PE20080067A1 - DERIVADOS DE TRIAZOLOPIRAZINA COMO MODULADORES DEL RECEPTOR DEL FACTOR DE CRECIMIENTO DE HEPATOCITO (c-MET O HGFR) - Google Patents
DERIVADOS DE TRIAZOLOPIRAZINA COMO MODULADORES DEL RECEPTOR DEL FACTOR DE CRECIMIENTO DE HEPATOCITO (c-MET O HGFR)Info
- Publication number
- PE20080067A1 PE20080067A1 PE2007000559A PE2007000559A PE20080067A1 PE 20080067 A1 PE20080067 A1 PE 20080067A1 PE 2007000559 A PE2007000559 A PE 2007000559A PE 2007000559 A PE2007000559 A PE 2007000559A PE 20080067 A1 PE20080067 A1 PE 20080067A1
- Authority
- PE
- Peru
- Prior art keywords
- hgfr
- modulators
- receptor
- met
- growth factor
- Prior art date
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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- 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)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Oncology (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
SE REFIERE A COMPUESTOS DERIVADOS DE TRIAZOLOPIRAZINA DE FORMULA (I) DONDE R1 Y R2 SON CADA UNO H, F, ALQUILO(C1-C6), CICLOALQUILO(C3-C8), ALQUENILO(C2-C6), ENTRE OTROS; R3 ES UN COMPUESTO DE FORMULA (i) DONDE R5, R6, R7, R8 Y R9 SON CADA UNO H, CN, NO2, ARILO(C6-C10), ALQUINILO(C2-C6), ENTRE OTROS; R4 ES H, F, ALQUILO(C1-C6) O ARILO(C6-C12). SON COMPUESTOS PREFERIDOS: 6-((6-(1-METIL-1H-PIRAZOL-4-IL)-1H-[1,2,3]TRIAZOLO[4,5-b]PIRAZIN-1-IL)METIL)QUINOLINA, N-(PIPERIDIN-4-IL)-4-(3-(QUINOLIN-6-ILMETIL)-3H-[1,2,3]TRIAZOLO[4,5-b]PIRAZIN-5-IL)BENZAMIDA, N-(2-AMINOETIL)-4-(3-(QUINOLIN-6-ILMETIL)-3H-[1,2,3]TRIAZOLO[4,5-b]PIRAZIN-5-IL)BENZAMIDA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON MODULADORES DEL RECEPTOR DEL FACTOR DE CRECIMIENTO DE HEPATOCITO (c-MET O HGFR) SIENDO UTILES EN EL TRATAMIENTO DE CANCER DE MAMA, GLIOMA, MELANOMA, LEUCEMIA
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US79996606P | 2006-05-11 | 2006-05-11 | |
US89323107P | 2007-03-06 | 2007-03-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20080067A1 true PE20080067A1 (es) | 2008-03-10 |
Family
ID=38441445
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2007000559A PE20080067A1 (es) | 2006-05-11 | 2007-05-09 | DERIVADOS DE TRIAZOLOPIRAZINA COMO MODULADORES DEL RECEPTOR DEL FACTOR DE CRECIMIENTO DE HEPATOCITO (c-MET O HGFR) |
Country Status (32)
Country | Link |
---|---|
US (2) | US7732604B2 (es) |
EP (1) | EP2018383B1 (es) |
JP (1) | JP4377962B2 (es) |
KR (1) | KR101099161B1 (es) |
CN (1) | CN101443331A (es) |
AP (1) | AP2008004674A0 (es) |
AR (1) | AR060994A1 (es) |
AT (1) | ATE532785T1 (es) |
AU (1) | AU2007251283A1 (es) |
BR (1) | BRPI0711809A2 (es) |
CA (1) | CA2651363C (es) |
CR (1) | CR10383A (es) |
EA (1) | EA016204B1 (es) |
EC (1) | ECSP088871A (es) |
ES (1) | ES2376913T3 (es) |
GE (1) | GEP20115174B (es) |
GT (1) | GT200700039A (es) |
HN (1) | HN2007015177A (es) |
IL (1) | IL194813A0 (es) |
MA (1) | MA30411B1 (es) |
ME (1) | MEP36508A (es) |
MX (1) | MX2008014399A (es) |
NL (1) | NL2000613C2 (es) |
NO (1) | NO20085060L (es) |
NZ (1) | NZ572361A (es) |
PE (1) | PE20080067A1 (es) |
RS (1) | RS20080533A (es) |
TN (1) | TNSN08445A1 (es) |
TW (1) | TWI346115B (es) |
UY (1) | UY30334A1 (es) |
WO (1) | WO2007132308A1 (es) |
ZA (1) | ZA200809020B (es) |
Families Citing this family (55)
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US8198448B2 (en) * | 2006-07-14 | 2012-06-12 | Amgen Inc. | Fused heterocyclic derivatives and methods of use |
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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 |
EP2253618A1 (en) * | 2008-02-27 | 2010-11-24 | Takeda Pharmaceutical Company Limited | Compound having 6-membered aromatic ring |
EP2265614A1 (en) * | 2008-02-28 | 2010-12-29 | Novartis AG | Imidazo [1,2-b]pyridazine derivatives for the treatment of c-met tyrosine kinase mediated disease |
AU2009222122A1 (en) * | 2008-03-03 | 2009-09-11 | Tiger Pharmatech | Tyrosine 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 |
JPWO2009157196A1 (ja) * | 2008-06-25 | 2011-12-08 | 武田薬品工業株式会社 | アミド化合物 |
DE102008037790A1 (de) * | 2008-08-14 | 2010-02-18 | Merck Patent Gmbh | Bicyclische Triazolderivate |
EP2356116A1 (en) | 2008-11-20 | 2011-08-17 | OSI Pharmaceuticals, Inc. | Substituted pyrroloý2,3-b¨-pyridines and-pyrazines |
CA2744563A1 (en) | 2008-12-12 | 2010-06-17 | Ariad Pharmaceuticals, Inc. | Azaindole derivatives as kinase inhibitors |
MX2011006682A (es) | 2008-12-22 | 2011-07-13 | Merck Patent Gmbh | Nuevas formas polimorficas de dihidrogeno-fosfato de 6-(1-metil-1h-pirazol-4-il)-2-{3-[5-(2-morfolin-4-il-etoxi)-pirim idin-2-il]-bencil}-2h-piridazin-3-ona y procesos para su preparacion. |
JOP20190231A1 (ar) | 2009-01-15 | 2017-06-16 | Incyte Corp | طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به |
CN102459283B (zh) * | 2009-05-28 | 2014-11-12 | 沃泰克斯药物股份有限公司 | C-met 蛋白激酶的氨基吡唑三唑并噻二唑抑制剂 |
US8389526B2 (en) | 2009-08-07 | 2013-03-05 | Novartis Ag | 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives |
WO2011018454A1 (en) | 2009-08-12 | 2011-02-17 | Novartis Ag | Heterocyclic hydrazone compounds and their uses to treat cancer and inflammation |
EA201200318A1 (ru) * | 2009-08-20 | 2012-09-28 | Новартис Аг | Гетероциклические оксимы |
DE102009056886A1 (de) * | 2009-12-03 | 2011-06-09 | Bayer Schering Pharma Aktiengesellschaft | cMet-Inhibitoren zur Behandlung der Endometriose |
RS61281B1 (sr) * | 2009-12-31 | 2021-02-26 | Hutchison Medipharma Ltd | Sintetički intermedijer koristan u pripremi triazolopiridinskih c-met inhibitora |
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 |
WO2011143646A1 (en) | 2010-05-14 | 2011-11-17 | OSI Pharmaceuticals, LLC | Fused bicyclic kinase inhibitors |
AR081039A1 (es) | 2010-05-14 | 2012-05-30 | Osi Pharmaceuticals Llc | Inhibidores biciclicos fusionados de quinasa |
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 |
JP2013532627A (ja) | 2010-07-01 | 2013-08-19 | 武田薬品工業株式会社 | cMET阻害剤とHGFおよび/またはcMETに対する抗体との組み合わせ |
WO2012042421A1 (en) | 2010-09-29 | 2012-04-05 | Pfizer Inc. | Method of treating abnormal cell growth |
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 |
WO2012158658A1 (en) | 2011-05-16 | 2012-11-22 | OSI Pharmaceuticals, LLC | Fused bicyclic kinase inhibitors |
EP2755976B1 (en) | 2011-09-15 | 2018-07-18 | Novartis AG | 6-substituted 3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyridines as c-met tyrosine kinase inhibitors |
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 |
CN104321322A (zh) | 2012-03-30 | 2015-01-28 | 理森制药股份公司 | 作为c-met蛋白激酶调节剂的新型3,5-二取代-3h-咪唑并[4,5-b]吡啶和3,5-二取代-3h-[1,2,3]三唑并[4,5-b]吡啶化合物 |
JP2015512425A (ja) | 2012-04-03 | 2015-04-27 | ノバルティス アーゲー | チロシンキナーゼ阻害剤との組合せ製品及びそれらの使用 |
JP2015512447A (ja) | 2012-04-03 | 2015-04-27 | ノバルティス アーゲー | チロシンキナーゼ阻害薬の組合せおよびその使用 |
CN105968115B (zh) * | 2013-04-17 | 2018-11-09 | 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 (en) | 2013-04-26 | 2014-10-30 | Novartis Ag | Pharmaceutical combinations of a pkc inhibitor and a c-met receptor tyrosine kinase inhibitor |
MX368311B (es) * | 2013-09-30 | 2019-09-27 | Korea Res Inst Chemical Tech | Nuevos derivados de triazolopirazina y usos de los mismos. |
ES2764299T3 (es) | 2014-12-09 | 2020-06-02 | Inst Nat Sante Rech Med | Anticuerpos monoclonales humanos contra AXL |
WO2016135041A1 (en) | 2015-02-26 | 2016-09-01 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Fusion proteins and antibodies comprising thereof for promoting apoptosis |
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 |
PE20180573A1 (es) | 2015-07-20 | 2018-04-04 | Genzyme Corp | Inhibidores del receptor del factor estimulador de colonias 1 (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 |
US10344035B2 (en) * | 2015-12-31 | 2019-07-09 | Shanghai Phaarmaceuticals Holding Co., Ltd. | Salt of quinolone compound, polymorphs thereof, preparation method therefor, composition, and applications |
EP3429571A1 (en) | 2016-03-15 | 2019-01-23 | Oryzon Genomics, S.A. | 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 (en) * | 2018-12-14 | 2020-06-18 | Beta Pharma, Inc. | Organophosphorus-substituted compounds as c-met inhibitors and therapeutic uses thereof |
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 |
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2007
- 2007-04-26 NL NL2000613A patent/NL2000613C2/nl not_active IP Right Cessation
- 2007-04-30 BR BRPI0711809-0A patent/BRPI0711809A2/pt not_active IP Right Cessation
- 2007-04-30 AT AT07734459T patent/ATE532785T1/de active
- 2007-04-30 EA EA200870423A patent/EA016204B1/ru not_active IP Right Cessation
- 2007-04-30 NZ NZ572361A patent/NZ572361A/en not_active IP Right Cessation
- 2007-04-30 JP JP2009508530A patent/JP4377962B2/ja not_active Expired - Fee Related
- 2007-04-30 RS RSP-2008/0533A patent/RS20080533A/sr unknown
- 2007-04-30 WO PCT/IB2007/001142 patent/WO2007132308A1/en active Application Filing
- 2007-04-30 AP AP2008004674A patent/AP2008004674A0/xx unknown
- 2007-04-30 EP EP07734459A patent/EP2018383B1/en active Active
- 2007-04-30 ES ES07734459T patent/ES2376913T3/es active Active
- 2007-04-30 AU AU2007251283A patent/AU2007251283A1/en not_active Abandoned
- 2007-04-30 MX MX2008014399A patent/MX2008014399A/es active IP Right Grant
- 2007-04-30 KR KR1020087027474A patent/KR101099161B1/ko not_active Expired - Fee Related
- 2007-04-30 GE GEAP200710971A patent/GEP20115174B/en unknown
- 2007-04-30 CA CA2651363A patent/CA2651363C/en not_active Expired - Fee Related
- 2007-04-30 CN CNA2007800170852A patent/CN101443331A/zh active Pending
- 2007-04-30 ME MEP-365/08A patent/MEP36508A/xx unknown
- 2007-05-08 US US11/745,921 patent/US7732604B2/en not_active Expired - Fee Related
- 2007-05-09 PE PE2007000559A patent/PE20080067A1/es not_active Application Discontinuation
- 2007-05-09 UY UY30334A patent/UY30334A1/es unknown
- 2007-05-09 GT GT200700039A patent/GT200700039A/es unknown
- 2007-05-09 AR ARP070102012A patent/AR060994A1/es not_active Application Discontinuation
- 2007-05-09 HN HN2007015177A patent/HN2007015177A/es unknown
- 2007-05-10 TW TW096116645A patent/TWI346115B/zh not_active IP Right Cessation
-
2008
- 2008-10-21 ZA ZA2008/09020A patent/ZA200809020B/en unknown
- 2008-10-21 CR CR10383A patent/CR10383A/es not_active Application Discontinuation
- 2008-10-22 IL IL194813A patent/IL194813A0/en unknown
- 2008-11-06 TN TNP2008000445A patent/TNSN08445A1/fr unknown
- 2008-11-07 EC EC2008008871A patent/ECSP088871A/es unknown
- 2008-11-11 MA MA31378A patent/MA30411B1/fr unknown
- 2008-12-03 NO NO20085060A patent/NO20085060L/no not_active Application Discontinuation
-
2010
- 2010-01-04 US US12/651,984 patent/US20100105656A1/en not_active Abandoned
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