AR045037A1 - Tetrahidro-1h-pirazolo [3,4-c] piridinas sustituidas, composiciones que las contienen y su utilizacion. - Google Patents
Tetrahidro-1h-pirazolo [3,4-c] piridinas sustituidas, composiciones que las contienen y su utilizacion.Info
- Publication number
- AR045037A1 AR045037A1 ARP040102391A ARP040102391A AR045037A1 AR 045037 A1 AR045037 A1 AR 045037A1 AR P040102391 A ARP040102391 A AR P040102391A AR P040102391 A ARP040102391 A AR P040102391A AR 045037 A1 AR045037 A1 AR 045037A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- heteroaryl
- aryl
- conh
- heterocyclyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000003222 pyridines Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 230000001225 therapeutic effect Effects 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
- 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
- A61P27/00—Drugs for disorders of the senses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
La presente se refiere principalmente a nuevas tetrahidro-1H-pirazolo[3,4-c]piridinas sustituidas que tienen una actividad terapéutica, utilizables en particular en oncología y composiciones que las contienen. Reivindicación 1: Producto de la fórmula general (1) siguiente, y sus tautómeros, caracterizado porque: L se elige entre enlace, -CH2, CO, SO2, CONH, COO, NHCO, NH, NHSO2, SO2NH, NHCONH, CH2NH y NHCH2; X se elige entre enlace, CH2, CO, SO2, CONH y COO; R1 se elige entre OH, H, alquilo, cicloalquilo, heterociclilo, arilo y heteroarilo, eventualmente sustituido y, cuando X es enlace, entonces R1 también puede ser halógeno; R2 es H o se elige entre alquilo, alquileno, cicloalquilo, heterociclilo, arilo y heteroarilo, eventualmente sustituido; y porque los sustituyentes se eligen independientemente entre R3, O-R3, halógeno, NO2, SO2-R3, CO-R3, SO2NH-R3, CONH-R3, N-(R3)2, NHCO-R3, NHSO2-R3, NHCONH-R3, NHSO2NH-R3, OCO-R3, COO-R3, OSO2-R3, SO2O-R3, OCONH-R3 y OSO2NH-R3, en el que cada R3 se elige independientemente entre H, alquilo, cicloalquilo, alquenilo, arilo, heteroarilo y heterociclilo, eventualmente sustituido con halógeno, arilo, heteroarilo, R4, OR4 y N(R4)2, en el que cada R4 se elige independientemente entre H, alquilo C1-4 y alquilo halogenado C1-4
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0308442A FR2857363B1 (fr) | 2003-07-10 | 2003-07-10 | 4,5,6,7-tetrahydro-1h-pyrazolo[3,4-c] pyridines substituees compositions les contenant et utilisation |
| FR0308441A FR2857362B1 (fr) | 2003-07-10 | 2003-07-10 | Tetrahydro-1h-pyrazolo[3,4-c] pyridines substituees, compositions les contenant et utilisation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR045037A1 true AR045037A1 (es) | 2005-10-12 |
Family
ID=34081983
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP040102391A AR045037A1 (es) | 2003-07-10 | 2004-07-07 | Tetrahidro-1h-pirazolo [3,4-c] piridinas sustituidas, composiciones que las contienen y su utilizacion. |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US7109340B2 (es) |
| EP (2) | EP1646632A2 (es) |
| JP (1) | JP4740841B2 (es) |
| KR (1) | KR20060054291A (es) |
| AR (1) | AR045037A1 (es) |
| AU (1) | AU2004256945B2 (es) |
| BR (1) | BRPI0412411A (es) |
| CA (1) | CA2532122A1 (es) |
| IL (1) | IL172994A0 (es) |
| MX (1) | MXPA06000247A (es) |
| TW (1) | TW200519110A (es) |
| WO (1) | WO2005007653A2 (es) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7524635B2 (en) | 2003-04-17 | 2009-04-28 | Biosite Incorporated | Methods and compositions for measuring natriuretic peptides and uses thereof |
| FR2888579A1 (fr) * | 2005-07-13 | 2007-01-19 | Aventis Pharma Sa | Pyrazolo pyridines substituees, compositions les contenant, procede de fabrication et utilisation |
| RU2404776C2 (ru) * | 2005-01-28 | 2010-11-27 | Новартис Аг | ПРИМЕНЕНИЕ ПИРИМИДИЛАМИНОБЕНЗАМИДОВ ДЛЯ ЛЕЧЕНИЯ ЗАБОЛЕВАНИЙ, ЧУВСТВИТЕЛЬНЫХ К МОДУЛЯЦИИ АКТИВНОСТИ КИНАЗЫ Тie-2 |
| ATE409190T1 (de) * | 2005-04-14 | 2008-10-15 | Hoffmann La Roche | Tricyclische azolderivate, ihre herstellung und ihre verwendung als pharmazeutische mittel |
| JP2009530337A (ja) * | 2006-03-23 | 2009-08-27 | エフ．ホフマン−ラ ロシュ アーゲー | 置換インダゾール誘導体、その製造方法、及びその薬剤としての利用法 |
| WO2008060568A2 (en) * | 2006-11-15 | 2008-05-22 | Neurogen Corporation | Amide-substituted aryl piperidines |
| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
| WO2013166037A1 (en) | 2012-05-01 | 2013-11-07 | The Trustees Of Columbia University In The City Of New York | Non-retinoid antagonists for treatment of eye disorders |
| UA125503C2 (uk) | 2012-06-13 | 2022-04-13 | Інсайт Холдинґс Корпорейшн | Заміщені трициклічні сполуки як інгібітори fgfr |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| EP2970271B1 (en) | 2013-03-14 | 2017-11-08 | Janssen Pharmaceutica NV | P2x7 modulators |
| US9938291B2 (en) | 2013-03-14 | 2018-04-10 | The Trustess Of Columbia University In The City Of New York | N-alkyl-2-phenoxyethanamines, their preparation and use |
| US9040534B2 (en) | 2013-03-14 | 2015-05-26 | Janssen Pharmaceutica Nv | [1,2,4]triazolo[4,3-a]pyrazines as P2X7 modulators |
| JO3509B1 (ar) | 2013-03-14 | 2020-07-05 | Janssen Pharmaceutica Nv | معدلات p2x7 |
| ES2700541T3 (es) | 2013-03-14 | 2019-02-18 | Univ Columbia | Octahidrociclopentapirroles, su preparación y uso |
| JO3773B1 (ar) | 2013-03-14 | 2021-01-31 | Janssen Pharmaceutica Nv | معدلات p2x7 |
| WO2014151936A1 (en) | 2013-03-14 | 2014-09-25 | The Trustees Of Columbia University In The City Of New York | Octahydropyrrolopyrroles, their preparation and use |
| EP2968304B1 (en) | 2013-03-14 | 2018-10-10 | The Trustees of Columbia University in the City of New York | 4-phenylpiperidines, their preparation and use |
| MY181497A (en) | 2013-04-19 | 2020-12-23 | Incyte Holdings Corp | Bicyclic heterocycles as fgfr inhibitors |
| WO2015168286A1 (en) * | 2014-04-30 | 2015-11-05 | The Trustees Of Columbia University In The City Of New York | Substituted 4-phenylpiperidines, their preparaiton and use |
| WO2016039977A1 (en) | 2014-09-12 | 2016-03-17 | Janssen Pharmaceutica Nv | P2x7 modulators |
| JP6625616B2 (ja) | 2014-09-12 | 2019-12-25 | ヤンセン ファーマシューティカ エヌ．ベー． | Ｐ２ｘ７調節ｎ−アシル−トリアゾロピラジン |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| CR20170390A (es) | 2015-02-20 | 2017-10-23 | Incyte Holdings Corp | Heterociclos biciclicos como inhibidores de fgfr |
| US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| BR112020022392A2 (pt) | 2018-05-04 | 2021-02-02 | Incyte Corporation | formas sólidas de um inibidor de fgfr e processos para preparação das mesmas |
| PE20210919A1 (es) | 2018-05-04 | 2021-05-19 | Incyte Corp | Sales de un inhibidor de fgfr |
| CA3111309A1 (en) | 2018-09-28 | 2020-04-02 | Janssen Pharmaceutica Nv | Monoacylglycerol lipase modulators |
| MX2021003737A (es) * | 2018-09-28 | 2021-05-14 | Janssen Pharmaceutica Nv | Moduladores de monoacilglicerol lipasa. |
| US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
| US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| MX2022003819A (es) | 2019-09-30 | 2022-05-11 | Janssen Pharmaceutica Nv | Ligandos de pet de mgl radiomarcados. |
| US12122767B2 (en) | 2019-10-01 | 2024-10-22 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| GEP20247679B (en) | 2019-10-14 | 2024-10-10 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| JP7720840B2 (ja) | 2019-12-04 | 2025-08-08 | インサイト・コーポレイション | Ｆｇｆｒ阻害剤としての三環式複素環 |
| PE20221504A1 (es) | 2019-12-04 | 2022-09-30 | Incyte Corp | Derivados de un inhibidor de fgfr |
| BR112022013849A2 (pt) * | 2020-01-13 | 2022-09-13 | Aptabio Therapeutics Inc | Novo derivado de pirazol |
| WO2021146424A1 (en) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| KR20220157999A (ko) | 2020-03-26 | 2022-11-29 | 얀센 파마슈티카 엔.브이. | 모노아실글리세롤 리파아제 조절제 |
| TW202304459A (zh) | 2021-04-12 | 2023-02-01 | 美商英塞特公司 | 包含ｆｇｆｒ抑制劑及ｎｅｃｔｉｎ－４靶向劑之組合療法 |
| CA3220155A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| TW202313611A (zh) | 2021-06-09 | 2023-04-01 | 美商英塞特公司 | 作為ｆｇｆｒ抑制劑之三環雜環 |
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| HUT77517A (hu) * | 1994-10-20 | 1998-05-28 | Pfizer Inc. | Biciklusos tetrahidro-pirazolo-piridin-származékok, alkalmazásuk és ilyen vegyületeket tartalmazó gyógyászati készítmények |
| AR007857A1 (es) | 1996-07-13 | 1999-11-24 | Glaxo Group Ltd | Compuestos heterociclicos fusionados como inhibidores de proteina tirosina quinasa, sus metodos de preparacion, intermediarios uso en medicina ycomposiciones farmaceuticas que los contienen. |
| ES2202827T3 (es) | 1997-03-19 | 2004-04-01 | ABBOTT GMBH & CO. KG | Pirrolo(2,3-d)pirimidinas y su uso como inhibidores de la tirosina kinasa. |
| GB9716557D0 (en) | 1997-08-06 | 1997-10-08 | Glaxo Group Ltd | Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity |
| WO1999017770A1 (en) | 1997-10-06 | 1999-04-15 | Basf Aktiengesellschaft | Indeno[1,2-c]pyrazole derivatives for inhibiting tyrosine kinase activity |
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| NZ510587A (en) | 1998-09-18 | 2003-11-28 | Abbott Gmbh & Co | 4-aminopyrrolopyrimidines as kinase inhibitors |
| PL348210A1 (en) | 1998-11-06 | 2002-05-06 | Basf Ag | Tricyclic pyrazole derivatives |
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| ES2228629T3 (es) | 1999-11-22 | 2005-04-16 | Smithkline Beecham Plc | Derivados de imidazol y su uso como inhibidores de raf-quinasa. |
| SK12712002A3 (sk) | 2000-02-07 | 2003-02-04 | Abbott Gmbh & Co. Kg | Deriváty 2-benzotiazolylmočoviny a ich použitie ako inhibítorov proteínkináz |
| WO2001072751A1 (en) | 2000-03-29 | 2001-10-04 | Knoll Gesellschaft Mit Beschraenkter Haftung | Pyrrolopyrimidines as tyrosine kinase inhibitors |
| EP1325006A2 (en) | 2000-08-07 | 2003-07-09 | Neurogen Corporation | Heterocyclic compounds as ligands of the gaba a? receptor |
| MXPA03001169A (es) * | 2000-08-10 | 2003-06-30 | Pharmacia Italia Spa | Biciclo-pirazoles activos como inhibidores de quinasa, proceso para su preparacion y composiciones farmaceuticas que comprenden los mismos. |
| EP1372648B1 (en) | 2001-01-19 | 2006-03-15 | Smithkline Beecham Corporation | Tie2 receptor kinase inhibitors for treating angiogenic diseases |
| WO2002076985A1 (en) | 2001-03-23 | 2002-10-03 | Smithkline Beecham Corporation | Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases |
| WO2002076463A1 (en) | 2001-03-23 | 2002-10-03 | Smithkline Beecham Corporation | Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases |
| WO2002076954A1 (en) | 2001-03-23 | 2002-10-03 | Smithkline Beecham Corporation | Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases |
| WO2002076984A1 (en) | 2001-03-23 | 2002-10-03 | Smithkline Beecham Corporation | Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases |
| AU2002303145A1 (en) | 2001-03-23 | 2002-10-08 | Smithkline Beecham Corporation | Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases |
| WO2003004488A1 (en) | 2001-07-03 | 2003-01-16 | Chiron Corporation | Indazole benzimidazole compounds as tyrosine and serine/threonine kinase inhibitors |
| FR2827861B1 (fr) * | 2001-07-27 | 2004-04-02 | Aventis Pharma Sa | Derives des indazoles ou des indoles, leur utilisation en medecine humaine et plus particulierement en cancerologie |
| US7101884B2 (en) * | 2001-09-14 | 2006-09-05 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| AU2002337142B2 (en) | 2001-09-19 | 2007-10-11 | Aventis Pharma S.A. | Indolizines as kinase protein inhibitors |
| MXPA04003954A (es) * | 2001-10-26 | 2004-11-29 | Aventis Pharma Inc | Bencimidazoles. |
| FR2831537B1 (fr) * | 2001-10-26 | 2008-02-29 | Aventis Pharma Sa | Nouveaux derives de benzimidazoles, leur procede de preparation, leur application a titre de medicament, compositions pharmaceutiques et nouvelle utilisation |
| US7265128B2 (en) * | 2003-01-17 | 2007-09-04 | Merck & Co., Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| CL2004000409A1 (es) * | 2003-03-03 | 2005-01-07 | Vertex Pharma | Compuestos derivados de 2-(cilo sustituido)-1-(amino u oxi sustituido)-quinazolina, inhibidores de canales ionicos de sodio y calcio dependientes de voltaje; composicion farmaceutica; y uso del compuesto en el tratamiento de dolor agudo, cronico, neu |
-
2004
- 2004-07-07 AR ARP040102391A patent/AR045037A1/es unknown
- 2004-07-08 KR KR1020067000505A patent/KR20060054291A/ko not_active Ceased
- 2004-07-08 BR BRPI0412411-1A patent/BRPI0412411A/pt not_active IP Right Cessation
- 2004-07-08 AU AU2004256945A patent/AU2004256945B2/en not_active Ceased
- 2004-07-08 CA CA002532122A patent/CA2532122A1/fr not_active Abandoned
- 2004-07-08 WO PCT/FR2004/001778 patent/WO2005007653A2/fr not_active Ceased
- 2004-07-08 MX MXPA06000247A patent/MXPA06000247A/es active IP Right Grant
- 2004-07-08 JP JP2006518294A patent/JP4740841B2/ja not_active Expired - Fee Related
- 2004-07-08 EP EP04767613A patent/EP1646632A2/fr not_active Withdrawn
- 2004-07-08 EP EP10173683A patent/EP2251340A1/fr not_active Withdrawn
- 2004-07-09 US US10/888,611 patent/US7109340B2/en not_active Expired - Fee Related
- 2004-07-09 TW TW093120534A patent/TW200519110A/zh unknown
-
2006
- 2006-01-05 IL IL172994A patent/IL172994A0/en unknown
- 2006-05-23 US US11/419,794 patent/US7435820B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP4740841B2 (ja) | 2011-08-03 |
| CA2532122A1 (fr) | 2005-01-27 |
| US7109340B2 (en) | 2006-09-19 |
| WO2005007653A2 (fr) | 2005-01-27 |
| JP2007516186A (ja) | 2007-06-21 |
| KR20060054291A (ko) | 2006-05-22 |
| IL172994A0 (en) | 2006-06-11 |
| US20060199837A1 (en) | 2006-09-07 |
| BRPI0412411A (pt) | 2006-08-22 |
| AU2004256945A1 (en) | 2005-01-27 |
| US20050096345A1 (en) | 2005-05-05 |
| TW200519110A (en) | 2005-06-16 |
| US7435820B2 (en) | 2008-10-14 |
| MXPA06000247A (es) | 2006-03-30 |
| EP2251340A1 (fr) | 2010-11-17 |
| AU2004256945B2 (en) | 2009-08-20 |
| EP1646632A2 (fr) | 2006-04-19 |
| WO2005007653A3 (fr) | 2005-03-24 |
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