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TNSN08445A1 - Derives de triazolopyrazine utiles comme agent anticancereux - Google Patents

Derives de triazolopyrazine utiles comme agent anticancereux

Info

Publication number
TNSN08445A1
TNSN08445A1 TNP2008000445A TNSN08445A TNSN08445A1 TN SN08445 A1 TNSN08445 A1 TN SN08445A1 TN P2008000445 A TNP2008000445 A TN P2008000445A TN SN08445 A TNSN08445 A TN SN08445A TN SN08445 A1 TNSN08445 A1 TN SN08445A1
Authority
TN
Tunisia
Prior art keywords
anticancer agent
derivatives useful
formula
compounds
triazolopyrazine derivatives
Prior art date
Application number
TNP2008000445A
Other languages
English (en)
Inventor
Robert Steven Kania
Mary Catherine Johnson
Phuong Thi Quy Le
Mitchell David Nambu
Mason Alan Pairish
Hong Shen
Michelle Bich Tran-Dube
Heng-Miao Chen
Jacqui Elizabeth Hoffman
Jingroung Jean Cui
Lei Jia
Original Assignee
Pfizer Prod 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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of TNSN08445A1 publication Critical patent/TNSN08445A1/fr

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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/5025Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

L'invention concerne des composés de formule (I) ou un de leurs sels pharmaceutiquement acceptables, formule dans laquelle R1, R2, R3 et R4 sont tels que definis dans le present memoire. L'invention concerne egalement des compositions pharmaceutiques contenant les composés de formule I, ainsi que des methodes pour le traitement de troubles hyperproliferatifs chez un mammifère par administration des composés de formule (I).
TNP2008000445A 2006-05-11 2008-11-06 Derives de triazolopyrazine utiles comme agent anticancereux TNSN08445A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US79996606P 2006-05-11 2006-05-11
US89323107P 2007-03-06 2007-03-06
PCT/IB2007/001142 WO2007132308A1 (fr) 2006-05-11 2007-04-30 Dérivés de triazolopyrazine utiles en tant qu'agents anti-cancereux

Publications (1)

Publication Number Publication Date
TNSN08445A1 true TNSN08445A1 (fr) 2010-04-14

Family

ID=38441445

Family Applications (1)

Application Number Title Priority Date Filing Date
TNP2008000445A TNSN08445A1 (fr) 2006-05-11 2008-11-06 Derives de triazolopyrazine utiles comme agent anticancereux

Country Status (32)

Country Link
US (2) US7732604B2 (fr)
EP (1) EP2018383B1 (fr)
JP (1) JP4377962B2 (fr)
KR (1) KR101099161B1 (fr)
CN (1) CN101443331A (fr)
AP (1) AP2008004674A0 (fr)
AR (1) AR060994A1 (fr)
AT (1) ATE532785T1 (fr)
AU (1) AU2007251283A1 (fr)
BR (1) BRPI0711809A2 (fr)
CA (1) CA2651363C (fr)
CR (1) CR10383A (fr)
EA (1) EA016204B1 (fr)
EC (1) ECSP088871A (fr)
ES (1) ES2376913T3 (fr)
GE (1) GEP20115174B (fr)
GT (1) GT200700039A (fr)
HN (1) HN2007015177A (fr)
IL (1) IL194813A0 (fr)
MA (1) MA30411B1 (fr)
ME (1) MEP36508A (fr)
MX (1) MX2008014399A (fr)
NL (1) NL2000613C2 (fr)
NO (1) NO20085060L (fr)
NZ (1) NZ572361A (fr)
PE (1) PE20080067A1 (fr)
RS (1) RS20080533A (fr)
TN (1) TNSN08445A1 (fr)
TW (1) TWI346115B (fr)
UY (1) UY30334A1 (fr)
WO (1) WO2007132308A1 (fr)
ZA (1) ZA200809020B (fr)

Families Citing this family (56)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8198448B2 (en) * 2006-07-14 2012-06-12 Amgen Inc. Fused heterocyclic derivatives and methods of use
PE20121506A1 (es) 2006-07-14 2012-11-26 Amgen Inc Compuestos triazolopiridinas como inhibidores de c-met
US8217177B2 (en) 2006-07-14 2012-07-10 Amgen Inc. Fused heterocyclic derivatives and methods of use
DE102007026341A1 (de) 2007-06-06 2008-12-11 Merck Patent Gmbh Benzoxazolonderivate
DE102007032507A1 (de) 2007-07-12 2009-04-02 Merck Patent Gmbh Pyridazinonderivate
US20110039856A1 (en) * 2007-11-29 2011-02-17 Pfizer Inc. Polymorphs of a c-met/hgfr inhibitor
DE102007061963A1 (de) 2007-12-21 2009-06-25 Merck Patent Gmbh Pyridazinonderivate
US20110009421A1 (en) * 2008-02-27 2011-01-13 Takeda Pharmaceutical Company Limited Compound having 6-membered aromatic ring
AR070487A1 (es) * 2008-02-28 2010-04-07 Novartis Ag Derivados de 3- metil- imidazo -( 1,2-b)- piridazina
US8598184B2 (en) * 2008-03-03 2013-12-03 Tiger Pharmatech Protein kinase inhibitors
DE102008019907A1 (de) 2008-04-21 2009-10-22 Merck Patent Gmbh Pyridazinonderivate
DE102008028905A1 (de) 2008-06-18 2009-12-24 Merck Patent Gmbh 3-(3-Pyrimidin-2-yl-benzyl)-[1,2,4]triazolo[4,3-b]pyridazinderivate
US20110130384A1 (en) * 2008-06-25 2011-06-02 Takeda Pharmaceutical Company Limited Amide compound
DE102008037790A1 (de) 2008-08-14 2010-02-18 Merck Patent Gmbh Bicyclische Triazolderivate
JP2012509342A (ja) * 2008-11-20 2012-04-19 オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド 置換ピロロ[2,3−b]−ピリジンおよび−ピラジン
CA2744563A1 (fr) * 2008-12-12 2010-06-17 Ariad Pharmaceuticals, Inc. Derives d'azaindole en tant qu'inhibiteurs de kinases
EA019320B1 (ru) 2008-12-22 2014-02-28 Мерк Патент Гмбх Новые полиморфные формы дигидрофосфата 6-(1-метил-1h-пиразол-4-ил)-2-{3-[5-(2-морфолин-4-илэтокси)пиримидин-2-ил]бензил}-2h-пиридазин-3-она и способы их получения
JOP20190230A1 (ar) 2009-01-15 2017-06-16 Incyte Corp طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به
SG176574A1 (en) * 2009-05-28 2012-01-30 Vertex Pharma Aminopyrazole triazolothiadiazole inhibitors of c-met protien kinase
US8389526B2 (en) 2009-08-07 2013-03-05 Novartis Ag 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives
JP5781510B2 (ja) * 2009-08-12 2015-09-24 ノバルティス アーゲー ヘテロ環式ヒドラゾン化合物および癌および炎症の処置のためのそれらの使用
MX2012002179A (es) 2009-08-20 2012-03-16 Novartis Ag Compuestos heterociclicos de oxima.
DE102009056886A1 (de) 2009-12-03 2011-06-09 Bayer Schering Pharma Aktiengesellschaft cMet-Inhibitoren zur Behandlung der Endometriose
EP2719699B1 (fr) 2009-12-31 2015-07-08 Hutchison Medipharma Limited Certaines triazolopyrazines, leurs compositions et leurs procédés d'utilisation
TWI423974B (zh) * 2010-02-11 2014-01-21 Hutchison Medipharma Ltd 三氮唑並吡啶和三氮唑並吡嗪化合物及其組合物和應用
AR081039A1 (es) 2010-05-14 2012-05-30 Osi Pharmaceuticals Llc Inhibidores biciclicos fusionados de quinasa
JP2013526570A (ja) 2010-05-14 2013-06-24 オーエスアイ・ファーマシューティカルズ,エルエルシー 縮合二環式キナーゼ阻害剤
ES2715611T3 (es) * 2010-05-17 2019-06-05 Incozen Therapeutics Pvt Ltd Compuestos novedosos de 3H-imidazo[4,5-b]piridina-3,5-disustituida y 3H-[1,2,3]triazolo[4,5-b]piridina 3,5-disustituida como moduladores de proteína cinasas
US20130315895A1 (en) 2010-07-01 2013-11-28 Takeda Pharmaceutical Company Limited COMBINATION OF A cMET INHIBITOR AND AN ANTIBODY TO HGF AND/OR cMET
WO2012042421A1 (fr) 2010-09-29 2012-04-05 Pfizer Inc. Procédé de traitement de la croissance cellulaire anormale
CN102532141A (zh) 2010-12-08 2012-07-04 中国科学院上海药物研究所 [1,2,4]三唑并[4,3-b][1,2,4]三嗪类化合物、其制备方法和用途
US20140088114A1 (en) 2011-05-16 2014-03-27 OSI Pharmaceuticals ,LLC Fused bicyclic kinase inhibitors
WO2013038362A1 (fr) 2011-09-15 2013-03-21 Novartis Ag 3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyradines substituées en position 6 à activité tyrosine kinase
CN102516263B (zh) * 2011-10-25 2015-04-08 南方医科大学 一种螺三环类化合物及其制备方法、以及含该类化合物的药物组合物及其应用
CN102503959B (zh) * 2011-10-25 2015-04-08 南方医科大学 一种稠三环类化合物及其制备方法、以及含该类化合物的药物组合物及其应用
CN103204844A (zh) * 2012-01-17 2013-07-17 上海艾力斯医药科技有限公司 氨基杂芳基化合物及其制备方法与应用
KR102164317B1 (ko) 2012-03-30 2020-10-13 리젠 파마슈티컬스 소시에떼 아노님 C-met 단백질 키나제의 조절제로서의 신규한 3,5-디치환-3h-이미다조[4,5-b]피리딘 및 3,5- 디치환 -3h-[1,2,3]트리아졸로[4,5-b] 피리딘 화합물
WO2013149581A1 (fr) 2012-04-03 2013-10-10 Novartis Ag Produits combinés comprenant des inhibiteurs de tyrosine kinase et leur utilisation
US20150051210A1 (en) 2012-04-03 2015-02-19 Novartis Ag Tyrosine Kinase Inhibitor Combinations and their Use
CN107312009B (zh) * 2013-04-17 2022-09-20 上海医药集团股份有限公司 喹啉类化合物、其制备方法、中间体、药物组合物和应用
WO2014174478A1 (fr) 2013-04-26 2014-10-30 Novartis Ag Combinaisons pharmaceutiques d'un inhibiteur de la pkc et d'un inhibiteur du récepteur tyrosine-kinase c-met
ES2675355T3 (es) * 2013-09-30 2018-07-10 Korea Research Institute Of Chemical Technology Derivados de triazolopirazina como inhibidores de tirosina cinasa
ES2764299T3 (es) 2014-12-09 2020-06-02 Inst Nat Sante Rech Med Anticuerpos monoclonales humanos contra AXL
WO2016135041A1 (fr) 2015-02-26 2016-09-01 INSERM (Institut National de la Santé et de la Recherche Médicale) Protéines de fusion et anticorps les contenant pour favoriser l'apoptose
JP2018123059A (ja) * 2015-06-10 2018-08-09 石原産業株式会社 1−シクロプロピルエチルアミン又はその塩の製造方法
WO2017015267A1 (fr) * 2015-07-20 2017-01-26 Genzyme Corporation Inhibiteurs du récepteur de facteur-1 de stimulation de colonies (csf-1r)
CN105272995B (zh) 2015-09-24 2017-10-27 上海海聚生物科技有限公司 喹啉类衍生物、其药物组合物、制备方法及应用
EP3398951B1 (fr) * 2015-12-31 2021-04-07 Shanghai Pharmaceuticals Holding Co., Ltd. Sel de composé de quinolone, ses polymorphes, son procédé de préparation, sa composition et les applications associées
SG11201807965YA (en) 2016-03-15 2018-10-30 Oryzon Genomics Sa Combinations of lsd1 inhibitors for use in the treatment of solid tumors
US11091489B2 (en) * 2016-06-20 2021-08-17 Novartis Ag Crystalline forms of a triazolopyrimidine compound
KR20180092096A (ko) * 2017-02-08 2018-08-17 에이비온 주식회사 트리아졸로 피라진 유도체의 신규한 다형체 및 이의 제조 방법
CN108570053A (zh) * 2017-03-13 2018-09-25 中国科学院上海药物研究所 五元并六元杂环化合物、制备方法、中间体、组合和应用
CN108276418A (zh) * 2018-03-20 2018-07-13 北京凯恩梅格医药科技有限公司 化合物、含有该化合物的药用组合物及其用途
CA3122575A1 (fr) 2018-12-14 2020-06-18 Beta Pharma, Inc. Composes substitues par organophosphore en tant qu'inhibiteurs de c-met et leurs utilisations therapeutiques
JP2024500919A (ja) 2020-12-23 2024-01-10 ジェンザイム・コーポレーション 重水素化コロニー刺激因子-1受容体(csf-1r)阻害剤
WO2025098425A1 (fr) * 2023-11-09 2025-05-15 浙江华海药业股份有限公司 Procédé de préparation de modulateur du récepteur de la chimiokine et utilisation

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI941572L (fi) 1991-10-07 1994-05-27 Oncologix Inc Anti-erbB-2-monoklonaalisten vasta-aineiden yhdistelmä ja käyttömenetelmä
ATE419355T1 (de) 1992-02-06 2009-01-15 Novartis Vaccines & Diagnostic Marker für krebs und biosynthetisches bindeprotein dafür
IL112248A0 (en) 1994-01-25 1995-03-30 Warner Lambert Co Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them
GB9520822D0 (en) 1995-10-11 1995-12-13 Wellcome Found Therapeutically active compounds
EP0912559B1 (fr) 1996-07-13 2002-11-06 Glaxo Group Limited Composes heterocycliques condenses en tant qu'inhibiteurs de la proteine tyrosine kinase
DE69718472T2 (de) 1996-07-13 2003-11-06 Glaxo Group Ltd., Greenford Bicyclische heteroaromatische verbindungen als protein tyrosine kinase inhibitoren
GB9800569D0 (en) 1998-01-12 1998-03-11 Glaxo Group Ltd Heterocyclic compounds
GB9800575D0 (en) 1998-01-12 1998-03-11 Glaxo Group Ltd Heterocyclic compounds
PT1212327E (pt) * 1999-09-17 2004-01-30 Abbott Gmbh & Co Kg Pirazolopirimidinas como agentes terapeuticos
JP2007516180A (ja) * 2003-07-02 2007-06-21 スゲン,インコーポレイティド c−Met阻害薬としてのアリールメチルトリアゾロおよびイミダゾピラジン類
WO2005028480A2 (fr) 2003-09-03 2005-03-31 Neurogen Corporation 5-aryl-pyrazolo[4,3-d]pyrimidines, pyridines, et pyrazines et composes associes
US9672526B2 (en) 2012-03-13 2017-06-06 American Express Travel Related Services Company, Inc. Systems and methods for tailoring marketing
US10884952B2 (en) 2016-09-30 2021-01-05 Intel Corporation Enforcing memory operand types using protection keys

Also Published As

Publication number Publication date
BRPI0711809A2 (pt) 2011-12-06
TW200804384A (en) 2008-01-16
JP4377962B2 (ja) 2009-12-02
US7732604B2 (en) 2010-06-08
AR060994A1 (es) 2008-07-30
NL2000613C2 (nl) 2007-11-20
US20070265272A1 (en) 2007-11-15
US20100105656A1 (en) 2010-04-29
MEP36508A (en) 2011-02-10
EP2018383B1 (fr) 2011-11-09
GEP20115174B (en) 2011-03-10
CA2651363C (fr) 2011-07-12
EA016204B1 (ru) 2012-03-30
HN2007015177A (es) 2010-06-09
ATE532785T1 (de) 2011-11-15
ECSP088871A (es) 2008-12-30
UY30334A1 (es) 2008-01-02
EP2018383A1 (fr) 2009-01-28
NO20085060L (no) 2008-12-03
JP2009536636A (ja) 2009-10-15
IL194813A0 (en) 2009-08-03
WO2007132308A1 (fr) 2007-11-22
AP2008004674A0 (en) 2008-12-31
EA200870423A1 (ru) 2009-04-28
MA30411B1 (fr) 2009-05-04
MX2008014399A (es) 2008-11-27
RS20080533A (sr) 2009-09-08
CR10383A (es) 2008-11-11
KR20090006187A (ko) 2009-01-14
AU2007251283A1 (en) 2007-11-22
GT200700039A (es) 2008-06-02
CN101443331A (zh) 2009-05-27
ES2376913T3 (es) 2012-03-20
NZ572361A (en) 2012-02-24
ZA200809020B (en) 2009-12-30
PE20080067A1 (es) 2008-03-10
TWI346115B (en) 2011-08-01
CA2651363A1 (fr) 2007-11-22
KR101099161B1 (ko) 2011-12-27

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