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
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 (40)
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FR2888579A1 (fr) * | 2005-07-13 | 2007-01-19 | Aventis Pharma Sa | Pyrazolo pyridines substituees, compositions les contenant, procede de fabrication et utilisation |
CN101203224B (zh) * | 2005-01-28 | 2010-11-03 | 诺瓦提斯公司 | 嘧啶基氨基苯甲酰胺在制备治疗对Tie-2激酶活性的调节有响应的疾病的药物中的用途 |
CN101160312A (zh) * | 2005-04-14 | 2008-04-09 | 霍夫曼-拉罗奇有限公司 | 三环吡咯衍生物、它们的制备和作为药剂的应用 |
EP2001882A1 (en) * | 2006-03-23 | 2008-12-17 | F. Hoffmann-La Roche AG | Substituted indazole derivatives, their manufacture and use as pharmaceutical agents |
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 |
US9333202B2 (en) | 2012-05-01 | 2016-05-10 | The Trustees Of Columbia University In The City Of New York | Non-retinoid antagonists for treatment of age-related macular degeneration and stargardt disease |
IL289834B1 (en) | 2012-06-13 | 2024-03-01 | Incyte Holdings Corp | Conversion of tricyclic compounds as FGFR inhibitors |
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 |
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 |
ES2666155T3 (es) | 2013-03-14 | 2018-05-03 | Janssen Pharmaceutica Nv | Moduladores de P2X7 |
US9040534B2 (en) | 2013-03-14 | 2015-05-26 | Janssen Pharmaceutica Nv | [1,2,4]triazolo[4,3-a]pyrazines as P2X7 modulators |
WO2014151936A1 (en) | 2013-03-14 | 2014-09-25 | The Trustees Of Columbia University In The City Of New York | Octahydropyrrolopyrroles, their preparation and use |
TWI599567B (zh) | 2013-03-14 | 2017-09-21 | 健生藥品公司 | P2x7調節劑 |
WO2014152018A1 (en) | 2013-03-14 | 2014-09-25 | The Trustees Of Columbia University In The City Of New York | Octahydrocyclopentapyrroles, 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 |
JO3509B1 (ar) | 2013-03-14 | 2020-07-05 | Janssen Pharmaceutica Nv | معدلات p2x7 |
SG10201708520YA (en) | 2013-04-19 | 2017-12-28 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
CN106794364B (zh) | 2014-04-30 | 2019-12-24 | 哥伦比亚大学董事会 | 取代的4-苯基哌啶及其制备和用途 |
EA034015B1 (ru) | 2014-09-12 | 2019-12-19 | Янссен Фармацевтика Нв | Модуляторы р2х7 |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
MX2017010673A (es) | 2015-02-20 | 2018-03-21 | Incyte Corp | Heterociclos biciclicos como inhibidores de receptores del factor de crecimiento fibroblastico (fgfr). |
MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
CR20200590A (es) | 2018-05-04 | 2021-04-26 | Incyte Corp | Formas sólidas de un inhibidor de fgfr y procesos para prepararlas |
US11174257B2 (en) | 2018-05-04 | 2021-11-16 | Incyte Corporation | Salts of an FGFR inhibitor |
KR20210069080A (ko) | 2018-09-28 | 2021-06-10 | 얀센 파마슈티카 엔.브이. | 모노아실글리세롤 리파아제 조절제 |
US20200102311A1 (en) | 2018-09-28 | 2020-04-02 | Janssen Pharmaceutica Nv | Monoacylglycerol Lipase Modulators |
US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
AU2020358948A1 (en) | 2019-09-30 | 2022-05-26 | Janssen Pharmaceutica Nv | Radiolabelled MGL PET ligands |
JP2022552324A (ja) | 2019-10-14 | 2022-12-15 | インサイト・コーポレイション | Fgfr阻害剤としての二環式複素環 |
WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
US11897891B2 (en) | 2019-12-04 | 2024-02-13 | Incyte Corporation | Tricyclic heterocycles as FGFR inhibitors |
BR112022010664A2 (pt) | 2019-12-04 | 2022-08-16 | Incyte Corp | Derivados de um inibidor de fgfr |
MX2022008665A (es) * | 2020-01-13 | 2022-08-10 | Aptabio Therapeutics Inc | Nuevo derivado de pirazol. |
CA3176946A1 (en) | 2020-03-26 | 2021-09-30 | Janssen Pharmaceutica Nv | Monoacylglycerol lipase modulators |
US11939331B2 (en) | 2021-06-09 | 2024-03-26 | Incyte Corporation | Tricyclic heterocycles as FGFR inhibitors |
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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 |
US6391874B1 (en) | 1996-07-13 | 2002-05-21 | Smithkline Beecham Corporation | Fused heterocyclic compounds as protein tyrosine kinase inhibitors |
CA2283961A1 (en) | 1997-03-19 | 1998-09-24 | Basf Aktiengesellschaft | Pyrrolo[2,3d]pyrimidines and their use as tyrosine kinase inhibitors |
GB9716557D0 (en) | 1997-08-06 | 1997-10-08 | Glaxo Group Ltd | Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity |
CN1278724A (zh) | 1997-10-06 | 2001-01-03 | 巴斯福股份公司 | 抑制酪氨酸激酶活性的茚并[1,2-c]吡唑衍生物 |
GB9721437D0 (en) | 1997-10-10 | 1997-12-10 | Glaxo Group Ltd | Heteroaromatic compounds and their use in medicine |
WO1999030710A1 (en) * | 1997-12-13 | 1999-06-24 | Bristol-Myers Squibb Company | USE OF PYRAZOLO [3,4-b] PYRIDINE AS CYCLIN DEPENDENT KINASE INHIBITORS |
EP1071658B1 (en) | 1998-04-17 | 2004-06-16 | Parker Hughes Institute | Btk inhibitors and methods for their identification and use |
DE69918542T2 (de) | 1998-04-30 | 2005-08-18 | Abbott Gmbh & Co. Kg | Substituierte trizyklische pyrazolderivate mit protein kinase aktivität |
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KR20010086005A (ko) | 1998-11-06 | 2001-09-07 | 스타르크, 카르크 | 트리사이클릭 피라졸 유도체 |
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WO2002076396A2 (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 |
WO2002076984A1 (en) | 2001-03-23 | 2002-10-03 | Smithkline Beecham Corporation | Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases |
EP1401831A1 (en) | 2001-07-03 | 2004-03-31 | 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 |
WO2003024969A1 (en) * | 2001-09-14 | 2003-03-27 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
ATE420879T1 (de) | 2001-09-19 | 2009-01-15 | Aventis Pharma Sa | Indolizine als kinaseproteinhemmer |
CA2465247C (en) * | 2001-10-26 | 2010-05-18 | Aventis Pharmaceuticals Inc. | Benzimidazoles and analogues and their use as protein kinases inhibitors |
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 |
CA2512546A1 (en) * | 2003-01-17 | 2004-08-05 | 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 CA CA002532122A patent/CA2532122A1/fr not_active Abandoned
- 2004-07-08 MX MXPA06000247A patent/MXPA06000247A/es active IP Right Grant
- 2004-07-08 EP EP04767613A patent/EP1646632A2/fr not_active Withdrawn
- 2004-07-08 KR KR1020067000505A patent/KR20060054291A/ko not_active Application Discontinuation
- 2004-07-08 BR BRPI0412411-1A patent/BRPI0412411A/pt not_active IP Right Cessation
- 2004-07-08 JP JP2006518294A patent/JP4740841B2/ja not_active Expired - Fee Related
- 2004-07-08 EP EP10173683A patent/EP2251340A1/fr not_active Withdrawn
- 2004-07-08 AU AU2004256945A patent/AU2004256945B2/en not_active Ceased
- 2004-07-08 WO PCT/FR2004/001778 patent/WO2005007653A2/fr active Application Filing
- 2004-07-09 TW TW093120534A patent/TW200519110A/zh unknown
- 2004-07-09 US US10/888,611 patent/US7109340B2/en not_active Expired - Fee Related
-
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 |
---|---|
WO2005007653A3 (fr) | 2005-03-24 |
TW200519110A (en) | 2005-06-16 |
AU2004256945A1 (en) | 2005-01-27 |
EP1646632A2 (fr) | 2006-04-19 |
JP4740841B2 (ja) | 2011-08-03 |
MXPA06000247A (es) | 2006-03-30 |
WO2005007653A2 (fr) | 2005-01-27 |
KR20060054291A (ko) | 2006-05-22 |
US20060199837A1 (en) | 2006-09-07 |
US7435820B2 (en) | 2008-10-14 |
US7109340B2 (en) | 2006-09-19 |
BRPI0412411A (pt) | 2006-08-22 |
JP2007516186A (ja) | 2007-06-21 |
AU2004256945B2 (en) | 2009-08-20 |
CA2532122A1 (fr) | 2005-01-27 |
IL172994A0 (en) | 2006-06-11 |
US20050096345A1 (en) | 2005-05-05 |
EP2251340A1 (fr) | 2010-11-17 |
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