ATE512972T1 - Pyrrolopyrazole als wirksame kinaseinhibitoren - Google Patents

Pyrrolopyrazole als wirksame kinaseinhibitoren

Info

Publication number
ATE512972T1
ATE512972T1 AT05850734T AT05850734T ATE512972T1 AT E512972 T1 ATE512972 T1 AT E512972T1 AT 05850734 T AT05850734 T AT 05850734T AT 05850734 T AT05850734 T AT 05850734T AT E512972 T1 ATE512972 T1 AT E512972T1
Authority
AT
Austria
Prior art keywords
pyrrolopyrazoles
kinase inhibitors
effective kinase
effective
inhibitors
Prior art date
Application number
AT05850734T
Other languages
English (en)
Inventor
Djamal Bouzida
Liming Dong
Chuangxing Guo
Yufeng Hong
Haitao Li
Joseph T Marakovits
Anle Yang
Junhu Zhang
Original Assignee
Pfizer
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
Application filed by Pfizer filed Critical Pfizer
Application granted granted Critical
Publication of ATE512972T1 publication Critical patent/ATE512972T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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
    • A61K31/437Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs 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)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
AT05850734T 2005-01-10 2005-12-28 Pyrrolopyrazole als wirksame kinaseinhibitoren ATE512972T1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US64290005P 2005-01-10 2005-01-10
US73377005P 2005-11-04 2005-11-04
PCT/IB2005/003975 WO2006072831A1 (en) 2005-01-10 2005-12-28 Pyrrolopyrazoles, potent kinase inhibitors

Publications (1)

Publication Number Publication Date
ATE512972T1 true ATE512972T1 (de) 2011-07-15

Family

ID=36463340

Family Applications (1)

Application Number Title Priority Date Filing Date
AT05850734T ATE512972T1 (de) 2005-01-10 2005-12-28 Pyrrolopyrazole als wirksame kinaseinhibitoren

Country Status (29)

Country Link
US (2) US8067591B2 (de)
EP (1) EP1838718B1 (de)
JP (1) JP4250195B2 (de)
KR (1) KR100919343B1 (de)
CN (1) CN101115760B (de)
AP (1) AP2007004061A0 (de)
AT (1) ATE512972T1 (de)
AU (1) AU2005323797B2 (de)
BR (1) BRPI0518509A2 (de)
CA (1) CA2593428C (de)
CU (1) CU23778B7 (de)
CY (1) CY1111752T1 (de)
DK (1) DK1838718T3 (de)
EA (1) EA011815B1 (de)
ES (1) ES2365245T3 (de)
GE (1) GEP20094785B (de)
HR (1) HRP20110485T1 (de)
IL (1) IL184275A0 (de)
MA (1) MA29141B1 (de)
MX (1) MX2007008385A (de)
NO (1) NO20073859L (de)
NZ (1) NZ556273A (de)
PL (1) PL1838718T3 (de)
PT (1) PT1838718E (de)
RS (1) RS51891B (de)
SI (1) SI1838718T1 (de)
TN (1) TNSN07254A1 (de)
WO (1) WO2006072831A1 (de)
ZA (1) ZA200705628B (de)

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GEP20104974B (en) 2005-12-21 2010-04-26 Pfizer Prod Inc Carbonylamino pyrrolopyrazoles, protent kinase inhibitors
KR101060892B1 (ko) 2007-02-07 2011-08-31 화이자 인코포레이티드 Pkc 억제제로서의 3-아미노-피롤로[3,4-c] 피라졸-5(1h,4h,6h) 카브알데하이드 유도체
CN101646673B (zh) * 2007-02-07 2014-06-25 辉瑞大药厂 作为pkc抑制剂的3-氨基-吡咯并[3,4-c]吡唑-5(1h,4h,6h)甲醛衍生物
MX2009010951A (es) * 2007-04-12 2009-10-29 Pfizer Derivados de 3-amino-pirrolo[3,4-c]pirazol-5(1h,4h,6h)-carbaldehid o como inhibidores de proteina quinasa c.
JP5282091B2 (ja) * 2007-07-25 2013-09-04 ブリストル−マイヤーズ スクイブ カンパニー トリアジンキナーゼ阻害剤
FR2928150A1 (fr) 2008-02-29 2009-09-04 Vetoquinol Sa Sa Nouveaux derives 7-substitues de 3-carboxy-oxadiazino-quinolones, leur preparation et leur application comme anti-bacteriens
JPWO2009130900A1 (ja) * 2008-04-24 2011-08-11 日本曹達株式会社 オキシム誘導体、中間体化合物および植物病害防除剤
EP2145891A1 (de) 2008-07-09 2010-01-20 Vetoquinol S.A. 9-substierte 5-Carboxy-Oxadiazin-Chinolon-Derivate, ihre Herstellung und ihre Anwendung als antibakterielle Mittel
US20120283296A1 (en) * 2009-10-06 2012-11-08 Afraxis, Inc. Pyrrolopyrazoles for treating cns disorders
KR101483215B1 (ko) 2010-01-29 2015-01-16 한미약품 주식회사 단백질 키나아제 저해활성을 갖는 비시클릭 헤테로아릴 유도체
CN103298461A (zh) 2010-11-17 2013-09-11 霍夫曼-拉罗奇有限公司 治疗肿瘤的方法
HK1198475A1 (en) 2011-07-19 2015-05-08 无限药品股份有限公司 Heterocyclic compounds and uses thereof
WO2013113716A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
US9055750B2 (en) 2012-02-03 2015-06-16 Basf Se Fungicidal pyrimidine compounds
WO2013113720A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
WO2013113791A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
WO2013113719A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds ii
WO2013113782A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
IN2014DN07224A (de) 2012-02-03 2015-04-24 Basf Se
WO2013113778A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
WO2013113773A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
WO2013113781A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds i
WO2013113776A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
WO2013135672A1 (en) 2012-03-13 2013-09-19 Basf Se Fungicidal pyrimidine compounds
EP2825533B1 (de) 2012-03-13 2016-10-19 Basf Se Fungizide pyrimidin-verbindungen
WO2013135745A1 (en) 2012-03-16 2013-09-19 F. Hoffmann-La Roche Ag Methods of treating melanoma with pak1 inhibitors
MX2015003535A (es) 2012-09-19 2015-07-14 Novartis Ag Dihidro-pirrolidino-pirimidinas como inhibidoras de cinasa.
CN104884450B (zh) * 2012-10-15 2017-03-29 辉瑞爱尔兰制药公司 制备伏立康唑及其类似物的方法
WO2015036059A1 (en) 2013-09-16 2015-03-19 Basf Se Fungicidal pyrimidine compounds
EP3046915A1 (de) 2013-09-16 2016-07-27 Basf Se Fungizide pyrimidinverbindungen
EP3236959B1 (de) 2014-12-23 2025-09-24 Dana-Farber Cancer Institute, Inc. Hemmer der cyclinabhängigen kinase 7 (cdk7)
JP6861166B2 (ja) 2015-03-27 2021-04-21 ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド サイクリン依存性キナーゼの阻害剤
US10273252B2 (en) 2015-06-15 2019-04-30 Ube Industries, Ltd. Substituted dihydropyrrolopyrazole derivative
CN104926735A (zh) * 2015-06-16 2015-09-23 上海合全药物研发有限公司 4-氯-5-氟-2-甲基嘧啶的工业化制备方法
CN109311868B (zh) 2015-12-22 2022-04-01 尚医治疗有限责任公司 用于治疗癌症和炎性疾病的化合物
WO2017144546A1 (en) 2016-02-23 2017-08-31 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and pharmaceutical compositions for the treatment of nasopharyngeal carcinoma
CA3041563C (en) 2016-11-22 2023-10-31 Dana-Farber Cancer Institute, Inc. Pyrimidin-2-amine derivatives and pharmaceutical compositions thereof useful as inhibitors of cyclin-dependent kinase 12 (cdk12)
BR112019027640A2 (pt) 2017-06-21 2020-07-07 SHY Therapeutics LLC composto, método para testar a capacidade de um ou mais compostos, método para inibir a função de ras, método para inibir a função de rho, método para inibir a função de rac, composição farmacêutica
US20210161943A1 (en) * 2018-04-16 2021-06-03 The Regents Of The University Of California Pak4 inhibitors and methods of use
CA3099763A1 (en) 2018-06-25 2020-01-02 Dana-Farber Cancer Institute, Inc. Taire family kinase inhibitors and uses thereof
US12391705B2 (en) 2018-12-19 2025-08-19 Shy Therapeutics, Llc Compounds that interact with the Ras superfamily for the treatment of cancers, inflammatory diseases, rasopathies, and fibrotic disease
US12281126B2 (en) 2018-12-28 2025-04-22 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 and uses thereof
EP3956446A1 (de) 2019-04-17 2022-02-23 INSERM (Institut National de la Santé et de la Recherche Médicale) Verfahren und zusammensetzungen zur behandlung von durch nlrp3-inflammasom vermittelten il-1-beta-abhängigen erkrankungen
JP7769388B2 (ja) 2019-12-12 2025-11-13 ティン セラピューティクス,インコーポレイテッド 聴覚損失の予防及び治療のための組成物及び方法
WO2021198511A1 (en) 2020-04-03 2021-10-07 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and compositions for treatment of sars-cov-2 infection
CN111454278B (zh) * 2020-05-15 2021-03-19 四川大学 Pak1抑制剂及其合成和在制备抗肿瘤药物中的应用
WO2022008597A1 (en) 2020-07-08 2022-01-13 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and pharmaceutical composition for the treatment of infectious diseases
WO2022143911A1 (zh) * 2020-12-31 2022-07-07 赛诺哈勃药业(成都)有限公司 一种纤溶酶抑制剂、其制备方法及应用
WO2024261302A1 (en) 2023-06-22 2024-12-26 Institut National de la Santé et de la Recherche Médicale Nlrp3 inhibitors, pak1/2 inhibitors and/or caspase 1 inhibitors for use in the treatment of rac2 monogenic disorders
WO2025078334A1 (en) 2023-10-09 2025-04-17 Institut National de la Santé et de la Recherche Médicale Combination of pak1 inhibitors and clk inhibitors for preventing resistance to chemotherapy in patients suffering from acute myeloid leukemia

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US3423414A (en) 1966-01-13 1969-01-21 Ciba Geigy Corp Pyrazolopyridines
US3526633A (en) 1968-03-06 1970-09-01 American Cyanamid Co Substituted 2,4,5,6-tetrahydropyrrolo(3,4-c)pyrazoles
US3947467A (en) 1973-08-02 1976-03-30 Eli Lilly And Company 3-(5-Nitro-2-imidazolyl) pyrazoles
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US6013500A (en) 1998-05-21 2000-01-11 The Trustees Of Columbia University In The City Of New York PAK4, a novel gene encoding a serine/threonine kinase
ATE480539T1 (de) 2000-08-10 2010-09-15 Pfizer Italia Srl Bizyklische pyrazole wirksam als kinase inhibitoren, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische zubereitungen
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Also Published As

Publication number Publication date
BRPI0518509A2 (pt) 2008-11-25
PL1838718T3 (pl) 2011-10-31
SI1838718T1 (sl) 2011-08-31
AU2005323797A1 (en) 2006-07-13
CN101115760A (zh) 2008-01-30
CU23778B7 (es) 2012-02-15
HK1114380A1 (en) 2008-10-31
US20100222342A1 (en) 2010-09-02
AP2007004061A0 (en) 2007-08-31
DK1838718T3 (da) 2011-07-25
NZ556273A (en) 2010-01-29
EA011815B1 (ru) 2009-06-30
CA2593428C (en) 2012-04-17
EA200701257A1 (ru) 2007-12-28
CN101115760B (zh) 2010-11-03
MX2007008385A (es) 2007-08-21
WO2006072831A1 (en) 2006-07-13
CA2593428A1 (en) 2006-07-13
CU20070160A7 (es) 2009-03-16
HRP20110485T1 (hr) 2011-07-31
CY1111752T1 (el) 2015-10-07
KR100919343B1 (ko) 2009-09-25
NO20073859L (no) 2007-10-03
ZA200705628B (en) 2008-11-26
GEP20094785B (en) 2009-09-25
PT1838718E (pt) 2011-08-17
JP2008526826A (ja) 2008-07-24
US8530652B2 (en) 2013-09-10
US8067591B2 (en) 2011-11-29
TNSN07254A1 (en) 2008-12-31
KR20070096007A (ko) 2007-10-01
AU2005323797B2 (en) 2009-07-09
ES2365245T3 (es) 2011-09-27
US20120264751A1 (en) 2012-10-18
MA29141B1 (fr) 2008-01-02
JP4250195B2 (ja) 2009-04-08
EP1838718B1 (de) 2011-06-15
RS51891B (sr) 2012-02-29
IL184275A0 (en) 2007-10-31
EP1838718A1 (de) 2007-10-03

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