CU20070160A7 - Pirrolopirazoles, inhibidores potentes de quinasa - Google Patents

Pirrolopirazoles, inhibidores potentes de quinasa

Info

Publication number
CU20070160A7
CU20070160A7 CU20070160A CU20070160A CU20070160A7 CU 20070160 A7 CU20070160 A7 CU 20070160A7 CU 20070160 A CU20070160 A CU 20070160A CU 20070160 A CU20070160 A CU 20070160A CU 20070160 A7 CU20070160 A7 CU 20070160A7
Authority
CU
Cuba
Prior art keywords
pirrolopirazoles
powerful
inhibitors
quinasa
quinasa inhibitors
Prior art date
Application number
CU20070160A
Other languages
English (en)
Other versions
CU23778B7 (es
Inventor
Anle Yang
Junhu Zhang
Haitao Li
Chuangxing Guo
Liming Dong
Djamal Bouzida
Yufeng Hong
Joseph Timothy Marakovits
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
Publication of CU20070160A7 publication Critical patent/CU20070160A7/es
Publication of CU23778B7 publication Critical patent/CU23778B7/es

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)

Abstract

Se proporcionan compuestos de pirrolo-pirazol de fórmula I, composiciones que incluyen estos compuestos y procedimientos de su uso. Los compuestos preferidos de fórmula I tienen actividad como inhibidores de proteína cinasa, incluyendo como inhibidores de PAK4.
CU20070160A 2005-01-10 2007-07-09 Pirrolopirazoles, inhibidores potentes de quinasa CU23778B7 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US64290005P 2005-01-10 2005-01-10
US73377005P 2005-11-04 2005-11-04

Publications (2)

Publication Number Publication Date
CU20070160A7 true CU20070160A7 (es) 2009-03-16
CU23778B7 CU23778B7 (es) 2012-02-15

Family

ID=36463340

Family Applications (1)

Application Number Title Priority Date Filing Date
CU20070160A CU23778B7 (es) 2005-01-10 2007-07-09 Pirrolopirazoles, inhibidores potentes de quinasa

Country Status (29)

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

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AU2008237660B2 (en) 2007-04-12 2011-12-22 Pfizer Inc. 3-amido-pyrrolo [3, 4-C] pyrazole-5 (1H, 4H, 6H) carbaldehyde derivatives as inhibitors of protein kinase C
US8415340B2 (en) 2007-07-25 2013-04-09 Bristol-Myers Squibb Company Triazine kinase inhibitors
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AR088218A1 (es) 2011-07-19 2014-05-21 Infinity Pharmaceuticals Inc Compuestos heterociclicos utiles como inhibidores de pi3k
WO2013113720A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
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WO2013113716A1 (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
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WO2013113776A1 (en) 2012-02-03 2013-08-08 Basf Se Fungicidal pyrimidine compounds
AU2013214353A1 (en) 2012-02-03 2014-08-21 Basf Se Fungicidal pyrimidine compounds
WO2013135672A1 (en) 2012-03-13 2013-09-19 Basf Se Fungicidal pyrimidine compounds
EP2825533B1 (en) 2012-03-13 2016-10-19 Basf Se Fungicidal pyrimidine compounds
JP2015511598A (ja) 2012-03-16 2015-04-20 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト Pak1阻害剤を用いて黒色腫を治療する方法
AU2013318283A1 (en) 2012-09-19 2015-03-05 Novartis Ag Dihydropyrrolidino-pyrimidines as kinase inhibitors
IN2015DN02877A (es) * 2012-10-15 2015-09-11 Pfizer Ireland Pharmaceuticals
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
JP6854762B2 (ja) 2014-12-23 2021-04-07 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7(cdk7)の阻害剤
USRE50776E1 (en) 2015-03-27 2026-02-03 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinases
MX394157B (es) 2015-06-15 2025-03-24 Ube Corp Derivado de dihidropirrolopirazol sustituido.
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
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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
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CA3097543A1 (en) * 2018-04-16 2019-10-24 The Regents Of The University Of California Pak4 inhibitors and methods of use
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EP3956446A1 (en) 2019-04-17 2022-02-23 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and compositions for treatment of nlrp3 inflammasome mediated il-1beta dependent disorders
CN118767143A (zh) 2019-12-12 2024-10-15 听治疗有限责任公司 用于预防和治疗听力损失的组合物和方法
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
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Also Published As

Publication number Publication date
AU2005323797B2 (en) 2009-07-09
KR100919343B1 (ko) 2009-09-25
US20100222342A1 (en) 2010-09-02
PT1838718E (pt) 2011-08-17
US8530652B2 (en) 2013-09-10
PL1838718T3 (pl) 2011-10-31
US20120264751A1 (en) 2012-10-18
DK1838718T3 (da) 2011-07-25
IL184275A0 (en) 2007-10-31
CA2593428A1 (en) 2006-07-13
CU23778B7 (es) 2012-02-15
RS51891B (sr) 2012-02-29
AU2005323797A1 (en) 2006-07-13
CA2593428C (en) 2012-04-17
TNSN07254A1 (en) 2008-12-31
HK1114380A1 (en) 2008-10-31
EP1838718A1 (en) 2007-10-03
EP1838718B1 (en) 2011-06-15
JP4250195B2 (ja) 2009-04-08
HRP20110485T1 (hr) 2011-07-31
CN101115760A (zh) 2008-01-30
US8067591B2 (en) 2011-11-29
KR20070096007A (ko) 2007-10-01
ES2365245T3 (es) 2011-09-27
NO20073859L (no) 2007-10-03
CN101115760B (zh) 2010-11-03
EA011815B1 (ru) 2009-06-30
NZ556273A (en) 2010-01-29
ATE512972T1 (de) 2011-07-15
AP2007004061A0 (en) 2007-08-31
MX2007008385A (es) 2007-08-21
GEP20094785B (en) 2009-09-25
ZA200705628B (en) 2008-11-26
WO2006072831A1 (en) 2006-07-13
EA200701257A1 (ru) 2007-12-28
CY1111752T1 (el) 2015-10-07
JP2008526826A (ja) 2008-07-24
MA29141B1 (fr) 2008-01-02
BRPI0518509A2 (pt) 2008-11-25
SI1838718T1 (sl) 2011-08-31

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