PE106300A1 - Imidazoquinoxalinas como inhibidores de la proteina tirosina cinasa - Google Patents
Imidazoquinoxalinas como inhibidores de la proteina tirosina cinasaInfo
- Publication number
- PE106300A1 PE106300A1 PE1998000776A PE00077698A PE106300A1 PE 106300 A1 PE106300 A1 PE 106300A1 PE 1998000776 A PE1998000776 A PE 1998000776A PE 00077698 A PE00077698 A PE 00077698A PE 106300 A1 PE106300 A1 PE 106300A1
- Authority
- PE
- Peru
- Prior art keywords
- alkynyl
- alkyl
- compound
- imidazoquinoxalins
- inhibitors
- Prior art date
Links
- 108091000080 Phosphotransferase Proteins 0.000 title abstract 2
- 102000020233 phosphotransferase Human genes 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- YELMWJNXDALKFE-UHFFFAOYSA-N 3h-imidazo[4,5-f]quinoxaline Chemical compound N1=CC=NC2=C(NC=N3)C3=CC=C21 YELMWJNXDALKFE-UHFFFAOYSA-N 0.000 abstract 1
- 201000004624 Dermatitis Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 229910006069 SO3H Inorganic materials 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 230000003110 anti-inflammatory effect Effects 0.000 abstract 1
- 230000001028 anti-proliverative effect Effects 0.000 abstract 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 229960003444 immunosuppressant agent Drugs 0.000 abstract 1
- 230000001861 immunosuppressant effect Effects 0.000 abstract 1
- 239000003018 immunosuppressive agent Substances 0.000 abstract 1
- 206010025135 lupus erythematosus Diseases 0.000 abstract 1
- SGQRUSCNUJBCNN-UHFFFAOYSA-N n-(2-chloro-6-methylphenyl)-8-nitroimidazo[1,5-a]quinoxalin-4-amine Chemical compound CC1=CC=CC(Cl)=C1NC1=NC2=CC=C([N+]([O-])=O)C=C2N2C1=CN=C2 SGQRUSCNUJBCNN-UHFFFAOYSA-N 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 1
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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- C07D491/12—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 three hetero rings
- C07D491/14—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
SE REFIERE A UNA IMIDAZOQUINOXALINA DE FORMULA I DONDE p ES 0-4; R1, R2 Y R3 SON H, R6, OH, OR6, SH, SR6, C(O)qH, -OC(O)qR6, SO3H, HALO, CIANO, ENTRE OTROS; q ES 1 o 2; R6 ES ALQUILO, ALQUENILO, ALQUINILO, ENTRE OTROS; R4 Y R5 SON H, R6 o -C(O)R6 o JUNTO CON N FORMAN UN ANILLO DE 3-8 MIEMBROS, OPCIONALMENTE SUSTITUIDO POR Z1, Z2 Y Z3; R7, R8, R9, R10, R11 Y R12 SON H, R6, O R7 Y R8 O R9, R10 Y R11 SON ALQUILENO O ALQUENILENO FORMANDO PARTE DE UN ANILLO DE 3-8 MIEMBROS; R13, R14 Y R15 SON ALQUILO O FENILO; Z1, Z2, Z3 SON H, Z6, OH, OZ6, SH, SZ6, C(O)qH, -OC(O)qZ6, ENTRE OTROS; Z6 ES ALQUILO, ALQUENILO, ALQUINILO, CICLOALQUILO, ENTRE OTROS. UN COMPUESTO PREFERIDO ES N-(2-CLORO-6-METILFENIL)-8-NITROIMIDAZO[1,5-a]-QUINOXALIN-4-AMINA, ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION. TAMBIEN JUNTO AL COMPUESTO I SE UTILIZA UN ANTIINFLAMATORIO, ANTIPROLIFERATIVO, INMUNOSUPRESOR. EL COMPUESTO I PUEDE SER UTIL PARA TRATAR UN PADECIMIENTO O DESORDEN ASOCIADO CON LA PROTEINA TIROSINA CINASA COMO RECHAZO DE TRANSPLANTE, ARTRITIS REUMATOIDE, ESCLEROSIS MULTIPLE, LUPUS, INJERTO, HIPERSENSIBILIDAD MEDIADA POR LAS CELULAS T, PSORIASIS, TIROIDITIS DE HASHIMOTO, SINDROME DE GUILLEN-BARRE, DERMATITIS, ASMA, CANCER
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5677097P | 1997-08-25 | 1997-08-25 | |
| US6915997P | 1997-12-09 | 1997-12-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE106300A1 true PE106300A1 (es) | 2000-01-23 |
Family
ID=26735691
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE1998000776A PE106300A1 (es) | 1997-08-25 | 1998-08-25 | Imidazoquinoxalinas como inhibidores de la proteina tirosina cinasa |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US6235740B1 (es) |
| AR (1) | AR013441A1 (es) |
| AU (1) | AU8681798A (es) |
| PE (1) | PE106300A1 (es) |
| WO (1) | WO1999009845A1 (es) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1066286B1 (en) * | 1998-03-04 | 2009-04-29 | Bristol-Myers Squibb Company | Heterocyclo-substituted imidazopyrazine protein tyrosine kinase inhibitors |
| US20060258686A1 (en) * | 1998-05-29 | 2006-11-16 | Cheresh David A | Method of treatment of myocardial infarction |
| US20030130209A1 (en) * | 1999-12-22 | 2003-07-10 | Cheresh David A. | Method of treatment of myocardial infarction |
| US20040214836A1 (en) * | 1998-05-29 | 2004-10-28 | Cheresh David A. | Method of treatment of myocardial infarction |
| AU6605200A (en) | 1999-06-30 | 2001-01-31 | Merck & Co., Inc. | Src kinase inhibitor compounds |
| EP1194152A4 (en) | 1999-06-30 | 2002-11-06 | Merck & Co Inc | Links to SRC kinase inhibition |
| WO2001000213A1 (en) | 1999-06-30 | 2001-01-04 | Merck & Co., Inc. | Src kinase inhibitor compounds |
| US6506769B2 (en) | 1999-10-06 | 2003-01-14 | Boehringer Ingelheim Pharmaceuticals, Inc. | Heterocyclic compounds useful as inhibitors of tyrosine kinases |
| US7101869B2 (en) | 1999-11-30 | 2006-09-05 | Pfizer Inc. | 2,4-diaminopyrimidine compounds useful as immunosuppressants |
| US20030176454A1 (en) * | 2000-05-15 | 2003-09-18 | Akira Yamada | N-coating heterocyclic compounds |
| CA2424303A1 (en) * | 2000-10-03 | 2002-04-11 | Bristol-Myers Squibb Company | Amino-substituted tetracyclic compounds useful as anti-inflammatory agents and pharmaceutical compositions comprising same |
| US6869956B2 (en) * | 2000-10-03 | 2005-03-22 | Bristol-Myers Squibb Company | Methods of treating inflammatory and immune diseases using inhibitors of IκB kinase (IKK) |
| HUP0304045A3 (en) * | 2001-02-01 | 2005-05-30 | Bristol Myers Squibb Company P | Use of ikb-kinase inhibitors for treating of inflammatory and immune diseases and pharmaceutical compositions containing them |
| GB0127922D0 (en) * | 2001-11-21 | 2002-01-16 | Novartis Ag | Organic compounds |
| AU2002359489B2 (en) * | 2001-11-27 | 2008-10-30 | Wyeth Holdings Corporation | 3-cyanoquinolines as inhibitors of EGF-R and Her2 kinases |
| AU2003258061A1 (en) * | 2002-08-02 | 2004-02-23 | Salmedix, Inc. | Therapeutic inhibitionof protein kinases in cancer cells |
| US20040180898A1 (en) * | 2003-03-03 | 2004-09-16 | Bang-Chi Chen | Processes for preparing imidazoquinoxalinones, heterocyclic-substituted imidazopyrazinones, imidazoquinoxalines and heterocyclic-substituted imidazopyrazines |
| US7880017B2 (en) * | 2003-11-11 | 2011-02-01 | Allergan, Inc. | Process for the synthesis of imidazoles |
| US7183305B2 (en) * | 2003-11-11 | 2007-02-27 | Allergan, Inc. | Process for the synthesis of imidazoles |
| US20060025419A1 (en) * | 2004-06-25 | 2006-02-02 | Ann Richmond | Imidazoquinoxaline compound for the treatment of melanoma |
| US8003657B2 (en) * | 2004-10-13 | 2011-08-23 | Merck Patent Gmbh | Heterocyclic substituted bisarylurea derivatives |
| CA2646316C (en) | 2006-03-15 | 2016-05-24 | Theralogics, Inc. | Methods of treating muscular wasting diseases using nf-kb activation inhibitors |
| ES2376492T3 (es) * | 2006-03-23 | 2012-03-14 | Novartis Ag | Compuestos de imidazoquinoxalina como inmunomoduladores. |
| JP2010504362A (ja) * | 2006-09-25 | 2010-02-12 | アレテ セラピューティクス, インコーポレイテッド | 可溶性エポキシドヒドロラーゼ阻害剤 |
| CN101616919B (zh) * | 2006-12-28 | 2012-10-10 | 雅培制药有限公司 | 聚(adp核糖)聚合酶抑制剂 |
| WO2008130619A2 (en) * | 2007-04-20 | 2008-10-30 | Trustees Of Boston College | A composition comprising an inhibitor of pde4 and/or pde7 |
| WO2009068320A1 (en) * | 2007-11-30 | 2009-06-04 | Elbion Gmbh | Aryl and heteroaryl fused imidazo (1,5-a) pyrazines as inhibitors of phosphodiesterase 10 |
| CN101918408A (zh) * | 2007-11-30 | 2010-12-15 | 惠氏有限责任公司 | 作为磷酸二酯酶10的抑制剂的芳基和杂芳基稠合的咪唑并[1,5-a]吡嗪 |
| US20090143361A1 (en) * | 2007-11-30 | 2009-06-04 | Elbion Gmbh | Pyrido[3,2-E]Pyrazines, Process For Preparing The Same, And Their Use As Inhibitors Of Phosphodiesterase 10 |
| US20100227853A1 (en) * | 2008-04-18 | 2010-09-09 | Trustees Of Boston College | Inhibitors of cyclic amp phosphodiesterases |
| US20100075973A1 (en) * | 2008-08-28 | 2010-03-25 | Takeda Pharmaceutical Company Limited | Polo-like kinase inhibitors |
| US8475790B2 (en) | 2008-10-06 | 2013-07-02 | Bristol-Myers Squibb Company | Combination of CD137 antibody and CTLA-4 antibody for the treatment of proliferative diseases |
| KR20110132559A (ko) | 2009-03-05 | 2011-12-08 | 아스텔라스세이야쿠 가부시키가이샤 | 퀴녹살린 화합물 |
| US8361962B2 (en) * | 2009-07-27 | 2013-01-29 | Roche Palo Alto Llc | Tricyclic inhibitors of JAK |
| MX2012002641A (es) * | 2009-09-10 | 2012-03-14 | Hoffmann La Roche | Inhibidores de cinasa janus (jak). |
| RU2012116003A (ru) * | 2009-09-21 | 2013-10-27 | Ф.Хоффманн-Ля Рош Аг | Макроциклические ингибиторы jak |
| GB201007286D0 (en) | 2010-04-30 | 2010-06-16 | Astex Therapeutics Ltd | New compounds |
| WO2012033101A1 (ja) | 2010-09-07 | 2012-03-15 | アステラス製薬株式会社 | キノキサリン化合物 |
| US9540379B2 (en) * | 2011-01-31 | 2017-01-10 | Boehringer Ingelheim International Gmbh | (1,2,4)triazolo[4,3-A]quinoxaline derivatives as inhibitors of phosphodiesterases |
| RU2715236C2 (ru) | 2014-03-26 | 2020-02-26 | Астекс Терапьютикс Лтд | Комбинации |
| JO3512B1 (ar) | 2014-03-26 | 2020-07-05 | Astex Therapeutics Ltd | مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز |
| CA2943687C (en) | 2014-03-26 | 2024-02-13 | Astex Therapeutics Ltd | Combinations of an fgfr inhibitor and an igf1r inhibitor |
| JOP20200201A1 (ar) | 2015-02-10 | 2017-06-16 | Astex Therapeutics Ltd | تركيبات صيدلانية تشتمل على n-(3.5- ثنائي ميثوكسي فينيل)-n'-(1-ميثيل إيثيل)-n-[3-(ميثيل-1h-بيرازول-4-يل) كينوكسالين-6-يل]إيثان-1.2-ثنائي الأمين |
| ES2811845T3 (es) | 2015-09-23 | 2021-03-15 | Janssen Pharmaceutica Nv | Heterociclos tricíclicos para el tratamiento del cáncer |
| US11542247B2 (en) | 2015-09-23 | 2023-01-03 | Janssen Pharmaceutica Nv | Bi-heteroaryl substitute 1,4-benzodiazepines and uses thereof for the treatment of cancer |
| WO2022166548A1 (zh) * | 2021-02-03 | 2022-08-11 | 苏州欧康维视生物科技有限公司 | 吡唑取代的咪唑并[1,2-a]喹喔啉衍生物的盐型及晶型 |
| CA3257212A1 (en) * | 2022-08-03 | 2025-03-19 | Abbisko Therapeutics Co., Ltd. | Fused three-cycle PRMT5 inhibitor containing nitrogen, its preparation process and its pharmaceutical use |
| AU2024222203A1 (en) * | 2023-02-17 | 2025-10-02 | Nanjing Synnocare Pharmaceutical Technology Co., Ltd. | Mir-124 inducer, and preparation method therefor and use thereof |
| CN116751198A (zh) * | 2023-05-15 | 2023-09-15 | 上海工程技术大学 | 含异硫脲片段的咪唑并六元氮杂化合物的制备方法 |
| WO2025077857A1 (zh) * | 2023-10-13 | 2025-04-17 | 上海湃隆生物科技有限公司 | Prmt5抑制剂在治疗肿瘤或癌症中的用途 |
| US12012414B1 (en) | 2024-01-04 | 2024-06-18 | King Faisal University | Imidazo[1,5-a]pyrido[4,3-e]pyrimidines as CK2 inhibitors |
| US12187726B1 (en) | 2024-02-06 | 2025-01-07 | King Faisal University | Imidazo[1,5-a]pyrido[4,3-e]pyrazines as CK2 inhibitors |
| WO2025180350A1 (zh) * | 2024-02-26 | 2025-09-04 | 上海湃隆生物科技有限公司 | 化合物盐的晶型及其制备方法和用途 |
| WO2025180349A1 (zh) * | 2024-02-26 | 2025-09-04 | 上海湃隆生物科技有限公司 | 化合物的固体及其制备方法和用途 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4197403A (en) | 1977-01-07 | 1980-04-08 | Westwood Pharmaceuticals Inc. | 4-Aminosubstituted imidazo(1,2-A)quinoxalines |
| US4191766A (en) | 1977-01-07 | 1980-03-04 | Westwood Pharmaceuticals, Inc. | Method for reducing immunological response |
| US4236015A (en) | 1977-01-07 | 1980-11-25 | Westwood Pharmaceuticals, Inc. | 1-(2-Acylaminophenyl)imidazoles |
| US4200750A (en) | 1977-01-07 | 1980-04-29 | Westwood Pharmaceuticals Inc. | 4-Substituted imidazo [1,2-a]quinoxalines |
| US4229452A (en) | 1977-01-07 | 1980-10-21 | Westwood Pharmaceuticals, Inc. | Treatment of inflammatory disorders with 4-trifluoromethylimidazo[1,2-a]quinoxaline |
| US4225724A (en) | 1977-01-07 | 1980-09-30 | Westwood Pharmaceuticals, Inc. | 1-(2-Phenylureylene)imidazoles |
| US4160097A (en) | 1977-01-07 | 1979-07-03 | Westwind Pharmaceuticals, Inc. | 1-(2-Phenylureylene)imidazoles |
| US4191767A (en) | 1977-01-07 | 1980-03-04 | Westwood Pharmaceuticals, Inc. | Method for treating fungal infection in mammals with imidazo [1,2-a]quinoxalines |
| US4198508A (en) | 1977-01-07 | 1980-04-15 | Westwood Pharmaceuticals Inc. | Process for preparing 4-substituted imidazo[1,2-a]quinoxalines |
| US4172947A (en) | 1977-01-07 | 1979-10-30 | Westwood Pharmaceuticals, Inc. | 1-(2-Acylaminophenyl)imidazoles |
| JPS5632549A (en) | 1979-08-27 | 1981-04-02 | Toyo Ink Mfg Co Ltd | Pigment composition |
| US4440929A (en) | 1981-07-16 | 1984-04-03 | Usv Pharmaceutical Corporation | Imidazoquinoxaline compounds |
| DK161148C (da) | 1988-06-14 | 1991-11-18 | Novo Nordisk As | Imidazoquinoxalinforbindelser, fremgangsmaade til fremstilling deraf samt farmaceutiske praeprater indeholdende forbindelserne |
| DK151890D0 (da) * | 1990-06-22 | 1990-06-22 | Ferrosan As | Heterocykliske forbindelser deres fremstilling og brug |
| US5276028A (en) | 1990-06-22 | 1994-01-04 | Nordisk A/S | Imidazoquinoxaline compounds |
| DE19506742A1 (de) | 1995-02-27 | 1996-08-29 | Bayer Ag | Verwendung von Chinoxalinen in Kombination mit Protease-Inhibitoren als Arzneimittel zur Behandlung von AIDS und/oder HIV-Infektionen |
| IT1276167B1 (it) | 1995-11-24 | 1997-10-27 | Foscama Biomed Chim Farma | Imidazo(1,2-alfa)chinossalin-4-ammine attivi come antagonisti adenosinici,procedimento per la loro preparazione e loro composizioni |
-
1998
- 1998-06-15 US US09/097,338 patent/US6235740B1/en not_active Expired - Lifetime
- 1998-08-03 AU AU86817/98A patent/AU8681798A/en not_active Abandoned
- 1998-08-03 WO PCT/US1998/016027 patent/WO1999009845A1/en not_active Ceased
- 1998-08-25 AR ARP980104209A patent/AR013441A1/es unknown
- 1998-08-25 PE PE1998000776A patent/PE106300A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| WO1999009845A1 (en) | 1999-03-04 |
| AR013441A1 (es) | 2000-12-27 |
| AU8681798A (en) | 1999-03-16 |
| US6235740B1 (en) | 2001-05-22 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |