MA30651B1 - Derive heterocyclique fusionne et son procede d'utilisation. - Google Patents
Derive heterocyclique fusionne et son procede d'utilisation.Info
- Publication number
- MA30651B1 MA30651B1 MA31647A MA31647A MA30651B1 MA 30651 B1 MA30651 B1 MA 30651B1 MA 31647 A MA31647 A MA 31647A MA 31647 A MA31647 A MA 31647A MA 30651 B1 MA30651 B1 MA 30651B1
- Authority
- MA
- Morocco
- Prior art keywords
- relates
- compound
- heterocyclic derivative
- fusioned
- formula
- 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
- 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
-
- 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
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P27/02—Ophthalmic agents
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Reproductive Health (AREA)
- Pulmonology (AREA)
- Ophthalmology & Optometry (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Gynecology & Obstetrics (AREA)
- Pregnancy & Childbirth (AREA)
- Immunology (AREA)
- Endocrinology (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Vascular Medicine (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
L'invention concerne un dérivé hétérocyclique fusionné présentant une puissante activité d'inhibition de kinase et son procédé d'utilisation. L'invention concerne un composé de formule (I). Dans cette formule, chaque symbole est tel qu'il est défini dans la description, à l'exception d'un composé particulier. L'invention concerne un sel du dérivé susmentionné et un agent pharmaceutique contenant ce composé ou un promédicament de celui-ci qui est un inhibiteur de kinase (VEGFR, VEGFR2, PDGFR, Raf), un inhibiteur d'angiogenèse, un agent de prophylaxie ou de traitement du cancer, un inhibiteur de croissance ou un suppresseur de métastases cancéreuses.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2006213981 | 2006-08-04 | ||
| JP2006331230 | 2006-12-07 | ||
| JP2007144072 | 2007-05-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30651B1 true MA30651B1 (fr) | 2009-08-03 |
Family
ID=38996616
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA31647A MA30651B1 (fr) | 2006-08-04 | 2009-02-17 | Derive heterocyclique fusionne et son procede d'utilisation. |
Country Status (18)
| Country | Link |
|---|---|
| US (4) | US8044049B2 (fr) |
| EP (1) | EP2049541B1 (fr) |
| JP (1) | JP5238697B2 (fr) |
| KR (1) | KR20090047509A (fr) |
| AR (1) | AR062207A1 (fr) |
| AU (1) | AU2007279595A1 (fr) |
| BR (1) | BRPI0714665A2 (fr) |
| CA (1) | CA2659971A1 (fr) |
| CL (1) | CL2007002261A1 (fr) |
| CO (1) | CO6150183A2 (fr) |
| CR (1) | CR10607A (fr) |
| IL (1) | IL196799A0 (fr) |
| MA (1) | MA30651B1 (fr) |
| MX (1) | MX2009001349A (fr) |
| NO (1) | NO20090986L (fr) |
| PE (1) | PE20080538A1 (fr) |
| TW (1) | TW200817409A (fr) |
| WO (1) | WO2008016192A2 (fr) |
Families Citing this family (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CL2008001626A1 (es) | 2007-06-05 | 2009-06-05 | Takeda Pharmaceuticals Co | Compuestos derivados de heterociclos fusionados, agente farmaceutico que los comprende y su uso en la profilaxis y tratamiento del cancer. |
| US8431608B2 (en) * | 2007-08-17 | 2013-04-30 | Icagen Inc. | Heterocycles as potassium channel modulators |
| ES2400604T3 (es) * | 2007-08-17 | 2013-04-11 | Icagen, Inc. | Heterociclos como moduladores del canal de potasio |
| JP5270553B2 (ja) | 2007-08-23 | 2013-08-21 | 武田薬品工業株式会社 | 複素環化合物およびその用途 |
| EP2240488B1 (fr) * | 2008-02-06 | 2016-11-02 | Bristol-Myers Squibb Company | Imidazopyridazines substituées utiles en tant qu'inhibiteurs de kinase |
| PE20091468A1 (es) | 2008-02-28 | 2009-10-22 | Novartis Ag | DERIVADOS DE 3-METIL-IMIDAZO-[1,2-b]-PIRIDAZINA |
| CN101372475B (zh) * | 2008-03-19 | 2012-01-04 | 南京工业大学 | 芳杂环取代的二苯脲类衍生物及其用途 |
| EP2277881A4 (fr) | 2008-04-18 | 2011-09-07 | Shionogi & Co | Composé hétérocyclique présentant une activité inhibitrice sur p13k |
| WO2009136663A1 (fr) * | 2008-05-08 | 2009-11-12 | Takeda Pharmaceutical Company Limited | Dérivés hétérocycliques fusionnés et leur utilisation |
| WO2010007099A1 (fr) * | 2008-07-15 | 2010-01-21 | Cellzome Limited | Dérivés de 2-aminoimidazo[1,2-b]pyridazine en tant qu’inhibiteurs de pi3k |
| UY32049A (es) | 2008-08-14 | 2010-03-26 | Takeda Pharmaceutical | Inhibidores de cmet |
| KR20110070887A (ko) | 2008-10-02 | 2011-06-24 | 레스피버트 리미티드 | P38 엠에이피 키나제 억제제 |
| GB0818033D0 (en) | 2008-10-02 | 2008-11-05 | Respivert Ltd | Novel compound |
| TWI491610B (zh) * | 2008-10-09 | 2015-07-11 | 必治妥美雅史谷比公司 | 作為激酶抑制劑之咪唑并嗒腈 |
| HRP20140309T1 (hr) | 2008-10-22 | 2014-05-09 | Array Biopharma, Inc. | SUPSTITUIRANI SPOJEVI PIRAZOLO[1,5-a]PIRIMIDINA KAO INHIBITORI TRK KINAZE |
| US8697874B2 (en) | 2008-12-01 | 2014-04-15 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| JO3101B1 (ar) | 2008-12-02 | 2017-09-20 | Takeda Pharmaceuticals Co | مشتقات بنزوثيازول كعوامل مضادة للسرطان |
| JP5670912B2 (ja) | 2008-12-11 | 2015-02-18 | レスピバート・リミテツド | p38MAPキナーゼ阻害剤 |
| CN102264705A (zh) * | 2008-12-24 | 2011-11-30 | 辛根塔有限公司 | 制备芳基酰胺的方法 |
| CN102388048B (zh) | 2009-02-10 | 2014-07-30 | 阿斯利康(瑞典)有限公司 | 三唑并[4,3-b]哒嗪衍生物及其用于前列腺癌的用途 |
| GB0905955D0 (en) | 2009-04-06 | 2009-05-20 | Respivert Ltd | Novel compounds |
| US8389526B2 (en) | 2009-08-07 | 2013-03-05 | Novartis Ag | 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives |
| WO2011137155A1 (fr) | 2010-04-28 | 2011-11-03 | Bristol-Myers Squibb Company | Composés d'imidazopyridazinyle et leurs utilisations pour le cancer |
| ES2620644T3 (es) * | 2011-04-01 | 2017-06-29 | Genentech, Inc. | Combinaciones de compuestos inhibidores de AKT y agentes quimioterapéuticos, y métodos de uso |
| KR20140103925A (ko) | 2011-12-09 | 2014-08-27 | 키에시 파르마슈티시 엣스. 피. 에이. | 4-히드록시-1,2,3,4-테트라히드로나프탈렌-1-일 우레아 및 호흡기 질환의 치료에서의 이들의 용도 |
| WO2014176259A1 (fr) | 2013-04-22 | 2014-10-30 | Icahn School Of Medicine At Mount Sinai | Mutations du gène pdgfrb et du gène notch3 responsables de la myofibromatose infantile autosomique dominante |
| AU2014275198B2 (en) * | 2013-05-30 | 2017-04-13 | KALA BIO, Inc. | Novel compounds and uses thereof |
| EP3077393A1 (fr) * | 2013-12-06 | 2016-10-12 | Vertex Pharmaceuticals Incorporated | Composés utiles en tant qu'inhibiteurs de la kinase atr |
| MX380237B (es) | 2013-12-13 | 2025-03-12 | Eurochem Agro Gmbh | Mezcla fertilizante que contiene inhibidor de la nitrificación. |
| US10253045B2 (en) | 2014-11-26 | 2019-04-09 | Kala Pharmaceuticals, Inc. | Crystalline forms of a therapeutic compound and uses thereof |
| WO2016093299A1 (fr) * | 2014-12-10 | 2016-06-16 | 千寿製薬株式会社 | Agent liquide aqueux |
| AU2017246554B2 (en) | 2016-04-04 | 2022-08-18 | Loxo Oncology, Inc. | Liquid formulations of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo(1,5-a)pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
| US10045991B2 (en) | 2016-04-04 | 2018-08-14 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
| KR102566858B1 (ko) | 2016-05-18 | 2023-08-11 | 어레이 바이오파마 인크. | (s)-n-(5-((r)-2-(2,5-디플루오로페닐)피롤리딘-1-일)-피라졸로[1,5-a]피리미딘-3-일)-3-히드록시피롤리딘-1-카르복사미드의 제조 방법 |
| EP3478676A1 (fr) | 2016-06-29 | 2019-05-08 | Orion Corporation | Dérivés de benzodioxane et leur utilisation pharmaceutique |
| JOP20190092A1 (ar) | 2016-10-26 | 2019-04-25 | Array Biopharma Inc | عملية لتحضير مركبات بيرازولو[1، 5-a]بيريميدين وأملاح منها |
| EP3541431B1 (fr) | 2016-11-16 | 2024-04-17 | The General Hospital Corporation | Agents d'imagerie de myéloperoxydase |
| DE102017201608A1 (de) | 2017-02-01 | 2018-08-02 | Eurochem Agro Gmbh | 3,4-Dimethylpyrazol enthaltende Mischung und ihre Verwendung |
| EP3942045A1 (fr) | 2019-03-21 | 2022-01-26 | Onxeo | Molécule dbait associée à un inhibiteur de kinase pour le traitement du cancer |
| US12523663B2 (en) | 2019-06-04 | 2026-01-13 | Inserm (Institut National De La Santé Et De La Rescherche Médicale) | Use of CD9 as a biomarker and as a biotarget in glomerulonephritis or glomerulosclerosis |
| CA3149917C (fr) | 2019-09-12 | 2024-06-25 | Nihon Nohyaku Co., Ltd. | Compose d'imidazopyridine comprenant un oxadiazole de cyclopropane substitue et utilisation comme insecticide ou pour controler les ectoparasites ou les endoparasites animaux |
| JP7618237B2 (ja) * | 2019-10-16 | 2025-01-21 | 国立大学法人京都大学 | 運動神経細胞変性阻害剤 |
| EP4054579A1 (fr) | 2019-11-08 | 2022-09-14 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Méthodes pour le traitement de cancers qui ont acquis une résistance aux inhibiteurs de kinase |
| WO2021148581A1 (fr) | 2020-01-22 | 2021-07-29 | Onxeo | Nouvelle molécule dbait et son utilisation |
| US12577244B2 (en) | 2020-09-30 | 2026-03-17 | Sumitomo Chemical Company, Limited | Heterocyclic compound and harmful arthropod-controlling composition containing same |
| US20220389488A1 (en) * | 2021-03-12 | 2022-12-08 | Gt Molecular, Llc | Multiplexed genotyping assays with a single probe using fluorescent amplitude tuning |
| KR20240115979A (ko) | 2021-11-08 | 2024-07-26 | 프로젠토스 테라퓨틱스, 인크. | 혈소판-유래 성장 인자 수용체(pdgfr) 알파 억제제 및 이의 용도 |
| CN120187435A (zh) * | 2022-10-27 | 2025-06-20 | 香港科技大学 | 肿瘤的治疗或预防方法 |
| WO2025086243A1 (fr) * | 2023-10-27 | 2025-05-01 | 深圳湾实验室坪山生物医药研发转化中心 | Inhibiteur de la tyrosine kinase du récepteur des leucocytes |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1989001478A1 (fr) | 1987-08-07 | 1989-02-23 | The Australian National University | IMIDAZO[1,2-b]PYRIDAZINES AVEC SUBSTITUANTS ARYLOXY ET ARALKYLTHIO |
| WO1989001333A1 (fr) | 1987-08-07 | 1989-02-23 | The Australian National University | IMIDAZO[1,2-b]PYRIDAZINES |
| GB8719368D0 (en) * | 1987-08-15 | 1987-09-23 | Wellcome Found | Heterocyclic compounds |
| JPH0820584A (ja) | 1994-07-04 | 1996-01-23 | Takeda Chem Ind Ltd | イミダゾール誘導体及びその用途 |
| CO4950519A1 (es) | 1997-02-13 | 2000-09-01 | Novartis Ag | Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion |
| EP1140840B1 (fr) | 1999-01-13 | 2006-03-22 | Bayer Pharmaceuticals Corp. | Diphenylurees a substituants -g(v)-carboxyaryles, inhibitrices de kinase raf |
| CA2361057C (fr) | 1999-01-22 | 2010-04-06 | Kazuo Kubo | Derives de quinoline et derives de quinazoline |
| CN100376567C (zh) | 1999-11-05 | 2008-03-26 | 阿斯特拉曾尼卡有限公司 | 作为vegf抑制剂的喹唑啉衍生物 |
| AR034118A1 (es) | 2000-02-15 | 2004-02-04 | Sugen Inc | Compuestos de 2-indolinonas sustituidas con pirroles inhibidoras de proteinquinasas; sus composiciones farmaceuticas e intermediarios de sintesis |
| EP1415987B1 (fr) | 2000-10-20 | 2007-02-28 | Eisai R&D Management Co., Ltd. | Composes heteroaromatiques azotes pour le traitement des maladies de cancer |
| JP2003137785A (ja) * | 2001-08-23 | 2003-05-14 | Takeda Chem Ind Ltd | Jnk活性化阻害剤 |
| PL380764A1 (pl) | 2003-12-31 | 2007-03-19 | Schering-Plough Ltd. | Kontrolowanie pasożytów u zwierząt za pomocą stosowania imidazo [1,2-b] pirydazynowych pochodnych |
| AU2005301568B2 (en) * | 2004-11-08 | 2011-06-09 | Msd K.K. | Novel fused imidazole derivative |
| WO2006070943A1 (fr) * | 2004-12-28 | 2006-07-06 | Takeda Pharmaceutical Company Limited | Derive condense d'imidazole et applications de ce dernier |
| JP2009502734A (ja) * | 2005-07-29 | 2009-01-29 | アステラス製薬株式会社 | Lck阻害剤としての縮合複素環 |
| US20070049591A1 (en) | 2005-08-25 | 2007-03-01 | Kalypsys, Inc. | Inhibitors of MAPK/Erk Kinase |
| DE102005042742A1 (de) * | 2005-09-02 | 2007-03-08 | Schering Ag | Substituierte Imidazo[1,2b]pyridazine als Kinase-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel |
| US7723336B2 (en) | 2005-09-22 | 2010-05-25 | Bristol-Myers Squibb Company | Fused heterocyclic compounds useful as kinase modulators |
| US20070078136A1 (en) * | 2005-09-22 | 2007-04-05 | Bristol-Myers Squibb Company | Fused heterocyclic compounds useful as kinase modulators |
| US20100029619A1 (en) * | 2006-08-04 | 2010-02-04 | Takeda Pharmaceutical Company Limted | Fused heterocyclic compound |
-
2007
- 2007-08-03 BR BRPI0714665-5A patent/BRPI0714665A2/pt not_active IP Right Cessation
- 2007-08-03 KR KR1020097004527A patent/KR20090047509A/ko not_active Withdrawn
- 2007-08-03 EP EP07792327.4A patent/EP2049541B1/fr active Active
- 2007-08-03 WO PCT/JP2007/065681 patent/WO2008016192A2/fr not_active Ceased
- 2007-08-03 AR ARP070103435A patent/AR062207A1/es unknown
- 2007-08-03 JP JP2009522492A patent/JP5238697B2/ja active Active
- 2007-08-03 CL CL200702261A patent/CL2007002261A1/es unknown
- 2007-08-03 CA CA002659971A patent/CA2659971A1/fr not_active Abandoned
- 2007-08-03 TW TW096128518A patent/TW200817409A/zh unknown
- 2007-08-03 PE PE2007001018A patent/PE20080538A1/es not_active Application Discontinuation
- 2007-08-03 AU AU2007279595A patent/AU2007279595A1/en not_active Abandoned
- 2007-08-03 US US12/064,903 patent/US8044049B2/en active Active
- 2007-08-03 MX MX2009001349A patent/MX2009001349A/es unknown
-
2008
- 2008-11-03 US US12/263,841 patent/US20100168424A1/en not_active Abandoned
- 2008-11-03 US US12/263,949 patent/US8273741B2/en active Active
- 2008-11-03 US US12/263,884 patent/US8034812B2/en active Active
-
2009
- 2009-01-29 IL IL196799A patent/IL196799A0/en unknown
- 2009-02-09 CR CR10607A patent/CR10607A/es not_active Application Discontinuation
- 2009-02-17 MA MA31647A patent/MA30651B1/fr unknown
- 2009-03-04 NO NO20090986A patent/NO20090986L/no not_active Application Discontinuation
- 2009-03-04 CO CO09022290A patent/CO6150183A2/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US20090306374A1 (en) | 2009-12-10 |
| US20090137595A1 (en) | 2009-05-28 |
| US8034812B2 (en) | 2011-10-11 |
| WO2008016192A2 (fr) | 2008-02-07 |
| WO2008016192A3 (fr) | 2008-05-08 |
| AU2007279595A2 (en) | 2009-03-19 |
| US8273741B2 (en) | 2012-09-25 |
| IL196799A0 (en) | 2009-11-18 |
| CO6150183A2 (es) | 2010-04-20 |
| US20100273788A1 (en) | 2010-10-28 |
| US20100168424A1 (en) | 2010-07-01 |
| MX2009001349A (es) | 2009-04-17 |
| BRPI0714665A2 (pt) | 2012-03-13 |
| PE20080538A1 (es) | 2008-06-18 |
| JP2009545583A (ja) | 2009-12-24 |
| AU2007279595A1 (en) | 2008-02-07 |
| EP2049541B1 (fr) | 2015-09-23 |
| CA2659971A1 (fr) | 2008-02-07 |
| EP2049541A2 (fr) | 2009-04-22 |
| KR20090047509A (ko) | 2009-05-12 |
| US8044049B2 (en) | 2011-10-25 |
| CL2007002261A1 (es) | 2008-05-02 |
| AR062207A1 (es) | 2008-10-22 |
| CR10607A (es) | 2009-03-12 |
| JP5238697B2 (ja) | 2013-07-17 |
| TW200817409A (en) | 2008-04-16 |
| NO20090986L (no) | 2009-05-04 |
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