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
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)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (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 |
JP2003513967A (ja) | 1999-11-05 | 2003-04-15 | サイトビア インコーポレイテッド | カスパーゼのアクチベーターおよびアポトーシスのインデューサーとしての置換4hクロメンおよびアナログ、ならびにその使用 |
AU4508601A (en) * | 1999-11-30 | 2001-06-18 | 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 |
AU2001236361A1 (en) * | 2000-10-20 | 2002-05-06 | Parker Hughes Institute | Treatment of asthma with lfm analogues |
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 |
AU2002306618B2 (en) * | 2001-03-07 | 2006-11-09 | 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 |
JP4382354B2 (ja) * | 2001-03-13 | 2009-12-09 | ヴァルブルク・グリコムド・ゲーエムベーハー | 1−ブタン酸誘導体およびその使用 |
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 |
WO2002092594A1 (en) | 2001-05-16 | 2002-11-21 | Cytovia, Inc. | Substituted 4h-chromenes 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 |
WO2003027276A2 (en) * | 2001-09-24 | 2003-04-03 | University Of Aarhus | Novel compositions and methods for diagnosis and treatment of lymphoma and leukemia |
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 |
CN100349887C (zh) | 2002-05-16 | 2007-11-21 | 西托维亚公司 | 取代的4-芳基-4h-吡咯并[2,3-h]色烯和类似物及其药物组合物和用途 |
AU2003258454A1 (en) | 2002-09-06 | 2004-04-30 | Schebo®Biotech Ag | Compounds for modulating the glycolosis enzyme complex and/or transaminase complex |
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. |
EP1804782A1 (de) * | 2004-10-19 | 2007-07-11 | Aventis Pharmaceuticals Inc. | Verwendung von (z)-2-cyano-3-hydroxy-but-2-ensäure-(4'-trifluoromethylphenyl)-amid zur behandlung entzündlicher darmerkrankungen |
EP2270200A3 (de) * | 2006-09-11 | 2011-07-13 | CGI Pharmaceuticals, Inc. | Kinasehemmer und Verfahren zur Verwendung und Identifizierung von Kinasehemmern |
SI2529622T1 (en) | 2006-09-22 | 2018-06-29 | Pharmacyclics Llc | Bruton tyrosine kinase inhibitors |
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 |
SG185330A1 (en) * | 2007-10-23 | 2012-11-29 | Hoffmann La Roche | Novel kinase inhibitors |
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 |
CA2724861A1 (en) | 2008-06-05 | 2009-12-10 | Alembic Limited | A process for preparing teriflunomide |
CA2730930C (en) | 2008-07-16 | 2015-01-13 | Pharmacyclics, Inc. | Inhibitors of bruton's tyrosine kinase for the treatment of solid tumors |
EP3409276B1 (de) | 2010-04-05 | 2020-12-30 | Fosun Orinove Pharmatech, Inc. | Ire-1a-inhibitoren |
BR112012030625A2 (pt) | 2010-06-03 | 2017-06-27 | Pharmacyclics Inc | uso de inibidores de tirosina quinase de bruton (btk) |
CN103857396A (zh) | 2011-07-13 | 2014-06-11 | 药品循环公司 | 布鲁顿酪氨酸激酶抑制剂 |
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 |
US9540382B2 (en) | 2012-06-04 | 2017-01-10 | Pharmacyclics Llc | Crystalline forms of a Bruton's tyrosine kinase inhibitor |
AU2013293087B2 (en) | 2012-07-24 | 2017-08-31 | Pharmacyclics Llc | Mutations associated with resistance to inhibitors of Bruton's tyrosine kinase (BTK) |
EA201590855A1 (ru) | 2012-11-15 | 2015-11-30 | Фармасайкликс, Инк. | Соединения пирролопиримидина как ингибиторы киназ |
WO2014085308A1 (en) * | 2012-11-28 | 2014-06-05 | Corning Incorporated | Cell culture medium for enhanced hepatocyte function |
JO3377B1 (ar) | 2013-03-11 | 2019-03-13 | Takeda Pharmaceuticals Co | مشتقات بيريدينيل وبيريدينيل مندمج |
CN105142640B (zh) * | 2013-04-02 | 2017-08-29 | 豪夫迈·罗氏有限公司 | 酪氨酸蛋白激酶抑制剂 |
JP6800750B2 (ja) | 2013-08-02 | 2020-12-16 | ファーマサイクリックス エルエルシー | 固形腫瘍の処置方法 |
EP2832358A1 (de) * | 2013-08-02 | 2015-02-04 | Bionsil S.r.l. | Pharmazeutisches Kit zur Verwendung bei der Behandlung von Darm- und kolorektalem Krebs |
EP3033079B1 (de) | 2013-08-12 | 2018-10-31 | Pharmacyclics LLC | Verfahren zur behandlung von her2-verstärktem krebs |
TN2016000094A1 (en) | 2013-09-30 | 2017-07-05 | Pharmacyclics Llc | Inhibitors of bruton's tyrosine kinase. |
EP3079682A4 (de) | 2013-12-13 | 2017-08-30 | Dana-Farber Cancer Institute, Inc. | Verfahren zur behandlung eines lymphoplasmazytischen lymphoms |
AU2014361798B2 (en) | 2013-12-13 | 2020-06-11 | Dana-Farber Cancer Institute, Inc. | Methods to treat lymphoplasmacytic lymphoma |
CA2942528A1 (en) | 2014-03-20 | 2015-09-24 | Pharmacyclics Inc. | 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 |
AU2015335788B2 (en) | 2014-10-22 | 2020-07-30 | 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 proton tyrosine kinase inhibitor |
AU2017240609B2 (en) | 2016-03-31 | 2021-07-15 | Takeda Pharmaceutical Company Limited | Isoquinolinyl triazolone complexes |
CA3046961A1 (en) | 2016-12-12 | 2018-06-21 | Multivir Inc. | Methods and compositions comprising viral gene therapy and an immune checkpoint inhibitor for treatment and prevention of cancer and infectious diseases |
AU2020242287A1 (en) | 2019-03-21 | 2021-09-02 | INSERM (Institut National de la Santé et de la Recherche Médicale) | 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 |
HU222234B1 (hu) * | 1990-05-18 | 2003-05-28 | Aventis Pharma Deutschland Gmbh. | Eljárás izoxazol-4-karbonsav-amidok és hidroxi-alkilidén-cián-ecetsav-amidok, a vegyületeket tartalmazó gyógyászati készítmények és az ismert vegyületeket tartalmazó rákellenes hatású gyógyszerkészítmények előállítására |
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 |
AU5958394A (en) * | 1992-12-23 | 1994-07-19 | 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 IL IL13908099A patent/IL139080A0/xx unknown
- 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 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 HU HU0102661A patent/HUP0102661A2/hu unknown
- 1999-04-19 AT AT99918673T patent/ATE269295T1/de not_active IP Right Cessation
- 1999-04-19 MX MXPA00010150A patent/MXPA00010150A/es unknown
- 1999-04-19 KR KR1020007011551A patent/KR20010042804A/ko not_active Application Discontinuation
- 1999-04-19 ES ES99918673T patent/ES2222705T3/es not_active Expired - Lifetime
-
2000
- 2000-10-17 NO NO20005224A patent/NO20005224L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
JP2002512216A (ja) | 2002-04-23 |
DE69918089T2 (de) | 2005-07-14 |
IL139080A0 (en) | 2001-11-25 |
NO20005224D0 (no) | 2000-10-17 |
DE69918089D1 (de) | 2004-07-22 |
EP1071658B1 (de) | 2004-06-16 |
HUP0102661A2 (hu) | 2001-11-28 |
KR20010042804A (ko) | 2001-05-25 |
EP1071658A2 (de) | 2001-01-31 |
AU3653099A (en) | 1999-11-08 |
MXPA00010150A (es) | 2002-05-14 |
WO1999054286A3 (en) | 2000-05-04 |
NO20005224L (no) | 2000-12-18 |
CA2328962A1 (en) | 1999-10-28 |
WO1999054286A2 (en) | 1999-10-28 |
ES2222705T3 (es) | 2005-02-01 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |