JP2008546753A - タンパク質キナーゼの阻害剤としてのアリール−アルキルアミンおよびヘテロアリール−アルキルアミン - Google Patents
タンパク質キナーゼの阻害剤としてのアリール−アルキルアミンおよびヘテロアリール−アルキルアミン Download PDFInfo
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- JP2008546753A JP2008546753A JP2008517591A JP2008517591A JP2008546753A JP 2008546753 A JP2008546753 A JP 2008546753A JP 2008517591 A JP2008517591 A JP 2008517591A JP 2008517591 A JP2008517591 A JP 2008517591A JP 2008546753 A JP2008546753 A JP 2008546753A
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- JP
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- Prior art keywords
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- phenyl
- compound
- hydrogen
- compound according
- 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.)
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- 0 *c1c(*I)c(*)n[n]1 Chemical compound *c1c(*I)c(*)n[n]1 0.000 description 16
- AIIKIZBWZDYCON-WSDLNYQXSA-N C/N=C/CC(c(cc1)ccc1-c1c[nH]nc1)(c(cc1)ccc1Cl)OC Chemical compound C/N=C/CC(c(cc1)ccc1-c1c[nH]nc1)(c(cc1)ccc1Cl)OC AIIKIZBWZDYCON-WSDLNYQXSA-N 0.000 description 1
- FUIHTSMKOYYBIV-UDWIEESQSA-N C/N=C/CC(c(cc1)ccc1Cl)(c(cc1)ccc1I)OC Chemical compound C/N=C/CC(c(cc1)ccc1Cl)(c(cc1)ccc1I)OC FUIHTSMKOYYBIV-UDWIEESQSA-N 0.000 description 1
- QEACSENDPXQEFE-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1(c1cc(Cl)ccc1)O)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1(c1cc(Cl)ccc1)O)=O QEACSENDPXQEFE-UHFFFAOYSA-N 0.000 description 1
- MCRIVSVOAUJKRH-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1(c1ccc(B2OC(C)(C)C(C)(C)O2)cc1)c(cc1)ccc1Cl)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1(c1ccc(B2OC(C)(C)C(C)(C)O2)cc1)c(cc1)ccc1Cl)=O MCRIVSVOAUJKRH-UHFFFAOYSA-N 0.000 description 1
- AOCSUUGBCMTKJH-UHFFFAOYSA-N CC(C)(C)OC(NCCN)=O Chemical compound CC(C)(C)OC(NCCN)=O AOCSUUGBCMTKJH-UHFFFAOYSA-N 0.000 description 1
- LOSOPOUNUQPWLP-UHFFFAOYSA-N CC(C)(C)OC(NCCNC(c1ccc(C)cc1)c(cc1)ccc1Cl)=O Chemical compound CC(C)(C)OC(NCCNC(c1ccc(C)cc1)c(cc1)ccc1Cl)=O LOSOPOUNUQPWLP-UHFFFAOYSA-N 0.000 description 1
- VLGGTNRSVQOSDI-UHFFFAOYSA-N CC(C)(C)c1ccccc1C1(CCNCC1)c(cc1)ccc1-c1c[nH]nc1 Chemical compound CC(C)(C)c1ccccc1C1(CCNCC1)c(cc1)ccc1-c1c[nH]nc1 VLGGTNRSVQOSDI-UHFFFAOYSA-N 0.000 description 1
- MJGTUYOCBQBORS-JXMROGBWSA-N CCOC(/C(/C#N)=C/c(cc1)ccc1Br)=O Chemical compound CCOC(/C(/C#N)=C/c(cc1)ccc1Br)=O MJGTUYOCBQBORS-JXMROGBWSA-N 0.000 description 1
- YTQAHFAWTIUFNQ-UHFFFAOYSA-N CCc([n](nc1)S(N(C)C)(=O)=O)c1-c1ccc(C(CC2)(CCN2C(OC(C)(C)C)=O)c(cc2)ccc2Cl)cc1 Chemical compound CCc([n](nc1)S(N(C)C)(=O)=O)c1-c1ccc(C(CC2)(CCN2C(OC(C)(C)C)=O)c(cc2)ccc2Cl)cc1 YTQAHFAWTIUFNQ-UHFFFAOYSA-N 0.000 description 1
- CNKPFPWSETVGBM-UHFFFAOYSA-N CCc([n](nc1)S(N(C)C)(=O)=O)c1Br Chemical compound CCc([n](nc1)S(N(C)C)(=O)=O)c1Br CNKPFPWSETVGBM-UHFFFAOYSA-N 0.000 description 1
- VWMFOOMEDFKJGH-UHFFFAOYSA-N CCc(c(Br)c1)n[n]1S(N(C)C)(=O)=O Chemical compound CCc(c(Br)c1)n[n]1S(N(C)C)(=O)=O VWMFOOMEDFKJGH-UHFFFAOYSA-N 0.000 description 1
- CSDWSKXRAXPRAP-UHFFFAOYSA-N CCc(cc1)n[n]1S(N(C)C)(=O)=O Chemical compound CCc(cc1)n[n]1S(N(C)C)(=O)=O CSDWSKXRAXPRAP-UHFFFAOYSA-N 0.000 description 1
- DAKXGOWVFIZXLK-JTQLQIEISA-N C[C@@H](CC1CC1)CN1CCOCC1 Chemical compound C[C@@H](CC1CC1)CN1CCOCC1 DAKXGOWVFIZXLK-JTQLQIEISA-N 0.000 description 1
- AYTPBAOKNBMTEH-GAJHUEQPSA-N C[C@@H](c1ccccc1)NC(C[C@H](c(cc1)ccc1-c1c[nH]nc1)c(cc1Cl)ccc1Cl)=O Chemical compound C[C@@H](c1ccccc1)NC(C[C@H](c(cc1)ccc1-c1c[nH]nc1)c(cc1Cl)ccc1Cl)=O AYTPBAOKNBMTEH-GAJHUEQPSA-N 0.000 description 1
- IETUJBHBQHSAGJ-UHFFFAOYSA-N Cc(c(-c1ccc(C(CN)(c2ccccc2)O)cc1)c1)n[n]1S(N(C)C)(=O)=O Chemical compound Cc(c(-c1ccc(C(CN)(c2ccccc2)O)cc1)c1)n[n]1S(N(C)C)(=O)=O IETUJBHBQHSAGJ-UHFFFAOYSA-N 0.000 description 1
- MWCUUYRCCBJOGX-UHFFFAOYSA-N Cc1ccc(C(CC(O)=O)(c(cc2)ccc2Cl)O)cc1 Chemical compound Cc1ccc(C(CC(O)=O)(c(cc2)ccc2Cl)O)cc1 MWCUUYRCCBJOGX-UHFFFAOYSA-N 0.000 description 1
- KJLGEVCAQUPFPX-UHFFFAOYSA-N NCC(c(cc1)ccc1Cl)(c(cc1)ccc1I)O Chemical compound NCC(c(cc1)ccc1Cl)(c(cc1)ccc1I)O KJLGEVCAQUPFPX-UHFFFAOYSA-N 0.000 description 1
- UKLYMSCNKMLFEQ-UHFFFAOYSA-N NCCC(c(cc1)ccc1-c1c[nH]nc1)c(cc1N2CCOCC2)ccc1Cl Chemical compound NCCC(c(cc1)ccc1-c1c[nH]nc1)c(cc1N2CCOCC2)ccc1Cl UKLYMSCNKMLFEQ-UHFFFAOYSA-N 0.000 description 1
- JNMRJCSPEARZBZ-UHFFFAOYSA-N NCCC(c(cc1)ccc1-c1c[nH]nc1)c1ccccc1Cl Chemical compound NCCC(c(cc1)ccc1-c1c[nH]nc1)c1ccccc1Cl JNMRJCSPEARZBZ-UHFFFAOYSA-N 0.000 description 1
- DTXFVYVTJKJFJV-UHFFFAOYSA-N NCCC(c(cc1)ccc1Cl)(c(cc1)cc(F)c1-c1c[nH]nc1)O Chemical compound NCCC(c(cc1)ccc1Cl)(c(cc1)cc(F)c1-c1c[nH]nc1)O DTXFVYVTJKJFJV-UHFFFAOYSA-N 0.000 description 1
- NJOGIGLBTLZKLU-UHFFFAOYSA-N NCCC(c1ccc[o]1)c(cc1)ccc1-c1c[nH]nc1 Chemical compound NCCC(c1ccc[o]1)c(cc1)ccc1-c1c[nH]nc1 NJOGIGLBTLZKLU-UHFFFAOYSA-N 0.000 description 1
- AVUDXLOVIBJFQA-UHFFFAOYSA-N O=C(C1)CN1C(c1ccccc1)c1ccccc1 Chemical compound O=C(C1)CN1C(c1ccccc1)c1ccccc1 AVUDXLOVIBJFQA-UHFFFAOYSA-N 0.000 description 1
- PCFIABOQFAFDAU-UHFFFAOYSA-N O=C(c(c(F)c1)ccc1Br)Cl Chemical compound O=C(c(c(F)c1)ccc1Br)Cl PCFIABOQFAFDAU-UHFFFAOYSA-N 0.000 description 1
- HKDDBMJLLJNLMT-UHFFFAOYSA-N O=C(c(cc1)ccc1Cl)c(c(F)c1)ccc1Br Chemical compound O=C(c(cc1)ccc1Cl)c(c(F)c1)ccc1Br HKDDBMJLLJNLMT-UHFFFAOYSA-N 0.000 description 1
- MMAJXKGUZYDTHV-UHFFFAOYSA-N OC(C1)CN1C(c1ccccc1)c1ccccc1 Chemical compound OC(C1)CN1C(c1ccccc1)c1ccccc1 MMAJXKGUZYDTHV-UHFFFAOYSA-N 0.000 description 1
- DUFWELWLZQVCJN-UHFFFAOYSA-N OC(CCC(c(cc1)ccc1-c1c[nH]nc1)c(cc1Cl)ccc1Cl)=O Chemical compound OC(CCC(c(cc1)ccc1-c1c[nH]nc1)c(cc1Cl)ccc1Cl)=O DUFWELWLZQVCJN-UHFFFAOYSA-N 0.000 description 1
- MSBOXWUPLWSATF-UHFFFAOYSA-N OC(c(cc1)ccc1Br)c(cc1N2CCOCC2)ccc1Cl Chemical compound OC(c(cc1)ccc1Br)c(cc1N2CCOCC2)ccc1Cl MSBOXWUPLWSATF-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- 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
- A61P11/02—Nasal agents, e.g. decongestants
-
- 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
- A61P11/04—Drugs for disorders of the respiratory system for throat disorders
-
- 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
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P11/16—Central respiratory analeptics
-
- A—HUMAN NECESSITIES
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- 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
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- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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- A—HUMAN NECESSITIES
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
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- A—HUMAN NECESSITIES
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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- 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
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- 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
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
- A61P37/02—Immunomodulators
-
- 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
- A61P9/06—Antiarrhythmics
-
- 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)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Otolaryngology (AREA)
- Psychiatry (AREA)
- Obesity (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Communicable Diseases (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69248205P | 2005-06-21 | 2005-06-21 | |
| GB0512642A GB0512642D0 (en) | 2005-06-21 | 2005-06-21 | Pharmaceutical compounds |
| US74414106P | 2006-04-03 | 2006-04-03 | |
| PCT/GB2006/002287 WO2006136830A1 (en) | 2005-06-21 | 2006-06-21 | Aryl-alkylamines and heteroaryl-alkylamines as protein kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008546753A true JP2008546753A (ja) | 2008-12-25 |
| JP2008546753A5 JP2008546753A5 (https=) | 2009-08-06 |
Family
ID=37103276
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008517591A Withdrawn JP2008546753A (ja) | 2005-06-21 | 2006-06-21 | タンパク質キナーゼの阻害剤としてのアリール−アルキルアミンおよびヘテロアリール−アルキルアミン |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20100210617A1 (https=) |
| EP (1) | EP1904451A1 (https=) |
| JP (1) | JP2008546753A (https=) |
| AR (1) | AR054485A1 (https=) |
| UY (1) | UY29610A1 (https=) |
| WO (1) | WO2006136830A1 (https=) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0418078A8 (pt) | 2003-12-23 | 2018-01-02 | Astex Therapeutics Ltd | composto ou um seu sal, solvato, tautômero ou n-óxido, uso de um composto, métodos para a profilaxia ou tratamento de um estado ou condição doentia mediada pela proteína quinase b e mediada pela proteína quinase a, para tratar uma doença ou condição, para inibir uma proteína quinase b e uma proteína quinase a, para modular um processo celular, para tratar um distúrbio imune em um mamífero e para induzir apoptose em uma célula cancerosa, composição farmacêutica, e, processo para a preparação de um composto |
| EP1902032A1 (en) | 2005-06-22 | 2008-03-26 | Astex Therapeutics Limited | Pharmaceutical compounds |
| JP5345842B2 (ja) | 2005-06-23 | 2013-11-20 | アステックス・セラピューティクス・リミテッド | プロテインキナーゼモジュレーターとしてのピラゾール誘導体を含む医薬組み合わせ |
| WO2007120574A2 (en) * | 2006-04-11 | 2007-10-25 | Merck & Co., Inc. | Diaryl substituted alkanes |
| US8329701B2 (en) | 2006-07-06 | 2012-12-11 | Array Biopharma Inc. | Dihydrofuro pyrimidines as AKT protein kinase inhibitors |
| EP2049500B1 (en) | 2006-07-06 | 2011-09-07 | Array Biopharma, Inc. | Cyclopenta [d] pyrimidines as akt protein kinase inhibitors |
| ATE532789T1 (de) | 2006-07-06 | 2011-11-15 | Array Biopharma Inc | Dihydrothienopyrimidine als akt-proteinkinase- inhibitoren |
| US8063050B2 (en) | 2006-07-06 | 2011-11-22 | Array Biopharma Inc. | Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
| ATE543810T1 (de) * | 2006-09-01 | 2012-02-15 | Merck Sharp & Dohme | Hemmer des 5-lipoxygenase aktivierenden proteins (flap) |
| GB0704932D0 (en) * | 2007-03-14 | 2007-04-25 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| CN101918373B (zh) | 2007-07-05 | 2013-06-05 | 阵列生物制药公司 | 作为akt蛋白激酶抑制剂的嘧啶基环戊烷 |
| US9409886B2 (en) | 2007-07-05 | 2016-08-09 | Array Biopharma Inc. | Pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
| CN103396409B (zh) | 2007-07-05 | 2015-03-11 | 阵列生物制药公司 | 作为akt蛋白激酶抑制剂的嘧啶基环戊烷 |
| US8846683B2 (en) | 2007-07-05 | 2014-09-30 | Array Biopharma, Inc. | Pyrimidyl cyclopentanes as Akt protein kinase inhibitors |
| NZ586346A (en) | 2008-01-09 | 2012-02-24 | Array Biopharma Inc | Hydroxylated pyrimidyl cyclopentanes as akt protein kinase inhibitors |
| US8853216B2 (en) | 2008-01-09 | 2014-10-07 | Array Biopharma, Inc. | Hydroxylated pyrimidyl cyclopentane as AKT protein kinase inhibitor |
| TR201815685T4 (tr) | 2011-04-01 | 2018-11-21 | Genentech Inc | Kanser tedavisi için akt ve mek inhibe edici bileşiklerin kombinasyonları. |
| KR102021157B1 (ko) | 2011-04-01 | 2019-09-11 | 제넨테크, 인크. | Akt 억제제 화합물 및 아비라테론의 조합물, 및 사용 방법 |
| CN110156786B (zh) * | 2018-02-13 | 2022-06-03 | 青煜医药研发(上海)有限公司 | 嘧啶并环化合物及其制备方法和应用 |
| BR112022021976A2 (pt) | 2020-04-30 | 2022-12-13 | Idorsia Pharmaceuticals Ltd | Composto, e, composição farmacêutica compreendendo um composto |
| WO2023057548A1 (en) | 2021-10-07 | 2023-04-13 | Idorsia Pharmaceuticals Ltd | Ccr6 receptor modulators |
| EP4423082A1 (en) | 2021-10-26 | 2024-09-04 | Idorsia Pharmaceuticals Ltd | Ccr6 receptor modulators |
| KR20240090693A (ko) | 2021-10-28 | 2024-06-21 | 이도르시아 파마슈티컬스 리미티드 | Ccr6 수용체 조절인자 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0418078A8 (pt) * | 2003-12-23 | 2018-01-02 | Astex Therapeutics Ltd | composto ou um seu sal, solvato, tautômero ou n-óxido, uso de um composto, métodos para a profilaxia ou tratamento de um estado ou condição doentia mediada pela proteína quinase b e mediada pela proteína quinase a, para tratar uma doença ou condição, para inibir uma proteína quinase b e uma proteína quinase a, para modular um processo celular, para tratar um distúrbio imune em um mamífero e para induzir apoptose em uma célula cancerosa, composição farmacêutica, e, processo para a preparação de um composto |
| UY29177A1 (es) * | 2004-10-25 | 2006-05-31 | Astex Therapeutics Ltd | Derivados sustituidos de purina, purinona y deazapurina, composiciones que los contienen métodos para su preparación y sus usos |
-
2006
- 2006-06-20 UY UY29610A patent/UY29610A1/es not_active Application Discontinuation
- 2006-06-20 AR ARP060102630A patent/AR054485A1/es not_active Application Discontinuation
- 2006-06-21 WO PCT/GB2006/002287 patent/WO2006136830A1/en not_active Ceased
- 2006-06-21 EP EP06755591A patent/EP1904451A1/en not_active Withdrawn
- 2006-06-21 US US11/993,835 patent/US20100210617A1/en not_active Abandoned
- 2006-06-21 JP JP2008517591A patent/JP2008546753A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| UY29610A1 (es) | 2007-01-31 |
| US20100210617A1 (en) | 2010-08-19 |
| WO2006136830A1 (en) | 2006-12-28 |
| EP1904451A1 (en) | 2008-04-02 |
| AR054485A1 (es) | 2007-06-27 |
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