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DK1838718T3 - Pyrrolopyrazoler, potente kinase inhibitorer - Google Patents

Pyrrolopyrazoler, potente kinase inhibitorer

Info

Publication number
DK1838718T3
DK1838718T3 DK05850734.4T DK05850734T DK1838718T3 DK 1838718 T3 DK1838718 T3 DK 1838718T3 DK 05850734 T DK05850734 T DK 05850734T DK 1838718 T3 DK1838718 T3 DK 1838718T3
Authority
DK
Denmark
Prior art keywords
pyrrolopyrazoles
kinase inhibitors
potent kinase
potent
inhibitors
Prior art date
Application number
DK05850734.4T
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 DK1838718T3 publication Critical patent/DK1838718T3/da

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)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (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)
DK05850734.4T 2005-01-10 2005-12-28 Pyrrolopyrazoler, potente kinase inhibitorer DK1838718T3 (da)

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
DK1838718T3 true DK1838718T3 (da) 2011-07-25

Family

ID=36463340

Family Applications (1)

Application Number Title Priority Date Filing Date
DK05850734.4T DK1838718T3 (da) 2005-01-10 2005-12-28 Pyrrolopyrazoler, potente kinase inhibitorer

Country Status (29)

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

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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
UA96618C2 (en) * 2007-02-07 2011-11-25 Пфайзер Инк. 3-amino-pyrrolo[3,4-c] pyrazole- 5 (1h, 4h, 6h) carbaldehyde derivatives as pkc inhibitors
EP2195321B1 (en) * 2007-04-12 2016-10-19 Pfizer Inc. 3-amido-pyrrolo[3,4-c]pyrazole-5(1h, 4h,6h) carbaldehyde derivatives as inhibitors of protein kinase c
KR20100038108A (ko) * 2007-07-25 2010-04-12 브리스톨-마이어스 스큅 컴퍼니 트리아진 키나제 억제제
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 (en) 2008-07-09 2010-01-20 Vetoquinol S.A. 9-substituted-5-carboxy-oxadiazino-quinolone derivatives, their preparation and their application as anti-bacterials
WO2011044264A2 (en) * 2009-10-06 2011-04-14 Afraxis, Inc. Pyrrolopyrazoles for treating cns disorders
KR101483215B1 (ko) 2010-01-29 2015-01-16 한미약품 주식회사 단백질 키나아제 저해활성을 갖는 비시클릭 헤테로아릴 유도체
EP2640369A1 (en) 2010-11-17 2013-09-25 F.Hoffmann-La Roche Ag Methods of treating tumors
WO2013012918A1 (en) 2011-07-19 2013-01-24 Infinity Pharmaceuticals Inc. Heterocyclic compounds and uses thereof
JP2015511940A (ja) 2012-02-03 2015-04-23 ビーエーエスエフ ソシエタス・ヨーロピアBasf Se 殺菌性ピリミジン化合物
CA2862346A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
WO2013113720A1 (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
WO2013113791A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
WO2013113716A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
WO2013113778A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
WO2013113782A1 (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
EP2825533B1 (en) 2012-03-13 2016-10-19 Basf Se Fungicidal pyrimidine compounds
WO2013135672A1 (en) 2012-03-13 2013-09-19 Basf Se Fungicidal pyrimidine compounds
CN104168898A (zh) * 2012-03-16 2014-11-26 霍夫曼-拉罗奇有限公司 以pak1抑制剂治疗黑色素瘤的方法
JP6186440B2 (ja) 2012-09-19 2017-08-23 ノバルティス アーゲー キナーゼ阻害剤としてのジヒドロピロリジノピリミジン
DK2906555T3 (da) * 2012-10-15 2017-02-06 Pfizer Ireland Pharmaceuticals Fremgangsmåde til fremstilling af voriconazol og analoger deraf
CA2923101A1 (en) 2013-09-16 2015-03-19 Basf Se Fungicidal pyrimidine compounds
WO2015036059A1 (en) 2013-09-16 2015-03-19 Basf Se Fungicidal pyrimidine compounds
EP3236959B1 (en) 2014-12-23 2025-09-24 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (cdk7)
CA2978518C (en) 2015-03-27 2023-11-21 Nathanael S. Gray Inhibitors of cyclin-dependent kinases
CN107735401B (zh) 2015-06-15 2021-08-31 宇部兴产株式会社 取代二氢吡咯并吡唑衍生物
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
AU2016378723B2 (en) 2015-12-22 2021-09-30 SHY Therapeutics LLC Compounds for the treatment of cancer and inflammatory disease
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
JP7258748B2 (ja) 2016-11-22 2023-04-17 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12(cdk12)の阻害剤およびその使用
MA49458A (fr) 2017-06-21 2020-04-29 SHY Therapeutics LLC Composés interagissant avec la superfamille ras destinés à être utilisés dans le traitement de cancers, de maladies inflammatoires, de rasopathies et de maladies fibrotiques
EP3781168A4 (en) * 2018-04-16 2022-10-05 The Regents of the University of California PAK4 INHIBITORS AND METHODS OF USE
WO2020005807A1 (en) 2018-06-25 2020-01-02 Dana-Farber Cancer Institute, Inc. Taire family kinase inhibitors and uses thereof
EP3898609A1 (en) 2018-12-19 2021-10-27 Shy Therapeutics LLC Compounds that interact with the ras superfamily for the treatment of cancers, inflammatory diseases, rasopathies, and fibrotic disease
EP3902542A4 (en) * 2018-12-28 2022-09-07 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 and uses thereof
US20220220480A1 (en) 2019-04-17 2022-07-14 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and compositions for treatment of nlrp3 inflammasome mediated il-1beta dependent disorders
EP4073102A4 (en) 2019-12-12 2024-05-08 Ting Therapeutics LLC Compositions and methods for the prevention and treatment of hearing loss
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
KR20230128085A (ko) * 2020-12-31 2023-09-01 시노허브 파마슈티컬 씨오., 엘티디 플라스민 억제제, 이를 제조하는 방법 및 이의 용도
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
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UA81790C2 (uk) 2002-12-19 2008-02-11 Фармация Италия С.П.А. Заміщені піролопіразольні похідні як інгібітори кінази
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Also Published As

Publication number Publication date
MA29141B1 (fr) 2008-01-02
PT1838718E (pt) 2011-08-17
CU23778B7 (es) 2012-02-15
US8067591B2 (en) 2011-11-29
BRPI0518509A2 (pt) 2008-11-25
HRP20110485T1 (hr) 2011-07-31
NO20073859L (no) 2007-10-03
HK1114380A1 (en) 2008-10-31
US20120264751A1 (en) 2012-10-18
CA2593428A1 (en) 2006-07-13
JP4250195B2 (ja) 2009-04-08
EP1838718A1 (en) 2007-10-03
EA200701257A1 (ru) 2007-12-28
IL184275A0 (en) 2007-10-31
CA2593428C (en) 2012-04-17
EA011815B1 (ru) 2009-06-30
WO2006072831A1 (en) 2006-07-13
PL1838718T3 (pl) 2011-10-31
NZ556273A (en) 2010-01-29
AU2005323797B2 (en) 2009-07-09
KR100919343B1 (ko) 2009-09-25
EP1838718B1 (en) 2011-06-15
US8530652B2 (en) 2013-09-10
US20100222342A1 (en) 2010-09-02
JP2008526826A (ja) 2008-07-24
TNSN07254A1 (en) 2008-12-31
CN101115760B (zh) 2010-11-03
AU2005323797A1 (en) 2006-07-13
SI1838718T1 (sl) 2011-08-31
KR20070096007A (ko) 2007-10-01
MX2007008385A (es) 2007-08-21
ES2365245T3 (es) 2011-09-27
CU20070160A7 (es) 2009-03-16
CN101115760A (zh) 2008-01-30
CY1111752T1 (el) 2015-10-07
AP2007004061A0 (en) 2007-08-31
ZA200705628B (en) 2008-11-26
GEP20094785B (en) 2009-09-25
RS51891B (sr) 2012-02-29
ATE512972T1 (de) 2011-07-15

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