente fórmula (1) (ver fórmula) como inhibidores de proteínas y/o Aurora quinasas, métodos de preparación de dichos compuestos, composiciones farmacéuticas que incluyen uno o más de dichos compuestos, métodos de preparación de formulaciones farmacéuticas que incluyen uno o más de dichos compuestos, y métodos de tratamiento, prevención, inhibición, o mejoría de una o más enfermedades asociadas con las proteínas o Aurora quinasas que utilizan dichos compuestos o composiciones farmacéuticas, tales como cáncer y leucemia.
MX2009005011A 2006-11-08 2007-11-06 Imidazopirazinas como inhibidores de proteina quinasa. MX2009005011A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US85824406P 2006-11-08 2006-11-08
PCT/US2007/023329 WO2008057512A2 (en) 2006-11-08 2007-11-06 Imidazopyrazines as protein kinase inhibitors

Publications (1)

Publication Number Publication Date
MX2009005011A true MX2009005011A (es) 2009-05-20

Family

ID=39276164

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2009005011A MX2009005011A (es) 2006-11-08 2007-11-06 Imidazopirazinas como inhibidores de proteina quinasa.

Country Status (11)

Country Link
US (1) US7511040B2 (es)
EP (1) EP2079746A2 (es)
JP (1) JP2010509328A (es)
CN (1) CN101589045A (es)
AR (1) AR063581A1 (es)
CA (1) CA2669465A1 (es)
CL (1) CL2007003212A1 (es)
MX (1) MX2009005011A (es)
PE (1) PE20080931A1 (es)
TW (1) TW200829588A (es)
WO (1) WO2008057512A2 (es)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0716292D0 (en) 2007-08-21 2007-09-26 Biofocus Dpi Ltd Imidazopyrazine compounds
CN102105147B (zh) * 2008-07-24 2013-07-03 内尔维阿诺医学科学有限公司 包含aurora激酶抑制剂和抗肿瘤药的治疗组合
JP5683462B2 (ja) * 2008-07-24 2015-03-11 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ オーロラキナーゼ阻害剤および抗増殖剤を含む治療用組み合わせ
US8394802B2 (en) * 2008-09-19 2013-03-12 Nerviano Medical Sciences S.R.L. 3,4-dihydro-2H-pyrrolo[1,2-a]pyrazin-1-one derivatives for the modulation of the activity of protein kinases
TW201107329A (en) * 2009-07-30 2011-03-01 Oncotherapy Science Inc Fused imidazole derivative having ttk inhibitory action
US8993535B2 (en) 2009-09-04 2015-03-31 Merck Sharp & Dohme Corp. Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors
CA2778949C (en) 2009-10-30 2018-02-27 Janssen Pharmaceutica Nv Imidazo[1,2-b]pyridazine derivatives and their use as pde10 inhibitors
AR080754A1 (es) 2010-03-09 2012-05-09 Janssen Pharmaceutica Nv Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10
CA2793279A1 (en) * 2010-03-18 2011-09-22 Ulrich Klar Imidazopyrazines
US9199999B2 (en) 2010-06-01 2015-12-01 Bayer Intellectual Property Gmbh Substituted imidazopyrazines
JP5813101B2 (ja) 2010-06-04 2015-11-17 アルバニー モレキュラー リサーチ， インコーポレイテッド グリシントランスポーター−１阻害剤、その作製方法および使用方法
WO2012080228A1 (en) 2010-12-17 2012-06-21 Bayer Pharma Aktiengesellschaft 6-thio-substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
EP2651950A1 (en) * 2010-12-17 2013-10-23 Bayer Intellectual Property GmbH 6 substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
EP2651945A1 (en) 2010-12-17 2013-10-23 Bayer Intellectual Property GmbH 6-substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
US8673905B2 (en) * 2011-03-17 2014-03-18 Hoffmann-La Roche Inc. Imidazo pyrazines
AU2012277912B2 (en) 2011-06-27 2017-03-23 Janssen Pharmaceutica Nv 1-aryl-4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline derivatives
CA2872216C (en) 2012-06-26 2021-07-20 Janssen Pharmaceutica Nv Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl-[1,2,4] triazolo [4,3-a] quinoxaline compounds and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders
CN104411314B (zh) 2012-07-09 2017-10-20 詹森药业有限公司 磷酸二酯酶10的抑制剂
EA201790086A1 (ru) 2014-07-14 2017-07-31 Джилид Сайэнс, Инк. Комбинации для лечения раковых заболеваний
US10118890B2 (en) 2014-10-10 2018-11-06 The Research Foundation For The State University Of New York Trifluoromethoxylation of arenes via intramolecular trifluoromethoxy group migration
CN107531710B (zh) * 2015-08-13 2020-02-14 北京韩美药品有限公司 Irak4抑制剂及其应用
CN107056789B (zh) * 2017-04-21 2019-03-29 陈剑 具有取代吡嗪并咪唑类衍生物,其制备及其在医药上的应用
WO2022061155A1 (en) * 2020-09-17 2022-03-24 The Translational Genomics Research Institute Imidazopyridazine and imidazopyrazine compounds as inhibitors of cdk7
CN117050085A (zh) * 2023-06-26 2023-11-14 广西大学 芳基取代的8-氨基咪唑并吡嗪类化合物及其制备方法和应用

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20050057520A (ko) * 2002-09-23 2005-06-16 쉐링 코포레이션 사이클린 의존성 키나제 억제제로서의 이미다조피라진
US7186832B2 (en) * 2003-02-20 2007-03-06 Sugen Inc. Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
WO2005085252A1 (en) * 2004-03-04 2005-09-15 Biofocus Discovery Limited Imidazo ‘1,2-a’ pyrazine compounds which interact with protein kinases
EP1812439B2 (en) * 2004-10-15 2017-12-06 Takeda Pharmaceutical Company Limited Kinase inhibitors
CA2628534A1 (en) * 2005-11-10 2007-05-18 Schering Corporation Methods for inhibiting protein kinases
AU2006315718B2 (en) * 2005-11-10 2012-10-04 Merck Sharp & Dohme Corp. Imidazopyrazines as protein kinase inhibitors

Also Published As

Publication number Publication date
WO2008057512A3 (en) 2008-06-26
CN101589045A (zh) 2009-11-25
JP2010509328A (ja) 2010-03-25
CL2007003212A1 (es) 2008-06-27
US7511040B2 (en) 2009-03-31
CA2669465A1 (en) 2008-05-15
EP2079746A2 (en) 2009-07-22
PE20080931A1 (es) 2008-07-19
AR063581A1 (es) 2009-02-04
WO2008057512A2 (en) 2008-05-15
TW200829588A (en) 2008-07-16
US20080139571A1 (en) 2008-06-12

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