EA200870454A1 - Способ ингибирования c-kit киназы - Google Patents
Способ ингибирования c-kit киназыInfo
- Publication number
- EA200870454A1 EA200870454A1 EA200870454A EA200870454A EA200870454A1 EA 200870454 A1 EA200870454 A1 EA 200870454A1 EA 200870454 A EA200870454 A EA 200870454A EA 200870454 A EA200870454 A EA 200870454A EA 200870454 A1 EA200870454 A1 EA 200870454A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- inhibiting
- kit
- subject
- compound
- kit kinase
- Prior art date
Links
- 108091000080 Phosphotransferase Proteins 0.000 title abstract 2
- 230000002401 inhibitory effect Effects 0.000 title abstract 2
- 102000020233 phosphotransferase Human genes 0.000 title abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- 230000002062 proliferating effect Effects 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Immunology (AREA)
- Cardiology (AREA)
- Oncology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurosurgery (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Psychiatry (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Способ снижения или ингибирования киназной активности С-KIT в клетке или у субъекта и применение такого соединения для профилактики или лечения у субъекта клеточно-пролиферативного расстройства и/или расстройств, связанных с С-KIT, с использованием соединения по настоящему изобретению (формула (I)) или его сольвата, гидрата, таутомера или фармацевтически приемлемой соли. Настоящее изобретение также направлено на способы лечения состояний, таких как различные типы рака и другие клеточно-пролиферативные расстройства.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US79347106P | 2006-04-20 | 2006-04-20 | |
PCT/US2007/066985 WO2007124369A2 (en) | 2006-04-20 | 2007-04-19 | Method of inhibiting c kit kinase |
Publications (2)
Publication Number | Publication Date |
---|---|
EA200870454A1 true EA200870454A1 (ru) | 2009-04-28 |
EA016611B1 EA016611B1 (ru) | 2012-06-29 |
Family
ID=38625740
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200870454A EA016611B1 (ru) | 2006-04-20 | 2007-04-19 | Способ лечения мастоцитоза |
Country Status (22)
Country | Link |
---|---|
EP (2) | EP2397138B1 (ru) |
JP (1) | JP5595727B2 (ru) |
KR (1) | KR101448052B1 (ru) |
CN (2) | CN102670605B (ru) |
AU (1) | AU2007240400B2 (ru) |
BR (1) | BRPI0710542B8 (ru) |
CA (1) | CA2649755C (ru) |
CO (1) | CO6382175A2 (ru) |
CR (1) | CR10450A (ru) |
EA (1) | EA016611B1 (ru) |
EC (1) | ECSP088842A (ru) |
ES (2) | ES2389678T3 (ru) |
GT (1) | GT200800225A (ru) |
HK (1) | HK1124766A1 (ru) |
IL (1) | IL194846A (ru) |
MX (1) | MX2008013528A (ru) |
MY (1) | MY147226A (ru) |
NO (1) | NO342001B1 (ru) |
NZ (1) | NZ572200A (ru) |
SG (1) | SG171592A1 (ru) |
WO (1) | WO2007124369A2 (ru) |
ZA (1) | ZA200809874B (ru) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2012288900B2 (en) | 2011-07-27 | 2016-10-06 | Ab Science | Selective protein kinase inhibitors |
CN104370880A (zh) * | 2013-01-24 | 2015-02-25 | 韩冰 | 一类蛋白酶抑制剂及其制备方法和用途 |
KR102295416B1 (ko) | 2013-07-22 | 2021-08-30 | 이도르시아 파마슈티컬스 리미티드 | 1-(피페라진-1-일)-2-([1,2,4]트리아졸-1-일)-에타논 유도체 |
AR103399A1 (es) | 2015-01-15 | 2017-05-10 | Actelion Pharmaceuticals Ltd | Derivados de (r)-2-metil-piperazina como moduladores del receptor cxcr3 |
KR101967083B1 (ko) | 2015-01-15 | 2019-04-08 | 이도르시아 파마슈티컬스 리미티드 | Cxcr3 수용체 조절제로서의 히드록시알킬-피페라진 유도체 |
CN105753770A (zh) * | 2015-05-27 | 2016-07-13 | 上海佐林生物医药有限公司 | 蛋白激酶抑制剂制备方法、中间体、制备方法及应用 |
KR20210142154A (ko) | 2019-03-21 | 2021-11-24 | 옹쎄오 | 암 치료를 위한 키나제 억제제와 조합된 dbait 분자 |
US20220401436A1 (en) | 2019-11-08 | 2022-12-22 | INSERM (Institute National de la Santé et de la Recherche Médicale) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PT627940E (pt) | 1992-03-05 | 2003-07-31 | Univ Texas | Utilizacao de imunoconjugados para o diagnostico e/ou terapia de tumores vascularizados |
BR0010017A (pt) | 1999-04-28 | 2002-06-11 | Univ Texas | Composições e processos para o tratamento de câncer por inibição seletiva de vegf |
DE19962924A1 (de) | 1999-12-24 | 2001-07-05 | Bayer Ag | Substituierte Oxazolidinone und ihre Verwendung |
ITMI992711A1 (it) * | 1999-12-27 | 2001-06-27 | Novartis Ag | Composti organici |
ATE375342T1 (de) * | 2002-08-02 | 2007-10-15 | Ab Science | 2-(3-aminoaryl)amino-4-aryl-thiazole und ihre verwendung als c-kit inhibitoren |
ATE465731T1 (de) * | 2003-10-23 | 2010-05-15 | Ab Science | 2-aminoaryloxazol-verbindungen als tyrosinkinase- hemmer |
GB0326601D0 (en) * | 2003-11-14 | 2003-12-17 | Novartis Ag | Organic compounds |
AU2005209485A1 (en) * | 2004-01-30 | 2005-08-11 | Ab Science | 2-(3-substituted-aryl)amino-4-aryl-thiazoles as tyrosine kinase inhibitors |
CA2585053C (en) * | 2004-10-22 | 2011-07-12 | Janssen Pharmaceutica N.V. | Substituted n-acyl (hetero)aryl compounds as c-fms kinase inhibitors |
US20060281788A1 (en) | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using a flt3 inhibitor and a farnesyl transferase inhibitor |
BRPI0617489A2 (pt) * | 2005-10-18 | 2011-07-26 | Janssen Pharmaceutica Nv | compostos, composiÇço e uso de ditos compostos para inibir a flt3 cinase |
AU2006342509A1 (en) * | 2006-04-20 | 2007-11-01 | Janssen Pharmaceutica, N.V. | c-fms kinase inhibitors |
US8815867B2 (en) * | 2006-04-20 | 2014-08-26 | Janssen Pharmaceutica Nv | Inhibitors of c-fms kinase |
US7414050B2 (en) * | 2006-04-20 | 2008-08-19 | Janssen Pharmaceutica, N.V. | Inhibitors of c-fms kinase |
-
2007
- 2007-04-19 ES ES07760927T patent/ES2389678T3/es active Active
- 2007-04-19 EP EP11161399.8A patent/EP2397138B1/en active Active
- 2007-04-19 JP JP2009506778A patent/JP5595727B2/ja not_active Expired - Fee Related
- 2007-04-19 SG SG201102829-7A patent/SG171592A1/en unknown
- 2007-04-19 CN CN201210022810.8A patent/CN102670605B/zh not_active Expired - Fee Related
- 2007-04-19 NZ NZ572200A patent/NZ572200A/en not_active IP Right Cessation
- 2007-04-19 KR KR1020087028216A patent/KR101448052B1/ko active IP Right Grant
- 2007-04-19 BR BRPI0710542A patent/BRPI0710542B8/pt not_active IP Right Cessation
- 2007-04-19 AU AU2007240400A patent/AU2007240400B2/en not_active Ceased
- 2007-04-19 EP EP07760927A patent/EP2015748B1/en active Active
- 2007-04-19 EA EA200870454A patent/EA016611B1/ru unknown
- 2007-04-19 WO PCT/US2007/066985 patent/WO2007124369A2/en active Application Filing
- 2007-04-19 MX MX2008013528A patent/MX2008013528A/es active IP Right Grant
- 2007-04-19 CN CN2007800231790A patent/CN101610768B/zh not_active Expired - Fee Related
- 2007-04-19 CA CA2649755A patent/CA2649755C/en active Active
- 2007-04-19 ES ES11161399.8T patent/ES2458291T3/es active Active
-
2008
- 2008-10-20 MY MYPI20084185A patent/MY147226A/en unknown
- 2008-10-21 GT GT200800225A patent/GT200800225A/es unknown
- 2008-10-22 IL IL194846A patent/IL194846A/en active IP Right Grant
- 2008-10-22 EC EC2008008842A patent/ECSP088842A/es unknown
- 2008-10-24 CO CO08113911A patent/CO6382175A2/es active IP Right Grant
- 2008-11-19 ZA ZA2008/09874A patent/ZA200809874B/en unknown
- 2008-11-20 NO NO20084892A patent/NO342001B1/no not_active IP Right Cessation
- 2008-11-20 CR CR10450A patent/CR10450A/es unknown
-
2009
- 2009-03-09 HK HK09102246.9A patent/HK1124766A1/xx not_active IP Right Cessation
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2007048088A3 (en) | Method of inhibiting flt3 kinase | |
EA200870454A1 (ru) | Способ ингибирования c-kit киназы | |
PH12018500792A1 (en) | Benzolactam compounds as protein kinase inhibitors | |
EA200970935A1 (ru) | Способы лечения с применением хинаксолиновых ингибиторов pi3k-альфа | |
EA200970447A1 (ru) | Соединения и композиции в качестве ингибиторов протеинкиназы | |
EA200970932A1 (ru) | Способы лечения с применением пиридопиримидиноновых ингибиторов pi3k альфа | |
TW200720268A (en) | 1h-benzimidazole-4-carboxamides substituted with a quaternary carbon at the 2-position are potent PARP inhibitors | |
IN2014KN02886A (ru) | ||
TW200736229A (en) | Substituted 1H-benzimidazole-4-carboxamides are potent PARP inhibitors | |
IL200793A0 (en) | Aminopyrimidines, compositions comprising the same and use thereof for inhibiting protein kinases | |
MX2009011810A (es) | Tiazoles y pirazoles utiles como inhibidores de cinasa. | |
MX2009012719A (es) | Tiazoles y pirazoles utiles como inhibidores de cinasa. | |
MX2009013077A (es) | Derivados dde benzoxazolona. | |
SI2054418T1 (sl) | Dihidrotieno pirimidini kot AKT protein kinazni inhibitorji | |
WO2008022024A3 (en) | Imidazole amines as inhibitors of beta-secretase | |
ATE493418T1 (de) | Dihydrofuropyrimidine als akt- proteinkinaseinhibitoren | |
MX2009011059A (es) | Aminopirimidinas utiles como inhibidores de cinasas. | |
MX2010004967A (es) | Uso de inhibidor de cfms para el tratamiento y la prevención del cancer de hueso, así como la perdida osea y el dolor de hueso asociados con el cancer de hueso. | |
MX2007004248A (es) | Derivados heterociclicos de bisarilurea sustituidos como inhibidores de cinasa. | |
TW200503722A (en) | Substituted 7-aza-quinazoline compounds | |
MX2009012079A (es) | Compuestos heterociclicos condensados como inhibidores de proteina cinasas. | |
TW200602023A (en) | Monocyclic heterocycles as kinase inhibitors | |
UA105483C2 (ru) | Производные изохинолинона, композиция на их основе и применение в качестве ингибиторов pi3k | |
NZ630353A (en) | Pyrazolopyrimidines and related heterocycles as ck2 inhibitors |