MA29141B1 - Pyrrolopyrazoles, servant de puissants inhibiteurs de kinases - Google Patents

Pyrrolopyrazoles, servant de puissants inhibiteurs de kinases

Info

Publication number
MA29141B1
MA29141B1 MA30059A MA30059A MA29141B1 MA 29141 B1 MA29141 B1 MA 29141B1 MA 30059 A MA30059 A MA 30059A MA 30059 A MA30059 A MA 30059A MA 29141 B1 MA29141 B1 MA 29141B1
Authority
MA
Morocco
Prior art keywords
kinases
pyrrolopyrazoles
inhibitors
powerful inhibitors
compounds
Prior art date
Application number
MA30059A
Other languages
English (en)
Inventor
Djamal Bouzida
Liming Dong
Chuangxing Guo
Yufeng Hong
Haitao Li
Joseph Timothy 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
Publication of MA29141B1 publication Critical patent/MA29141B1/fr

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
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/4353—Heterocyclic 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
    • A61K31/437—Heterocyclic 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
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Abstract

L'INVENTION DES COMPOSÉS DE PYRROLOPYRAZOLES DE FORMULE (I), DES COMPOSITIONS COMPRENANT LESDITS COMPOSÉS, AINSI QUE LEURS MÉTHODES D'UTILISATION. LES COMPOSÉS PRÉFÉRÉS DE FORMULE I PRÉSENTENT UNE ACTIVITÉ EN TANT QU'INHIBITEURS DE PROTÉINES KINASES, NOTAMMENT EN TANT QU'INHIBITEURS DE PAK4.
MA30059A 2005-01-10 2007-07-10 Pyrrolopyrazoles, servant de puissants inhibiteurs de kinases MA29141B1 (fr)

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 (1)

Publication Number Publication Date
MA29141B1 true MA29141B1 (fr) 2008-01-02

Family

ID=36463340

Family Applications (1)

Application Number Title Priority Date Filing Date
MA30059A MA29141B1 (fr) 2005-01-10 2007-07-10 Pyrrolopyrazoles, servant de puissants inhibiteurs de kinases

Country Status (30)

Country Link
US (2) US8067591B2 (fr)
EP (1) EP1838718B1 (fr)
JP (1) JP4250195B2 (fr)
KR (1) KR100919343B1 (fr)
CN (1) CN101115760B (fr)
AP (1) AP2007004061A0 (fr)
AT (1) ATE512972T1 (fr)
AU (1) AU2005323797B2 (fr)
BR (1) BRPI0518509A2 (fr)
CA (1) CA2593428C (fr)
CU (1) CU23778B7 (fr)
CY (1) CY1111752T1 (fr)
DK (1) DK1838718T3 (fr)
EA (1) EA011815B1 (fr)
ES (1) ES2365245T3 (fr)
GE (1) GEP20094785B (fr)
HK (1) HK1114380A1 (fr)
HR (1) HRP20110485T1 (fr)
IL (1) IL184275A0 (fr)
MA (1) MA29141B1 (fr)
MX (1) MX2007008385A (fr)
NO (1) NO20073859L (fr)
NZ (1) NZ556273A (fr)
PL (1) PL1838718T3 (fr)
PT (1) PT1838718E (fr)
RS (1) RS51891B (fr)
SI (1) SI1838718T1 (fr)
TN (1) TNSN07254A1 (fr)
WO (1) WO2006072831A1 (fr)
ZA (1) ZA200705628B (fr)

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AP2369A (en) 2005-12-21 2012-02-29 Pfizer Prod Inc Carbonylamino pyrrolopyrazoles, potent kinase inhibitors.
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MX2009008546A (es) 2007-02-07 2009-10-08 Pfizer Derivados de 3-amino-pirrolo[3,4-c]pirazol-5(1h,4h,6h)carbaldehido como inhibidores de la proteina quinasa c.
JP5404601B2 (ja) 2007-04-12 2014-02-05 ファイザー・インク 新規な３−アミド−ピロロ［３，４−ｃ］ピラゾール−５（１Ｈ，４Ｈ，６Ｈ）カルバルデヒド誘導体
EP2175933B1 (fr) * 2007-07-25 2012-08-22 Bristol-Myers Squibb Company Inhibiteurs de triazine kinase
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 (fr) 2008-07-09 2010-01-20 Vetoquinol S.A. Dérivés de 9-substitués-5-carboxy-oxadiazino-quinolone, leur préparation et leur application en tant qu'antibactériens
EP2485727A4 (fr) * 2009-10-06 2013-05-01 Afraxis Inc Pyrrolopyrazoles pour le traitement de troubles du snc
KR101483215B1 (ko) * 2010-01-29 2015-01-16 한미약품 주식회사 단백질 키나아제 저해활성을 갖는 비시클릭 헤테로아릴 유도체
RU2013126036A (ru) 2010-11-17 2014-12-27 Ф. Хоффманн-Ля Рош Аг Способ лечения опухолей
CA2842190A1 (fr) 2011-07-19 2013-01-24 Infinity Pharmaceuticals Inc. Composes heterocycliques et leurs utilisations
EP2809659A1 (fr) 2012-02-03 2014-12-10 Basf Se Composés de pyrimidine fongicides
WO2013113778A1 (fr) 2012-02-03 2013-08-08 Basf Se Composés de pyrimidine fongicides
WO2013113773A1 (fr) 2012-02-03 2013-08-08 Basf Se Composés fongicides de pyrimidine
WO2013113776A1 (fr) 2012-02-03 2013-08-08 Basf Se Composés de pyrimidine fongicides
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
WO2013113782A1 (fr) 2012-02-03 2013-08-08 Basf Se Composés de pyrimidine fongicides
WO2013113781A1 (fr) 2012-02-03 2013-08-08 Basf Se Composés de pyrimidine fongicides i
WO2013113716A1 (fr) 2012-02-03 2013-08-08 Basf Se Composés de pyrimidine fongicides
WO2013113788A1 (fr) 2012-02-03 2013-08-08 Basf Se Composés de pyrimidine fongicides
WO2013113720A1 (fr) 2012-02-03 2013-08-08 Basf Se Composés de pyrimidine fongicides
WO2013113719A1 (fr) 2012-02-03 2013-08-08 Basf Se Composés de pyrimidine fongicides ii
US9462809B2 (en) 2012-03-13 2016-10-11 Basf Se Fungicidal pyrimidine compounds
WO2013135672A1 (fr) 2012-03-13 2013-09-19 Basf Se Composés de pyrimidine fongicides
WO2013135745A1 (fr) 2012-03-16 2013-09-19 F. Hoffmann-La Roche Ag Procédés de traitement d'un mélanome avec des inhibiteurs de pak1
CN104640865B (zh) 2012-09-19 2018-05-11 诺华股份有限公司 作为激酶抑制剂的二氢吡咯烷子基-嘧啶
ES2615743T3 (es) * 2012-10-15 2017-06-08 Pfizer Ireland Pharmaceuticals Procedimiento de preparación de voriconazol y análogos de los mismos
WO2015036059A1 (fr) 2013-09-16 2015-03-19 Basf Se Composés fongicides de pyrimidine
CN105722833A (zh) 2013-09-16 2016-06-29 巴斯夫欧洲公司 杀真菌的嘧啶化合物
RU2765718C1 (ru) * 2015-06-15 2022-02-02 Убе Индастриз, Лтд. Замещенное производное дигидропирролопиразола
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
CA3008171A1 (fr) 2015-12-22 2017-06-29 SHY Therapeutics LLC Composes pour le traitement du cancer et de maladies inflammatoires
WO2017144546A1 (fr) 2016-02-23 2017-08-31 INSERM (Institut National de la Santé et de la Recherche Médicale) Méthodes et compositions pharmaceutiques pour le traitement d'un carcinome de rhinopharyngite
CA3041563C (fr) 2016-11-22 2023-10-31 Dana-Farber Cancer Institute, Inc. Derives de pyrimidine-2-amine et compositions pharmaceutiques connexes utiles comme inhibiteurs de kinase 12 dependante des cyclines (cdk12)
IL310023A (en) 2017-06-21 2024-03-01 SHY Therapeutics LLC Compounds interacting with the RAS superfamily for the treatment of cancer, inflammation, RAS pathology and fibrotic diseases
US20210161943A1 (en) * 2018-04-16 2021-06-03 The Regents Of The University Of California Pak4 inhibitors and methods of use
EP3956446A1 (fr) 2019-04-17 2022-02-23 INSERM (Institut National de la Santé et de la Recherche Médicale) Procédés et compositions de traitement de troubles dépendants de il-1beta mediés par inflamasome nlrp3
WO2021198511A1 (fr) 2020-04-03 2021-10-07 INSERM (Institut National de la Santé et de la Recherche Médicale) Méthodes et compositions pour le traitement d'une infection par sars-cov-2
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 (fr) 2020-07-08 2022-01-13 INSERM (Institut National de la Santé et de la Recherche Médicale) Méthodes et composition pharmaceutique pour le traitement de maladies infectieuses
JP2024507433A (ja) * 2020-12-31 2024-02-20 シノハブ ファーマシューティカルズ カンパニー リミテッド プラスミン阻害剤、そのための調製方法及びその応用

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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
JPS5163193A (ja) 1974-11-26 1976-06-01 Yoshitomi Pharmaceutical Tetorahidoropirazoropirijinkagobutsuno seizoho
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
EA006381B1 (ru) 2000-08-10 2005-12-29 Фармация Италия С.П.А. Бициклопиразолы, активные в качестве ингибиторов киназы, способ их получения и включающие их фармацевтические композиции
JP2005537290A (ja) * 2002-07-25 2005-12-08 ファルマシア・イタリア・エス・ピー・エー キナーゼ阻害剤として活性なビシクロピラゾール類、その製造方法、およびそれを含有する薬学的組成物
UA81790C2 (uk) 2002-12-19 2008-02-11 Фармация Италия С.П.А. Заміщені піролопіразольні похідні як інгібітори кінази
US7141568B2 (en) 2003-07-09 2006-11-28 Pfizer Italia S.R.L. Pyrrolo[3,4-c]pyrazole derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them

Also Published As

Publication number Publication date
AU2005323797A1 (en) 2006-07-13
US20120264751A1 (en) 2012-10-18
AU2005323797B2 (en) 2009-07-09
HRP20110485T1 (hr) 2011-07-31
NZ556273A (en) 2010-01-29
AP2007004061A0 (en) 2007-08-31
EA200701257A1 (ru) 2007-12-28
US8530652B2 (en) 2013-09-10
US8067591B2 (en) 2011-11-29
TNSN07254A1 (en) 2008-12-31
KR100919343B1 (ko) 2009-09-25
NO20073859L (no) 2007-10-03
EP1838718A1 (fr) 2007-10-03
BRPI0518509A2 (pt) 2008-11-25
CA2593428A1 (fr) 2006-07-13
CN101115760A (zh) 2008-01-30
CU23778B7 (es) 2012-02-15
KR20070096007A (ko) 2007-10-01
HK1114380A1 (en) 2008-10-31
EA011815B1 (ru) 2009-06-30
ATE512972T1 (de) 2011-07-15
PL1838718T3 (pl) 2011-10-31
CU20070160A7 (es) 2009-03-16
EP1838718B1 (fr) 2011-06-15
IL184275A0 (en) 2007-10-31
US20100222342A1 (en) 2010-09-02
ES2365245T3 (es) 2011-09-27
SI1838718T1 (sl) 2011-08-31
MX2007008385A (es) 2007-08-21
JP4250195B2 (ja) 2009-04-08
DK1838718T3 (da) 2011-07-25
CN101115760B (zh) 2010-11-03
RS51891B (en) 2012-02-29
ZA200705628B (en) 2008-11-26
GEP20094785B (en) 2009-09-25
CY1111752T1 (el) 2015-10-07
CA2593428C (fr) 2012-04-17
JP2008526826A (ja) 2008-07-24
PT1838718E (pt) 2011-08-17
WO2006072831A1 (fr) 2006-07-13

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