NO20005224L - BTK inhibitorer og fremgangsmåter for deres identifikasjon og anvendelse - Google Patents
BTK inhibitorer og fremgangsmåter for deres identifikasjon og anvendelseInfo
- Publication number
- NO20005224L NO20005224L NO20005224A NO20005224A NO20005224L NO 20005224 L NO20005224 L NO 20005224L NO 20005224 A NO20005224 A NO 20005224A NO 20005224 A NO20005224 A NO 20005224A NO 20005224 L NO20005224 L NO 20005224L
- Authority
- NO
- Norway
- Prior art keywords
- identification
- methods
- btk inhibitors
- inhibitors
- btk
- Prior art date
Links
- 229940124291 BTK inhibitor Drugs 0.000 title abstract 3
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/06—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2
- C07D311/08—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring
- C07D311/18—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring substituted otherwise than in position 3 or 7
-
- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/23—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and carboxyl groups, other than cyano groups, bound to the same unsaturated acyclic carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/26—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C317/32—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C317/34—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having sulfone or sulfoxide groups and amino groups bound to carbon atoms of six-membered aromatic rings being part of the same non-condensed ring or of a condensed ring system containing that ring
- C07C317/38—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having sulfone or sulfoxide groups and amino groups bound to carbon atoms of six-membered aromatic rings being part of the same non-condensed ring or of a condensed ring system containing that ring with the nitrogen atom of at least one amino group being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfones
- C07C317/40—Y being a hydrogen or a carbon atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Oncology (AREA)
- Transplantation (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyrane Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US8209498P | 1998-04-17 | 1998-04-17 | |
US09/273,191 US6303652B1 (en) | 1998-08-21 | 1999-03-19 | BTK inhibitors and methods for their identification and use |
PCT/US1999/008556 WO1999054286A2 (en) | 1998-04-17 | 1999-04-19 | Btk inhibitors and methods for their identification and use |
Publications (2)
Publication Number | Publication Date |
---|---|
NO20005224D0 NO20005224D0 (no) | 2000-10-17 |
NO20005224L true NO20005224L (no) | 2000-12-18 |
Family
ID=26767041
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20005224A NO20005224L (no) | 1998-04-17 | 2000-10-17 | BTK inhibitorer og fremgangsmåter for deres identifikasjon og anvendelse |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP1071658B1 (de) |
JP (1) | JP2002512216A (de) |
KR (1) | KR20010042804A (de) |
AT (1) | ATE269295T1 (de) |
AU (1) | AU3653099A (de) |
CA (1) | CA2328962A1 (de) |
DE (1) | DE69918089T2 (de) |
ES (1) | ES2222705T3 (de) |
HU (1) | HUP0102661A2 (de) |
IL (1) | IL139080A0 (de) |
MX (1) | MXPA00010150A (de) |
NO (1) | NO20005224L (de) |
WO (1) | WO1999054286A2 (de) |
Families Citing this family (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6303652B1 (en) | 1998-08-21 | 2001-10-16 | Hughes Institute | BTK inhibitors and methods for their identification and use |
WO2002034251A1 (en) * | 2000-10-20 | 2002-05-02 | Parker Hughes Institute | Treatment of asthma with lfm analogues |
US6306897B1 (en) | 1999-03-19 | 2001-10-23 | Parker Hughes Institute | Calanolides for inhibiting BTK |
DE60008574T2 (de) | 1999-11-05 | 2009-10-01 | Cytovia, Inc., San Diego | Substituierte 4H-Chromene und Analoga als Caspase-Aktivatoren und Apoptose-Induktoren und deren Verwendung |
WO2001041754A2 (en) * | 1999-11-30 | 2001-06-14 | Parker Hughes Institute | Inhibitors of collagen-induced platelet aggregation |
US6589992B2 (en) | 1999-11-30 | 2003-07-08 | Parker Hughes Institute | Inhibiting collagen-induced platelet aggregation |
GB0005345D0 (en) * | 2000-03-06 | 2000-04-26 | Mathilda & Terence Kennedy Ins | Methods of treating sepsis septic shock and inflammation |
AU2002236692A1 (en) * | 2000-10-23 | 2002-05-21 | Bristol-Myers Squibb Company | Modulators of bruton's tyrosine kinase and bruton's tyrosine kinase, their identification and use |
CA2434020A1 (en) * | 2001-03-07 | 2002-10-03 | Telik, Inc. | Substituted diarylureas as stimulators for fas-mediated apoptosis |
DE10112924A1 (de) * | 2001-03-13 | 2002-10-02 | Erich Eigenbrodt | 1-Butansäurederivate, pharmazeutische Zusammensetzungen enthaltend solche Derivate und Verwendungen solcher Derivate |
EP1377291A2 (de) * | 2001-03-13 | 2004-01-07 | Protagen AG | 1-butansäuderivate wie z.b. carbomethoxypropionylcyanid oder leflunomidderivate und deren therapeutische anwendung |
US7015328B2 (en) | 2001-05-16 | 2006-03-21 | Cytovia, Inc. | Substituted coumarins and quinolines and analogs as activators of caspases and inducers of apoptosis and the use thereof |
EP1392683B1 (de) | 2001-05-16 | 2009-12-02 | Cytovia, Inc. | Substituierte 4h-chromene und analoga als aktivatoren von caspasen und induktoren von apoptose, und deren verwendung als antikrebsmittel |
US6858607B1 (en) | 2001-05-16 | 2005-02-22 | Cytovia, Inc. | 7,8-fused 4H-chromene and analogs as activators of caspases and inducers of apoptosis and the use thereof |
WO2003043565A2 (en) * | 2001-09-24 | 2003-05-30 | University Of Aarhus | Methods for diagnosis and treatment of diseases associated with altered expression of nrf2 |
WO2003096982A2 (en) | 2002-05-16 | 2003-11-27 | Cytovia, Inc. | Substituted 4h-chromenes, 2h-chromenes, chromans and analogs as activators of caspases and inducers of apoptosis and the use thereof |
EP1509515A4 (de) | 2002-05-16 | 2006-07-05 | Cytovia Inc | SUBSTITUIERTE 4-ARYL-4H-PYRROLO ç2,3-H]CHROMENE UND ANALOGA ALS AKTIVATOREN VON CASPASEN UND APOPTOSEINDUKTOREN UND DEREN VERWENDUNG |
WO2004024676A1 (de) * | 2002-09-06 | 2004-03-25 | Schebo®Biotech Ag | Verbindungen zur modulation des glykolyse-enzym-und/oder transaminase-komplexes |
AR045037A1 (es) | 2003-07-10 | 2005-10-12 | Aventis Pharma Sa | Tetrahidro-1h-pirazolo [3,4-c] piridinas sustituidas, composiciones que las contienen y su utilizacion. |
BRPI0518205A (pt) * | 2004-10-19 | 2008-11-04 | Aventis Pharma Inc | uso de (4'-trifluorometilfenil)-amida de ácido (z)-2-ciano-3-hidróxi-but-2-enóico para o tratamento de doença inflamatória do intestino |
JP2010502751A (ja) * | 2006-09-11 | 2010-01-28 | シージーアイ ファーマシューティカルズ,インコーポレイティド | キナーゼ阻害物質、およびキナーゼ阻害物質の使用および同定方法 |
KR101464424B1 (ko) | 2006-09-22 | 2014-11-27 | 파마시클릭스, 인코포레이티드 | 브루톤 티로신 키나제 억제제 |
PL2134374T3 (pl) * | 2007-03-14 | 2014-11-28 | Bionsil S R L In Liquidazione | Inhibitory btk w chemoterapeutycznym leczeniu nowotworów nabłonka |
US8809273B2 (en) | 2007-03-28 | 2014-08-19 | Pharmacyclics, Inc. | Inhibitors of Bruton's tyrosine kinase |
EP2426109B1 (de) * | 2007-10-23 | 2013-12-18 | F. Hoffmann-La Roche AG | Neue Kinaseinhibitoren |
JP5479105B2 (ja) * | 2007-11-05 | 2014-04-23 | 国立大学法人佐賀大学 | 新規ユビキリン結合性小分子 |
US8389757B2 (en) | 2008-06-05 | 2013-03-05 | Alembic Ltd. | Process for preparing teriflunomide |
ES2660418T3 (es) | 2008-07-16 | 2018-03-22 | Pharmacyclics Llc | Inhibidores de la tirosina quinasa de Bruton para el tratamiento de tumores sólidos |
CN107082770B (zh) | 2010-04-05 | 2019-04-23 | 复星弘创(苏州)医药科技有限公司 | IRE-1α抑制剂 |
IL300955A (en) | 2010-06-03 | 2023-04-01 | Pharmacyclics Llc | (R)-1-(3-(4-amino-3-(4-phenoxyphenyl)-H1-pyrazolo[4,3-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1- Indicated for use as a drug to treat chronic lymphocytic leukemia or small lymphocytic lymphoma |
CA2841080A1 (en) | 2011-07-13 | 2013-01-17 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase |
US8377946B1 (en) | 2011-12-30 | 2013-02-19 | Pharmacyclics, Inc. | Pyrazolo[3,4-d]pyrimidine and pyrrolo[2,3-d]pyrimidine compounds as kinase inhibitors |
WO2013148603A1 (en) | 2012-03-27 | 2013-10-03 | Takeda Pharmaceutical Company Limited | Cinnoline derivatives as as btk inhibitors |
CN104736178A (zh) | 2012-06-04 | 2015-06-24 | 药品循环公司 | 布鲁顿酪氨酸激酶抑制剂的晶形 |
JP6575950B2 (ja) | 2012-07-24 | 2019-09-18 | ファーマサイクリックス エルエルシー | Bruton型チロシンキナーゼ(Btk)阻害剤に対する耐性を伴う変異 |
WO2014078578A1 (en) | 2012-11-15 | 2014-05-22 | Pharmacyclics, Inc. | Pyrrolopyrimidine compounds as kinase inhibitors |
US10876096B2 (en) | 2012-11-28 | 2020-12-29 | Corning Incorporated | Cell culture medium for enhanced hepatocyte function |
JO3377B1 (ar) | 2013-03-11 | 2019-03-13 | Takeda Pharmaceuticals Co | مشتقات بيريدينيل وبيريدينيل مندمج |
EP2981264B1 (de) * | 2013-04-02 | 2018-04-25 | F.Hoffmann-La Roche Ag | Brutons tyrosin kinase inhibitoren |
US9421208B2 (en) | 2013-08-02 | 2016-08-23 | Pharmacyclics Llc | Methods for the treatment of solid tumors |
EP2832358A1 (de) * | 2013-08-02 | 2015-02-04 | Bionsil S.r.l. | Pharmazeutisches Kit zur Verwendung bei der Behandlung von Darm- und kolorektalem Krebs |
JP6429292B2 (ja) | 2013-08-12 | 2018-11-28 | ファーマサイクリックス エルエルシー | Her2増幅性癌の処置のための方法 |
KR20160062103A (ko) | 2013-09-30 | 2016-06-01 | 파마싸이클릭스 엘엘씨 | 브루톤 티로신 키나제의 억제제 |
USRE50030E1 (en) | 2013-12-13 | 2024-07-02 | Dana-Farber Cancer Institute, Inc. | Methods to treat lymphoplasmacytic lymphoma |
JP6878004B2 (ja) | 2013-12-13 | 2021-05-26 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | リンパ形質細胞性リンパ腫を処置する方法 |
US9885086B2 (en) | 2014-03-20 | 2018-02-06 | Pharmacyclics Llc | Phospholipase C gamma 2 and resistance associated mutations |
CN105272882B (zh) * | 2014-07-23 | 2019-05-31 | 欣凯医药化工中间体(上海)有限公司 | 一种环保简便制备泰瑞米特的方法 |
CA2959602A1 (en) | 2014-08-01 | 2016-02-04 | Pharmacyclics Llc | Inhibitors of bruton's tyrosine kinase |
EP3193877A4 (de) | 2014-08-07 | 2018-04-04 | Pharmacyclics LLC | Neuartige formen eines bruton-tyrosinkinase-hemmers |
CA2965178C (en) | 2014-10-22 | 2023-09-26 | Dana-Farber Cancer Institute, Inc. | Thiazolyl-containing compounds for treating proliferative diseases |
IL315294A (en) | 2015-03-03 | 2024-10-01 | Pharmacyclics Llc | Pharmaceutical formulations of bruton's tyrosine kinase inhibitor |
AU2017240609B2 (en) | 2016-03-31 | 2021-07-15 | Takeda Pharmaceutical Company Limited | Isoquinolinyl triazolone complexes |
CN110381997A (zh) | 2016-12-12 | 2019-10-25 | 茂体外尔公司 | 用于治疗和预防癌症和感染性疾病的包含病毒基因治疗和免疫检查点抑制剂的方法和组合物 |
WO2020188015A1 (en) | 2019-03-21 | 2020-09-24 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
WO2021089791A1 (en) | 2019-11-08 | 2021-05-14 | INSERM (Institut 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 (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2555685A1 (de) * | 1975-12-11 | 1977-06-23 | Hoechst Ag | Neue cyanessigsaeureanilid-derivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende mittel |
DK0527736T3 (da) * | 1990-05-18 | 1997-10-20 | Hoechst Ag | Isoxazol-4-carboxylsyreamider og hydroxyalkyliden-cyanoacetamider, lægemidler indeholdende disse forbindelser og anvendelsen af disse lægemidler. |
CA2080554A1 (en) * | 1991-10-15 | 1993-04-16 | Mitsubishi Chemical Corporation | Styrene derivatives |
GB9200275D0 (en) * | 1992-01-08 | 1992-02-26 | Roussel Lab Ltd | Chemical compounds |
WO1994014789A1 (en) * | 1992-12-23 | 1994-07-07 | Smithkline Beecham Corporation | Coumarin derivatives as retroviral inhibitors |
GB9322781D0 (en) * | 1993-11-04 | 1993-12-22 | Roussel Lab Ltd | Aromatic amides |
US5700823A (en) * | 1994-01-07 | 1997-12-23 | Sugen, Inc. | Treatment of platelet derived growth factor related disorders such as cancers |
US5489697A (en) * | 1994-08-03 | 1996-02-06 | Medichem Research, Inc. | Method for the preparation of (+)-calanolide A and intermediates thereof |
US5608085A (en) * | 1995-02-27 | 1997-03-04 | The University Of Tennessee Research Corporation | Synthesis of optically active calanolides A and B and enantiomers and related compounds |
AU5259296A (en) * | 1995-04-07 | 1996-10-23 | Warner-Lambert Company | Flavones and coumarins as agents for the treatment of athero sclerosis |
IT1289238B1 (it) * | 1996-12-10 | 1998-09-29 | Bio S S P A Ora Bio S S R L | Composizioni farmaceutiche per il trattamento di infezioni virali comprendenti una 4 arilcumarina |
-
1999
- 1999-04-19 HU HU0102661A patent/HUP0102661A2/hu unknown
- 1999-04-19 AU AU36530/99A patent/AU3653099A/en not_active Abandoned
- 1999-04-19 JP JP2000544627A patent/JP2002512216A/ja active Pending
- 1999-04-19 EP EP99918673A patent/EP1071658B1/de not_active Expired - Lifetime
- 1999-04-19 ES ES99918673T patent/ES2222705T3/es not_active Expired - Lifetime
- 1999-04-19 DE DE69918089T patent/DE69918089T2/de not_active Expired - Fee Related
- 1999-04-19 WO PCT/US1999/008556 patent/WO1999054286A2/en not_active Application Discontinuation
- 1999-04-19 IL IL13908099A patent/IL139080A0/xx unknown
- 1999-04-19 CA CA002328962A patent/CA2328962A1/en not_active Abandoned
- 1999-04-19 AT AT99918673T patent/ATE269295T1/de not_active IP Right Cessation
- 1999-04-19 KR KR1020007011551A patent/KR20010042804A/ko not_active Application Discontinuation
- 1999-04-19 MX MXPA00010150A patent/MXPA00010150A/es unknown
-
2000
- 2000-10-17 NO NO20005224A patent/NO20005224L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
HUP0102661A2 (hu) | 2001-11-28 |
MXPA00010150A (es) | 2002-05-14 |
ATE269295T1 (de) | 2004-07-15 |
WO1999054286A3 (en) | 2000-05-04 |
DE69918089D1 (de) | 2004-07-22 |
NO20005224D0 (no) | 2000-10-17 |
IL139080A0 (en) | 2001-11-25 |
AU3653099A (en) | 1999-11-08 |
EP1071658B1 (de) | 2004-06-16 |
KR20010042804A (ko) | 2001-05-25 |
ES2222705T3 (es) | 2005-02-01 |
EP1071658A2 (de) | 2001-01-31 |
JP2002512216A (ja) | 2002-04-23 |
CA2328962A1 (en) | 1999-10-28 |
DE69918089T2 (de) | 2005-07-14 |
WO1999054286A2 (en) | 1999-10-28 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC2A | Withdrawal, rejection or dismissal of laid open patent application |