DE69434294D1 - Proteinkinase c-inhibitoren - Google Patents
Proteinkinase c-inhibitorenInfo
- Publication number
- DE69434294D1 DE69434294D1 DE69434294T DE69434294T DE69434294D1 DE 69434294 D1 DE69434294 D1 DE 69434294D1 DE 69434294 T DE69434294 T DE 69434294T DE 69434294 T DE69434294 T DE 69434294T DE 69434294 D1 DE69434294 D1 DE 69434294D1
- Authority
- DE
- Germany
- Prior art keywords
- beta
- protein kinase
- inhibitors
- isozyme
- present
- 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 - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
- A61P17/06—Antipsoriatics
-
- 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
- A61P25/28—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]
-
- 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
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/26—Acyclic or carbocyclic radicals, substituted by hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Hospice & Palliative Care (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Psychiatry (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17374193A | 1993-12-23 | 1993-12-23 | |
US173741 | 1993-12-23 | ||
US08/324,948 US5545636A (en) | 1993-12-23 | 1994-10-18 | Protein kinase C inhibitors |
US324948 | 1994-10-18 | ||
PCT/US1994/014313 WO1995017182A1 (en) | 1993-12-23 | 1994-12-14 | Protein kinase c inhibitors |
Publications (2)
Publication Number | Publication Date |
---|---|
DE69434294D1 true DE69434294D1 (de) | 2005-04-14 |
DE69434294T2 DE69434294T2 (de) | 2005-12-29 |
Family
ID=26869484
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE69434294T Expired - Lifetime DE69434294T2 (de) | 1993-12-23 | 1994-12-14 | Proteinkinase c-inhibitoren |
Country Status (13)
Country | Link |
---|---|
US (3) | US5668152A (de) |
EP (2) | EP0817627B1 (de) |
JP (4) | JP3998261B2 (de) |
AT (2) | ATE456367T1 (de) |
AU (1) | AU1339895A (de) |
CA (1) | CA2179650C (de) |
DE (1) | DE69434294T2 (de) |
DK (1) | DK0817627T3 (de) |
ES (1) | ES2236702T3 (de) |
HK (1) | HK1008183A1 (de) |
PT (1) | PT817627E (de) |
SI (1) | SI0817627T1 (de) |
WO (1) | WO1995017182A1 (de) |
Families Citing this family (76)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20000064764A (ko) * | 1996-03-20 | 2000-11-06 | 피터지.스트링거 | 인돌릴말레이미드의제조방법 |
US6232299B1 (en) * | 1996-05-01 | 2001-05-15 | Eli Lilly And Company | Use of protein kinase C inhibitors to enhance the clinical efficacy of oncolytic agents and radiation therapy |
SE9603285D0 (sv) * | 1996-09-10 | 1996-09-10 | Astra Ab | New compounds |
SE9603284D0 (sv) * | 1996-09-10 | 1996-09-10 | Astra Ab | New compounds |
SE9603283D0 (sv) * | 1996-09-10 | 1996-09-10 | Astra Ab | New compounds |
TW472045B (en) | 1996-09-25 | 2002-01-11 | Astra Ab | Protein kinase C inhibitor compounds, method for their preparation, pharmaceutical composition thereof and intermediate used for their preparation |
US5859261A (en) * | 1997-03-20 | 1999-01-12 | Eli Lilly And Company | Synthesis of indolylmaleimides |
AR017200A1 (es) | 1997-12-23 | 2001-08-22 | Astrazeneca Ab | Compuestos inhibidores de la proteina cinasa c, sales farmaceuticamente aceptables de los mismos, formulaciones farmaceuitcas que los comprenden, usode las mismas y proceso para la sintesis de dichos compuestos |
SE9800835D0 (sv) | 1998-03-13 | 1998-03-13 | Astra Ab | New Compounds |
TR200002580T2 (tr) * | 1998-03-17 | 2000-11-21 | F.Hoffmann-La Roche Ag | Hücre çoğalmasının engellenmesinde kullanılan ikameli bisindolimaleimitler |
EP1109785B1 (de) | 1998-05-04 | 2003-01-02 | Zentaris AG | Indolderivate und deren verwendung zur behandlung von malignen und anderen, auf pathologischen zellproliferationen beruhenden erkrankungen |
US6127401A (en) * | 1998-06-05 | 2000-10-03 | Cephalon, Inc. | Bridged indenopyrrolocarbazoles |
US6013646A (en) * | 1998-07-02 | 2000-01-11 | Bayer Corporation | Indolocarbazole derivatives useful for the treatment of neurodegenerative diseases and cancer |
US6841567B1 (en) | 1999-02-12 | 2005-01-11 | Cephalon, Inc. | Cyclic substituted fused pyrrolocarbazoles and isoindolones |
US6492406B1 (en) | 1999-05-21 | 2002-12-10 | Astrazeneca Ab | Pharmaceutically active compounds |
US6284783B1 (en) | 1999-06-09 | 2001-09-04 | The Uab Research Foundation | Use of bisindolylmaleimide compounds to induce Fas-mediated apoptosis |
US6346625B1 (en) | 1999-06-23 | 2002-02-12 | Astrazeneca Ab | Protein kinase inhibitors |
CN1158258C (zh) | 1999-06-24 | 2004-07-21 | 东丽株式会社 | 肾上腺素能α1B受体拮抗药 |
US6399780B1 (en) | 1999-08-20 | 2002-06-04 | Cephalon, Inc. | Isomeric fused pyrrolocarbazoles and isoindolones |
EP1242420A2 (de) * | 1999-12-16 | 2002-09-25 | Eli Lilly And Company | Mittel und verfahren zur behandlung von proliferativen erkrankungen |
US6743785B2 (en) | 1999-12-16 | 2004-06-01 | Eli Lilly And Company | Agents and methods for the treatment of proliferative diseases |
DE60010934T2 (de) * | 1999-12-16 | 2005-05-19 | Eli Lilly And Co., Indianapolis | Medikamente geeignet zur Behandlung von proliferativen Erkrankungen |
ATE366238T1 (de) * | 2000-05-11 | 2007-07-15 | Consejo Superior Investigacion | Heterocyclischen inhibitoren von glycogen synthase kinase gsk-3 |
ES2166328B1 (es) * | 2000-05-11 | 2003-09-16 | Consejo Superior Investigacion | Inhibidores heterociclicos del enzima gsk 3 utiles en el tratamiento de procesos neurodegenerativos e hiperproliferativos |
AU2001271257A1 (en) * | 2000-06-29 | 2002-01-14 | Eli Lilly And Company | Use of a protein kinase c inhibitor to enhance the clinical efficacy of anti-neoplastic chemotherapeutic agents and radiation therapy |
AU2001271261A1 (en) * | 2000-06-29 | 2002-01-14 | Eli Lilly And Company | Therapeutic treatment of cancer with a protein kinase c inhibitor |
PT1362047E (pt) | 2000-12-08 | 2006-09-29 | Ortho Mcneil Pharm Inc | Compostos de pirrolina substituidos com indazolilo como inibidores de cinase |
WO2003103663A2 (en) | 2002-06-05 | 2003-12-18 | Janssen Pharmaceutica N.V. | Substituted pyrrolines as kinase inhibitors |
KR20050008787A (ko) * | 2002-06-05 | 2005-01-21 | 얀센 파마슈티카 엔.브이. | 키나제 저해제로서의 비스인돌릴-말레이미드 유도체 |
CA2393720C (en) * | 2002-07-12 | 2010-09-14 | Eli Lilly And Company | Crystalline 2,5-dione-3-(1-methyl-1h-indol-3-yl)-4-[1-(pyridin-2-ylmethyl)piperidin-4-yl]-1h-indol-3-yl]-1h-pyrrole mono-hydrochloride |
DE10244453A1 (de) | 2002-09-24 | 2004-04-01 | Phenomiques Gmbh | Hemmung der Proteinkinase C-alpha zur Behandlung von Krankheiten |
ATE400268T1 (de) * | 2003-10-24 | 2008-07-15 | Lilly Co Eli | Bisindolylmaleimid zur behandlung von prostatakrebs und akt-vermittelten erkrankungen |
GB0513881D0 (en) | 2005-07-06 | 2005-08-10 | Btg Int Ltd | Core 2 GLCNAC-T Inhibitors III |
GB0329667D0 (en) | 2003-12-22 | 2004-01-28 | King S College London | Core 2 GlcNAc-T inhibitor |
US20080182801A1 (en) | 2003-12-22 | 2008-07-31 | Btg International Limited | Core 2 glcnac-t inhibitors |
WO2006002422A2 (en) | 2004-06-24 | 2006-01-05 | Novartis Vaccines And Diagnostics Inc. | Compounds for immunopotentiation |
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KR20080023732A (ko) * | 2005-07-11 | 2008-03-14 | 노파르티스 아게 | 인돌릴말레이미드 유도체 |
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JP5425060B2 (ja) | 2007-06-22 | 2014-02-26 | アークル インコーポレイテッド | ピロリジノン、ピロリジン−2,5−ジオン、ピロリジンおよびチオスクシンイミド誘導体、癌の治療のための組成物および方法 |
PE20091523A1 (es) | 2007-12-20 | 2009-10-29 | Novartis Ag | Derivados de tiazol como inhibidores de la enzima fosfatidilinositol 3-cinasa (pi3k) |
WO2010019225A1 (en) * | 2008-08-15 | 2010-02-18 | Robert Shorr | Pharmaceutical composition |
CN102245184A (zh) | 2008-12-15 | 2011-11-16 | 伊莱利利公司 | 用于治疗癌症的恩扎妥林 |
US8293753B2 (en) | 2009-07-02 | 2012-10-23 | Novartis Ag | Substituted 2-carboxamide cycloamino ureas |
EP2552428A1 (de) | 2010-03-30 | 2013-02-06 | Novartis AG | Pkc-hemmer zur behandlung von b-zell-lymphom mit chronischer aktiver b-zell-rezeptorsignalisierung |
AR082418A1 (es) | 2010-08-02 | 2012-12-05 | Novartis Ag | Formas cristalinas de 1-(4-metil-5-[2-(2,2,2-trifluoro-1,1-dimetil-etil)-piridin-4-il]-tiazol-2-il)-amida de 2-amida del acido (s)-pirrolidin-1,2-dicarboxilico |
PT2670753T (pt) | 2011-01-31 | 2017-01-10 | Novartis Ag | Novos derivados heterocíclicos |
EP2567959B1 (de) | 2011-09-12 | 2014-04-16 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridin-4-carbonsäureamid-derivate als kinaseinhibitoren |
WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
US8846712B2 (en) | 2011-09-12 | 2014-09-30 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
EP2760862B1 (de) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridin-4-carbonsäureamidderivate als kinaseinhibitoren |
CN104039790B (zh) | 2011-10-28 | 2016-04-13 | 诺华股份有限公司 | 嘌呤衍生物及它们在治疗疾病中的应用 |
HUE029402T2 (en) | 2012-03-16 | 2017-02-28 | Vitae Pharmaceuticals Inc | Liver X receptor modulators |
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WO2013167403A1 (en) | 2012-05-09 | 2013-11-14 | Sanofi | Substituted 6-(4-hydroxy-phenyl)-1h-pyrazolo[3,4-b]pyridine derivatives as kinase inhibitors |
EP2849756A1 (de) | 2012-05-16 | 2015-03-25 | Novartis AG | Dosierungsplan für einen pi-3-kinaseinhibitor |
EP2925366B1 (de) | 2012-11-29 | 2018-02-21 | Novartis AG | Pharmazeutische kombinationen |
WO2014174478A1 (en) | 2013-04-26 | 2014-10-30 | Novartis Ag | Pharmaceutical combinations of a pkc inhibitor and a c-met receptor tyrosine kinase inhibitor |
EP3076969B1 (de) | 2013-12-06 | 2021-09-01 | Novartis AG | Dosierungsschema für einen alpha-isoform-selektiven phosphatidylinositol-3-kinase-hemmer |
US20170216286A1 (en) | 2014-01-28 | 2017-08-03 | Mayo Foundation For Medical Education And Research | Killing senescent cells and treating senescence-associated conditions using a src inhibitor and a flavonoid |
JO3589B1 (ar) | 2014-08-06 | 2020-07-05 | Novartis Ag | مثبطات كيناز البروتين c وطرق استخداماتها |
CN104398508B (zh) * | 2014-11-28 | 2017-06-13 | 上海交通大学 | 双吲哚马来酰亚胺衍生物在制备治疗慢性粒细胞白血病药物中的应用 |
KR20180073674A (ko) | 2015-11-02 | 2018-07-02 | 노파르티스 아게 | 포스파티딜이노시톨 3-키나제 억제제에 대한 투여 요법 |
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EP4455145A2 (de) * | 2015-12-02 | 2024-10-30 | Astraea Therapeutics, LLC | Piperidinyl-nociceptin-rezeptorverbindungen |
CN106083830B (zh) * | 2016-06-01 | 2019-07-12 | 中国海洋大学 | 双吲哚马来酰亚胺衍生物及其制备方法和用途 |
CN106146475B (zh) * | 2016-06-01 | 2019-05-17 | 中国海洋大学 | 双吲哚马来酰亚胺衍生物及其制备方法和用途 |
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WO2018060833A1 (en) | 2016-09-27 | 2018-04-05 | Novartis Ag | Dosage regimen for alpha-isoform selective phosphatidylinositol 3-kinase inhibitor alpelisib |
WO2019000224A1 (zh) * | 2017-06-27 | 2019-01-03 | 中国海洋大学 | 双吲哚马来酰亚胺衍生物及其制备方法和用途 |
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SK278989B6 (sk) * | 1988-02-10 | 1998-05-06 | F. Hoffmann-La Roche Ag | Substituované pyroly, ich použitie na výrobu lieči |
MC2096A1 (fr) | 1989-02-23 | 1991-02-15 | Hoffmann La Roche | Pyrroles substitues |
CA2015996C (en) | 1989-05-05 | 2001-08-28 | Hartmut Osswald | Bis-(1h-indol-3-yl)-maleinimide derivatives and their use as pharmaceuticals |
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DE3942991A1 (de) * | 1989-12-27 | 1991-07-04 | Goedecke Ag | Maleinimid-derivate und deren verwendung als arzneimittel |
DE3914764A1 (de) * | 1989-05-05 | 1990-11-08 | Goedecke Ag | Maleinimid-derivate und deren verwendung als arzneimittel |
DE3942296A1 (de) * | 1989-12-21 | 1991-06-27 | Goedecke Ag | Indolocarbazol-derivate, verfahren zu deren herstellung und deren verwendung |
DE4005970A1 (de) * | 1990-02-26 | 1991-08-29 | Boehringer Mannheim Gmbh | Neue trisubstituierte maleinimide, verfahren zu ihrer herstellung sowie arzneimittel, die diese verbindungen enthalten |
DE4005969A1 (de) * | 1990-02-26 | 1991-08-29 | Boehringer Mannheim Gmbh | Neue trisubstituierte pyrrole, verfahren zu ihrer herstellung sowie arzneimittel, die diese verbindungen enthalten |
CA2046801C (en) * | 1990-08-07 | 2002-02-26 | Peter D. Davis | Substituted pyrroles |
US5292747A (en) * | 1990-08-07 | 1994-03-08 | Hoffman-La Roche Inc. | Substituted pyrroles |
EP0580609A1 (de) * | 1991-03-22 | 1994-02-02 | Xenova Limited | Pharmazeutische xanthonderivate |
GB9123396D0 (en) * | 1991-11-04 | 1991-12-18 | Hoffmann La Roche | A process for the manufacture of substituted maleimides |
AU3761393A (en) * | 1992-03-20 | 1993-10-21 | Wellcome Foundation Limited, The | Indole derivatives with antiviral activity |
US5461146A (en) * | 1992-07-24 | 1995-10-24 | Cephalon, Inc. | Selected protein kinase inhibitors for the treatment of neurological disorders |
DE4243321A1 (de) * | 1992-12-21 | 1994-06-23 | Goedecke Ag | Aminosäurederivate von Heterocyclen als PKC-Inhibitoren |
AU678435B2 (en) * | 1993-05-10 | 1997-05-29 | F. Hoffmann-La Roche Ag | Substituted pyrroles |
US5481003A (en) * | 1994-06-22 | 1996-01-02 | Eli Lilly And Company | Protein kinase C inhibitors |
-
1994
- 1994-12-14 AT AT04102054T patent/ATE456367T1/de not_active IP Right Cessation
- 1994-12-14 PT PT95904892T patent/PT817627E/pt unknown
- 1994-12-14 EP EP95904892A patent/EP0817627B1/de not_active Expired - Lifetime
- 1994-12-14 SI SI9430475T patent/SI0817627T1/xx unknown
- 1994-12-14 AT AT95904892T patent/ATE290378T1/de active
- 1994-12-14 JP JP51747995A patent/JP3998261B2/ja not_active Expired - Lifetime
- 1994-12-14 AU AU13398/95A patent/AU1339895A/en not_active Abandoned
- 1994-12-14 ES ES95904892T patent/ES2236702T3/es not_active Expired - Lifetime
- 1994-12-14 WO PCT/US1994/014313 patent/WO1995017182A1/en active IP Right Grant
- 1994-12-14 DK DK95904892T patent/DK0817627T3/da active
- 1994-12-14 EP EP04102054A patent/EP1449529B1/de not_active Expired - Lifetime
- 1994-12-14 CA CA002179650A patent/CA2179650C/en not_active Expired - Lifetime
- 1994-12-14 DE DE69434294T patent/DE69434294T2/de not_active Expired - Lifetime
-
1995
- 1995-05-25 US US08/452,617 patent/US5668152A/en not_active Expired - Lifetime
- 1995-05-25 US US08/450,320 patent/US5661173A/en not_active Expired - Lifetime
- 1995-05-25 US US08/452,606 patent/US5672618A/en not_active Expired - Lifetime
-
1998
- 1998-07-14 HK HK98109161A patent/HK1008183A1/xx not_active IP Right Cessation
-
2005
- 2005-05-09 JP JP2005135900A patent/JP4369397B2/ja not_active Expired - Lifetime
- 2005-05-09 JP JP2005135896A patent/JP4365803B2/ja not_active Expired - Lifetime
-
2006
- 2006-07-20 JP JP2006198260A patent/JP4490400B2/ja not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US5661173A (en) | 1997-08-26 |
WO1995017182A1 (en) | 1995-06-29 |
ATE456367T1 (de) | 2010-02-15 |
ES2236702T3 (es) | 2005-07-16 |
EP1449529A1 (de) | 2004-08-25 |
JPH09507066A (ja) | 1997-07-15 |
EP0817627A1 (de) | 1998-01-14 |
DE69434294T2 (de) | 2005-12-29 |
US5672618A (en) | 1997-09-30 |
JP4490400B2 (ja) | 2010-06-23 |
PT817627E (pt) | 2005-07-29 |
SI0817627T1 (de) | 2005-08-31 |
EP0817627A4 (de) | 2002-07-17 |
JP4365803B2 (ja) | 2009-11-18 |
CA2179650A1 (en) | 1995-06-29 |
AU1339895A (en) | 1995-07-10 |
DK0817627T3 (da) | 2005-06-06 |
ATE290378T1 (de) | 2005-03-15 |
JP3998261B2 (ja) | 2007-10-24 |
EP1449529B1 (de) | 2010-01-27 |
JP2005225895A (ja) | 2005-08-25 |
JP4369397B2 (ja) | 2009-11-18 |
HK1008183A1 (en) | 1999-05-07 |
EP0817627B1 (de) | 2005-03-09 |
US5668152A (en) | 1997-09-16 |
JP2005225896A (ja) | 2005-08-25 |
JP2006316068A (ja) | 2006-11-24 |
CA2179650C (en) | 2007-10-30 |
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