HRP20120490T1 - Spojevi za inhibiciju napredovanja mitoze - Google Patents

Spojevi za inhibiciju napredovanja mitoze Download PDF

Info

Publication number
HRP20120490T1
HRP20120490T1 HRP20120490TT HRP20120490T HRP20120490T1 HR P20120490 T1 HRP20120490 T1 HR P20120490T1 HR P20120490T T HRP20120490T T HR P20120490TT HR P20120490 T HRP20120490 T HR P20120490T HR P20120490 T1 HRP20120490 T1 HR P20120490T1
Authority
HR
Croatia
Prior art keywords
aliphatic
group
fluoroaliphatic
compound according
fluoro
Prior art date
Application number
HRP20120490TT
Other languages
English (en)
Croatian (hr)
Inventor
Christopher@F@@Claiborne
Todd@B@@Sells
Stephen@G@@Stroud
Original Assignee
Millennium@Pharmaceuticals
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=39315133&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HRP20120490(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Millennium@Pharmaceuticals filed Critical Millennium@Pharmaceuticals
Publication of HRP20120490T1 publication Critical patent/HRP20120490T1/hr

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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • 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)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
HRP20120490TT 2006-11-16 2007-11-14 Spojevi za inhibiciju napredovanja mitoze HRP20120490T1 (hr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US85934006P 2006-11-16 2006-11-16
PCT/US2007/023948 WO2008063525A1 (en) 2006-11-16 2007-11-14 Compounds for inhibiting mitotic progression

Publications (1)

Publication Number Publication Date
HRP20120490T1 true HRP20120490T1 (hr) 2012-07-31

Family

ID=39315133

Family Applications (2)

Application Number Title Priority Date Filing Date
HRP20120490TT HRP20120490T1 (hr) 2006-11-16 2007-11-14 Spojevi za inhibiciju napredovanja mitoze
HRP20150047TT HRP20150047T1 (en) 2006-11-16 2015-01-13 Compound for inhibiting mitotic progression

Family Applications After (1)

Application Number Title Priority Date Filing Date
HRP20150047TT HRP20150047T1 (en) 2006-11-16 2015-01-13 Compound for inhibiting mitotic progression

Country Status (34)

Country Link
US (7) US8026246B2 (Direct)
EP (4) EP2497772B1 (Direct)
JP (3) JP5102839B2 (Direct)
KR (2) KR101110458B1 (Direct)
CN (2) CN103483343B (Direct)
AR (1) AR064246A1 (Direct)
AT (1) ATE556076T1 (Direct)
AU (1) AU2007322046B2 (Direct)
BR (1) BRPI0718803B8 (Direct)
CA (1) CA2669680C (Direct)
CL (1) CL2007003244A1 (Direct)
CR (3) CR10782A (Direct)
CY (1) CY1112828T1 (Direct)
DK (2) DK2497772T3 (Direct)
EA (1) EA015779B1 (Direct)
ES (3) ES2384123T3 (Direct)
GE (1) GEP20125459B (Direct)
HR (2) HRP20120490T1 (Direct)
IL (1) IL198690A0 (Direct)
MA (1) MA30988B1 (Direct)
MX (3) MX343391B (Direct)
MY (1) MY153243A (Direct)
NO (1) NO343338B1 (Direct)
NZ (3) NZ611898A (Direct)
PH (1) PH12012502057B1 (Direct)
PL (2) PL2086981T3 (Direct)
PT (2) PT2497772E (Direct)
RS (2) RS52313B (Direct)
SG (2) SG176443A1 (Direct)
SI (2) SI2086981T1 (Direct)
TW (1) TWI401255B (Direct)
UA (1) UA94129C2 (Direct)
WO (1) WO2008063525A1 (Direct)
ZA (1) ZA200903279B (Direct)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20120091275A (ko) 2004-05-14 2012-08-17 밀레니엄 파머슈티컬스 인코퍼레이티드 아우로라 키나아제의 억제에 의해 유사분열 진행을 억제하기 위한 화합물 및 그 방법
CL2007003244A1 (es) 2006-11-16 2008-04-04 Millennium Pharm Inc Compuestos derivados de pirimido[5,4-d][2]benzazepina; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento del cancer.
WO2010065134A1 (en) * 2008-12-05 2010-06-10 Millennium Pharmaceuticals, Inc. 5, 7-dihydro- 6h-pyrimido [ 5, 4-d] [ 1 ] benzazepin-6-thiones as plk inhibitors
KR101741168B1 (ko) * 2008-12-22 2017-05-29 밀레니엄 파머슈티컬스 인코퍼레이티드 오로라 키나아제 억제제 및 항­cd 항체의 병용
JO3635B1 (ar) * 2009-05-18 2020-08-27 Millennium Pharm Inc مركبات صيدلانية صلبة وطرق لانتاجها
JO3434B1 (ar) * 2009-07-31 2019-10-20 Millennium Pharm Inc مركبات صيدلانية لمعالجة السرطان وامراض واضطرابات اخري
CN104031049A (zh) * 2010-02-19 2014-09-10 米伦纽姆医药公司 极光激酶抑制剂的结晶形式
US20120107304A1 (en) 2010-04-27 2012-05-03 Boehringer Ingelheim International Gmbh Combination therapy in treatment of oncological and fibrotic diseases
US9085582B2 (en) * 2010-06-22 2015-07-21 Glaxosmithkline Llc Benzotriazolodiazepine compounds inhibitors of bromodomains
TW201316991A (zh) * 2011-06-03 2013-05-01 Millennium Pharm Inc Mek抑制劑與奧諾拉(aurora)a激酶選擇性抑制劑之組合
US20130303519A1 (en) 2012-03-20 2013-11-14 Millennium Pharmaceuticals, Inc. Methods of treating cancer using aurora kinase inhibitors
CN103772391A (zh) * 2012-10-23 2014-05-07 杨子娇 一类治疗房角狭窄的化合物及其用途
CN105209042B (zh) * 2013-03-22 2019-03-08 米伦纽姆医药公司 催化性mtorc 1/2抑制剂与选择性极光a激酶抑制剂的组合
JP6525474B2 (ja) 2013-12-06 2019-06-05 ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. オーロラキナーゼ阻害剤と抗cd30抗体の併用
EP3236948A4 (en) * 2014-12-23 2018-10-03 Millennium Pharmaceuticals, Inc. Combination of raf inhibitors and aurora kinase inhibitors
JP2018524292A (ja) 2015-07-21 2018-08-30 ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. オーロラキナーゼインヒビターと化学療法剤の投与
JP6955485B2 (ja) 2015-09-09 2021-10-27 アイカーン スクール オブ メディスン アット マウント サイナイIcahn School of Medicine at Mt. Sinai 抗がん剤としての複素環式の限定された三環系スルホンアミド
JP6966425B2 (ja) 2015-09-09 2021-11-17 アイカーン スクール オブ メディスン アット マウント サイナイIcahn School of Medicine at Mt. Sinai 抗がん剤としての複素環式の限定された三環系スルホンアミド
WO2017146253A1 (ja) 2016-02-26 2017-08-31 公益財団法人がん研究会 Hp1の機能に着目した抗癌剤のスクリーニング方法及び評価系
CN109195593A (zh) 2016-03-15 2019-01-11 奥莱松基因组股份有限公司 用于治疗实体瘤的lsd1抑制剂的组合
JP6188986B1 (ja) * 2017-03-23 2017-08-30 株式会社ノエビア 時計遺伝子発現量調整剤及びエラスチン産生促進剤
US11874276B2 (en) 2018-04-05 2024-01-16 Dana-Farber Cancer Institute, Inc. STING levels as a biomarker for cancer immunotherapy
WO2020049208A1 (es) 2018-09-09 2020-03-12 Fundacio Privada Institut De Recerca De La Sida - Caixa Aurora cinasa como diana para tratar, prevenir o curar una infección por vih o sida
WO2021041532A1 (en) 2019-08-26 2021-03-04 Dana-Farber Cancer Institute, Inc. Use of heparin to promote type 1 interferon signaling
WO2023196959A1 (en) 2022-04-07 2023-10-12 Eli Lilly And Company Process for making a kras g12c inhibitor
CN119546309A (zh) 2022-04-08 2025-02-28 伊莱利利公司 包括kras g12c抑制剂和aurora a抑制剂的治疗方法
WO2024006424A1 (en) 2022-06-30 2024-01-04 Eli Lilly And Company Kras g12c inhibitor for treating cancer
WO2025075211A1 (en) 2023-10-03 2025-04-10 Takeda Pharmaceutical Company Limited Alisertib and paclitaxel for treating small cell lung cancer
WO2025245045A1 (en) 2024-05-21 2025-11-27 The Regents Of The University Of California Methods of treating lung cancer

Family Cites Families (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4099012A (en) * 1975-08-28 1978-07-04 Ciba-Geigy Corporation 2-pyrazolyl-benzophenones
US4481142A (en) * 1979-02-07 1984-11-06 Hoffmann-La Roche Inc. Pyrimido-2-benzazepines
CA1138863A (en) 1979-02-07 1983-01-04 Norman W. Gilman Benzazepine-derivatives
US4469633A (en) * 1980-05-16 1984-09-04 Hoffmann-La Roche Inc. N-oxides of 5-oxo-1-phenyl-2-benzazepines
EP0273697A3 (en) 1986-12-30 1989-11-29 Merck & Co. Inc. 2-benzazepines with 5- and 6- membered heterocyclic rings
US5166151A (en) * 1988-03-25 1992-11-24 Merck & Co., Inc. 2-Benzazepines with 5- and 6-membered heterocyclic rings, compositions and medical methods of use thereof
US5210082A (en) * 1991-05-16 1993-05-11 Merck & Co., Inc. 2-benzazepines with 5- and 6-membered heterocyclic rings to treat pain and anxiety disorders
GB9523675D0 (en) 1995-11-20 1996-01-24 Celltech Therapeutics Ltd Chemical compounds
US6124281A (en) * 1996-03-08 2000-09-26 Zeneca Limited Azolobenzazepine derivatives as neurologically active agents
WO1998028281A1 (en) * 1996-12-23 1998-07-02 Celltech Therapeutics Limited Fused polycyclic 2-aminopyrimidine derivatives, their preparation and their use as protein tyrosine kinase inhibitors
GB9713087D0 (en) 1997-06-20 1997-08-27 Celltech Therapeutics Ltd Chemical compounds
WO1999016770A1 (en) * 1997-09-29 1999-04-08 Meiji Seika Kaisha, Ltd. Tricyclic triazolobenzazepine derivatives, process for producing the same, and antiallergic
US6277844B1 (en) * 1998-09-14 2001-08-21 Sydney Spector Compound for selective treatment of malignant cells by inhibiting cell cycle progression, decreasing Bcl2, and increasing apoptosis
US6417207B1 (en) 1999-05-12 2002-07-09 Nitromed, Inc. Nitrosated and nitrosylated potassium channel activators, compositions and methods of use
DE60039782D1 (de) 1999-12-06 2008-09-18 Ajinomoto Kk Amidinophenylbrenztraubensäure-derivat
WO2002059111A2 (en) * 2000-12-21 2002-08-01 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
US6686352B2 (en) 2001-05-18 2004-02-03 Hoffmann-La Roche Inc. Substituted imidazo [1,5-a] pyrimido [5,4-d] [1] benzazepine derivatives
DE10135457A1 (de) * 2001-07-20 2003-02-06 Adc Automotive Dist Control Optische Sensoranordnung
KR100909122B1 (ko) 2001-08-09 2009-07-23 액테리온 파마슈티칼 리미티드 신규한 벤조-융합된 헤테로환
CN1897950A (zh) 2003-10-14 2007-01-17 惠氏公司 稠合芳基和杂芳基衍生物及其使用方法
KR20120091275A (ko) 2004-05-14 2012-08-17 밀레니엄 파머슈티컬스 인코퍼레이티드 아우로라 키나아제의 억제에 의해 유사분열 진행을 억제하기 위한 화합물 및 그 방법
BRPI0517737A (pt) 2004-11-17 2008-10-21 Miikana Therapeutics Inc inibidores de quinase
JP2008526723A (ja) 2004-12-30 2008-07-24 アステックス、セラピューティックス、リミテッド Cdk、gsk及びオーロラキナーゼの活性を調節するピラゾール誘導体
BRPI0620341A2 (pt) 2005-12-23 2011-11-08 Smithkline Beecham Corparation azaindóis inibidores de cinases aurora
US7718648B2 (en) 2006-08-09 2010-05-18 Millennium Pharmaceuticals, Inc. Pyridobenzazepine compounds and methods for inhibiting mitotic progression
CL2007003244A1 (es) 2006-11-16 2008-04-04 Millennium Pharm Inc Compuestos derivados de pirimido[5,4-d][2]benzazepina; composicion farmaceutica que comprende a dicho compuesto; y uso del compuesto para el tratamiento del cancer.
JO3635B1 (ar) 2009-05-18 2020-08-27 Millennium Pharm Inc مركبات صيدلانية صلبة وطرق لانتاجها

Also Published As

Publication number Publication date
WO2008063525A1 (en) 2008-05-29
KR101110458B1 (ko) 2012-03-13
BRPI0718803B1 (pt) 2020-11-17
US20110312942A1 (en) 2011-12-22
CR20140154A (es) 2014-07-23
ZA200903279B (en) 2010-07-28
EP2086981A1 (en) 2009-08-12
CN101547924B (zh) 2013-09-25
PL2497772T3 (pl) 2015-05-29
CR20140544A (es) 2015-01-12
PL2086981T3 (pl) 2012-09-28
MX2009004670A (es) 2009-05-15
PT2086981E (pt) 2012-06-20
SG176443A1 (en) 2011-12-29
US8026246B2 (en) 2011-09-27
RS53788B1 (sr) 2015-06-30
PH12012502057A1 (en) 2015-09-14
ES2537451T3 (es) 2015-06-08
EA015779B1 (ru) 2011-12-30
JP5102839B2 (ja) 2012-12-19
US9988384B2 (en) 2018-06-05
EP2944639B1 (en) 2017-01-04
MX348568B (es) 2017-06-20
PH12012502057B1 (en) 2018-10-24
EP2497772B1 (en) 2014-10-29
KR101342014B1 (ko) 2013-12-19
AR064246A1 (es) 2009-03-25
US20240400567A1 (en) 2024-12-05
US20210214361A1 (en) 2021-07-15
EP2497773A1 (en) 2012-09-12
DK2086981T3 (da) 2012-08-06
EA200970486A1 (ru) 2009-10-30
SI2086981T1 (sl) 2012-12-31
HRP20150047T1 (en) 2015-03-13
TWI401255B (zh) 2013-07-11
UA94129C2 (ru) 2011-04-11
JP2014055166A (ja) 2014-03-27
JP5452811B2 (ja) 2014-03-26
CA2669680C (en) 2012-04-10
NO343338B1 (no) 2019-02-04
EP2086981B1 (en) 2012-05-02
CN103483343B (zh) 2016-06-01
ES2384123T3 (es) 2012-06-29
RS52313B (sr) 2012-12-31
BRPI0718803B8 (pt) 2021-05-25
TW200829589A (en) 2008-07-16
US20080167292A1 (en) 2008-07-10
HK1175777A1 (en) 2013-07-12
EP2944639A1 (en) 2015-11-18
PT2497772E (pt) 2015-02-05
MY153243A (en) 2015-01-29
CN103483343A (zh) 2014-01-01
US11958855B2 (en) 2024-04-16
SG10201503350TA (en) 2015-06-29
US10836766B2 (en) 2020-11-17
EP2497772A1 (en) 2012-09-12
KR20090091173A (ko) 2009-08-26
US20110312943A1 (en) 2011-12-22
DK2497772T3 (en) 2015-01-19
US9765076B2 (en) 2017-09-19
CL2007003244A1 (es) 2008-04-04
ATE556076T1 (de) 2012-05-15
HK1134672A1 (en) 2010-05-07
AU2007322046B2 (en) 2012-04-05
CY1112828T1 (el) 2016-02-10
GEP20125459B (en) 2012-03-26
AU2007322046A1 (en) 2008-05-29
CA2669680A1 (en) 2008-05-29
NZ597252A (en) 2013-06-28
CR10782A (es) 2009-06-24
ES2528793T3 (es) 2015-02-12
KR20110113210A (ko) 2011-10-14
JP2012006965A (ja) 2012-01-12
US20150166545A1 (en) 2015-06-18
EP2497773B1 (en) 2015-02-25
CN101547924A (zh) 2009-09-30
HK1217699A1 (en) 2017-01-20
MX343391B (es) 2016-11-04
US20190031662A1 (en) 2019-01-31
NZ611898A (en) 2015-01-30
NO20091864L (no) 2009-06-15
MA30988B1 (fr) 2009-12-01
NZ577042A (en) 2012-03-30
HK1175778A1 (en) 2013-07-12
IL198690A0 (en) 2010-02-17
BRPI0718803A2 (pt) 2013-12-03
SI2497772T1 (sl) 2015-03-31
JP2010510215A (ja) 2010-04-02

Similar Documents

Publication Publication Date Title
HRP20120490T1 (hr) Spojevi za inhibiciju napredovanja mitoze
ES2970074T3 (es) Inhibidor de ATR y su aplicación
RU2345996C1 (ru) Аннелированные азагетероциклические амиды, включающие пиримидиновый фрагмент, способ их получения и применения
JP2010510215A5 (Direct)
HRP20131051T1 (hr) Inhibitori proteinskih kinaza
HRP20120785T1 (hr) Spojevi i postupci za inhibiciju napredovanja mitoze putem inhibicije aurora kinaze
ATE361916T1 (de) Pyrimidine verbindungen
NZ578876A (en) 3-amino-pyrrolo[3,4-c]pyrazole-5 (1h, 4h, 6h) carbaldehyde derivatives as pkc inhibitors
HRP20160967T1 (hr) Heterociklički spojevi korisni kao pdk1 inhibitori
HRP20140437T1 (hr) Bicikliäśki spojevi i njihove uporabe kao dualnih c-src/jak inhibitora
JO3108B1 (ar) بيرروليدينونات أروماتية مخلطة مندمجة كمثبطات syk
EA200601350A1 (ru) Азотсодержащие гетероциклические производные и их фармацевтические применения
RU2341527C1 (ru) Аннелированные азагетероциклы, включающие пиримидиновый фрагмент, способ их получения и ингибиторы pi3k киназ
ATE307810T1 (de) Imidazol-2-carbonsäureamid derivate als raf- kinase-inhibitoren
RU2005135338A (ru) Замещенные 3-цианотиофенацетамиды в качестве антагонистов рецептора глюкагона
AR086100A1 (es) Compuestos de cromenona y composiciones farmaceuticas que los contienen
NO20070837L (no) Pyrido-pyrido pyrimidinderivater, fremstilling derav samt terapeutisk anvendelse for behandling av cancer.
EA201991025A1 (ru) Липосомальный препарат для применения для лечения злокачественного новообразования
WO2010002779A2 (en) Naphthyridininones as aurora kinase inhibitors
JP2015502371A5 (Direct)
SE0300091D0 (sv) Novel compounds
JP2014524449A5 (Direct)
AR054863A1 (es) DERIVADOS DE 1H-PIRROLO[3, 4-C]PIRAZOL, UN PROCESO PARA SU PREPARACION, COMPOSICIONES FARMACEUTICAS QUE LOS COMPRENDEN Y SU USO EN LA FABRICACION DE UN MEDICAMENTO PARA EL TRATAMIENTO O PROFILAXIS DE ENFERMEDADES ASOCIADAS CON EL FACTOR DE COAGULACIoN XA
RU2007125661A (ru) Арилоксиэтиламиновые и фенилпиперазиновые производные с сочетанием свойств неполного агонизма к рецепторам дофимина-d2 и ингибирования повторного поглощения серотонина
RU2011153613A (ru) Аминопиразол триазолотиадиазольные ингибиторы протеинкиназы с-мет