PE20091414A1 - FURO [3,2-c] PIRIDINA Y TIENO [3,2-c] PIRIDINAS - Google Patents
FURO [3,2-c] PIRIDINA Y TIENO [3,2-c] PIRIDINASInfo
- Publication number
- PE20091414A1 PE20091414A1 PE2009000178A PE2009000178A PE20091414A1 PE 20091414 A1 PE20091414 A1 PE 20091414A1 PE 2009000178 A PE2009000178 A PE 2009000178A PE 2009000178 A PE2009000178 A PE 2009000178A PE 20091414 A1 PE20091414 A1 PE 20091414A1
- Authority
- PE
- Peru
- Prior art keywords
- furo
- alkyl
- pyridine
- ilamine
- pirazol
- Prior art date
Links
- WJDMEHCIRPKRRQ-UHFFFAOYSA-N furo[3,2-c]pyridine Chemical compound N1=CC=C2OC=CC2=C1 WJDMEHCIRPKRRQ-UHFFFAOYSA-N 0.000 title abstract 2
- RQMWVVBHJMUJNZ-UHFFFAOYSA-N 4-chloropyridin-2-amine Chemical compound NC1=CC(Cl)=CC=N1 RQMWVVBHJMUJNZ-UHFFFAOYSA-N 0.000 title 1
- -1 2,6-DICHLORO-3-FLUOROPHENYL Chemical class 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 206010009944 Colon cancer Diseases 0.000 abstract 1
- 201000008808 Fibrosarcoma Diseases 0.000 abstract 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 102000004022 Protein-Tyrosine Kinases Human genes 0.000 abstract 1
- 108090000412 Protein-Tyrosine Kinases Proteins 0.000 abstract 1
- 208000029742 colonic neoplasm Diseases 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 201000005202 lung cancer Diseases 0.000 abstract 1
- 208000020816 lung neoplasm Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
REFERIDA A UN COMPUESTO DERIVADO DE FURO[3,2-c]PIRIDINA Y TIENO[3,2-c]PIRIDINA DE FORMULA (I) DONDE X1 ES O, S; X2 ES O, S(O)m, NR5; R5 ES H, ALQUILO(C1-C12), CICLOALQUILO(C3-C12)ALQUILO(C1-C12), ENTRE OTROS; R1 ES H, HALO, CN, CF3, ENTRE OTROS; R2 ES H, CF3, NO2, ENTRE OTROS; R3 ES H O ALQUILO(C1-C12); R4 ES H, ALQUILO(C1-C12), HETEROCICLOALQUILO(C3-C12)ALQUILO(C1-C12), ENTRE OTROS; m ES 0-2; q ES 0-1. SON COMPUESTOS SELECCIONADOS: 7-[(R)-1-(2,6-DICLORO-3-FLUOROFENIL)-ETOXI]-3-(1-METIL-1H-PIRAZOL-4-IL)-FURO[3,2-c]PIRIDIN-6-ILAMINA; 7-[(R)-1-(2,6-DICLORO-3-FLUOROFENIL)-ETOXI]-3-(1-PIPERIDIN-4-IL-1H-PIRAZOL-4-IL)-FURO[3,2-c]PIRIDIN-6-ILAMINA; 7-[(R)-1-(2,6-DICLORO-3-FLUOROFENIL)-ETOXI]-3-(1H-PIRAZOL-4-IL)-FURO[3,2-c]PIRIDIN-6-ILAMINA; ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA ACTIVIDAD DE TIROSINA CINASA, SIENDO UTILES EN EL TRATAMIENTO DE CANCER COMO FIBROSARCOMA, CANCER DE PULMON, CANCER DE COLON, ENTRE OTROS
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US6380008P | 2008-02-06 | 2008-02-06 | |
US11955308P | 2008-12-03 | 2008-12-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20091414A1 true PE20091414A1 (es) | 2009-09-23 |
Family
ID=40524808
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2009000178A PE20091414A1 (es) | 2008-02-06 | 2009-02-05 | FURO [3,2-c] PIRIDINA Y TIENO [3,2-c] PIRIDINAS |
Country Status (19)
Country | Link |
---|---|
US (1) | US8022206B2 (es) |
EP (1) | EP2265616B8 (es) |
JP (1) | JP2011511094A (es) |
KR (1) | KR20110014971A (es) |
CN (1) | CN102007127A (es) |
AR (1) | AR070317A1 (es) |
AU (1) | AU2009212338A1 (es) |
BR (1) | BRPI0908050A2 (es) |
CA (1) | CA2711078A1 (es) |
CL (1) | CL2009000275A1 (es) |
EA (1) | EA201070929A1 (es) |
ES (1) | ES2451024T3 (es) |
IL (1) | IL206758A0 (es) |
MX (1) | MX2010008638A (es) |
PE (1) | PE20091414A1 (es) |
TW (1) | TW200944201A (es) |
UY (1) | UY31638A1 (es) |
WO (1) | WO2009100282A1 (es) |
ZA (1) | ZA201005554B (es) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2013519681A (ja) * | 2010-02-11 | 2013-05-30 | オーエスアイ・ファーマシューティカルズ,エルエルシー | 7−アミノフロピリジン誘導体 |
WO2011109593A1 (en) | 2010-03-03 | 2011-09-09 | OSI Pharmaceuticals, LLC | Substituted-5-aminopyrrolo/pyrazolopyridines |
US8916593B2 (en) * | 2010-05-04 | 2014-12-23 | Pfizer Inc. | Alkoxy-substituted 2-aminopyridines as ALK inhibitors |
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 |
TWI504350B (zh) * | 2010-09-01 | 2015-10-21 | Du Pont | 殺真菌吡唑及其混合物 |
US10614666B2 (en) | 2011-04-20 | 2020-04-07 | Video Gaming Technologies, Inc. | Gaming machines with free play bonus mode presenting only winning outcomes |
WO2013151584A1 (en) * | 2011-10-31 | 2013-10-10 | The Methodist Hospital Research Institute | Compound comprising a mao targeting/ seeker moiety for treating human gliomas |
JP6117334B2 (ja) * | 2012-03-23 | 2017-04-19 | メモリアル スローン−ケタリング キャンサー センター | 膵臓癌および関連するがんの5−アシル−6,7−ジヒドロチエノ[3,2−c]ピリジンでの処置 |
WO2013152252A1 (en) | 2012-04-06 | 2013-10-10 | OSI Pharmaceuticals, LLC | Combination anti-cancer therapy |
KR101582852B1 (ko) | 2012-05-24 | 2016-01-07 | 서울대학교 산학협력단 | 타우 단백질 매개 신경 퇴행성 질환 치료제 |
UY35630A (es) | 2013-06-26 | 2015-01-30 | Abbvie Inc | Carboxamidas primarias como inhibidores de btk |
US9907791B2 (en) * | 2014-03-14 | 2018-03-06 | University Of Utah Research Foundation | Ron inhibitors for use in preventing and treating bone loss |
CN103923081B (zh) * | 2014-04-14 | 2017-06-27 | 武汉光谷人福生物医药有限公司 | 化合物及其制备方法和应用 |
US10398774B2 (en) | 2014-12-09 | 2019-09-03 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Human monoclonal antibodies against 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 |
CN106866447A (zh) * | 2017-03-30 | 2017-06-20 | 成都绿林科技有限公司 | 一种合成对乙酰基苯甲酰胺的方法 |
US10957159B2 (en) | 2018-04-12 | 2021-03-23 | Aristocrat Technologies Australia Pty Limited | Gaming machine and method for displaying a free spin count-up |
US11427596B2 (en) * | 2019-07-19 | 2022-08-30 | Indian Institute of Technology Indore | Metal-free solvent-free synthesis of fused-pyrido heterocycles and biomedical applications |
WO2024124464A1 (zh) * | 2022-12-15 | 2024-06-20 | 武汉睿健医药科技有限公司 | 一种诱导间质细胞向上皮细胞转化及重编程的诱导剂 |
Family Cites Families (33)
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KR100875380B1 (ko) * | 2001-06-23 | 2008-12-23 | 아벤티스 파마슈티칼스 인크. | 단백질 키나제 억제제로서의 피롤로피리미딘 |
US20040235867A1 (en) * | 2001-07-24 | 2004-11-25 | Bilodeau Mark T. | Tyrosine kinase inhibitors |
EP1465900B1 (en) | 2002-01-10 | 2008-05-14 | Bayer HealthCare AG | Rho-kinase inhibitors |
US7704995B2 (en) * | 2002-05-03 | 2010-04-27 | Exelixis, Inc. | Protein kinase modulators and methods of use |
US7276519B2 (en) * | 2002-11-25 | 2007-10-02 | Wyeth | Thieno[3,2-b]pyridine-6-carbonitriles and thieno[2,3-b]pyridine-5-carbonitriles as protein kinase inhibitors |
CL2003002287A1 (es) * | 2002-11-25 | 2005-01-14 | Wyeth Corp | COMPUESTOS DERIVADOS DE TIENO[3,2-b]-PIRIDINA-6-CARBONITRILOS Y TIENEO[2,3-b]-PIRIDINA-5-CARBONITRILOS, COMPOSICION FARMACEUTICA, PROCEDIMIENTO DE PREPARACION Y COMPUESTOS INTERMEDIARIOS, Y SU USO EN EL TRATAMIENTO DEL CANCER, APOPLEJIA, OSTEOPOROSIS |
EP1590339A4 (en) | 2003-01-28 | 2007-07-25 | Smithkline Beecham Corp | CHEMICAL COMPOUNDS |
MEP52808A (en) * | 2003-02-26 | 2011-05-10 | Sugen Inc | Aminoheteroaryl compounds as protein kinase inhibitors |
EP1620094A4 (en) * | 2003-05-06 | 2010-04-28 | Glaxosmithkline Llc | NEW CHEMICAL COMPOUNDS |
US20050026944A1 (en) * | 2003-07-24 | 2005-02-03 | Patrick Betschmann | Thienopyridine and furopyridine kinase inhibitors |
US7674907B2 (en) * | 2004-07-23 | 2010-03-09 | Amgen Inc. | Furanopyridine derivatives and methods of use |
US7361764B2 (en) * | 2004-07-27 | 2008-04-22 | Sgx Pharmaceuticals, Inc. | Pyrrolo-pyridine kinase modulators |
US7709645B2 (en) | 2004-07-27 | 2010-05-04 | Sgx Pharmaceuticals, Inc. | Pyrrolo-pyridine kinase modulators |
BRPI0514687A (pt) * | 2004-08-26 | 2008-06-17 | Pfizer | compostos amino heteroarila como inibidores de proteìna tirosina cinase |
MX2007002312A (es) * | 2004-08-26 | 2007-04-16 | Pfizer | Compuestos de aminoheteroarilo enantiomericamente puros como inhibidores de proteina quinasa. |
BRPI0514537B8 (pt) | 2004-08-26 | 2021-05-25 | Pfizer | compostos de aminoeteroarila substituídos com pirazol e composição farmacêutica que os compreende |
CA2601983A1 (en) * | 2005-04-06 | 2006-10-12 | Astrazeneca Ab | Substituted heterocycles and their use as chk1, pdk1 and pak inhibitors |
JP2009504692A (ja) * | 2005-08-16 | 2009-02-05 | エフ.ホフマン−ラ ロシュ アーゲー | 新規4−アミノ−チエノ[3,2−c]ピリジン−7−カルボン酸アミド |
RU2008112313A (ru) | 2005-09-01 | 2009-10-10 | Эррэй Биофарма Инк. (Us) | Соединения ингибиторы raf и способы их применения |
WO2007056625A2 (en) * | 2005-11-04 | 2007-05-18 | Smithkline Beecham Corporation | Thienopyridine b-raf kinase inhibitors |
KR101146852B1 (ko) * | 2005-12-05 | 2012-05-16 | 화이자 프로덕츠 인크. | C?met/hgfr 억제제의 다형체 |
US7989461B2 (en) * | 2005-12-23 | 2011-08-02 | Amgen Inc. | Substituted quinazolinamine compounds for the treatment of cancer |
AU2007231577B2 (en) | 2006-03-22 | 2012-07-19 | Vertex Pharmaceuticals Incorporated | c-MET protein kinase inhibitors for the treatment of proliferative disorders |
US7745449B2 (en) | 2006-04-21 | 2010-06-29 | Amgen Inc. | Thieno-[2,3-d]pyrimidine and thieno-pyridazine compounds and methods of use |
US7601716B2 (en) * | 2006-05-01 | 2009-10-13 | Cephalon, Inc. | Pyridopyrazines and derivatives thereof as ALK and c-Met inhibitors |
WO2008080001A2 (en) * | 2006-12-21 | 2008-07-03 | Plexxikon, Inc. | Compounds and methods for kinase modulation, and indications therefor |
GB0625659D0 (en) | 2006-12-21 | 2007-01-31 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
PE20121126A1 (es) * | 2006-12-21 | 2012-08-24 | Plexxikon Inc | Compuestos pirrolo [2,3-b] piridinas como moduladores de quinasa |
TW200908968A (en) * | 2007-05-29 | 2009-03-01 | Sgx Pharmaceuticals Inc | Substituted pyrrolopyridines and pyrazolopyridines as kinase modulators |
KR20100089090A (ko) | 2007-10-25 | 2010-08-11 | 아스트라제네카 아베 | 세포 증식 장애의 치료에 유용한 피리딘 및 피라진 유도체 |
UY31478A1 (es) | 2007-11-21 | 2009-07-17 | Inhibicion del receptor para la proteina estimulante del macrofago (ron) y métodos para el tratamiento de lo mismo | |
WO2009140549A1 (en) | 2008-05-14 | 2009-11-19 | Amgen Inc. | Combinations vegf(r) inhibitors and hepatocyte growth factor (c-met) inhibitors for the treatment of cancer |
KR101034351B1 (ko) | 2008-05-14 | 2011-05-16 | 한국화학연구원 | 신규 벤즈옥사졸로 치환된 피리딘 유도체 또는 이의약학적으로 허용가능한 염, 이의 제조방법 및 이를유효성분으로 함유하는 이상세포 성장 질환의 예방 및치료용 약학적 조성물 |
-
2009
- 2009-01-29 AR ARP090100283A patent/AR070317A1/es unknown
- 2009-02-04 TW TW098103558A patent/TW200944201A/zh unknown
- 2009-02-05 PE PE2009000178A patent/PE20091414A1/es not_active Application Discontinuation
- 2009-02-05 UY UY031638A patent/UY31638A1/es not_active Application Discontinuation
- 2009-02-06 WO PCT/US2009/033311 patent/WO2009100282A1/en active Application Filing
- 2009-02-06 CL CL2009000275A patent/CL2009000275A1/es unknown
- 2009-02-06 JP JP2010546027A patent/JP2011511094A/ja not_active Ceased
- 2009-02-06 US US12/366,743 patent/US8022206B2/en not_active Expired - Fee Related
- 2009-02-06 CN CN2009801092027A patent/CN102007127A/zh active Pending
- 2009-02-06 EA EA201070929A patent/EA201070929A1/ru unknown
- 2009-02-06 MX MX2010008638A patent/MX2010008638A/es active IP Right Grant
- 2009-02-06 EP EP09709265.4A patent/EP2265616B8/en active Active
- 2009-02-06 BR BRPI0908050-3A patent/BRPI0908050A2/pt not_active IP Right Cessation
- 2009-02-06 ES ES09709265.4T patent/ES2451024T3/es active Active
- 2009-02-06 KR KR1020107019308A patent/KR20110014971A/ko not_active Ceased
- 2009-02-06 AU AU2009212338A patent/AU2009212338A1/en not_active Abandoned
- 2009-02-06 CA CA2711078A patent/CA2711078A1/en not_active Abandoned
-
2010
- 2010-07-01 IL IL206758A patent/IL206758A0/en unknown
- 2010-08-04 ZA ZA2010/05554A patent/ZA201005554B/en unknown
Also Published As
Publication number | Publication date |
---|---|
CL2009000275A1 (es) | 2009-06-12 |
AU2009212338A1 (en) | 2009-08-13 |
CN102007127A (zh) | 2011-04-06 |
TW200944201A (en) | 2009-11-01 |
IL206758A0 (en) | 2010-12-30 |
EA201070929A1 (ru) | 2011-04-29 |
WO2009100282A1 (en) | 2009-08-13 |
EP2265616A1 (en) | 2010-12-29 |
US8022206B2 (en) | 2011-09-20 |
KR20110014971A (ko) | 2011-02-14 |
BRPI0908050A2 (pt) | 2015-08-11 |
MX2010008638A (es) | 2010-08-30 |
ES2451024T3 (es) | 2014-03-26 |
US20090197864A1 (en) | 2009-08-06 |
EP2265616B1 (en) | 2013-11-20 |
JP2011511094A (ja) | 2011-04-07 |
AR070317A1 (es) | 2010-03-31 |
EP2265616B8 (en) | 2014-01-08 |
ZA201005554B (en) | 2011-04-28 |
CA2711078A1 (en) | 2009-08-13 |
UY31638A1 (es) | 2009-09-30 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD | Application declared void or lapsed |