MX2009013948A - Derivados de 6-cicloamino-3-(piridin-4-il)imidazo[1,2-b] piridazina, su preparacion y uso terapéutico. - Google Patents
Derivados de 6-cicloamino-3-(piridin-4-il)imidazo[1,2-b] piridazina, su preparacion y uso terapéutico.Info
- Publication number
- MX2009013948A MX2009013948A MX2009013948A MX2009013948A MX2009013948A MX 2009013948 A MX2009013948 A MX 2009013948A MX 2009013948 A MX2009013948 A MX 2009013948A MX 2009013948 A MX2009013948 A MX 2009013948A MX 2009013948 A MX2009013948 A MX 2009013948A
- Authority
- MX
- Mexico
- Prior art keywords
- group
- groups
- optionally substituted
- cycloamino
- imidazo
- Prior art date
Links
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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Oncology (AREA)
- Hospice & Palliative Care (AREA)
- Hematology (AREA)
- Addiction (AREA)
- Anesthesiology (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
La presente invención se refiere a derivados de 6-cicloamino-3-(piridin-4-il)imidazo[1,2-b]piridazina que corresponden a la fórmula general de (I), en el cual cuya fórmula (I) R2 es un grupo arilo opcionalmente substituido por uno o más substituyentes seleccionados de los átomos de halógeno, y C1-6 alquilo, C1-6 alquiloxi, C1-6 alquiltio, C1-6 fluoroalquilo, C1-6 fluoroalquiloxi y grupos -CN; R3 es un átomo de hidrógeno o un C1-3 alquilo, -NR4R5, hidroxilo o un grupo C1-4 alquiloxi; -A es un grupo C1-7 alquileno opcionalmente substituido por uno o dos grupos Ra; B es un grupo C1-7 alquileno opcionalmente substituido por un grupo Ra; L es cualquiera de un átomo de nitrógeno opcionalmente substituido por un grupo R, o Ra o un átomo de carbono substituido por un grupo R y un grupo Ra o dos grupos Re2; los átomos de carbono de A y de B o de los grupos Re2 son opcionalmente substituidos por uno o más grupos Rf los cuales pueden ser idénticos o diferentes entre ellos; R7 y Ra son, independientemente entre ellos, un átomo de hidrógeno o un grupo C1-6-alquilo. Método de preparación y uso terapéutico.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US94678507P | 2007-06-28 | 2007-06-28 | |
FR0704661A FR2918061B1 (fr) | 2007-06-28 | 2007-06-28 | Derives de 6-cycloamino-3-(pyridin-4-yl)imidazo°1,2-b!- pyridazine,leur preparation et leur application en therapeutique. |
PCT/FR2008/000902 WO2009016286A2 (fr) | 2007-06-28 | 2008-06-26 | Derives de 6-cycloamino-3-(pyridin-4-yl)imidazo[1, 2-b]-pyridazine, leur preparation et leur application en therapeutique |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2009013948A true MX2009013948A (es) | 2010-03-09 |
Family
ID=39203151
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2009013948A MX2009013948A (es) | 2007-06-28 | 2008-06-26 | Derivados de 6-cicloamino-3-(piridin-4-il)imidazo[1,2-b] piridazina, su preparacion y uso terapéutico. |
Country Status (22)
Country | Link |
---|---|
US (2) | US8354405B2 (es) |
EP (1) | EP2170889B1 (es) |
JP (1) | JP5537424B2 (es) |
KR (1) | KR20100050492A (es) |
CN (1) | CN101765602A (es) |
AR (1) | AR069269A1 (es) |
AU (1) | AU2008281662A1 (es) |
BR (1) | BRPI0814807A2 (es) |
CA (1) | CA2691866A1 (es) |
CL (1) | CL2008001932A1 (es) |
CO (1) | CO6251269A2 (es) |
EA (1) | EA201070072A1 (es) |
FR (1) | FR2918061B1 (es) |
MA (1) | MA31572B1 (es) |
MX (1) | MX2009013948A (es) |
NZ (1) | NZ582677A (es) |
PA (1) | PA8786101A1 (es) |
PE (1) | PE20090556A1 (es) |
TW (1) | TW200911812A (es) |
UY (1) | UY31193A1 (es) |
WO (1) | WO2009016286A2 (es) |
ZA (1) | ZA200909186B (es) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7868001B2 (en) * | 2007-11-02 | 2011-01-11 | Hutchison Medipharma Enterprises Limited | Cytokine inhibitors |
ES2548135T3 (es) | 2008-05-13 | 2015-10-14 | Novartis Ag | Heterociclos condensados que contienen nitrógeno y composiciones de los mismos como inhibidores de quinasa |
FR2934994B1 (fr) * | 2008-08-12 | 2010-09-17 | Sanofi Aventis | Derives de 2-alkyl-6cycloamino-3-(pyridin-4-yl)imidaz°1,2-b! pyridazine, leur preparation et leur application en therapeutique |
FR2939134A1 (fr) * | 2008-12-01 | 2010-06-04 | Sanofi Aventis | Derives de 6-cycloamino-3-(1h-pyrrolo°2,3-b!pyridin-4-yl) imidazo°1,2-b!-pyridazine, leur preparation et leur application en therapeutique |
FR2940285A1 (fr) * | 2008-12-19 | 2010-06-25 | Sanofi Aventis | Derives de 6-cycloamino-2-thienyl-3-(pyridin-4-yl)imidazo °1,2-b!-pyridazine et 6-cycloamino-2-furanyl-3- (pyridin-4-yl)imidazo°1,2-b!-pyridazine, leur preparation et leur application en therapeutique |
FR2940284B1 (fr) * | 2008-12-19 | 2011-02-18 | Sanofi Aventis | Derives de 6-cycloamino-2,3-di-pyridinyl-imidazo°1,2-b!- pyridazine,leur preparation et leur application en therapeutique |
US8680275B2 (en) | 2009-10-23 | 2014-03-25 | Janssen Pharmaceutica Nv | Fused heterocyclic compounds as orexin receptor modulators |
JP5848251B2 (ja) | 2009-10-23 | 2016-01-27 | ヤンセン ファーマシューティカ エヌ.ベー. | オレキシン受容体調節因子としての縮合複素環式化合物 |
MX2012004753A (es) | 2009-10-23 | 2012-09-07 | Janssen Pharmaceutica Nv | Octahidropirrolo[3,4-c]pirrolos disustituidos como moduladores del receptor de orexina. |
CA2778949C (en) | 2009-10-30 | 2018-02-27 | Janssen Pharmaceutica Nv | Imidazo[1,2-b]pyridazine derivatives and their use as pde10 inhibitors |
AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
JP2013525283A (ja) * | 2010-04-06 | 2013-06-20 | フレッド ハッチンソン キャンサー リサーチ センター | MYC駆動型腫瘍細胞の成長および/または増殖を阻害するためのカゼインキナーゼ1εアイソフォームのインヒビターを同定および使用するための方法 |
US8637516B2 (en) | 2010-09-09 | 2014-01-28 | Irm Llc | Compounds and compositions as TRK inhibitors |
EP2651404B1 (en) * | 2010-12-14 | 2015-10-14 | Electrophoretics Limited | Casein kinase 1delta (ck1delta) inhibitors |
TWI617559B (zh) * | 2010-12-22 | 2018-03-11 | 江蘇恆瑞醫藥股份有限公司 | 2-芳基咪唑并[1,2-b]嗒.2-苯基咪唑并[1,2-a]吡啶,和2-苯基咪唑并[1,2-a]吡衍生物 |
US9586962B2 (en) | 2011-04-20 | 2017-03-07 | Janssen Pharmaceutica Nv | Disubstituted octahydropyrrolo [3,4-C] pyrroles as orexin receptor modulators |
CN103619846B (zh) | 2011-06-27 | 2016-08-17 | 詹森药业有限公司 | 1-芳基-4-甲基-[1,2,4]三唑[4,3-a]喹喔啉衍生物 |
WO2013023084A2 (en) | 2011-08-09 | 2013-02-14 | Fred Hutchinson Cancer Research Center | Methods and compositions for inhibiting the growth and/or proliferation of myc-driven tumor cells |
JP6426603B2 (ja) | 2012-06-26 | 2018-11-21 | ヤンセン ファーマシューティカ エヌ.ベー. | 神経障害または代謝障害の治療に使用するための、1−アリール−4−メチル−[1,2,4]トリアゾロ[4,3−a]−キノキサリン化合物などのPDE2阻害剤とPDE10阻害剤との組合せ |
UA116541C2 (uk) | 2012-06-27 | 2018-04-10 | 4Ск Діскавері Гмбх | Біфтордіоксаланамінобензімідазольні інгібітори кінази для лікування злоякісного новоутворення, аутоімунного запалення і порушень цнс |
EP2869822B1 (en) | 2012-07-09 | 2016-09-14 | Janssen Pharmaceutica, N.V. | Inhibitors of phosphodiesterase 10 enzyme |
CZ2012538A3 (cs) * | 2012-08-08 | 2014-02-19 | Masarykova Univerzita | Inhibitory pro léčbu B-buněčné chronické lymfocytární leukémie |
US10676746B2 (en) | 2013-11-22 | 2020-06-09 | Fred Hutchinson Cancer Research Center | Methods for identifying therapeutic targets and treating monitoring cancers |
US9944648B2 (en) * | 2014-01-09 | 2018-04-17 | Intra-Cellular Therapies, Inc. | Organic compounds |
JP2017506259A (ja) | 2014-02-03 | 2017-03-02 | イッスム・リサーチ・ディベロップメント・カンパニー・オブ・ザ・ヘブルー・ユニバーシティ・オブ・エルサレム・リミテッドYissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | 幹細胞を枯渇させるためのカゼインキナーゼi阻害剤の使用 |
WO2017156266A1 (en) | 2016-03-10 | 2017-09-14 | Janssen Pharmaceutica Nv | Methods of treating depression using orexin-2 receptor antagonists |
RS64354B1 (sr) * | 2017-03-14 | 2023-08-31 | Daiichi Sankyo Co Ltd | Postupak za proizvodnju derivata 3, 6-disupstituisanog imidazo[1, 2-b]piridazina |
EP3680241A1 (en) | 2017-03-20 | 2020-07-15 | Forma Therapeutics, Inc. | Pyrrolopyrrole compositions as pyruvate kinase (pkr) activators |
US10973820B2 (en) * | 2017-12-13 | 2021-04-13 | Facio Intellectual Property B.V. | Compounds for treatment of diseases related to DUX4 expression |
US20230055923A1 (en) | 2018-09-19 | 2023-02-23 | Forma Therapeutics, Inc. | Activating pyruvate kinase r |
WO2020061378A1 (en) | 2018-09-19 | 2020-03-26 | Forma Therapeutics, Inc. | Treating sickle cell disease with a pyruvate kinase r activating compound |
WO2020151682A1 (zh) * | 2019-01-23 | 2020-07-30 | 成都先导药物开发股份有限公司 | 一种大环类免疫调节剂 |
TW202112368A (zh) * | 2019-06-13 | 2021-04-01 | 荷蘭商法西歐知識產權股份有限公司 | 用於治療有關dux4表現之疾病的抑制劑組合 |
US11193891B2 (en) | 2019-12-20 | 2021-12-07 | Robert Bosch Gmbh | Receptors and spacers for a fluorescence-based lead ion chemosensor |
CN115335057A (zh) * | 2020-03-27 | 2022-11-11 | 北京原基华毅生物科技有限公司 | 抑制酪蛋白激酶的方法 |
EP4126878A4 (en) * | 2020-03-27 | 2024-07-10 | Gritscience Biopharmaceuticals Co Ltd | COMPOUNDS USED AS CASEIN KINASE INHIBITORS |
WO2023064857A1 (en) | 2021-10-14 | 2023-04-20 | Incyte Corporation | Quinoline compounds as inhibitors of kras |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0103926D0 (en) * | 2001-02-17 | 2001-04-04 | Astrazeneca Ab | Chemical compounds |
EP1388541A1 (en) * | 2002-08-09 | 2004-02-11 | Centre National De La Recherche Scientifique (Cnrs) | Pyrrolopyrazines as kinase inhibitors |
JP4691506B2 (ja) | 2003-12-11 | 2011-06-01 | アベンティス・ファーマスーティカルズ・インコーポレイテツド | カゼインキナーゼIεの阻害剤としての置換1H−ピロロ[3,2−b,3,2−c,及び2,3−c]ピリジン−2−カルボキシアミド及び関連類似物 |
EP1790650B1 (en) * | 2004-08-31 | 2014-03-26 | Msd Kk | NEW SUBSTITUTED IMIDAZOLE DERIVATIVES |
EP1832588A4 (en) * | 2004-12-28 | 2009-09-02 | Takeda Pharmaceutical | IMIDAZOLE CONDENSE DERIVATIVE AND APPLICATIONS THEREOF |
US20100216798A1 (en) * | 2005-07-29 | 2010-08-26 | Astellas Pharma Inc | Fused heterocycles as lck inhibitors |
EP1845098A1 (en) * | 2006-03-29 | 2007-10-17 | Ferrer Internacional, S.A. | Imidazo[1,2-b]pyridazines, their processes of preparation and their use as GABA receptor ligands |
SG176461A1 (en) * | 2006-11-06 | 2011-12-29 | Supergen Inc | Imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine derivatives and their use as protein kinase inhibitors |
AR064420A1 (es) * | 2006-12-21 | 2009-04-01 | Alcon Mfg Ltd | Composiciones farmaceuticas oftalmicas que comprenden una cantidad efectiva de analogos de 6-aminoimidazo[1,2b]piridazinas, utiles para el tratamiento del glaucoma y/o controlar la presion intraocular normal o elevada(iop). |
-
2007
- 2007-06-28 FR FR0704661A patent/FR2918061B1/fr active Active
-
2008
- 2008-06-25 TW TW097123772A patent/TW200911812A/zh unknown
- 2008-06-26 KR KR1020107001891A patent/KR20100050492A/ko not_active Application Discontinuation
- 2008-06-26 PE PE2008001090A patent/PE20090556A1/es not_active Application Discontinuation
- 2008-06-26 MX MX2009013948A patent/MX2009013948A/es unknown
- 2008-06-26 EP EP08826677.0A patent/EP2170889B1/fr active Active
- 2008-06-26 WO PCT/FR2008/000902 patent/WO2009016286A2/fr active Application Filing
- 2008-06-26 NZ NZ582677A patent/NZ582677A/en not_active IP Right Cessation
- 2008-06-26 AU AU2008281662A patent/AU2008281662A1/en not_active Abandoned
- 2008-06-26 JP JP2010514033A patent/JP5537424B2/ja not_active Expired - Fee Related
- 2008-06-26 EA EA201070072A patent/EA201070072A1/ru unknown
- 2008-06-26 CA CA002691866A patent/CA2691866A1/fr not_active Abandoned
- 2008-06-26 BR BRPI0814807-4A2A patent/BRPI0814807A2/pt not_active IP Right Cessation
- 2008-06-26 CN CN200880100885A patent/CN101765602A/zh active Pending
- 2008-06-27 PA PA20088786101A patent/PA8786101A1/es unknown
- 2008-06-27 UY UY31193A patent/UY31193A1/es not_active Application Discontinuation
- 2008-06-27 CL CL2008001932A patent/CL2008001932A1/es unknown
- 2008-06-27 AR ARP080102783A patent/AR069269A1/es unknown
-
2009
- 2009-12-23 ZA ZA2009/09186A patent/ZA200909186B/en unknown
- 2009-12-24 US US12/647,059 patent/US8354405B2/en not_active Expired - Fee Related
- 2009-12-28 CO CO09148262A patent/CO6251269A2/es not_active Application Discontinuation
-
2010
- 2010-01-26 MA MA32556A patent/MA31572B1/fr unknown
-
2012
- 2012-09-14 US US13/617,678 patent/US8846676B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
AR069269A1 (es) | 2010-01-13 |
CA2691866A1 (fr) | 2009-02-05 |
US20130012516A1 (en) | 2013-01-10 |
WO2009016286A2 (fr) | 2009-02-05 |
WO2009016286A3 (fr) | 2009-04-09 |
PA8786101A1 (es) | 2009-01-23 |
ZA200909186B (en) | 2011-02-23 |
NZ582677A (en) | 2011-12-22 |
CL2008001932A1 (es) | 2009-09-25 |
JP2010531342A (ja) | 2010-09-24 |
MA31572B1 (fr) | 2010-08-02 |
FR2918061B1 (fr) | 2010-10-22 |
US8354405B2 (en) | 2013-01-15 |
FR2918061A1 (fr) | 2009-01-02 |
CN101765602A (zh) | 2010-06-30 |
US8846676B2 (en) | 2014-09-30 |
EP2170889A2 (fr) | 2010-04-07 |
BRPI0814807A2 (pt) | 2015-02-03 |
US20100179154A1 (en) | 2010-07-15 |
EA201070072A1 (ru) | 2010-08-30 |
KR20100050492A (ko) | 2010-05-13 |
EP2170889B1 (fr) | 2016-08-17 |
PE20090556A1 (es) | 2009-06-01 |
AU2008281662A1 (en) | 2009-02-05 |
TW200911812A (en) | 2009-03-16 |
CO6251269A2 (es) | 2011-02-21 |
UY31193A1 (es) | 2009-01-30 |
JP5537424B2 (ja) | 2014-07-02 |
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