ATE279413T1 - Pyrazolobenzodiazepine mit cdk2 hemmender wirkung - Google Patents

Pyrazolobenzodiazepine mit cdk2 hemmender wirkung

Info

Publication number
ATE279413T1
ATE279413T1 AT00929360T AT00929360T ATE279413T1 AT E279413 T1 ATE279413 T1 AT E279413T1 AT 00929360 T AT00929360 T AT 00929360T AT 00929360 T AT00929360 T AT 00929360T AT E279413 T1 ATE279413 T1 AT E279413T1
Authority
AT
Austria
Prior art keywords
pyrazolobenzodiazepines
inhibiting effect
cdk2
cdk2 inhibiting
effect
Prior art date
Application number
AT00929360T
Other languages
English (en)
Inventor
Qingjie Ding
Jin-Jun Liu
Vincent Stewart Madison
Giacomo Pizzolato
Chung-Chen Wei
Peter Michael Wovkulich
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
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Application granted granted Critical
Publication of ATE279413T1 publication Critical patent/ATE279413T1/de

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
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/08—Drugs for disorders of the urinary system of the prostate
    • 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
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
    • C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
    • C07D243/10—Heterocyclic 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
    • C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
    • C07D243/16—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
    • C07D243/18—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
    • C07D243/22—Sulfur 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)
AT00929360T 1999-04-21 2000-04-14 Pyrazolobenzodiazepine mit cdk2 hemmender wirkung ATE279413T1 (de)

Applications Claiming Priority (2)

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

Publications (1)

Publication Number Publication Date
ATE279413T1 true ATE279413T1 (de) 2004-10-15

Family

ID=22444382

Family Applications (1)

Application Number Title Priority Date Filing Date
AT00929360T ATE279413T1 (de) 1999-04-21 2000-04-14 Pyrazolobenzodiazepine mit cdk2 hemmender wirkung

Country Status (33)

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

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HUP0402003A3 (en) * 2001-11-13 2005-06-28 Dimensional Pharm Inc Substituted 1,4-benzodiazepines, pharmaceutical compositions containing them and uses thereof
FR2847253B1 (fr) * 2002-11-19 2007-05-18 Aventis Pharma Sa Nouveaux derives de pyridazinones a titre de medicaments et compositions pharmaceutiques les renfermant
EP1606268B1 (de) * 2003-02-27 2015-05-20 AbbVie Inc. 5,10-dihydro-11h-dibenzo[b,e][1,4]diazepin-11-on verbindungen als kinase inhibitoren
DK1802625T3 (da) * 2004-10-13 2008-09-01 Hoffmann La Roche Disubstituerede pyrazolobenzodiazepiner der er nyttige som inhibitorer af CDK2 og angiogenese og til behandling af bryst-, tyktarms-, lunge- og prostatacancer
WO2007042430A1 (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
PL2081921T3 (pl) 2006-07-10 2011-03-31 Paion Uk Ltd Krótko działające sole benzodiazepiny i ich formy polimorficzne
KR20100073454A (ko) * 2008-12-23 2010-07-01 국립암센터 트란스글루타미나제 억제제로 사용되는 신규한 피라졸로디아제핀계 화합물, 이의 제조방법 및 이를 포함하는 조성물
EP2305647A1 (de) * 2009-09-18 2011-04-06 PAION UK Limited Verfahren zur Herstellung von 3-[(4S)-8-brom-1-methyl-6-(2-pyridinyl)-4 H-imidazo[1,2-a][1,4]benzodiazepin-4-yl]propionsäuremethylester oder das Benzensulfonatsalz davon und in diesem Prozess nützliche Verbindungen
EP2450039A1 (de) 2010-11-08 2012-05-09 PAION UK Ltd. Dosierschema zur Sedierung mit 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
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
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
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
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
JP7139323B2 (ja) * 2016-11-01 2022-09-20 エフ．ホフマン－ラ ロシュ アーゲー Ｃｎｓ関連疾患を処置するための１，３－ジヒドロ－１，４－ベンゾジアゼピン－２－チオン
JP6594571B2 (ja) * 2016-12-13 2019-10-23 南京薬捷安康生物科技有限公司 マルチキナーゼ阻害剤化合物、並びにその結晶形及びその使用
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
TW202100520A (zh) 2019-03-05 2021-01-01 美商英塞特公司 作為cdk2 抑制劑之吡唑基嘧啶基胺化合物
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
CR20220066A (es) 2019-08-14 2022-11-28 Incyte Corp Compuestos de imidazolil pirimidinilamina como inhibidores de cdk2
CN115298177A (zh) 2019-10-11 2022-11-04 因赛特公司 作为cdk2抑制剂的双环胺
JP2023525732A (ja) * 2020-05-08 2023-06-19 薬捷安康（南京）科技股▲分▼有限公司 抗腫瘍化合物の合成方法及びその中間体
TW202237585A (zh) 2020-11-27 2022-10-01 瑞士商瑞森製藥公司 Ｃｄｋ抑制劑
WO2022149057A1 (en) 2021-01-05 2022-07-14 Rhizen Pharmaceuticals Ag Cdk inhibitors
WO2022237765A1 (zh) * 2021-05-10 2022-11-17 药捷安康(南京)科技股份有限公司 多激酶抑制剂的药物组合物及其用途
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
DE69732780T2 (de) 1996-10-02 2006-04-06 Novartis Ag 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
US20020183514A1 (en) 2002-12-05
TR200103016T2 (tr) 2002-04-22
PT1185529E (pt) 2005-02-28
JP2002543081A (ja) 2002-12-17
AU768667B2 (en) 2003-12-18
KR100481757B1 (ko) 2005-04-11
TW585866B (en) 2004-05-01
PE20010054A1 (es) 2001-02-07
HK1046278B (zh) 2005-08-12
SI1185529T1 (en) 2005-02-28
KR20010112435A (ko) 2001-12-20
DE60014893T2 (de) 2005-10-13
US20040198976A1 (en) 2004-10-07
CZ20013738A3 (cs) 2002-08-14
JP3746680B2 (ja) 2006-02-15
CN1196703C (zh) 2005-04-13
AR023542A1 (es) 2002-09-04
NO20015065D0 (no) 2001-10-18
IL145764A0 (en) 2002-07-25
MA26782A1 (fr) 2004-12-20
JO2248B1 (en) 2004-10-07
ZA200108016B (en) 2003-03-26
BR0009887A (pt) 2002-01-22
CA2367704A1 (en) 2000-11-02
EP1185529B1 (de) 2004-10-13
CN1279029C (zh) 2006-10-11
NO20015065L (no) 2001-10-18
HK1046278A1 (en) 2003-01-03
CN1603314A (zh) 2005-04-06
HRP20010742A2 (en) 2002-12-31
HUP0300318A3 (en) 2004-11-29
YU73101A (sh) 2004-05-12
AU4748000A (en) 2000-11-10
US6440959B1 (en) 2002-08-27
CO5170444A1 (es) 2002-06-27
WO2000064900A1 (en) 2000-11-02
ES2228522T3 (es) 2005-04-16
DE60014893D1 (de) 2004-11-18
DK1185529T3 (da) 2005-02-07
RU2249593C2 (ru) 2005-04-10
EP1185529A1 (de) 2002-03-13
CA2367704C (en) 2008-06-17
PL354405A1 (en) 2004-01-12
US6838558B2 (en) 2005-01-04
US6916923B2 (en) 2005-07-12
HUP0300318A2 (hu) 2003-06-28
PL200933B1 (pl) 2009-02-27
CN1348455A (zh) 2002-05-08
NZ514523A (en) 2003-11-28

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