ATE269295T1 - Btk inhibitoren und verfahren zur identifizierung und verwendung - Google Patents
Btk inhibitoren und verfahren zur identifizierung und verwendungInfo
- Publication number
- ATE269295T1 ATE269295T1 AT99918673T AT99918673T ATE269295T1 AT E269295 T1 ATE269295 T1 AT E269295T1 AT 99918673 T AT99918673 T AT 99918673T AT 99918673 T AT99918673 T AT 99918673T AT E269295 T1 ATE269295 T1 AT E269295T1
- Authority
- AT
- Austria
- 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
- 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
- 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
- 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)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Pulmonology (AREA)
- Hematology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrane 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 (1)
| Publication Number | Publication Date |
|---|---|
| ATE269295T1 true ATE269295T1 (de) | 2004-07-15 |
Family
ID=26767041
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT99918673T ATE269295T1 (de) | 1998-04-17 | 1999-04-19 | Btk inhibitoren und verfahren zur identifizierung und verwendung |
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 |
| US6306897B1 (en) | 1999-03-19 | 2001-10-23 | Parker Hughes Institute | Calanolides for inhibiting BTK |
| SI1230232T1 (en) | 1999-11-05 | 2004-08-31 | Cytovia, Inc. | Substituted 4h-chromene and analogs as activators of caspases and inducers of apoptosis and the use thereof |
| CA2390857A1 (en) * | 1999-11-30 | 2001-06-14 | Fatih M. Uckun | 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 |
| AU2001236361A1 (en) * | 2000-10-20 | 2002-05-06 | Parker Hughes Institute | Treatment of asthma with lfm analogues |
| CA2426508A1 (en) * | 2000-10-23 | 2002-05-16 | Bristol-Myers Squibb Company | Modulators of bruton's tyrosine kinase and bruton's tyrosine kinase intermediates and methods for their identification and use in the treatment and prevention of osteoporosis and related disease states |
| JP2004528311A (ja) * | 2001-03-07 | 2004-09-16 | テリック,インコーポレイテッド | Fas媒介アポトーシスの刺激剤としての置換ジアリールウレア |
| DE10112924A1 (de) * | 2001-03-13 | 2002-10-02 | Erich Eigenbrodt | 1-Butansäurederivate, pharmazeutische Zusammensetzungen enthaltend solche Derivate und Verwendungen solcher Derivate |
| WO2002072527A2 (de) * | 2001-03-13 | 2002-09-19 | Protagen Aktiengesellschaft | 1-butansäurederivate wie z.b. carbomethoxypropionylcyanid oder leflunomidderivate und deren therapeutische anwendung |
| 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 |
| EP1392283A4 (de) | 2001-05-16 | 2004-10-20 | Cytovia Inc | Substituierte cumarine und chinoline als caspase-aktivatoren |
| AU2002329000A1 (en) * | 2001-09-24 | 2003-04-07 | University Of Aarhus | Methods for diagnosis and treatment of diseases associated with altered expression of pik3r1 |
| JP2005531566A (ja) | 2002-05-16 | 2005-10-20 | サイトビア インコーポレイティッド | カスパーゼ活性化剤およびアポトーシス誘導物質としての置換4−アリール−4h−ピロロ[2,3−h]クロメンおよび類似体ならびにそれらの使用 |
| EP1513515A2 (de) | 2002-05-16 | 2005-03-16 | Cytovia, Inc. | Substitutierte 4h-chromene, 2h-chromene, chromane und analoga als aktivatoren von caspasen und induktoren von apoptose und ihre verwendung |
| JP2005538165A (ja) * | 2002-09-06 | 2005-12-15 | シェボ ビオテック アクティエン ゲゼルシャフト | 解糖酵素及び/又はアミノ基転移酵素錯体調節用化合物 |
| 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. |
| SG142305A1 (en) * | 2004-10-19 | 2008-05-28 | Aventis Pharma Inc | Use of (z)-2-cyano-3-hydroxy-but-2-enoic acid-(4'- trifluoromethylphenyl)-amide for treating inflammatory bowel disease |
| EP2270200A3 (de) * | 2006-09-11 | 2011-07-13 | CGI Pharmaceuticals, Inc. | Kinasehemmer und Verfahren zur Verwendung und Identifizierung von Kinasehemmern |
| EA018573B1 (ru) | 2006-09-22 | 2013-09-30 | Фармасайкликс, Инк. | Ингибиторы тирозинкиназы брутона |
| US8232085B2 (en) * | 2007-03-14 | 2012-07-31 | Bionsil S.R.L. | Isoform of bruton's tyrosine kinase (BTK) protein |
| US8809273B2 (en) | 2007-03-28 | 2014-08-19 | Pharmacyclics, Inc. | Inhibitors of Bruton's tyrosine kinase |
| EP2205564B1 (de) * | 2007-10-23 | 2014-07-30 | 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 |
| CN105362277A (zh) | 2008-07-16 | 2016-03-02 | 药品循环有限公司 | 用于实体肿瘤的治疗的布鲁顿酪氨酸激酶的抑制剂 |
| US9040714B2 (en) | 2010-04-05 | 2015-05-26 | Mannkind Corporation | IRE-1α inhibitors |
| CA3007787C (en) | 2010-06-03 | 2020-03-10 | Pharmacyclics Llc | The use of inhibitors of bruton's tyrosine kinase (btk) |
| BR112014000653A2 (pt) | 2011-07-13 | 2017-02-14 | Pharmacyclics Inc | inibidores de tirosina quinase de bruton |
| 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 |
| EA201492082A1 (ru) | 2012-06-04 | 2015-03-31 | Фармасайкликс, Инк. | Кристаллические формы ингибитора тирозинкиназы брутона |
| CA2879570A1 (en) | 2012-07-24 | 2014-01-30 | Pharmacyclics, Inc. | Mutations associated with resistance to inhibitors of bruton's tyrosine kinase (btk) |
| MX2015006168A (es) | 2012-11-15 | 2015-08-10 | Pharmacyclics Inc | Compuestos de pirrolopirimidina como inhibidores de quinasas. |
| CN105189737B (zh) * | 2012-11-28 | 2019-02-12 | 康宁股份有限公司 | 用于增强肝细胞功能的细胞培养基 |
| JO3377B1 (ar) | 2013-03-11 | 2019-03-13 | Takeda Pharmaceuticals Co | مشتقات بيريدينيل وبيريدينيل مندمج |
| RU2634723C2 (ru) * | 2013-04-02 | 2017-11-03 | Ф. Хоффманн-Ля Рош Аг | Ингибиторы тирозинкиназы брутона |
| TWI649081B (zh) | 2013-08-02 | 2019-02-01 | 製藥公司 | 治療固態腫瘤之方法 |
| EP2832358A1 (de) * | 2013-08-02 | 2015-02-04 | Bionsil S.r.l. | Pharmazeutisches Kit zur Verwendung bei der Behandlung von Darm- und kolorektalem Krebs |
| ES2709509T3 (es) | 2013-08-12 | 2019-04-16 | Pharmacyclics Llc | Procedimientos para el tratamiento de cáncer amplificado por HER2 |
| KR20160062103A (ko) | 2013-09-30 | 2016-06-01 | 파마싸이클릭스 엘엘씨 | 브루톤 티로신 키나제의 억제제 |
| US9908872B2 (en) | 2013-12-13 | 2018-03-06 | Dana-Farber Cancer Institute, Inc. | Methods to treat lymphoplasmacytic lymphoma |
| JP6879740B2 (ja) | 2013-12-13 | 2021-06-02 | 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 |
| EP3119910A4 (de) | 2014-03-20 | 2018-02-21 | Pharmacyclics LLC | Phospholipase c gamma 2 und resistenzassoziierte mutationen |
| 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 |
| CN106999494A (zh) | 2014-08-01 | 2017-08-01 | 药品循环有限公司 | 布鲁顿酪氨酸激酶的抑制剂 |
| JP2017523206A (ja) | 2014-08-07 | 2017-08-17 | ファーマサイクリックス エルエルシー | ブルトン型チロシンキナーゼ阻害剤の新規製剤 |
| JP6788583B2 (ja) | 2014-10-22 | 2020-11-25 | 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 | 増殖性疾患を処置するためのチアゾリル含有化合物 |
| IL315294A (en) | 2015-03-03 | 2024-10-01 | Pharmacyclics Llc | Pharmaceutical formulations of bruton's tyrosine kinase inhibitor |
| ES2886080T3 (es) | 2016-03-31 | 2021-12-16 | Takeda Pharmaceuticals Co | Complejos de isoquinolinil triazolona |
| JP2020510624A (ja) | 2016-12-12 | 2020-04-09 | マルチビア インコーポレイテッド | がんおよび感染性疾患の治療および予防のための、ウイルス遺伝子治療および免疫チェックポイント阻害剤を含む方法および組成物 |
| BR112021018168B1 (pt) | 2019-03-21 | 2023-11-28 | Onxeo | Composição farmacêutica, combinação e kit compreendendo uma molécula dbait e um inibidor de quinase para o tratamento de câncer |
| CA3159348A1 (en) | 2019-11-08 | 2021-05-14 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | 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 |
| WO1991017748A1 (de) * | 1990-05-18 | 1991-11-28 | Hoechst Aktiengesellschaft | Isoxazol-4-carbonsäureamide und hydroxyalkyliden-cyanessigsäureamide, diese verbindungen enthaltende arzneimittel und deren verwendung |
| 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 |
| WO1996031206A2 (en) * | 1995-04-07 | 1996-10-10 | Warner-Lambert Company | Flavones and coumarins as agents for the treatment of atherosclerosis |
| 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 CA CA002328962A patent/CA2328962A1/en not_active Abandoned
- 1999-04-19 AU AU36530/99A patent/AU3653099A/en not_active Abandoned
- 1999-04-19 EP EP99918673A patent/EP1071658B1/de not_active Expired - Lifetime
- 1999-04-19 WO PCT/US1999/008556 patent/WO1999054286A2/en not_active Ceased
- 1999-04-19 DE DE69918089T patent/DE69918089T2/de not_active Expired - Fee Related
- 1999-04-19 ES ES99918673T patent/ES2222705T3/es not_active Expired - Lifetime
- 1999-04-19 MX MXPA00010150A patent/MXPA00010150A/es unknown
- 1999-04-19 JP JP2000544627A patent/JP2002512216A/ja active Pending
- 1999-04-19 KR KR1020007011551A patent/KR20010042804A/ko not_active Ceased
- 1999-04-19 AT AT99918673T patent/ATE269295T1/de not_active IP Right Cessation
- 1999-04-19 HU HU0102661A patent/HUP0102661A2/hu unknown
- 1999-04-19 IL IL13908099A patent/IL139080A0/xx unknown
-
2000
- 2000-10-17 NO NO20005224A patent/NO20005224L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| WO1999054286A3 (en) | 2000-05-04 |
| KR20010042804A (ko) | 2001-05-25 |
| NO20005224L (no) | 2000-12-18 |
| HUP0102661A2 (hu) | 2001-11-28 |
| DE69918089D1 (de) | 2004-07-22 |
| DE69918089T2 (de) | 2005-07-14 |
| NO20005224D0 (no) | 2000-10-17 |
| AU3653099A (en) | 1999-11-08 |
| IL139080A0 (en) | 2001-11-25 |
| MXPA00010150A (es) | 2002-05-14 |
| ES2222705T3 (es) | 2005-02-01 |
| CA2328962A1 (en) | 1999-10-28 |
| WO1999054286A2 (en) | 1999-10-28 |
| JP2002512216A (ja) | 2002-04-23 |
| EP1071658A2 (de) | 2001-01-31 |
| EP1071658B1 (de) | 2004-06-16 |
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