KR101448052B1 - Ｃ-ｋｉｔ 키나아제 억제 방법 - Google Patents
Ｃ-ｋｉｔ 키나아제 억제 방법 Download PDFInfo
- Publication number
- KR101448052B1 KR101448052B1 KR1020087028216A KR20087028216A KR101448052B1 KR 101448052 B1 KR101448052 B1 KR 101448052B1 KR 1020087028216 A KR1020087028216 A KR 1020087028216A KR 20087028216 A KR20087028216 A KR 20087028216A KR 101448052 B1 KR101448052 B1 KR 101448052B1
- Authority
- KR
- South Korea
- Prior art keywords
- mmol
- phenyl
- carboxylic acid
- enyl
- cyclohex
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 CCN(C)C(N/C1=C(\*)/CCC*(*)/C=C1)=O Chemical compound CCN(C)C(N/C1=C(\*)/CCC*(*)/C=C1)=O 0.000 description 10
- BKGAAMAFOWYKJB-UHFFFAOYSA-N Cc1c(-c(cc(cc2)N3CCN(C)CC3)c2NC(c2ccc(C#N)[o]2)=O)[s]cc1 Chemical compound Cc1c(-c(cc(cc2)N3CCN(C)CC3)c2NC(c2ccc(C#N)[o]2)=O)[s]cc1 BKGAAMAFOWYKJB-UHFFFAOYSA-N 0.000 description 2
- PKYRLRVLXYAKPM-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CC=C1c(cc1)ccc1[N+]([O-])=O)=O Chemical compound CC(C)(C)OC(N(CC1)CC=C1c(cc1)ccc1[N+]([O-])=O)=O PKYRLRVLXYAKPM-UHFFFAOYSA-N 0.000 description 1
- YRLQFRXDWBFGMK-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1c(cc1)ccc1N)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1c(cc1)ccc1N)=O YRLQFRXDWBFGMK-UHFFFAOYSA-N 0.000 description 1
- AEUFQWRXSRWAGD-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1c(cc1)nc(C2=CCCCC2)c1NC(c1nc(C#N)c[n]1COCC[Si+](C)(C)C)=O)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1c(cc1)nc(C2=CCCCC2)c1NC(c1nc(C#N)c[n]1COCC[Si+](C)(C)C)=O)=O AEUFQWRXSRWAGD-UHFFFAOYSA-N 0.000 description 1
- JTFJPZUTHAZKCK-UHFFFAOYSA-N CC(C)(C)OC(NC(C)(C)CC(N(CC1)CCC1c(cc1)cc(C2=CCCCC2)c1NC(c1nc(C#N)c[nH]1)=O)=O)=O Chemical compound CC(C)(C)OC(NC(C)(C)CC(N(CC1)CCC1c(cc1)cc(C2=CCCCC2)c1NC(c1nc(C#N)c[nH]1)=O)=O)=O JTFJPZUTHAZKCK-UHFFFAOYSA-N 0.000 description 1
- MYSVNRUEZQUSTA-UHFFFAOYSA-N CC(C)(CC1)CC=C1c(nc(C1CCN(CCS(C)(=O)=O)CC1)cc1)c1NC(c1nc(C#N)c[nH]1)=O Chemical compound CC(C)(CC1)CC=C1c(nc(C1CCN(CCS(C)(=O)=O)CC1)cc1)c1NC(c1nc(C#N)c[nH]1)=O MYSVNRUEZQUSTA-UHFFFAOYSA-N 0.000 description 1
- NARDFLCWIXQUGJ-UHFFFAOYSA-N CN(CC1)CCN1c(cc1)cc(C2=CCCCC2)c1[N+]([O-])=O Chemical compound CN(CC1)CCN1c(cc1)cc(C2=CCCCC2)c1[N+]([O-])=O NARDFLCWIXQUGJ-UHFFFAOYSA-N 0.000 description 1
- MBDRFJPJBRFKSM-UHFFFAOYSA-N CS(CCN(CC1)CCC1c(cc1)nc(C2=CCCCC2)c1NC(c1nc(C#N)c[nH]1)=O)(=O)=O Chemical compound CS(CCN(CC1)CCC1c(cc1)nc(C2=CCCCC2)c1NC(c1nc(C#N)c[nH]1)=O)(=O)=O MBDRFJPJBRFKSM-UHFFFAOYSA-N 0.000 description 1
- ZEYUMPKHRZXSEC-UHFFFAOYSA-N C[Si+](C)(C)CCOC[n]1c(C(Nc(ccc(C(CC2)CCS2(=O)=O)c2)c2C2=CCCCC2)=O)nc(C#N)c1 Chemical compound C[Si+](C)(C)CCOC[n]1c(C(Nc(ccc(C(CC2)CCS2(=O)=O)c2)c2C2=CCCCC2)=O)nc(C#N)c1 ZEYUMPKHRZXSEC-UHFFFAOYSA-N 0.000 description 1
- NCGAWJMJSZBSLI-UHFFFAOYSA-N N#CCCN(CC1)CCC1c(cc1C2=CCCCC2)ccc1NC(c1nc(C#N)c[nH]1)=O Chemical compound N#CCCN(CC1)CCC1c(cc1C2=CCCCC2)ccc1NC(c1nc(C#N)c[nH]1)=O NCGAWJMJSZBSLI-UHFFFAOYSA-N 0.000 description 1
- QPSVRPUGGFUWCH-UHFFFAOYSA-N N#Cc1c[nH]c(C(Nc2ccc(C3CCN(CCO)CC3)cc2C2=CCCCC2)=O)n1 Chemical compound N#Cc1c[nH]c(C(Nc2ccc(C3CCN(CCO)CC3)cc2C2=CCCCC2)=O)n1 QPSVRPUGGFUWCH-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Psychiatry (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Oncology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79347106P | 2006-04-20 | 2006-04-20 | |
| US60/793,471 | 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 |
|---|---|
| KR20080111545A KR20080111545A (ko) | 2008-12-23 |
| KR101448052B1 true KR101448052B1 (ko) | 2014-10-07 |
Family
ID=38625740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020087028216A Expired - Fee Related KR101448052B1 (ko) | 2006-04-20 | 2007-04-19 | Ｃ-ｋｉｔ 키나아제 억제 방법 |
Country Status (21)
| Country | Link |
|---|---|
| EP (2) | EP2397138B1 (enExample) |
| JP (1) | JP5595727B2 (enExample) |
| KR (1) | KR101448052B1 (enExample) |
| CN (2) | CN102670605B (enExample) |
| AU (1) | AU2007240400B2 (enExample) |
| BR (1) | BRPI0710542B8 (enExample) |
| CA (1) | CA2649755C (enExample) |
| CO (1) | CO6382175A2 (enExample) |
| CR (1) | CR10450A (enExample) |
| EA (1) | EA016611B1 (enExample) |
| EC (1) | ECSP088842A (enExample) |
| ES (2) | ES2458291T3 (enExample) |
| GT (1) | GT200800225A (enExample) |
| IL (1) | IL194846A (enExample) |
| MX (1) | MX2008013528A (enExample) |
| MY (1) | MY147226A (enExample) |
| NO (1) | NO342001B1 (enExample) |
| NZ (1) | NZ572200A (enExample) |
| SG (1) | SG171592A1 (enExample) |
| WO (1) | WO2007124369A2 (enExample) |
| ZA (1) | ZA200809874B (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112014001977A2 (pt) | 2011-07-27 | 2017-02-21 | Ab Science | inibidores seletivos de proteína quinase |
| 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 |
| CN105658649B (zh) | 2013-07-22 | 2019-03-22 | 爱杜西亚药品有限公司 | 1-(哌嗪-1-基)-2-([1,2,4]三唑-1-基)-乙酮衍生物 |
| PE20171100A1 (es) | 2015-01-15 | 2017-08-07 | Idorsia Pharmaceuticals Ltd | Derivados de hidroxialquil-piperazina como moduladores del receptor cxcr3 |
| AR103399A1 (es) | 2015-01-15 | 2017-05-10 | Actelion Pharmaceuticals Ltd | Derivados de (r)-2-metil-piperazina como moduladores del receptor cxcr3 |
| 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 |
| CN114761006A (zh) | 2019-11-08 | 2022-07-15 | Inserm(法国国家健康医学研究院) | 对激酶抑制剂产生耐药性的癌症的治疗方法 |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006047277A2 (en) | 2004-10-22 | 2006-05-04 | Janssen Pharmaceutica, N.V. | Inhibitors of c-fms kinase |
| WO2006138155A1 (en) | 2005-06-10 | 2006-12-28 | Janssen Pharmaceutica N.V. | Synergistic modulation of flt3 kinase using a flt3 inhibitor and a farnesyl transferase inhibitor |
| WO2007048088A2 (en) | 2005-10-18 | 2007-04-26 | Janssen Pharmaceutica N.V. | Method of inhibiting flt3 kinase |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1993017715A1 (en) | 1992-03-05 | 1993-09-16 | Board Of Regents, The University Of Texas System | Diagnostic and/or therapeutic agents, targeted to neovascular endothelial cells |
| WO2000064946A2 (en) | 1999-04-28 | 2000-11-02 | Board Of Regents, The University Of Texas System | Compositions and methods for cancer treatment by selectively inhibiting 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 |
| US7718676B2 (en) * | 2003-10-23 | 2010-05-18 | Ab Science | 2-aminoaryloxazole compounds as tyrosine kinase inhibitors |
| GB0326601D0 (en) * | 2003-11-14 | 2003-12-17 | Novartis Ag | Organic compounds |
| NZ548884A (en) * | 2004-01-30 | 2010-06-25 | Ab Science | 2-(3-substituted-aryl)amino-4-aryl-thiazoles as tyrosine kinase inhibitors |
| NZ572072A (en) * | 2006-04-20 | 2011-09-30 | Janssen Pharmaceutica Nv | Inhibitors of c-fms kinase |
| WO2007124316A1 (en) * | 2006-04-20 | 2007-11-01 | Janssen Pharmaceutica N.V. | Heterocyclic compounds as inhibitors of c-fms kinase |
| EP2016057A1 (en) * | 2006-04-20 | 2009-01-21 | Janssen Pharmaceutica N.V. | C-fms kinase inhibitors |
-
2007
- 2007-04-19 BR BRPI0710542A patent/BRPI0710542B8/pt not_active IP Right Cessation
- 2007-04-19 NZ NZ572200A patent/NZ572200A/en not_active IP Right Cessation
- 2007-04-19 CA CA2649755A patent/CA2649755C/en active Active
- 2007-04-19 ES ES11161399.8T patent/ES2458291T3/es active Active
- 2007-04-19 WO PCT/US2007/066985 patent/WO2007124369A2/en not_active Ceased
- 2007-04-19 CN CN201210022810.8A patent/CN102670605B/zh not_active Expired - Fee Related
- 2007-04-19 EP EP11161399.8A patent/EP2397138B1/en active Active
- 2007-04-19 ES ES07760927T patent/ES2389678T3/es active Active
- 2007-04-19 JP JP2009506778A patent/JP5595727B2/ja not_active Expired - Fee Related
- 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 AU AU2007240400A patent/AU2007240400B2/en not_active Ceased
- 2007-04-19 EA EA200870454A patent/EA016611B1/ru unknown
- 2007-04-19 KR KR1020087028216A patent/KR101448052B1/ko not_active Expired - Fee Related
- 2007-04-19 EP EP07760927A patent/EP2015748B1/en active Active
- 2007-04-19 SG SG201102829-7A patent/SG171592A1/en unknown
-
2008
- 2008-10-20 MY MYPI20084185A patent/MY147226A/en unknown
- 2008-10-21 GT GT200800225A patent/GT200800225A/es unknown
- 2008-10-22 EC EC2008008842A patent/ECSP088842A/es unknown
- 2008-10-22 IL IL194846A patent/IL194846A/en active IP Right Grant
- 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
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006047277A2 (en) | 2004-10-22 | 2006-05-04 | Janssen Pharmaceutica, N.V. | Inhibitors of c-fms kinase |
| WO2006138155A1 (en) | 2005-06-10 | 2006-12-28 | Janssen Pharmaceutica N.V. | Synergistic modulation of flt3 kinase using a flt3 inhibitor and a farnesyl transferase inhibitor |
| WO2007048088A2 (en) | 2005-10-18 | 2007-04-26 | Janssen Pharmaceutica N.V. | Method of inhibiting flt3 kinase |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
St.27 status event code: A-0-1-A10-A15-nap-PA0105 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
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