[go: up one dir, main page]

TN2009000399A1 - Procedes de traitement impliquant l'inhibition de pi3k-alpha au moyen d'inhibiteurs de type quinaxoline - Google Patents

Procedes de traitement impliquant l'inhibition de pi3k-alpha au moyen d'inhibiteurs de type quinaxoline

Info

Publication number
TN2009000399A1
TN2009000399A1 TNP2009000399A TN2009000399A TN2009000399A1 TN 2009000399 A1 TN2009000399 A1 TN 2009000399A1 TN P2009000399 A TNP2009000399 A TN P2009000399A TN 2009000399 A TN2009000399 A TN 2009000399A TN 2009000399 A1 TN2009000399 A1 TN 2009000399A1
Authority
TN
Tunisia
Prior art keywords
quinaxolin
pi3k
alpha
treatment methods
methods involving
Prior art date
Application number
TNP2009000399A
Other languages
English (en)
Inventor
Peter Lamb
David Matthews
Original Assignee
Exelixis 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
Application filed by Exelixis Inc filed Critical Exelixis Inc
Publication of TN2009000399A1 publication Critical patent/TN2009000399A1/fr

Links

Classifications

    • 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
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
    • 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
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/436—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
    • 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
    • A61K31/4965—Non-condensed pyrazines
    • A61K31/497—Non-condensed pyrazines containing further 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
    • A61K31/495—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
    • A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
    • 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
    • A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring 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
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • 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
    • A61K31/555—Heterocyclic compounds containing heavy metals, e.g. hemin, hematin, melarsoprol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61P35/02—Antineoplastic agents specific for leukemia
    • 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

  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La présente invention concerne des procédés de traitement du cancer impliquant l'administration d'un composé de formule I ou, éventuellement, d'un sel, solvate et/ou hydrate de celui-ci acceptable sur le plan pharmaceutique, en association avec d'autres traitements anticancéreux
TNP2009000399A 2007-04-11 2009-09-30 Procedes de traitement impliquant l'inhibition de pi3k-alpha au moyen d'inhibiteurs de type quinaxoline TN2009000399A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US92316407P 2007-04-11 2007-04-11
PCT/US2008/004570 WO2008127594A2 (fr) 2007-04-11 2008-04-08 Procédés de traitement impliquant l'inhibition de pi3k-alpha au moyen d'inhibiteurs de type quinaxoline

Publications (1)

Publication Number Publication Date
TN2009000399A1 true TN2009000399A1 (fr) 2010-12-31

Family

ID=39864581

Family Applications (1)

Application Number Title Priority Date Filing Date
TNP2009000399A TN2009000399A1 (fr) 2007-04-11 2009-09-30 Procedes de traitement impliquant l'inhibition de pi3k-alpha au moyen d'inhibiteurs de type quinaxoline

Country Status (33)

Country Link
US (1) US8481001B2 (fr)
EP (1) EP2139483B9 (fr)
JP (2) JP5726515B2 (fr)
KR (1) KR101586774B1 (fr)
CN (2) CN103202842A (fr)
AU (1) AU2008239668B2 (fr)
BR (1) BRPI0810208A2 (fr)
CA (1) CA2684056A1 (fr)
CO (1) CO6140024A2 (fr)
CR (1) CR11099A (fr)
CY (1) CY1114608T1 (fr)
DK (1) DK2139483T3 (fr)
EA (1) EA019064B1 (fr)
EC (1) ECSP099723A (fr)
ES (1) ES2438998T3 (fr)
GT (1) GT200900263A (fr)
HR (1) HRP20131081T1 (fr)
IL (1) IL201211A (fr)
MA (1) MA31335B1 (fr)
ME (1) ME00937B (fr)
MX (1) MX2009010929A (fr)
MY (1) MY150797A (fr)
NI (1) NI200900184A (fr)
NZ (1) NZ580009A (fr)
PL (1) PL2139483T3 (fr)
PT (1) PT2139483E (fr)
RS (1) RS53020B (fr)
SI (1) SI2139483T1 (fr)
SV (1) SV2009003390A (fr)
TN (1) TN2009000399A1 (fr)
UA (1) UA98141C2 (fr)
WO (1) WO2008127594A2 (fr)
ZA (1) ZA200906765B (fr)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2623768C (fr) * 2005-10-07 2016-04-12 Exelixis, Inc. Derives de n-(3-amino-quinoxalin-2-yl) -sulfonamide et leur utilisation comme inhibiteurs de phosphatidylinositol 3-kinase
KR20140105621A (ko) * 2005-10-07 2014-09-01 엑셀리시스, 인코포레이티드 ＰＩ３Ｋα의 피리도피리미디논 억제제
ATE539752T1 (de) 2006-08-16 2012-01-15 Exelixis Inc Verwendung von pi3k- und mek-modulatoren bei der krebsbehandlung
RS52939B (sr) * 2007-04-10 2014-02-28 Exelixis Inc. Postupci za lečenje kancera upotrebom piridopirimidinonskih inhibitora pi3k alfa
PT2374802E (pt) * 2008-11-10 2014-07-10 Kyowa Hakko Kirin Co Ltd Inibidor de produção de quinurenina
DE102009049679A1 (de) 2009-10-19 2011-04-21 Merck Patent Gmbh Pyrazolopyrimidinderivate
UY33221A (es) 2010-02-09 2011-09-30 Univ California MÉTODOS PARA TRATAR CÁNCER USANDO INHIBIDORES DE PI3K Y mTOR EN COMBINACIÓN CON INHIBIDORES DE AUTOFAGIA
AR084469A1 (es) 2010-07-09 2013-05-22 Exelixis Inc Combinaciones de inhibidores de quinasas para el tratamiento del cancer
CA2812089C (fr) 2010-09-14 2020-02-18 Exelixis Inc. Inhibiteurs de pi3k-delta et leurs procedes d'utilisation et fabrication
KR20130141528A (ko) 2010-10-20 2013-12-26 메르크 세로노 에스에이 제네바 치환 ｎ-(3-아미노-퀴녹살린-2-일)-술폰아미드 및 이들의 중간체인 ｎ-(3-클로로-퀴녹살린-2-일)술폰아미드의 제조 방법
DE102010048800A1 (de) 2010-10-20 2012-05-10 Merck Patent Gmbh Chinoxalinderivate
DE102010049595A1 (de) 2010-10-26 2012-04-26 Merck Patent Gmbh Chinazolinderivate
WO2012065057A2 (fr) 2010-11-12 2012-05-18 Exelixis, Inc. Inhibiteurs de la phosphatidylinositol 3-kinase et leurs procédés d'utilisation
IN2014CN02671A (fr) * 2011-09-14 2015-07-03 Exelixis Inc
WO2013052699A2 (fr) * 2011-10-04 2013-04-11 Gilead Calistoga Llc Nouveaux inhibiteurs de quinoxaline de la voie pi3k
WO2013056067A1 (fr) 2011-10-13 2013-04-18 Exelixis, Inc. Composés pour une utilisation dans le traitement de carcinome des cellules basales
PH12014500897A1 (en) * 2011-10-28 2019-10-07 Novartis Ag Method of treating gastrointestinal stromal tumors
HK1201480A1 (en) * 2011-11-01 2015-09-04 Exelixis, Inc. N-(3-{[(3-{[2-chloro-5-(methoxy)phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}phenyl)-2-methylalaninamide as phosphatidylinositol 3-kinase inhibitor for the treatment of lymphoproliferative malignancies
WO2013067306A1 (fr) * 2011-11-02 2013-05-10 Exelixis, Inc. Inhibiteurs de la phosphatidylinositol 3-kinase pour le traitement de cancers chez les enfants
WO2013101964A1 (fr) * 2011-12-27 2013-07-04 Kadmon Corporation, Llc Procédés de traitement d'un cancer du sein ne répondant pas au trastuzumab
WO2013152717A1 (fr) 2012-04-10 2013-10-17 上海昀怡健康管理咨询有限公司 Composé de pyrimidine condensé, et procédé de préparation, intermédiaire, composition et utilisations dudit composé
US9487526B2 (en) 2012-08-13 2016-11-08 Takeda Pharmaceutical Company Limited Quinoxaline derivatives as GPR6 modulators
CN104513254B (zh) 2013-09-30 2019-07-26 上海璎黎药业有限公司 稠合嘧啶类化合物、中间体、其制备方法、组合物和应用
CN104557872B (zh) 2013-10-16 2017-05-24 上海璎黎药业有限公司 稠合杂环化合物、其制备方法、药物组合物和用途
WO2015123505A1 (fr) 2014-02-14 2015-08-20 Takeda Pharmaceutical Company Limited Modulateurs pyridopyrazines de gpr6
US9950194B2 (en) 2014-09-09 2018-04-24 Mevion Medical Systems, Inc. Patient positioning system
WO2019119206A1 (fr) 2017-12-18 2019-06-27 Merck Sharp & Dohme Corp. Inhibiteurs puriques de la phosphatidylinositol 3-kinase delta humaine

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006515885A (ja) * 2003-01-17 2006-06-08 スレッシュオールド ファーマシューティカルズ， インコーポレイテッド 癌の処置のための併用療法
EP2351745A1 (fr) * 2005-08-26 2011-08-03 Merck Serono S.A. Dérivés de pyrazine et leurs utilisations en tant qu'inhibiteurs de PI3K
KR20140105621A (ko) * 2005-10-07 2014-09-01 엑셀리시스, 인코포레이티드 ＰＩ３Ｋα의 피리도피리미디논 억제제
CA2623768C (fr) * 2005-10-07 2016-04-12 Exelixis, Inc. Derives de n-(3-amino-quinoxalin-2-yl) -sulfonamide et leur utilisation comme inhibiteurs de phosphatidylinositol 3-kinase
ATE539752T1 (de) 2006-08-16 2012-01-15 Exelixis Inc Verwendung von pi3k- und mek-modulatoren bei der krebsbehandlung
BRPI0808013A2 (pt) 2007-02-22 2014-06-17 Merck Serono Sa Compostos de quinoxalina e uso dos mesmos
RS52939B (sr) * 2007-04-10 2014-02-28 Exelixis Inc. Postupci za lečenje kancera upotrebom piridopirimidinonskih inhibitora pi3k alfa
JP4623164B2 (ja) * 2008-08-21 2011-02-02 セイコーエプソン株式会社 プロジェクタ

Also Published As

Publication number Publication date
IL201211A0 (en) 2010-05-31
HK1140141A1 (en) 2010-10-08
EP2139483B9 (fr) 2014-05-21
NI200900184A (es) 2011-09-08
CR11099A (es) 2010-01-19
US8481001B2 (en) 2013-07-09
MA31335B1 (fr) 2010-04-01
AU2008239668A1 (en) 2008-10-23
JP2014074031A (ja) 2014-04-24
IL201211A (en) 2015-09-24
HRP20131081T1 (hr) 2013-12-20
CN103202842A (zh) 2013-07-17
BRPI0810208A2 (pt) 2014-10-21
CY1114608T1 (el) 2016-10-05
EP2139483A2 (fr) 2010-01-06
JP5726515B2 (ja) 2015-06-03
PT2139483E (pt) 2013-12-27
CN101959516B (zh) 2013-05-08
CN101959516A (zh) 2011-01-26
NZ580009A (en) 2012-06-29
ES2438998T3 (es) 2014-01-21
UA98141C2 (ru) 2012-04-25
DK2139483T3 (da) 2014-01-13
US20110123434A1 (en) 2011-05-26
KR20100019436A (ko) 2010-02-18
AU2008239668B2 (en) 2013-11-07
JP2010523669A (ja) 2010-07-15
WO2008127594A3 (fr) 2009-04-30
KR101586774B1 (ko) 2016-01-19
GT200900263A (es) 2014-01-15
SV2009003390A (es) 2010-05-21
SI2139483T1 (sl) 2013-11-29
MX2009010929A (es) 2010-01-20
CA2684056A1 (fr) 2008-10-23
PL2139483T3 (pl) 2014-02-28
EA200970935A1 (ru) 2010-04-30
ZA200906765B (en) 2010-05-26
ECSP099723A (es) 2010-03-31
CO6140024A2 (es) 2010-03-19
RS53020B (sr) 2014-04-30
EP2139483B1 (fr) 2013-09-18
MY150797A (en) 2014-02-28
EA019064B1 (ru) 2013-12-30
WO2008127594A2 (fr) 2008-10-23
ME00937B (fr) 2012-06-20

Similar Documents

Publication Publication Date Title
TN2009000399A1 (fr) Procedes de traitement impliquant l'inhibition de pi3k-alpha au moyen d'inhibiteurs de type quinaxoline
MA31358B1 (fr) Méthodes de traitement du cancer à l'aide d'inhibiteurs de pi3k alpha à base de pyridopyrimidinone
MY146111A (en) Acylaminopyrazoles as fgfr inhibitors
MA34207B1 (fr) Inhibiteurs de la pi3 kinase et/ou du mtor
SG179418A1 (en) Inhibitors of the hedgehog pathway
MA32903B1 (fr) Inhibiteurs de proteine-kinases
ATE534377T1 (de) Verfahren und zusammensetzungen zur behandlung von hämatologischen erkrankungen
MY148688A (en) 2-methylmorpholine pyrido-, pyrazo- and pyrimido-pyrimidine derivatives as mtor inhibitors
MA33076B1 (fr) Utilisation d'un inhibiteur de la gamma-secretase pour le traitement du cancer
MA32135B1 (fr) Inhibiteurs de pim kinase et leurs procedes d'utilisation
EA200802329A1 (ru) Производные триазола ii
EA200802223A1 (ru) 1,5-дифенилпиразолы ii в качестве ингибиторов hsp90
IL192100A0 (en) Use of benzo-fused heterocycle sulfamide derivatives for the treatment of pain
MA38315A1 (fr) Composés tétracycliques substitués par un hétérocycle et procédés pour les utiliser pour le traitement de maladies virales
UA104148C2 (ru) [4-(5-аминометил-2-фторфенил)-пиперидин-1-ил]-[7-фтор-1-(2-метоксиэтил)-4-трифторметокси-1h-индол-3-ил]-метанон как ингибитор триптазы тучных клеток
UA96969C2 (en) Acylaminopyrazoles as fgfr inhibitors
ATE543492T1 (de) Behandlung von lungenkrebs
MA35347B1 (fr) Procedes therapeuiques
UA96304C2 (en) 2-METHYLMORPHOLINE PYRIDO-, PYRAZO- AND PYRIMIDO-PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS
TW200602035A (en) [4-(5-Aminomethyl-2-fluoro-phenyl)-piperidin-1-yl]-(4-bromo-3-methyl-5-propoxy-thiophen-2-yl)-methanone hydrochloride as an inhibitor of mast cell tryptase
MY156278A (en) Disubstituted [4-(5-aminomethyl-phenyl)-piperidin-1-yl]-1h-indol-3-yl]-methanones
NO20070250L (no) S-Tenatoprazol-natriummonohydratsalt og dennes anvendelse i form av en protonpumpe-inhibitor
SE0402591D0 (sv) Novel use
UA99612C2 (en) Inhibitors of the hedgehog pathway
UA89242C2 (ru) Способ лечения эндометриоза с применением ингибитора jnk, которым является производное бензотиазола