ATE389653T1 - 4-substituierte derivate von pyrazolo 3,4-d pyrimidin und deren verwendungen - Google Patents

4-substituierte derivate von pyrazolo 3,4-d pyrimidin und deren verwendungen

Info

Publication number
ATE389653T1
ATE389653T1 AT04734885T AT04734885T ATE389653T1 AT E389653 T1 ATE389653 T1 AT E389653T1 AT 04734885 T AT04734885 T AT 04734885T AT 04734885 T AT04734885 T AT 04734885T AT E389653 T1 ATE389653 T1 AT E389653T1
Authority
AT
Austria
Prior art keywords
pyrazolo
pyrimidine
substituted derivatives
nhch2c6h5
nhc4h9
Prior art date
Application number
AT04734885T
Other languages
English (en)
Inventor
Francesco Bondavalli
Maurizio Botta
Olga Bruno
Fabrizio Manetti
Silvia Schenone
Fabio Carraro
Original Assignee
Univ Siena
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
Priority claimed from IT000263A external-priority patent/ITRM20030263A1/it
Priority claimed from IT000264A external-priority patent/ITRM20030264A1/it
Application filed by Univ Siena filed Critical Univ Siena
Application granted granted Critical
Publication of ATE389653T1 publication Critical patent/ATE389653T1/de

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
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
AT04734885T 2003-05-28 2004-05-26 4-substituierte derivate von pyrazolo 3,4-d pyrimidin und deren verwendungen ATE389653T1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT000263A ITRM20030263A1 (it) 2003-05-28 2003-05-28 Derivati 4-sostituiti della 1-(2-cloro-2-feniletil)-
IT000264A ITRM20030264A1 (it) 2003-05-28 2003-05-28 Derivati 4-sostituiti della 1-(2-cloro-2-feniletil)-

Publications (1)

Publication Number Publication Date
ATE389653T1 true ATE389653T1 (de) 2008-04-15

Family

ID=33492308

Family Applications (1)

Application Number Title Priority Date Filing Date
AT04734885T ATE389653T1 (de) 2003-05-28 2004-05-26 4-substituierte derivate von pyrazolo 3,4-d pyrimidin und deren verwendungen

Country Status (8)

Country Link
US (1) US7589086B2 (de)
EP (1) EP1638966B1 (de)
JP (1) JP4642766B2 (de)
AT (1) ATE389653T1 (de)
CA (1) CA2527496C (de)
DE (1) DE602004012559T2 (de)
ES (1) ES2304252T3 (de)
WO (2) WO2004106339A2 (de)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1746099A1 (de) 2004-12-23 2007-01-24 DeveloGen Aktiengesellschaft Mnk1 or Mnk2 Inhibitoren
US7994172B2 (en) * 2004-12-28 2011-08-09 Exelixis, Inc. [1H-pyrazolo[3, 4-D]pyrimidin-4-yl]-piperidine or -piperazine compounds as serine-theoronine kinase modulators (P70s6k, Atk1 and Atk2) for the treatment of immunological, inflammatory and proliferative diseases
US7558755B2 (en) * 2005-07-13 2009-07-07 Mott Antony R Methods and systems for valuing investments, budgets and decisions
GB0524436D0 (en) * 2005-11-30 2006-01-11 Novartis Ag Organic compounds
JP5302883B2 (ja) 2006-04-07 2013-10-02 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 医薬組成物用のmnk1/mnk2阻害活性を有するチエノピリミジン
EP1889847A1 (de) 2006-07-10 2008-02-20 DeveloGen Aktiengesellschaft Pyrrolopyrimidine zur pharmazeutischen Anwendung
EP2201013B1 (de) 2007-09-14 2014-11-19 Universita Degli Studi di Siena Neue 4-substituierte derivate von pyrazolo[3,4-d]pyrimidin und pyrrolo[2,3-d]pyrimidin und anwendungen davon
KR20110045019A (ko) 2008-08-26 2011-05-03 베링거 인겔하임 인터내셔날 게엠베하 약제학적 조성물을 위한 티에노피리미딘
UY33241A (es) 2010-02-26 2011-09-30 Boehringer Ingelheim Int ?Tienopirimidinas que contienen heterocicloalquilo para composiciones farmacéuticas?.
AR080328A1 (es) 2010-02-26 2012-03-28 Boehringer Ingelheim Int Tienopirimidinas que contienen un grupo alquilo sustituido inhibidoras de quinasas mnk1 y/o mnk2, composiciones farmaceuticas que las contienen y uso de las mismas para el tratamiento de trastornos metabolicos tales como diabetes y obesidad, y trastornos hiperproliferativos, entre otros
EA201201191A1 (ru) 2010-02-26 2013-04-30 Бёрингер Ингельхайм Интернациональ Гмбх 4-[циклоалкилокси(гетеро)ариламино]тиено[2,3-d]пиримидины, обладающие ингибирующей активностью по отношению к mnkl/mnk2, предназначенные для фармацевтических композиций
WO2011146313A1 (en) * 2010-05-19 2011-11-24 The University Of North Carolina At Chapel Hill Pyrazolopyrimidine compounds for the treatment of cancer
WO2012056319A1 (en) 2010-10-27 2012-05-03 Dynamix Pharmaceuticals Ltd. Sulfonamides for the modulation of pkm2
US9273056B2 (en) 2011-10-03 2016-03-01 The University Of North Carolina At Chapel Hill Pyrrolopyrimidine compounds for the treatment of cancer
HK1206338A1 (en) 2012-05-22 2016-01-08 北卡罗来纳大学教堂山分校 Pyrimidine compounds for the treatment of cancer
CN103570723B (zh) 2012-07-27 2016-07-13 广西梧州制药(集团)股份有限公司 吡唑并嘧啶衍生物及其制备方法和在药物制备中的用途
EP2909211A4 (de) 2012-10-17 2016-06-22 Univ North Carolina Pyrazolopyrimidinverbindungen zur krebsbehandlung
WO2014085225A1 (en) 2012-11-27 2014-06-05 The University Of North Carolina At Chapel Hill Pyrimidine compounds for the treatment of cancer
CN106459063A (zh) 2014-04-11 2017-02-22 北卡罗来纳-查佩尔山大学 Mertk‑特异性嘧啶化合物
US10709708B2 (en) 2016-03-17 2020-07-14 The University Of North Carolina At Chapel Hill Method of treating cancer with a combination of MER tyrosine kinase inhibitor and an epidermal growth factor receptor (EGFR) inhibitor

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58208293A (ja) * 1982-05-20 1983-12-03 Lion Corp 1H−ピラゾロ〔3,4−d〕ピリミジン誘導体及び該化合物を含有する抗腫瘍剤
JP4249804B2 (ja) 1995-04-03 2009-04-08 ノバルティス・アクチエンゲゼルシャフト ピラゾール誘導体およびその製造法
ES2309206T3 (es) * 2001-10-02 2008-12-16 Smithkline Beecham Corporation Compuestos quimicos.

Also Published As

Publication number Publication date
ES2304252T3 (es) 2008-10-01
JP4642766B2 (ja) 2011-03-02
US7589086B2 (en) 2009-09-15
WO2004106339A3 (en) 2005-02-17
DE602004012559D1 (de) 2008-04-30
WO2004106340A3 (en) 2005-02-17
US20070010510A1 (en) 2007-01-11
WO2004106339A2 (en) 2004-12-09
JP2007500206A (ja) 2007-01-11
EP1638966B1 (de) 2008-03-19
CA2527496C (en) 2012-08-14
DE602004012559T2 (de) 2009-04-30
CA2527496A1 (en) 2004-12-09
WO2004106340A2 (en) 2004-12-09
EP1638966A2 (de) 2006-03-29

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