HRP20120490T1 - Spojevi za inhibiciju napredovanja mitoze - Google Patents

Spojevi za inhibiciju napredovanja mitoze Download PDF

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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

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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)
  • 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)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (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 2012-06-12 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 2012-06-12 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 (35)

Country Link
US (6) US8026246B2 (es)
EP (4) EP2497772B1 (es)
JP (3) JP5102839B2 (es)
KR (2) KR101110458B1 (es)
CN (2) CN103483343B (es)
AR (1) AR064246A1 (es)
AT (1) ATE556076T1 (es)
AU (1) AU2007322046B2 (es)
BR (1) BRPI0718803B8 (es)
CA (1) CA2669680C (es)
CL (1) CL2007003244A1 (es)
CR (3) CR10782A (es)
CY (1) CY1112828T1 (es)
DK (2) DK2086981T3 (es)
EA (1) EA015779B1 (es)
ES (3) ES2537451T3 (es)
GE (1) GEP20125459B (es)
HK (4) HK1134672A1 (es)
HR (2) HRP20120490T1 (es)
IL (1) IL198690A0 (es)
MA (1) MA30988B1 (es)
MX (3) MX348568B (es)
MY (1) MY153243A (es)
NO (1) NO343338B1 (es)
NZ (3) NZ597252A (es)
PH (1) PH12012502057A1 (es)
PL (2) PL2086981T3 (es)
PT (2) PT2497772E (es)
RS (2) RS52313B (es)
SG (2) SG176443A1 (es)
SI (2) SI2497772T1 (es)
TW (1) TWI401255B (es)
UA (1) UA94129C2 (es)
WO (1) WO2008063525A1 (es)
ZA (1) ZA200903279B (es)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005111039A2 (en) * 2004-05-14 2005-11-24 Millennium Pharmaceuticals, Inc. Compounds and methods for inhibiting mitotic progression by inhibition of aurora kinase
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.
AR074487A1 (es) * 2008-12-05 2011-01-19 Millennium Pharm Inc Tiolactamas inhibidoras de proteinquinasas plk, composiciones farmaceuticas que las contienen y usos de las mismas para el tratamiento de trastornos proliferativos e inflamatorios, en particular cancer.
MX2011006725A (es) 2008-12-22 2011-09-15 Millennium Pharm Inc Combinacion de inhibidores de aurora cinasa y anticuerpos anti-cd20.
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
CA2788774A1 (en) * 2010-02-19 2011-08-25 Millennium Pharmaceuticals, Inc. Crystalline forms of sodium 4-{[9-chloro-7-(2-fluoro-6-methoxyphenyl)-5h-pyrimido[5,4-d][2]benzazepin-2-yl]amino}-2-methoxybenzoate
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
CA2907726A1 (en) 2013-03-22 2014-09-25 Millennium Pharmaceuticals, Inc. Combination of catalytic mtorc1/2 inhibitors and selective inhibitors of aurora a kinase
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
JP2018502089A (ja) * 2014-12-23 2018-01-25 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. Raf阻害剤及びauroraキナーゼ阻害剤の組み合わせ
WO2017015316A1 (en) 2015-07-21 2017-01-26 Millennium Pharmaceuticals, Inc. Administration of aurora kinase inhibitor and chemotherapeutic agents
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
CN108349943A (zh) 2015-09-09 2018-07-31 西奈山伊坎医学院 杂环受限三环磺酰胺作为抗癌试剂
JP6591036B2 (ja) 2016-02-26 2019-10-16 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
KR20230042756A (ko) 2016-03-15 2023-03-29 오리존 지노믹스 에스.에이. 고형 종양의 치료에 사용하기 위한 lsd1 억제제의 조합물
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
WO2023196887A1 (en) 2022-04-08 2023-10-12 Eli Lilly And Company Method of treatment including kras g12c inhibitors and aurora a inhibitors
US20240108618A1 (en) 2022-06-30 2024-04-04 Eli Lilly And Company Kras g12c inhibitor dosing regimens

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
FR2450833A1 (fr) 1979-02-07 1980-10-03 Hoffmann La Roche Derives de benzazepine
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
CA2247453A1 (en) * 1996-03-08 1997-09-12 Joseph James Lewis Azolobenzazepine derivatives as neurologically active agents
JP2001507349A (ja) * 1996-12-23 2001-06-05 セルテック セラピューティックス リミテッド 縮合多環式2−アミノピリミジン誘導体、それらの製造およびたんぱく質チロシンキナーゼ抑制因子としてのそれらの使用
GB9713087D0 (en) 1997-06-20 1997-08-27 Celltech Therapeutics Ltd Chemical compounds
US6372735B1 (en) * 1997-09-29 2002-04-16 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
WO2000067754A1 (en) 1999-05-12 2000-11-16 Nitromed, Inc. Nitrosated and nitrosylated potassium channel activators, compositions and methods of use
ATE403644T1 (de) 1999-12-06 2008-08-15 Ajinomoto Kk Amidinophenylbrenztraubensäure-derivat
JP4160395B2 (ja) 2000-12-21 2008-10-01 バーテックス ファーマシューティカルズ インコーポレイテッド プロテインキナーゼインヒビターとして有用なピラゾール化合物
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
JP4364637B2 (ja) 2001-08-09 2009-11-18 アクテリオン ファーマシューティカルズ リミテッド 新規なベンゾ縮合へテロ環化合物
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
WO2005111039A2 (en) 2004-05-14 2005-11-24 Millennium Pharmaceuticals, Inc. Compounds and methods for inhibiting mitotic progression by inhibition of aurora kinase
RU2007122485A (ru) 2004-11-17 2008-12-27 Мийкана Терапьютикс Ингибиторы киназы
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
WO2008021038A2 (en) 2006-08-09 2008-02-21 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
PL2086981T3 (pl) 2012-09-28
NO20091864L (no) 2009-06-15
EP2086981B1 (en) 2012-05-02
EP2944639B1 (en) 2017-01-04
IL198690A0 (en) 2010-02-17
KR101110458B1 (ko) 2012-03-13
US20110312943A1 (en) 2011-12-22
CY1112828T1 (el) 2016-02-10
JP5452811B2 (ja) 2014-03-26
WO2008063525A1 (en) 2008-05-29
JP2012006965A (ja) 2012-01-12
US10836766B2 (en) 2020-11-17
CA2669680C (en) 2012-04-10
CN103483343B (zh) 2016-06-01
NZ577042A (en) 2012-03-30
NZ597252A (en) 2013-06-28
EA015779B1 (ru) 2011-12-30
CN103483343A (zh) 2014-01-01
EA200970486A1 (ru) 2009-10-30
MX348568B (es) 2017-06-20
AR064246A1 (es) 2009-03-25
ATE556076T1 (de) 2012-05-15
SI2086981T1 (sl) 2012-12-31
BRPI0718803B1 (pt) 2020-11-17
JP2014055166A (ja) 2014-03-27
HRP20150047T1 (en) 2015-03-13
KR20090091173A (ko) 2009-08-26
CL2007003244A1 (es) 2008-04-04
US11958855B2 (en) 2024-04-16
NZ611898A (en) 2015-01-30
NO343338B1 (no) 2019-02-04
SI2497772T1 (sl) 2015-03-31
DK2497772T3 (en) 2015-01-19
EP2497773B1 (en) 2015-02-25
US9988384B2 (en) 2018-06-05
US8026246B2 (en) 2011-09-27
ES2537451T3 (es) 2015-06-08
BRPI0718803B8 (pt) 2021-05-25
ES2384123T3 (es) 2012-06-29
SG10201503350TA (en) 2015-06-29
AU2007322046A1 (en) 2008-05-29
EP2497772B1 (en) 2014-10-29
EP2944639A1 (en) 2015-11-18
EP2497772A1 (en) 2012-09-12
CA2669680A1 (en) 2008-05-29
KR101342014B1 (ko) 2013-12-19
BRPI0718803A2 (pt) 2013-12-03
DK2086981T3 (da) 2012-08-06
CN101547924A (zh) 2009-09-30
CR20140544A (es) 2015-01-12
PH12012502057B1 (en) 2015-09-14
TWI401255B (zh) 2013-07-11
MA30988B1 (fr) 2009-12-01
JP2010510215A (ja) 2010-04-02
UA94129C2 (ru) 2011-04-11
PL2497772T3 (pl) 2015-05-29
MX343391B (es) 2016-11-04
US20080167292A1 (en) 2008-07-10
KR20110113210A (ko) 2011-10-14
GEP20125459B (en) 2012-03-26
US20190031662A1 (en) 2019-01-31
ZA200903279B (en) 2010-07-28
ES2528793T3 (es) 2015-02-12
TW200829589A (en) 2008-07-16
US20150166545A1 (en) 2015-06-18
MX2009004670A (es) 2009-05-15
PT2086981E (pt) 2012-06-20
AU2007322046B2 (en) 2012-04-05
EP2086981A1 (en) 2009-08-12
HK1175778A1 (en) 2013-07-12
RS53788B1 (en) 2015-06-30
HK1134672A1 (en) 2010-05-07
JP5102839B2 (ja) 2012-12-19
EP2497773A1 (en) 2012-09-12
RS52313B (en) 2012-12-31
CR10782A (es) 2009-06-24
HK1217699A1 (zh) 2017-01-20
SG176443A1 (en) 2011-12-29
MY153243A (en) 2015-01-29
CR20140154A (es) 2014-07-23
CN101547924B (zh) 2013-09-25
US9765076B2 (en) 2017-09-19
HK1175777A1 (en) 2013-07-12
US20210214361A1 (en) 2021-07-15
PH12012502057A1 (en) 2015-09-14
PT2497772E (pt) 2015-02-05
US20110312942A1 (en) 2011-12-22

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Amr et al. Anti-cancer and kinases inhibitor activities of synthesized heterocyclic substituted thiophene fused with cyclohexane derivatives