NO20060678L - Triazolopyrimidinderivater som glykogensyntase-kinase 3-inhibitorer - Google Patents
Triazolopyrimidinderivater som glykogensyntase-kinase 3-inhibitorerInfo
- Publication number
- NO20060678L NO20060678L NO20060678A NO20060678A NO20060678L NO 20060678 L NO20060678 L NO 20060678L NO 20060678 A NO20060678 A NO 20060678A NO 20060678 A NO20060678 A NO 20060678A NO 20060678 L NO20060678 L NO 20060678L
- Authority
- NO
- Norway
- Prior art keywords
- optionally substituted
- alkyl
- alkyloxy
- polyhaloci
- polyhaloc
- Prior art date
Links
Classifications
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- 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
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- 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
- A61P15/16—Masculine contraceptives
-
- 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
-
- 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
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
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- 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
- A61P25/24—Antidepressants
-
- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- 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
- 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 Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Diabetes (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dermatology (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Psychology (AREA)
- Rheumatology (AREA)
- Oncology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Denne oppfinnelse vedrører en forbindelse med formel etN-oksid, et farmasøytisk akseptabelt addisjonssalt, et kvatemært amin og en stereokjemisk isomer form derav, hvori ring A representerer fenyl, pyridyl, pyrimidinyl, pyridazinyl eller pyrazinyl; R' representerer hydrogen; aryl; formyl; Ci.6alkylkarbonyl; Ci.6alkyl; Ci.6alkyloksykarbonyl; Ci.6alkyl substituert med formyl, Ci.6aUcyULarbonyl, Ci.6aUsyloksykarbonyl, Ci.6aUcylkarbonyloksy; eUer Ci-ealkyloksyCi-ealkylkarbonyl eventuelt substituert med Ci-ealkyloksykarbonyl; X representerer en direktebinding; -(CH2)n3- eller -(CH2)n4-Xia-Xib-; R^ representerer Cs-vcykloalkyl; fenyl; en 4, 5, 6- eller 7- leddet monocyklisk heterocykel inneholdende minst ett heteroatom valgt fra O, S eller N; benzoksazolyl eller et radikal med formel hvori R^ -substituenten eventuelt kan være substituert; R^ representerer halo; hydroksy; eventuelt substituert Ci.6aUcyl; C2.6aUcenyl eUer C2.6alkynyl, hver eventuelt substituert; eventuelt substituert polyhaloCi-eaUcyl; eventuelt substituert Ci-eaUcyloksy; eventuelt substituert polyhaloCi-ealkyloksy; Ci-ealkyltio; polyhaloCi-eaUcyltio; Ci-eaUcyl-oksykarbonyl; Ci-ealkyUcarbonyloksy; Ci-ealkyUcarbonyl; polyhaloCi-eaULyUcarbonyl; cyano; karboksyl; aiyloksy; aiyltio; aiyUcarbonyl; NR^R^^; C(=0)-NR^'^; -NR'-C(=0)-NR'^*; -NR'-C(=0)-R'; -S(=0)bi,-R^ -NR'-S(=0>,i- R**; -S-CN; -NR^-CN; R'^ representerer hydrogen; halo; hydroksy; eventuelt substituert Ci.4aUsyl; C2.4aUcenyl eller C2.4aUcynyl, hver eventuelt substituert; polyhaloCualkyl; eventuelt substituert Ci.4alkyloksy; polyhalo-CuaUsyloksy; Ci.4alkyltio; polyhaloCi.salkyltio; Ci.4alkyloksykarbonyl; Ci.4alkyULarbonyloksy; Ci.4alkyULarbonyl; polyhaloCi.4aUcyl-karbonyl; nitio; cyano; karboksyl; NR'°R"; C(=0)NR'°R"; -NR'-C(=0)-NR'°R"; -NR'-C(-0)-R'; -S(=0)ni-R''; -NR'-S(=0)ni-R''; -S-CN; -NR'-CN; deres anvendelse, farmasøytiske sammensetninger omfattende dem og fremgangsmåter for deres fremstiUing.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP0350310 | 2003-07-16 | ||
PCT/EP2004/051455 WO2005012307A1 (en) | 2003-07-16 | 2004-07-12 | Triazolopyrimidine derivatives as glycogen synthase kinase 3 inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
NO20060678L true NO20060678L (no) | 2006-02-10 |
Family
ID=34112425
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20060678A NO20060678L (no) | 2003-07-16 | 2006-02-10 | Triazolopyrimidinderivater som glykogensyntase-kinase 3-inhibitorer |
Country Status (26)
Country | Link |
---|---|
US (2) | US7560458B2 (no) |
EP (1) | EP1658292B1 (no) |
JP (1) | JP2009514782A (no) |
KR (1) | KR20060120393A (no) |
CN (1) | CN100404536C (no) |
AP (1) | AP2006003486A0 (no) |
AR (1) | AR045698A1 (no) |
AT (1) | ATE370142T1 (no) |
AU (1) | AU2004260738B2 (no) |
BR (1) | BRPI0412596A (no) |
CA (1) | CA2531333A1 (no) |
DE (1) | DE602004008303T2 (no) |
DK (1) | DK1658292T3 (no) |
EA (1) | EA010109B1 (no) |
ES (1) | ES2290754T3 (no) |
IL (1) | IL173139A (no) |
JO (1) | JO2460B1 (no) |
MX (1) | MXPA06000540A (no) |
NO (1) | NO20060678L (no) |
NZ (1) | NZ545058A (no) |
PA (1) | PA8607001A1 (no) |
PL (1) | PL1658292T3 (no) |
PT (1) | PT1658292E (no) |
TW (1) | TW200524935A (no) |
WO (1) | WO2005012307A1 (no) |
ZA (1) | ZA200600385B (no) |
Families Citing this family (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
CN103169708B (zh) | 2002-07-29 | 2018-02-02 | 里格尔药品股份有限公司 | 用2,4‑嘧啶二胺化合物治疗或者预防自体免疫性疾病的方法 |
AU2004260738B2 (en) * | 2003-07-16 | 2009-07-16 | Janssen Pharmaceutica N.V. | Triazolopyrimidine derivatives as glycogen synthase kinase 3 inhibitors |
RS53109B (en) | 2003-07-30 | 2014-06-30 | Rigel Pharmaceuticals Inc. | 2,4 PIRIMIDINDIAMINE COMPOUNDS FOR USE IN TREATMENT OR PREVENTION OF AUTOIMMUNE DISEASES |
DK1660458T3 (da) * | 2003-08-15 | 2012-05-07 | Irm Llc | 2, 4-pyrimidindiaminer egnede i behandling af neoplastiske sygdomme, in-flammatoriske lidelser og lidelser i immunsystemet. |
WO2005028434A2 (en) * | 2003-09-18 | 2005-03-31 | Conforma Therapeutics Corporation | Novel heterocyclic compounds as hsp90-inhibitors |
CA2580857A1 (en) | 2004-09-20 | 2006-09-28 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
JP5094398B2 (ja) | 2004-09-20 | 2012-12-12 | ゼノン・ファーマシューティカルズ・インコーポレイテッド | 複素環式誘導体およびステアロイル−CoAデサチュラーゼのメディエータとしてのそれらの使用 |
WO2006034440A2 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
WO2006034341A2 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives for inhibiting human stearoyl-coa-desaturase |
TW200626138A (en) | 2004-09-20 | 2006-08-01 | Xenon Pharmaceuticals Inc | Heterocyclic derivatives and their use as therapeutic agents |
WO2006034441A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
MX2007003318A (es) | 2004-09-20 | 2007-05-18 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como agentes terapeuticos. |
EP1812439B2 (en) | 2004-10-15 | 2017-12-06 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
CA2577588C (en) | 2004-10-29 | 2013-09-10 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting bicyclic pyrimidine derivatives |
US7563781B2 (en) | 2005-01-14 | 2009-07-21 | Janssen Pharmaceutica Nv | Triazolopyrimidine derivatives |
AU2006343359A1 (en) | 2005-06-03 | 2007-11-15 | Xenon Pharmaceuticals Inc. | Aminothiazole derivatives as human stearoyl-coa desaturase inhibitors |
US20070203161A1 (en) * | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
NZ563454A (en) * | 2005-06-08 | 2011-03-31 | Rigel Pharmaceuticals Inc | 2,4-diaminopyrimidine derivatives for inhibition of the JAK pathway |
EP2275095A3 (en) | 2005-08-26 | 2011-08-17 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
EP2258358A3 (en) | 2005-08-26 | 2011-09-07 | Braincells, Inc. | Neurogenesis with acetylcholinesterase inhibitor |
US8119655B2 (en) * | 2005-10-07 | 2012-02-21 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
JP2009512711A (ja) | 2005-10-21 | 2009-03-26 | ブレインセルス,インコーポレイティド | Pde阻害による神経新生の調節 |
CA2625210A1 (en) | 2005-10-31 | 2007-05-10 | Braincells, Inc. | Gaba receptor mediated modulation of neurogenesis |
EP1991532B1 (en) | 2006-02-24 | 2017-01-11 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
AU2007249399A1 (en) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
US20100120717A1 (en) | 2006-10-09 | 2010-05-13 | Brown Jason W | Kinase inhibitors |
JP2010532381A (ja) * | 2007-06-29 | 2010-10-07 | サネシス ファーマシューティカルズ, インコーポレイテッド | Rafキナーゼ阻害剤として有用な複素環式化合物 |
CL2008001933A1 (es) * | 2007-06-29 | 2009-09-25 | Millennium Pharm Inc | Compuestos derivados de pirimidina, inhibidores de la raf quinasa; compuestos intermediarios; procedimiento de preparacion; composicion farmaceutica; y su uso para tratar trastornos proliferativos, cardiacos, neurodegenerativos, inflamatorios, oseos, inmunologicos enfermedad viral, entre otros. |
WO2010099217A1 (en) | 2009-02-25 | 2010-09-02 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
AU2011254550B2 (en) | 2010-05-21 | 2013-11-07 | Noviga Research Ab | Novel pyrimidine derivatives |
EP2688883B1 (en) | 2011-03-24 | 2016-05-18 | Noviga Research AB | Pyrimidine derivatives |
ES2655264T3 (es) | 2012-01-28 | 2018-02-19 | Merck Patent Gmbh | Derivados de triazolo[4,5-d]pirimidina |
AU2013230286B2 (en) | 2012-03-07 | 2016-12-22 | Merck Patent Gmbh | Triazolopyrazine derivatives |
ES2636936T3 (es) * | 2013-03-05 | 2017-10-10 | Merck Patent Gmbh | Derivados de triazolo[4,5-d]pirimidina para el tratamiento de enfermedades tales como cáncer |
ES2614872T3 (es) | 2013-03-05 | 2017-06-02 | Merck Patent Gmbh | Derivados de 9-(aril o heteroaril)-2-(pirazolilo, pirrolidinilo o ciclopentilo) aminopurina como agentes anticancer |
CA2911259A1 (en) | 2013-05-06 | 2014-11-13 | Merck Patent Gmbh | Macrocycles as kinase inhibitors |
US10414768B2 (en) * | 2014-12-05 | 2019-09-17 | Centre National De La Recherche Scientifique (Cnrs) | Compounds for treating cystic fibrosis |
WO2017035528A1 (en) | 2015-08-27 | 2017-03-02 | Nantneuro, Llc | Triazolopyridines and triazolopyrimidines that lower stress-induced p-tau |
WO2017156527A1 (en) * | 2016-03-11 | 2017-09-14 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Aurora kinase and janus kinase inhibitors for prevention of graft versus host disease |
US20220133740A1 (en) | 2019-02-08 | 2022-05-05 | Frequency Therapeutics, Inc. | Valproic acid compounds and wnt agonists for treating ear disorders |
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JPS5962594A (ja) * | 1982-09-30 | 1984-04-10 | Ss Pharmaceut Co Ltd | 3,5―ジ置換―トリアゾロピリミジン誘導体 |
US20020040031A1 (en) * | 2000-07-07 | 2002-04-04 | Glasky Michelle S. | Methods for prevention of accumulation of amyloid beta peptide in the central nervous system |
US6737085B2 (en) * | 2000-11-01 | 2004-05-18 | Tokiwa Phytochemical Co., Ltd. | Apocynum venetum extract for use as antidepressant |
US7105532B2 (en) * | 2000-12-19 | 2006-09-12 | Smithkline Beecham Corporation | Pyrazolo[3,4-c]pyridines as gsk-3 inhibitors |
AU2004260738B2 (en) * | 2003-07-16 | 2009-07-16 | Janssen Pharmaceutica N.V. | Triazolopyrimidine derivatives as glycogen synthase kinase 3 inhibitors |
-
2004
- 2004-07-12 AU AU2004260738A patent/AU2004260738B2/en not_active Ceased
- 2004-07-12 AT AT04766189T patent/ATE370142T1/de active
- 2004-07-12 DE DE602004008303T patent/DE602004008303T2/de not_active Expired - Lifetime
- 2004-07-12 PT PT04766189T patent/PT1658292E/pt unknown
- 2004-07-12 KR KR1020057024541A patent/KR20060120393A/ko not_active Application Discontinuation
- 2004-07-12 AP AP2006003486A patent/AP2006003486A0/xx unknown
- 2004-07-12 CA CA002531333A patent/CA2531333A1/en not_active Abandoned
- 2004-07-12 JO JO200496A patent/JO2460B1/en active
- 2004-07-12 MX MXPA06000540A patent/MXPA06000540A/es active IP Right Grant
- 2004-07-12 US US10/564,844 patent/US7560458B2/en not_active Expired - Fee Related
- 2004-07-12 EA EA200600258A patent/EA010109B1/ru not_active IP Right Cessation
- 2004-07-12 JP JP2006519926A patent/JP2009514782A/ja not_active Withdrawn
- 2004-07-12 BR BRPI0412596-7A patent/BRPI0412596A/pt not_active IP Right Cessation
- 2004-07-12 PL PL04766189T patent/PL1658292T3/pl unknown
- 2004-07-12 CN CNB2004800201486A patent/CN100404536C/zh not_active Expired - Fee Related
- 2004-07-12 ES ES04766189T patent/ES2290754T3/es not_active Expired - Lifetime
- 2004-07-12 EP EP04766189A patent/EP1658292B1/en not_active Expired - Lifetime
- 2004-07-12 DK DK04766189T patent/DK1658292T3/da active
- 2004-07-12 WO PCT/EP2004/051455 patent/WO2005012307A1/en active IP Right Grant
- 2004-07-12 NZ NZ545058A patent/NZ545058A/en unknown
- 2004-07-15 PA PA20048607001A patent/PA8607001A1/es unknown
- 2004-07-15 TW TW093121066A patent/TW200524935A/zh unknown
- 2004-07-15 AR ARP040102496A patent/AR045698A1/es not_active Application Discontinuation
-
2006
- 2006-01-12 IL IL173139A patent/IL173139A/en not_active IP Right Cessation
- 2006-01-13 ZA ZA200600385A patent/ZA200600385B/en unknown
- 2006-02-10 NO NO20060678A patent/NO20060678L/no not_active Application Discontinuation
-
2008
- 2008-09-16 US US12/211,361 patent/US20090036471A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
ES2290754T3 (es) | 2008-02-16 |
US7560458B2 (en) | 2009-07-14 |
EA010109B1 (ru) | 2008-06-30 |
EP1658292A1 (en) | 2006-05-24 |
AU2004260738B2 (en) | 2009-07-16 |
AR045698A1 (es) | 2005-11-09 |
CN100404536C (zh) | 2008-07-23 |
TW200524935A (en) | 2005-08-01 |
AU2004260738A1 (en) | 2005-02-10 |
ATE370142T1 (de) | 2007-09-15 |
IL173139A0 (en) | 2006-06-11 |
BRPI0412596A (pt) | 2006-09-19 |
EA200600258A1 (ru) | 2006-06-30 |
US20060205721A1 (en) | 2006-09-14 |
PT1658292E (pt) | 2007-10-25 |
DE602004008303T2 (de) | 2008-05-08 |
US20090036471A1 (en) | 2009-02-05 |
NZ545058A (en) | 2008-05-30 |
WO2005012307A1 (en) | 2005-02-10 |
ZA200600385B (en) | 2007-05-30 |
CA2531333A1 (en) | 2005-02-10 |
MXPA06000540A (es) | 2006-03-30 |
EP1658292B1 (en) | 2007-08-15 |
DE602004008303D1 (de) | 2007-09-27 |
PA8607001A1 (es) | 2005-05-10 |
CN1823068A (zh) | 2006-08-23 |
AP2006003486A0 (en) | 2006-02-28 |
KR20060120393A (ko) | 2006-11-27 |
JP2009514782A (ja) | 2009-04-09 |
PL1658292T3 (pl) | 2008-01-31 |
IL173139A (en) | 2010-04-29 |
JO2460B1 (en) | 2009-01-20 |
DK1658292T3 (da) | 2007-11-12 |
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