PL1802625T3 - Dwupodstawione pirazolobenzodiazepiny użyteczne jako inhibitory CDK2 i angiogenezy oraz w leczeniu raka sutka, okrężnicy, płuca i gruczołu krokowego - Google Patents

Dwupodstawione pirazolobenzodiazepiny użyteczne jako inhibitory CDK2 i angiogenezy oraz w leczeniu raka sutka, okrężnicy, płuca i gruczołu krokowego

Info

Publication number
PL1802625T3
PL1802625T3 PL05792946T PL05792946T PL1802625T3 PL 1802625 T3 PL1802625 T3 PL 1802625T3 PL 05792946 T PL05792946 T PL 05792946T PL 05792946 T PL05792946 T PL 05792946T PL 1802625 T3 PL1802625 T3 PL 1802625T3
Authority
PL
Poland
Prior art keywords
angiogesis
cdk2
colon
breast
lung
Prior art date
Application number
PL05792946T
Other languages
English (en)
Inventor
Jin-Jun Liu
Kin-Chun Luk
Giacomo Pizzolato
Yi Ren
Kshitij Chhabilbhai Thakkar
Peter Michael Wovkulich
Zhuming Zhang
Original Assignee
Hoffmann La Roche
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35311946&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PL1802625(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PL1802625T3 publication Critical patent/PL1802625T3/pl

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
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
    • A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system

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)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
PL05792946T 2004-10-13 2005-10-04 Dwupodstawione pirazolobenzodiazepiny użyteczne jako inhibitory CDK2 i angiogenezy oraz w leczeniu raka sutka, okrężnicy, płuca i gruczołu krokowego PL1802625T3 (pl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US61817404P 2004-10-13 2004-10-13
PCT/EP2005/010653 WO2006040036A1 (en) 2004-10-13 2005-10-04 Disubstituted pyrazolobenzodiazepines useful as inhibitors for cdk2 and angiogesis, and for the treatment of breast, colon, lung and prostate cancer
EP05792946A EP1802625B1 (en) 2004-10-13 2005-10-04 Disubstituted pyrazolobenzodiazepines useful as inhibitors for cdk2 and angiogesis, and for the treatment of breast, colon, lung and prostate cancer

Publications (1)

Publication Number Publication Date
PL1802625T3 true PL1802625T3 (pl) 2008-12-31

Family

ID=35311946

Family Applications (1)

Application Number Title Priority Date Filing Date
PL05792946T PL1802625T3 (pl) 2004-10-13 2005-10-04 Dwupodstawione pirazolobenzodiazepiny użyteczne jako inhibitory CDK2 i angiogenezy oraz w leczeniu raka sutka, okrężnicy, płuca i gruczołu krokowego

Country Status (25)

Country Link
US (1) US7524840B2 (pl)
EP (1) EP1802625B1 (pl)
JP (1) JP2008515939A (pl)
KR (1) KR100858262B1 (pl)
CN (2) CN101899049A (pl)
AR (1) AR051326A1 (pl)
AT (1) ATE398619T1 (pl)
AU (1) AU2005293818A1 (pl)
BR (1) BRPI0518152A (pl)
CA (1) CA2582985A1 (pl)
DE (1) DE602005007623D1 (pl)
DK (1) DK1802625T3 (pl)
ES (1) ES2308551T3 (pl)
HR (1) HRP20080429T3 (pl)
IL (1) IL182423A0 (pl)
MX (1) MX2007004464A (pl)
NO (1) NO20071794L (pl)
NZ (1) NZ554353A (pl)
PL (1) PL1802625T3 (pl)
PT (1) PT1802625E (pl)
RU (1) RU2394826C2 (pl)
SI (1) SI1802625T1 (pl)
TW (1) TWI309652B (pl)
WO (1) WO2006040036A1 (pl)
ZA (1) ZA200702973B (pl)

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BRPI1012108B8 (pt) 2009-05-22 2021-05-25 Incyte Corp composto 3-[4-(7h-pirrolo[2,3-d]pirimidin-4-il)-1h-pirazol-1-il]octa no- ou heptano-nitrila, sua composição, seus usos e processo para preparar um sal de ácido fosfórico
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TW201113285A (en) * 2009-09-01 2011-04-16 Incyte Corp Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors
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EA202091303A3 (ru) 2010-05-21 2021-05-31 Инсайт Холдингс Корпорейшн Композиция ингибитора jak для местного применения
ES2536415T3 (es) 2010-11-19 2015-05-25 Incyte Corporation Pirrolopiridinas y pirrolopirimidinas sustituidas heterocíclicas como inhibidores de JAK
CA2818542A1 (en) 2010-11-19 2012-05-24 Incyte Corporation Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors
US8691807B2 (en) 2011-06-20 2014-04-08 Incyte Corporation Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as JAK inhibitors
TW201313721A (zh) 2011-08-18 2013-04-01 Incyte Corp 作為jak抑制劑之環己基氮雜環丁烷衍生物
UA111854C2 (uk) 2011-09-07 2016-06-24 Інсайт Холдінгс Корпорейшн Способи і проміжні сполуки для отримання інгібіторів jak
CN102603743B (zh) * 2012-02-24 2014-05-28 南京天易生物科技有限公司 抗肿瘤的氮杂苯并[f]薁衍生物其制备方法及其用途
TW201406761A (zh) 2012-05-18 2014-02-16 Incyte Corp 做爲jak抑制劑之哌啶基環丁基取代之吡咯并吡啶及吡咯并嘧啶衍生物
CN103626761B (zh) * 2012-08-24 2015-07-29 上海医药工业研究院 苯并吡啶氮杂卓类化合物及其作为抗肿瘤药物的应用
KR102242077B1 (ko) 2012-11-15 2021-04-20 인사이트 홀딩스 코포레이션 룩솔리티니브의 서방성 제형
EP3489239B1 (en) 2013-03-06 2021-09-15 Incyte Holdings Corporation Processes and intermediates for making a jak inhibitor
MX376856B (es) 2013-08-07 2025-03-07 Incyte Holdings Corp Formas de dosificacion de liberacion prolongada para un inhibidor de jak 1 (cinasa de janus 1).
WO2015184305A1 (en) 2014-05-30 2015-12-03 Incyte Corporation TREATMENT OF CHRONIC NEUTROPHILIC LEUKEMIA (CNL) AND ATYPICAL CHRONIC MYELOID LEUKEMIA (aCML) BY INHIBITORS OF JAK1
HUE050567T2 (hu) 2015-09-23 2020-12-28 Janssen Pharmaceutica Nv Triciklusos heterociklusok rák kezelésére
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CN106928040A (zh) * 2015-12-31 2017-07-07 上海医药工业研究院 Sglt2抑制剂中间体的制备方法
RU2019120162A (ru) * 2016-12-12 2021-01-12 Де Юниверсити Оф Сидней Непептидные агонисты рецепторов окситоцина
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TW201924683A (zh) 2017-12-08 2019-07-01 美商英塞特公司 用於治療骨髓增生性贅瘤的低劑量組合療法
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Also Published As

Publication number Publication date
RU2394826C2 (ru) 2010-07-20
TWI309652B (en) 2009-05-11
US7524840B2 (en) 2009-04-28
MX2007004464A (es) 2007-05-07
TW200628469A (en) 2006-08-16
SI1802625T1 (sl) 2008-10-31
CA2582985A1 (en) 2006-04-20
NO20071794L (no) 2007-07-10
WO2006040036A1 (en) 2006-04-20
HRP20080429T3 (en) 2008-09-30
CN101899049A (zh) 2010-12-01
AR051326A1 (es) 2007-01-03
ES2308551T3 (es) 2008-12-01
NZ554353A (en) 2010-01-29
PT1802625E (pt) 2008-08-06
ATE398619T1 (de) 2008-07-15
EP1802625A1 (en) 2007-07-04
KR20070054243A (ko) 2007-05-28
KR100858262B1 (ko) 2008-09-11
BRPI0518152A (pt) 2008-11-04
RU2007117770A (ru) 2008-11-20
CN101039946B (zh) 2010-12-08
DK1802625T3 (da) 2008-09-01
EP1802625B1 (en) 2008-06-18
CN101039946A (zh) 2007-09-19
IL182423A0 (en) 2007-07-24
US20060079511A1 (en) 2006-04-13
AU2005293818A1 (en) 2006-04-20
DE602005007623D1 (de) 2008-07-31
HK1108284A1 (en) 2008-05-02
JP2008515939A (ja) 2008-05-15
ZA200702973B (en) 2009-09-30

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