PE20070212A1 - Heterociclos de 1,4-dihidropiridina-condensados, procesos para preparar los mismos, uso y composiciones que los contienen - Google Patents
Heterociclos de 1,4-dihidropiridina-condensados, procesos para preparar los mismos, uso y composiciones que los contienenInfo
- Publication number
- PE20070212A1 PE20070212A1 PE2006000862A PE2006000862A PE20070212A1 PE 20070212 A1 PE20070212 A1 PE 20070212A1 PE 2006000862 A PE2006000862 A PE 2006000862A PE 2006000862 A PE2006000862 A PE 2006000862A PE 20070212 A1 PE20070212 A1 PE 20070212A1
- Authority
- PE
- Peru
- Prior art keywords
- hexahydro
- dihydropyridine
- prepare
- processes
- same
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- -1 4-HYDROXY-3-METHYL-PHENYL Chemical class 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—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
- A61K31/435—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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
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)
- Dermatology (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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
SE REFIERE A UN COMPUESTO DE FORMULA I, DONDE R1 ES H, METILO; R2 ES ARILO SUSTITUIDO, HETEROARILO SUSTITUIDO; R3 ES H, R4; X ES N, CR7; Y, Y' E Y'' SON CADA UNO CH2, C=O, O, S, NH, NR7, ENTRE OTROS; R4 Y R7 SON CADA UNO H, ALQUILO SUSTITUIDO, ALQUIL-ALQUENILO SUSTITUIDO, ARILO, HETEROARILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 4-(4-HIDROXI-3-METIL-FENIL)-2,4,6,7,8,9-HEXAHIDRO-PIRAZOLO[3,4-b]-1,7-NAFTIRIDIN-5-ONA; 4-[5-(1H-BENCIMIDAZOL-2-ILSULFANIL)-FURAN-2-IL]-1,4,6,7,8,9-HEXAHIDRO-PIRAZOLO[3,4-b]QUINOLIN-5-ONA; 4-CLORO-N-[3-(5-OXO-2,4,6,7,8,9-HEXAHIDRO-PIRAZOLO[3,4-b]-1,7-NAFTIRIDIN-4-IL)-TIAZOL-2-IL]-BENZAMIDA; ENTRE OTROS. REFERIDA TAMBIEN A UNA COMPOSICION FARMACEUTICA Y A UN PROCEDIMIENTO DE PREPARACION. DICHOS COMPUESTOS ACTUAN COMO INHIBIDORES DE AURORA A Y/O B QUINASAS Y SON UTILES EN EL TRATAMIENTO DE ENFERMEDADES CANCEROSAS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05291558A EP1746097B1 (en) | 2005-07-20 | 2005-07-20 | 1,4-dihydropyridine-fused heterocycles, process for preparing the same, use and compositions containing them |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20070212A1 true PE20070212A1 (es) | 2007-03-21 |
Family
ID=35510894
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2010000153A PE20100718A1 (es) | 2005-07-20 | 2006-07-18 | Derivados triciclicos de 1, 4-dihidropiridina [b, e]-condensados como inhibidores de aurora quinasas |
| PE2006000862A PE20070212A1 (es) | 2005-07-20 | 2006-07-18 | Heterociclos de 1,4-dihidropiridina-condensados, procesos para preparar los mismos, uso y composiciones que los contienen |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2010000153A PE20100718A1 (es) | 2005-07-20 | 2006-07-18 | Derivados triciclicos de 1, 4-dihidropiridina [b, e]-condensados como inhibidores de aurora quinasas |
Country Status (37)
| Country | Link |
|---|---|
| US (1) | US8163768B2 (es) |
| EP (2) | EP1746097B1 (es) |
| JP (2) | JP2009501778A (es) |
| KR (1) | KR101286796B1 (es) |
| CN (1) | CN101243087B (es) |
| AR (1) | AR054845A1 (es) |
| AT (2) | ATE455115T1 (es) |
| AU (1) | AU2006273692B8 (es) |
| BR (1) | BRPI0614002A2 (es) |
| CA (1) | CA2615700C (es) |
| CR (1) | CR9663A (es) |
| CY (1) | CY1109964T1 (es) |
| DE (1) | DE602005018911D1 (es) |
| DK (1) | DK1746097T3 (es) |
| DO (1) | DOP2006000175A (es) |
| EA (1) | EA016815B1 (es) |
| EC (1) | ECSP078062A (es) |
| ES (1) | ES2339676T3 (es) |
| HN (1) | HN2008000088A (es) |
| HR (1) | HRP20100195T1 (es) |
| IL (1) | IL188861A0 (es) |
| MA (1) | MA29634B1 (es) |
| MX (1) | MX2008000902A (es) |
| MY (1) | MY148617A (es) |
| NO (1) | NO20080831L (es) |
| NZ (1) | NZ592766A (es) |
| PE (2) | PE20100718A1 (es) |
| PL (1) | PL1746097T3 (es) |
| PT (1) | PT1746097E (es) |
| RS (1) | RS51351B (es) |
| SI (1) | SI1746097T1 (es) |
| TN (1) | TNSN08020A1 (es) |
| TW (1) | TWI386411B (es) |
| UA (1) | UA98928C2 (es) |
| UY (1) | UY29685A1 (es) |
| WO (1) | WO2007012972A2 (es) |
| ZA (1) | ZA200800542B (es) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2945535B1 (fr) * | 2009-05-18 | 2011-06-10 | Sanofi Aventis | Compose anticancereux et composition pharmaceutique le contenant |
| FR2967413A1 (fr) * | 2010-11-17 | 2012-05-18 | Sanofi Aventis | Compose 8-oxo-9-[3-(1h-benzimidazol-2-yloxy)-phenyl]-4,5,6,7,8,9-hexahydro-2h-pyrrolo[3,4-b]quinoline-3-carboxylate d'ethyle, sel, forme cristalline, co-cristal, formulation, procedes de preparation, application a titre de medicaments, compositions pharmaceutiques et nouvelle utilisation notamment comme inhibiteur des kinases aurora. |
| WO2013171641A1 (en) | 2012-05-15 | 2013-11-21 | Novartis Ag | Compounds and compositions for inhibiting the activity of abl1, abl2 and bcr-abl1 |
| JP6078640B2 (ja) | 2012-05-15 | 2017-02-08 | ノバルティス アーゲー | Ａｂｌ１、ａｂｌ２およびｂｃｒ−ａｂｌ１の活性を阻害するためのベンズアミド誘導体 |
| ES2665539T3 (es) | 2012-05-15 | 2018-04-26 | Novartis Ag | Derivados de benzamida para inhibir la actividad de ABL1, ABL2 y BCR-ABL1 |
| AP3613A (en) | 2012-05-15 | 2016-02-29 | Novartis Ag | Benzamide derivatives for inhibiting the activity of abl1, abl2 and bcr-abl1 abl1abl2 bcr-abl1 |
| PL2909204T3 (pl) | 2012-10-12 | 2019-07-31 | The Broad Institute, Inc. | Inhibitory GSK3 i sposoby ich stosowania |
| JP2017537940A (ja) * | 2014-12-10 | 2017-12-21 | マサチューセッツ インスティテュート オブ テクノロジー | 増殖性疾患の処置に有用な融合１，３−アゾール誘導体 |
| CA2983314C (en) | 2015-04-30 | 2024-11-12 | Memorial Sloan-Kettering Cancer Center | Mitragynine analogues and their uses |
| RU2619932C1 (ru) * | 2015-11-25 | 2017-05-22 | федеральное государственное бюджетное образовательное учреждение высшего образования "Воронежский государственный университет" (ФГБОУ ВО "ВГУ") | ЗАМЕЩЕННЫЕ ПИРАЗОЛО[1,5-а]ПИРИДО[3,4-е]ПИРИМИДИНЫ И ИХ ИСПОЛЬЗОВАНИЕ В КАЧЕСТВЕ ИНГИБИТОРОВ ПРОТЕИНКИНАЗ |
| US11180492B2 (en) | 2016-01-15 | 2021-11-23 | University Of Central Florida Research Foundation, Inc. | Anti-parasitic compounds and uses thereof |
| RU2018132559A (ru) | 2016-02-16 | 2020-03-17 | Массачусетс Инститьют Оф Текнолоджи | Связывающие молекулы для max в качестве модуляторов myc и их применения |
| KR20190136063A (ko) | 2017-04-05 | 2019-12-09 | 더 브로드 인스티튜트, 인코퍼레이티드 | 글리코겐 신타제 키나제 3 (gsk3) 억제제로서의 트리시클릭 화합물 및 그의 용도 |
| JP7455581B2 (ja) * | 2017-05-12 | 2024-03-26 | リサーチ トライアングル インスティテュート | Ｃｂ１アロステリック・モジュレーターとしてのジアリール尿素 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU747705C (en) * | 1997-12-13 | 2004-09-23 | Bristol-Myers Squibb Company | Use of pyrazolo (3,4-b) pyridine as cyclin dependent kinase inhibitors |
| JP2003529552A (ja) | 1999-11-19 | 2003-10-07 | アボット・ラボラトリーズ | 三環性ジヒドロピリミジンカリウムチャンネル開口剤 |
| MXPA02008615A (es) | 2000-03-03 | 2003-04-14 | Abbott Lab | Abridores de canales de potasio de dihidropirazolona triciclica y dihidroisoxazolona triciclica. |
| US6538004B2 (en) | 2000-03-03 | 2003-03-25 | Abbott Laboratories | Tricyclic dihydropyrazolone and tricyclic dihydroisoxazolone potassium channel openers |
| JP2005501800A (ja) | 2001-02-02 | 2005-01-20 | 三菱ウェルファーマ株式会社 | ジヒドロピラゾロピリジン化合物およびその医薬用途 |
| FR2823854A1 (fr) | 2001-04-18 | 2002-10-25 | Centre Nat Rech Scient | Nouveau procede de criblage d'inhibiteurs de la liaison entre la proteine oxyde nitrique synthase neuronale et la proteine inhibitrice de l'oxyde nitrique synthase neuronale |
| FR2825091B1 (fr) | 2001-05-23 | 2003-07-04 | Servier Lab | Nouveaux derives tricycliques de dihydro-quinnoleines, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| US7037902B2 (en) * | 2002-07-03 | 2006-05-02 | Receptron, Inc. | Affinity small molecules for the EPO receptor |
| SE0301371D0 (sv) | 2003-05-09 | 2003-05-09 | Astrazeneca Ab | New Compounds |
| EP1648463A2 (en) * | 2003-06-13 | 2006-04-26 | Zentaris GmbH | Compounds having inhibitive activity of phosphatidylinositol 3-kinase and methods of use thereof |
-
2005
- 2005-07-20 AT AT05291558T patent/ATE455115T1/de active
- 2005-07-20 PL PL05291558T patent/PL1746097T3/pl unknown
- 2005-07-20 RS RSP-2010/0159A patent/RS51351B/sr unknown
- 2005-07-20 EP EP05291558A patent/EP1746097B1/en not_active Expired - Lifetime
- 2005-07-20 ES ES05291558T patent/ES2339676T3/es not_active Expired - Lifetime
- 2005-07-20 PT PT05291558T patent/PT1746097E/pt unknown
- 2005-07-20 DE DE602005018911T patent/DE602005018911D1/de not_active Expired - Lifetime
- 2005-07-20 SI SI200530964T patent/SI1746097T1/sl unknown
- 2005-07-20 DK DK05291558.4T patent/DK1746097T3/da active
-
2006
- 2006-07-18 MX MX2008000902A patent/MX2008000902A/es active IP Right Grant
- 2006-07-18 AT AT06808922T patent/ATE521611T1/de not_active IP Right Cessation
- 2006-07-18 MY MYPI20063429A patent/MY148617A/en unknown
- 2006-07-18 EP EP06808922A patent/EP1910366B1/en active Active
- 2006-07-18 UA UAA200802146A patent/UA98928C2/ru unknown
- 2006-07-18 CA CA2615700A patent/CA2615700C/en not_active Expired - Fee Related
- 2006-07-18 AU AU2006273692A patent/AU2006273692B8/en not_active Ceased
- 2006-07-18 JP JP2008522098A patent/JP2009501778A/ja not_active Withdrawn
- 2006-07-18 PE PE2010000153A patent/PE20100718A1/es not_active Application Discontinuation
- 2006-07-18 CN CN2006800303826A patent/CN101243087B/zh not_active Expired - Fee Related
- 2006-07-18 BR BRPI0614002-5A patent/BRPI0614002A2/pt not_active IP Right Cessation
- 2006-07-18 PE PE2006000862A patent/PE20070212A1/es not_active Application Discontinuation
- 2006-07-18 NZ NZ592766A patent/NZ592766A/xx not_active IP Right Cessation
- 2006-07-18 KR KR1020087003945A patent/KR101286796B1/ko not_active Expired - Fee Related
- 2006-07-18 WO PCT/IB2006/002734 patent/WO2007012972A2/en not_active Ceased
- 2006-07-18 ZA ZA200800542A patent/ZA200800542B/xx unknown
- 2006-07-18 EA EA200800374A patent/EA016815B1/ru not_active IP Right Cessation
- 2006-07-18 AR ARP060103065A patent/AR054845A1/es not_active Application Discontinuation
- 2006-07-19 TW TW095126453A patent/TWI386411B/zh not_active IP Right Cessation
- 2006-07-20 UY UY29685A patent/UY29685A1/es unknown
- 2006-07-20 DO DO2006000175A patent/DOP2006000175A/es unknown
-
2007
- 2007-12-27 EC EC2007008062A patent/ECSP078062A/es unknown
-
2008
- 2008-01-15 CR CR9663A patent/CR9663A/es unknown
- 2008-01-15 US US12/014,516 patent/US8163768B2/en active Active
- 2008-01-16 MA MA30580A patent/MA29634B1/fr unknown
- 2008-01-17 IL IL188861A patent/IL188861A0/en unknown
- 2008-01-18 TN TNP2008000020A patent/TNSN08020A1/en unknown
- 2008-01-21 HN HN2008000088A patent/HN2008000088A/es unknown
- 2008-02-15 NO NO20080831A patent/NO20080831L/no not_active Application Discontinuation
-
2010
- 2010-04-07 HR HR20100195T patent/HRP20100195T1/hr unknown
- 2010-04-09 CY CY20101100327T patent/CY1109964T1/el unknown
-
2012
- 2012-11-05 JP JP2012243375A patent/JP2013063987A/ja not_active Withdrawn
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