SI1185529T1 - Pirazolobenzodiazepini kot inhibitorji cdk2 - Google Patents

Pirazolobenzodiazepini kot inhibitorji cdk2

Info

Publication number
SI1185529T1
SI1185529T1 SI200030524T SI200030524T SI1185529T1 SI 1185529 T1 SI1185529 T1 SI 1185529T1 SI 200030524 T SI200030524 T SI 200030524T SI 200030524 T SI200030524 T SI 200030524T SI 1185529 T1 SI1185529 T1 SI 1185529T1
Authority
SI
Slovenia
Prior art keywords
pyrazolobenzodiazepines
cdk2 inhibitors
cdk2
inhibitors
Prior art date
Application number
SI200030524T
Other languages
English (en)
Inventor
Qingjie Ding
Jin-Jun Liu
Vincent Stewart Madison
Giacomo Pizzolato
Chung-Chen Wei
Peter Michael Wovkulich
Original Assignee
F. Hoffmann-La Roche Ag
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 F. Hoffmann-La Roche Ag filed Critical F. Hoffmann-La Roche Ag
Publication of SI1185529T1 publication Critical patent/SI1185529T1/sl

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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D243/00Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
    • C07D243/06Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
    • C07D243/10Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D243/141,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
    • C07D243/161,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
    • C07D243/181,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
    • C07D243/22Sulfur atoms

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Oncology (AREA)
  • Urology & Nephrology (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
SI200030524T 1999-04-21 2000-04-14 Pirazolobenzodiazepini kot inhibitorji cdk2 SI1185529T1 (sl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US13037099P 1999-04-21 1999-04-21
PCT/EP2000/003394 WO2000064900A1 (en) 1999-04-21 2000-04-14 Pyrazolobenzodiazepines as cdk2 inhibitors
EP00929360A EP1185529B1 (en) 1999-04-21 2000-04-14 Pyrazolobenzodiazepines as cdk2 inhibitors

Publications (1)

Publication Number Publication Date
SI1185529T1 true SI1185529T1 (sl) 2005-02-28

Family

ID=22444382

Family Applications (1)

Application Number Title Priority Date Filing Date
SI200030524T SI1185529T1 (sl) 1999-04-21 2000-04-14 Pirazolobenzodiazepini kot inhibitorji cdk2

Country Status (33)

Country Link
US (3) US6440959B1 (sl)
EP (1) EP1185529B1 (sl)
JP (1) JP3746680B2 (sl)
KR (1) KR100481757B1 (sl)
CN (2) CN1196703C (sl)
AR (1) AR023542A1 (sl)
AT (1) ATE279413T1 (sl)
AU (1) AU768667B2 (sl)
BR (1) BR0009887A (sl)
CA (1) CA2367704C (sl)
CO (1) CO5170444A1 (sl)
CZ (1) CZ20013738A3 (sl)
DE (1) DE60014893T2 (sl)
DK (1) DK1185529T3 (sl)
ES (1) ES2228522T3 (sl)
HK (1) HK1046278B (sl)
HR (1) HRP20010742A2 (sl)
HU (1) HUP0300318A3 (sl)
IL (1) IL145764A0 (sl)
JO (1) JO2248B1 (sl)
MA (1) MA26782A1 (sl)
NO (1) NO20015065L (sl)
NZ (1) NZ514523A (sl)
PE (1) PE20010054A1 (sl)
PL (1) PL200933B1 (sl)
PT (1) PT1185529E (sl)
RU (1) RU2249593C2 (sl)
SI (1) SI1185529T1 (sl)
TR (1) TR200103016T2 (sl)
TW (1) TW585866B (sl)
WO (1) WO2000064900A1 (sl)
YU (1) YU73101A (sl)
ZA (1) ZA200108016B (sl)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL370176A1 (en) * 2001-11-13 2005-05-16 3-Dimensional Pharmaceuticals, Inc. Substituted 1,4-benzodiazepines and uses thereof for the treatment of cancer
FR2847253B1 (fr) * 2002-11-19 2007-05-18 Aventis Pharma Sa Nouveaux derives de pyridazinones a titre de medicaments et compositions pharmaceutiques les renfermant
BRPI0407841A (pt) * 2003-02-27 2006-11-14 Abbott Lab inibidores heterocìclicos de quinase
BRPI0518152A (pt) * 2004-10-13 2008-11-04 Hoffmann La Roche pirazolbenzodiazepinas dissubstituìdas úteis como inibidores para cdk2 e angiogênese e para o tratamento de cánceres de mama, cólon, pulmão e próstata
CA2624025A1 (en) * 2005-10-14 2007-04-19 F. Hoffmann-La Roche Ag Regimen of administration for 5-(2-chlorophenyl)-1 ,2-dihydro-7-fluoro-8-methoxy-3-methyl-pyrazolo [3, 4.-b] [1, 4] benzodiazepine
CA2657347C (en) 2006-07-10 2014-11-18 Paion Uk Limited Short-acting benzodiazepine salts and their polymorphic forms
KR20100073454A (ko) * 2008-12-23 2010-07-01 국립암센터 트란스글루타미나제 억제제로 사용되는 신규한 피라졸로디아제핀계 화합물, 이의 제조방법 및 이를 포함하는 조성물
EP2305647A1 (en) 2009-09-18 2011-04-06 PAION UK Limited Process for preparing 3-[(4S)-8-bromo-1-methyl-6-(2-pyridinyl)-4 H-imidazo[1,2-a][1,4]benzodiazepine-4-yl] propionic acid methyl ester or the benzene sulfonate salt thereof, and compounds useful in that process
EP2450039A1 (en) 2010-11-08 2012-05-09 PAION UK Ltd. Dosing regimen for sedation with CNS 7056 (Remimazolam)
UA117342C2 (uk) * 2012-02-02 2018-07-25 Сенекс Біотекнолоджи Інк. Селективні інгібітори cdk8/cdk19 та їх застосування як протиметастатичних та хіміопрофілактичних засобів у способах лікування раку
CN103288830A (zh) * 2012-02-24 2013-09-11 中国科学院大连化学物理研究所 一种合成手性二氢-5H-吡咯并[2,1-c][1,4]-苯并二氮杂卓的方法
CN103288828A (zh) * 2012-02-24 2013-09-11 中国科学院大连化学物理研究所 一种合成手性二氢-6H-吲哚并[2,1-c][1,4]-苯并二氮杂卓的方法
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
AR094963A1 (es) 2013-03-04 2015-09-09 Ono Pharmaceutical Co Reacción de oxidación excelente en el índice de conversión
CN106608877B (zh) * 2015-10-21 2018-11-13 新发药业有限公司 一种依鲁替尼中间体4-氨基-3-(4-苯氧基)苯基-1H-吡唑并[3,4-d]嘧啶的制备方法
CN109906220A (zh) * 2016-11-01 2019-06-18 豪夫迈·罗氏有限公司 用于治疗cns相关疾病的1,3-二氢-1,4-苯并二氮杂*-2-硫酮化合物
WO2018108079A1 (zh) 2016-12-13 2018-06-21 南京药捷安康生物科技有限公司 多激酶抑制剂化合物、其晶型及用途
CN109020980B (zh) * 2017-06-09 2020-11-20 华东师范大学 一类抗肿瘤作用的吡唑并嘧啶二氮*衍生物
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
US11384083B2 (en) 2019-02-15 2022-07-12 Incyte Corporation Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors
US11472791B2 (en) 2019-03-05 2022-10-18 Incyte Corporation Pyrazolyl pyrimidinylamine compounds as CDK2 inhibitors
WO2020205560A1 (en) 2019-03-29 2020-10-08 Incyte Corporation Sulfonylamide compounds as cdk2 inhibitors
WO2020223469A1 (en) 2019-05-01 2020-11-05 Incyte Corporation N-(1-(methylsulfonyl)piperidin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine derivatives and related compounds as cyclin-dependent kinase 2 (cdk2) inhibitors for treating cancer
WO2020223558A1 (en) * 2019-05-01 2020-11-05 Incyte Corporation Tricyclic amine compounds as cdk2 inhibitors
AU2020328025A1 (en) 2019-08-14 2022-03-03 Incyte Corporation Imidazolyl pyrimidinylamine compounds as CDK2 inhibitors
KR20220099970A (ko) 2019-10-11 2022-07-14 인사이트 코포레이션 Cdk2 억제제로서의 이환식 아민
KR20230008792A (ko) * 2020-05-08 2023-01-16 트랜스테라 사이언시즈 (난징), 인크. 항종양 화합물의 합성방법 및 그 중간체
WO2022113003A1 (en) 2020-11-27 2022-06-02 Rhizen Pharmaceuticals Ag Cdk inhibitors
WO2022149057A1 (en) 2021-01-05 2022-07-14 Rhizen Pharmaceuticals Ag Cdk inhibitors
BR112023023223A2 (pt) 2021-05-07 2024-01-30 Kymera Therapeutics Inc Degradadores de cdk2 e usos dos mesmos
TW202304427A (zh) * 2021-05-10 2023-02-01 大陸商藥捷安康(南京)科技股份有限公司 多激酶抑制劑的藥物組合物及其用途
US11981671B2 (en) 2021-06-21 2024-05-14 Incyte Corporation Bicyclic pyrazolyl amines as CDK2 inhibitors
US11976073B2 (en) 2021-12-10 2024-05-07 Incyte Corporation Bicyclic amines as CDK2 inhibitors
WO2024030399A2 (en) * 2022-08-02 2024-02-08 Lab1636, Llc Use of a gaba-a pam for reduction of tactile hypersensitivity

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE291022T1 (de) 1996-10-02 2005-04-15 Novartis Pharma Gmbh Pyrimiderivate und verfahren zu ihrer herstellung
US6350786B1 (en) * 1998-09-22 2002-02-26 Hoffmann-La Roche Inc. Stable complexes of poorly soluble compounds in ionic polymers

Also Published As

Publication number Publication date
ATE279413T1 (de) 2004-10-15
CZ20013738A3 (cs) 2002-08-14
HK1046278A1 (en) 2003-01-03
TW585866B (en) 2004-05-01
PT1185529E (pt) 2005-02-28
DE60014893T2 (de) 2005-10-13
US20020183514A1 (en) 2002-12-05
DK1185529T3 (da) 2005-02-07
HK1046278B (zh) 2005-08-12
CN1348455A (zh) 2002-05-08
CA2367704C (en) 2008-06-17
CO5170444A1 (es) 2002-06-27
WO2000064900A1 (en) 2000-11-02
US6838558B2 (en) 2005-01-04
US20040198976A1 (en) 2004-10-07
YU73101A (sh) 2004-05-12
CN1279029C (zh) 2006-10-11
EP1185529A1 (en) 2002-03-13
IL145764A0 (en) 2002-07-25
JO2248B1 (en) 2004-10-07
DE60014893D1 (de) 2004-11-18
CN1196703C (zh) 2005-04-13
PL354405A1 (en) 2004-01-12
CN1603314A (zh) 2005-04-06
PE20010054A1 (es) 2001-02-07
MA26782A1 (fr) 2004-12-20
NZ514523A (en) 2003-11-28
EP1185529B1 (en) 2004-10-13
US6916923B2 (en) 2005-07-12
KR100481757B1 (ko) 2005-04-11
NO20015065D0 (no) 2001-10-18
HUP0300318A2 (hu) 2003-06-28
HUP0300318A3 (en) 2004-11-29
AU4748000A (en) 2000-11-10
KR20010112435A (ko) 2001-12-20
AU768667B2 (en) 2003-12-18
RU2249593C2 (ru) 2005-04-10
TR200103016T2 (tr) 2002-04-22
JP2002543081A (ja) 2002-12-17
NO20015065L (no) 2001-10-18
JP3746680B2 (ja) 2006-02-15
HRP20010742A2 (en) 2002-12-31
ES2228522T3 (es) 2005-04-16
PL200933B1 (pl) 2009-02-27
BR0009887A (pt) 2002-01-22
CA2367704A1 (en) 2000-11-02
ZA200108016B (en) 2003-03-26
AR023542A1 (es) 2002-09-04
US6440959B1 (en) 2002-08-27

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