MA30988B1 - Composes destines a inhiber la progression mitotique - Google Patents

Composes destines a inhiber la progression mitotique

Info

Publication number
MA30988B1
MA30988B1 MA31985A MA31985A MA30988B1 MA 30988 B1 MA30988 B1 MA 30988B1 MA 31985 A MA31985 A MA 31985A MA 31985 A MA31985 A MA 31985A MA 30988 B1 MA30988 B1 MA 30988B1
Authority
MA
Morocco
Prior art keywords
compounds
mitotic progression
inhibiting mitotic
cancer
treatment
Prior art date
Application number
MA31985A
Other languages
English (en)
Inventor
Christopher F Claiborne
Todd B Sells
Stephen G Stroud
Original Assignee
Millennium Pharm Inc
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=MA30988(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Millennium Pharm Inc filed Critical Millennium Pharm Inc
Publication of MA30988B1 publication Critical patent/MA30988B1/fr

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
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • 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
    • 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

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)

Abstract

LA PRÉSENTE INVENTION CONCERNE DES COMPOSÉS REPRÉSENTÉS PAR LA FORMULE GÉNÉRALE (I), AINSI QUE DES PROCÉDÉS DESTINÉS AU TRAITEMENT DU CANCER. L'INVENTION CONCERNE PLUS PARTICULIÈREMENT DE PUISSANTS INHIBITEURS DE LA KINASE AURORA A, DES COMPOSITIONS PHARMACEUTIQUES COMPRENANT LES COMPOSÉS, AINSI QUE DES PROCÉDÉS D'UTILISATION DE CES COMPOSÉS POUR LE TRAITEMENT DU CANCER.
MA31985A 2006-11-16 2009-06-12 Composes destines a inhiber la progression mitotique MA30988B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US85934006P 2006-11-16 2006-11-16

Publications (1)

Publication Number Publication Date
MA30988B1 true MA30988B1 (fr) 2009-12-01

Family

ID=39315133

Family Applications (1)

Application Number Title Priority Date Filing Date
MA31985A MA30988B1 (fr) 2006-11-16 2009-06-12 Composes destines a inhiber la progression mitotique

Country Status (34)

Country Link
US (7) US8026246B2 (fr)
EP (4) EP2497773B1 (fr)
JP (3) JP5102839B2 (fr)
KR (2) KR101110458B1 (fr)
CN (2) CN101547924B (fr)
AR (1) AR064246A1 (fr)
AT (1) ATE556076T1 (fr)
AU (1) AU2007322046B2 (fr)
BR (1) BRPI0718803B8 (fr)
CA (1) CA2669680C (fr)
CL (1) CL2007003244A1 (fr)
CR (3) CR10782A (fr)
CY (1) CY1112828T1 (fr)
DK (2) DK2086981T3 (fr)
EA (1) EA015779B1 (fr)
ES (3) ES2384123T3 (fr)
GE (1) GEP20125459B (fr)
HR (2) HRP20120490T1 (fr)
IL (1) IL198690A0 (fr)
MA (1) MA30988B1 (fr)
MX (3) MX348568B (fr)
MY (1) MY153243A (fr)
NO (1) NO343338B1 (fr)
NZ (3) NZ611898A (fr)
PH (1) PH12012502057B1 (fr)
PL (2) PL2497772T3 (fr)
PT (2) PT2086981E (fr)
RS (2) RS52313B (fr)
SG (2) SG10201503350TA (fr)
SI (2) SI2086981T1 (fr)
TW (1) TWI401255B (fr)
UA (1) UA94129C2 (fr)
WO (1) WO2008063525A1 (fr)
ZA (1) ZA200903279B (fr)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101792651B1 (ko) 2004-05-14 2017-11-20 밀레니엄 파머슈티컬스 인코퍼레이티드 아우로라 키나아제의 억제에 의해 유사분열 진행을 억제하기 위한 화합물 및 그 화합물을 포함하는 약학적 조성물
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.
US7998952B2 (en) * 2008-12-05 2011-08-16 Millennium Pharmaceuticals, Inc. Thiolactams and uses thereof
CN102264368B (zh) 2008-12-22 2014-09-10 米伦纽姆医药公司 极光激酶抑制剂与抗cd20抗体的组合
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
WO2011103089A1 (fr) 2010-02-19 2011-08-25 Millennium Pharmaceuticals, Inc. Formes cristallines de 4-{[9-chloro-7-(2-fluoro-6--méthoxyphényl)-5h-pyrimido[5,4-d][2]benzazépin-2yl]amino}-2-méthoxybenzoate de sodium
US20120107304A1 (en) 2010-04-27 2012-05-03 Boehringer Ingelheim International Gmbh Combination therapy in treatment of oncological and fibrotic diseases
EP2585465B1 (fr) * 2010-06-22 2014-11-12 GlaxoSmithKline LLC Composés de benzotriazolodiazépine inhibiteurs de bromodomaines
AR086656A1 (es) * 2011-06-03 2014-01-15 Millennium Pharm Inc Combinacion de inhibidores de mek e inhibidores selectivos de la quinasa aurora a
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
EP2976086B1 (fr) * 2013-03-22 2020-10-14 Millennium Pharmaceuticals, Inc. Combinaison d'inhibiteurs catalytiques de mtorc1/2 et inhibiteurs sélectifs de la kinase aurora a
US10335494B2 (en) 2013-12-06 2019-07-02 Millennium Pharmaceuticals, Inc. Combination of aurora kinase inhibitors and anti-CD30 antibodies
EP3236948A4 (fr) * 2014-12-23 2018-10-03 Millennium Pharmaceuticals, Inc. Combinaison d'inhibiteurs de raf et d'inhibiteurs de kinases aurora
EP3324976A4 (fr) 2015-07-21 2019-03-27 Millennium Pharmaceuticals, Inc. Administration d'inhibiteur de kinase aurora et d'agents chimiothérapeutiques
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 (fr) 2016-02-26 2017-08-31 公益財団法人がん研究会 Procédé de criblage d'agent anticancéreux focalisé sur la fonction de hp1, et système d'évaluation
CN120661674A (zh) 2016-03-15 2025-09-19 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
WO2019195658A1 (fr) 2018-04-05 2019-10-10 Dana-Farber Cancer Institute, Inc. Niveaux sting comme biomarqueur pour l'immunothérapie du cancer
WO2020049208A1 (fr) 2018-09-09 2020-03-12 Fundacio Privada Institut De Recerca De La Sida - Caixa Aurora cinasa comme cible pour traiter, prévenir ou soigner une infection par vih ou le sida
WO2021041532A1 (fr) 2019-08-26 2021-03-04 Dana-Farber Cancer Institute, Inc. Utilisation d'héparine pour favoriser la signalisation de l'interféron de type 1
US20250228848A1 (en) 2022-04-07 2025-07-17 Eli Lilly And Company Process for making a kras g12c inhibitor
CA3247183A1 (fr) 2022-04-08 2023-10-12 Eli Lilly And Company Méthode de traitement comprenant des inhibiteurs de kras g12c et des inhibiteurs d’aurora a
KR20250027777A (ko) 2022-06-30 2025-02-27 일라이 릴리 앤드 캄파니 암을 치료하기 위한 kras g12c 억제제
IL327467A (en) 2023-10-03 2026-05-01 Takeda Pharmaceutical Co Limited Elisartib and paclitaxel for the treatment of small cell lung cancer
WO2025245045A1 (fr) 2024-05-21 2025-11-27 The Regents Of The University Of California Méthodes de traitement du cancer du poumon

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
SU1181547A3 (ru) 1979-02-07 1985-09-23 Ф.Хоффманн-Ля Рош Унд Ко,Аг (Фирма) Способ получени пиримидо-2-бензазепинов или их фармакологически совместимых кислотно-аддитивных солей (и его вариант)
US4469633A (en) * 1980-05-16 1984-09-04 Hoffmann-La Roche Inc. N-oxides of 5-oxo-1-phenyl-2-benzazepines
EP0273697A3 (fr) 1986-12-30 1989-11-29 Merck & Co. Inc. 2-Benzazépines à cycles hétérocycliques de 5 et 6 côtés
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
EP0888350A1 (fr) 1996-03-08 1999-01-07 Zeneca Limited Principes actifs neurologiques derives d'azolobenzazepine
AU5330698A (en) * 1996-12-23 1998-07-17 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
DK1026167T3 (da) * 1997-09-29 2003-05-26 Meiji Seika Kaisha Tricykliske triazolobenzazepinderivater, fremgangsmåde til fremstilling af disse samt antiallergiske midler
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
BR0116493A (pt) * 2000-12-21 2003-09-30 Vertex Pharma Compostos de pirazol úteis como inibidores de proteìna cinase
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
HUP0401107A3 (en) 2001-08-09 2004-10-28 Actelion Pharmaceuticals Ltd Novel benzo-fused heterocycles, their use process for their preparation and pharmaceutical compositions containing them
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
KR101792651B1 (ko) 2004-05-14 2017-11-20 밀레니엄 파머슈티컬스 인코퍼레이티드 아우로라 키나아제의 억제에 의해 유사분열 진행을 억제하기 위한 화합물 및 그 화합물을 포함하는 약학적 조성물
MX2007005857A (es) 2004-11-17 2007-10-10 Mikana Therapeutics Inc Inhibidores de cinasa.
EP1836188A1 (fr) 2004-12-30 2007-09-26 Astex Therapeutics Limited Derives pyrazoliques modulant l'activite des kinases cdk, gsk et aurora
WO2007076348A2 (fr) 2005-12-23 2007-07-05 Smithkline Beecham Corporation Inhibiteurs azaindoliques des kinases aurora
WO2008021038A2 (fr) 2006-08-09 2008-02-21 Millennium Pharmaceuticals, Inc. Pyridobenzazépines et méthodes d'inhibition de la progression mitotique
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
JP5452811B2 (ja) 2014-03-26
HK1134672A1 (en) 2010-05-07
BRPI0718803B1 (pt) 2020-11-17
PT2497772E (pt) 2015-02-05
ZA200903279B (en) 2010-07-28
MX348568B (es) 2017-06-20
RS53788B1 (sr) 2015-06-30
KR20090091173A (ko) 2009-08-26
BRPI0718803B8 (pt) 2021-05-25
PL2086981T3 (pl) 2012-09-28
WO2008063525A1 (fr) 2008-05-29
IL198690A0 (en) 2010-02-17
DK2086981T3 (da) 2012-08-06
EP2086981A1 (fr) 2009-08-12
AR064246A1 (es) 2009-03-25
ES2528793T3 (es) 2015-02-12
PH12012502057A1 (en) 2015-09-14
EP2944639A1 (fr) 2015-11-18
US20150166545A1 (en) 2015-06-18
MY153243A (en) 2015-01-29
HRP20120490T1 (hr) 2012-07-31
MX343391B (es) 2016-11-04
SI2086981T1 (sl) 2012-12-31
KR101342014B1 (ko) 2013-12-19
US9765076B2 (en) 2017-09-19
US20240400567A1 (en) 2024-12-05
US20210214361A1 (en) 2021-07-15
US20190031662A1 (en) 2019-01-31
CR10782A (es) 2009-06-24
NZ577042A (en) 2012-03-30
NO343338B1 (no) 2019-02-04
NZ611898A (en) 2015-01-30
SI2497772T1 (sl) 2015-03-31
US8026246B2 (en) 2011-09-27
EP2497772A1 (fr) 2012-09-12
NO20091864L (no) 2009-06-15
PL2497772T3 (pl) 2015-05-29
CL2007003244A1 (es) 2008-04-04
AU2007322046A1 (en) 2008-05-29
HK1175777A1 (en) 2013-07-12
RS52313B (sr) 2012-12-31
US10836766B2 (en) 2020-11-17
GEP20125459B (en) 2012-03-26
EP2497773A1 (fr) 2012-09-12
US20110312943A1 (en) 2011-12-22
JP5102839B2 (ja) 2012-12-19
EA200970486A1 (ru) 2009-10-30
EP2497773B1 (fr) 2015-02-25
US20080167292A1 (en) 2008-07-10
EP2086981B1 (fr) 2012-05-02
CN103483343B (zh) 2016-06-01
SG10201503350TA (en) 2015-06-29
NZ597252A (en) 2013-06-28
ES2384123T3 (es) 2012-06-29
CR20140544A (es) 2015-01-12
JP2014055166A (ja) 2014-03-27
MX2009004670A (es) 2009-05-15
PT2086981E (pt) 2012-06-20
EP2497772B1 (fr) 2014-10-29
AU2007322046B2 (en) 2012-04-05
TWI401255B (zh) 2013-07-11
CA2669680C (fr) 2012-04-10
US11958855B2 (en) 2024-04-16
HK1175778A1 (en) 2013-07-12
CA2669680A1 (fr) 2008-05-29
ATE556076T1 (de) 2012-05-15
CN101547924A (zh) 2009-09-30
TW200829589A (en) 2008-07-16
UA94129C2 (ru) 2011-04-11
EP2944639B1 (fr) 2017-01-04
CN103483343A (zh) 2014-01-01
US20110312942A1 (en) 2011-12-22
DK2497772T3 (en) 2015-01-19
EA015779B1 (ru) 2011-12-30
CY1112828T1 (el) 2016-02-10
BRPI0718803A2 (pt) 2013-12-03
HRP20150047T1 (en) 2015-03-13
JP2012006965A (ja) 2012-01-12
KR101110458B1 (ko) 2012-03-13
KR20110113210A (ko) 2011-10-14
JP2010510215A (ja) 2010-04-02
CR20140154A (es) 2014-07-23
HK1217699A1 (en) 2017-01-20
SG176443A1 (en) 2011-12-29
ES2537451T3 (es) 2015-06-08
PH12012502057B1 (en) 2018-10-24
US9988384B2 (en) 2018-06-05
CN101547924B (zh) 2013-09-25

Similar Documents

Publication Publication Date Title
TNSN07305A1 (fr) Agonistes de pyy et leurs utilisations
MA31574B1 (fr) Dérivés de pyrazole et leur utilisation comme inhibiteurs de raf
MA30166B1 (fr) Imidazoles substitues et leur utilisation comme pesticides.
MA30781B1 (fr) Inhibiteur de kinase
MA31906B1 (fr) Inhibiteurs de la replication du virus de limmunodeficience humaine
MA33275B1 (fr) Inhibiteurs de la replication du virus de l'immunodeficience humaine
MA29688B1 (fr) Formulation d'un inhibiteur de l'agregation plaquettaire thienopyridine
TN2011000454A1 (fr) Derives de benzofurannyle utilises comme inhibiteurs de glucokinase
PH12012502057A1 (en) Compounds for inhibiting mitotic progression
MA32104B1 (fr) Dérivés d'oxime en tant qu'inhibiteurs de hsp90
MA40225B1 (fr) Composés dihydroisoquinolinone substitués
MA34361B1 (fr) Dérivés de tétrahydro-pyrido-pyrimidine
MA32135B1 (fr) Inhibiteurs de pim kinase et leurs procedes d'utilisation
MA31433B1 (fr) Inhibiteurs de la p70 s6 kinase
MA29160B1 (fr) Derives de triazole substitues, servant d'antagonistes d'ocytocine
WO2006123113A3 (fr) Composes chimiques
MA32468B1 (fr) Derives de thiophene ou de thiazole et leur utilisation comme inhibiteurs de pi3k
MA32904B1 (fr) Composes de purine
MA31741B1 (fr) Derives fongicides de 2-alkylthio-2-quinolinyloxy- acetamide
TN2009000428A1 (fr) Derives de sulfonylamides destines au traitement d'une croissance cellulaire anormale
MA33730B1 (fr) Procédés de synthèse pour des composés spiro-oxindoles
TNSN08444A1 (en) Bicyclic derivatives as cetp inhibitors
MY149512A (en) Pyrazolylaminopyridine derivatives useful as kinase inhibitors
MA30351B1 (fr) Composes de tetrahydropyridothienopyrimidine et leurs procedes d'utilisation
MA29377B1 (fr) Derives de la pyrimidine pour traitement de troubles a caractere hyperproliferatif