HK1006021A1 - 4h-1-benzopyran-4-one derivatives, process for their preparation and their use as medicaments - Google Patents
4h-1-benzopyran-4-one derivatives, process for their preparation and their use as medicaments Download PDFInfo
- Publication number
- HK1006021A1 HK1006021A1 HK98105203A HK98105203A HK1006021A1 HK 1006021 A1 HK1006021 A1 HK 1006021A1 HK 98105203 A HK98105203 A HK 98105203A HK 98105203 A HK98105203 A HK 98105203A HK 1006021 A1 HK1006021 A1 HK 1006021A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- methyl
- alkyl
- formula
- compound
- cis
- Prior art date
Links
Classifications
-
- 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
- C07D405/02—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 two hetero rings
- C07D405/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/40—Oxygen atoms
- C07D211/42—Oxygen atoms attached in position 3 or 5
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Transplantation (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19863612337 DE3612337A1 (de) | 1986-04-11 | 1986-04-11 | 4h-1-benzopyran-4-on-derivate, ein verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
| DE3612337 | 1986-04-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| HK1006021B HK1006021B (en) | 1999-02-05 |
| HK1006021A1 true HK1006021A1 (en) | 1999-02-05 |
Family
ID=6298535
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HK98105203A HK1006021A1 (en) | 1986-04-11 | 1998-06-11 | 4h-1-benzopyran-4-one derivatives, process for their preparation and their use as medicaments |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US4900727A (enExample) |
| EP (1) | EP0241003B1 (enExample) |
| JP (1) | JPH0686446B2 (enExample) |
| KR (1) | KR950009861B1 (enExample) |
| AT (2) | ATE95519T1 (enExample) |
| AU (1) | AU602891B2 (enExample) |
| CA (1) | CA1332238C (enExample) |
| DE (2) | DE3612337A1 (enExample) |
| DK (1) | DK169760B1 (enExample) |
| ES (1) | ES2060582T3 (enExample) |
| HK (1) | HK1006021A1 (enExample) |
| IE (1) | IE62244B1 (enExample) |
| IL (1) | IL82149A (enExample) |
| IN (1) | IN164232B (enExample) |
| PT (1) | PT84654B (enExample) |
| ZA (1) | ZA872555B (enExample) |
Families Citing this family (59)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3836676A1 (de) * | 1988-10-28 | 1990-05-03 | Hoechst Ag | Die verwendung von 4h-1-benzopyran-4-on-derivaten, neue 4h-1-benzopyran-4-on-derivate und diese enthaltende arzneimittel |
| US5284856A (en) * | 1988-10-28 | 1994-02-08 | Hoechst Aktiengesellschaft | Oncogene-encoded kinases inhibition using 4-H-1-benzopyran-4-one derivatives |
| US5278174A (en) * | 1990-06-04 | 1994-01-11 | Scios Nova, Inc. | Sigma binding site agents |
| EP0508347A1 (en) * | 1991-04-10 | 1992-10-14 | Hoechst Aktiengesellschaft | 5,7-Dihydroxy-2-methyl-8-[4-(3-hydroxy-1-(1-propyl)) piperidinyl]-4H-1-benzopyran-4-one, its preparation and its use |
| US6476011B1 (en) | 1991-08-28 | 2002-11-05 | Sterix Limited | Methods for introducing an estrogenic compound |
| US6011024A (en) | 1991-08-28 | 2000-01-04 | Imperial College Of Science Technology & Medicine | Steroid sulphatase inhibitors |
| GB9604709D0 (en) * | 1996-03-05 | 1996-05-01 | Imperial College | A compound |
| US6903084B2 (en) * | 1991-08-28 | 2005-06-07 | Sterix Limited | Steroid sulphatase inhibitors |
| SK280617B6 (sk) * | 1992-01-16 | 2000-05-16 | Hoechst Aktiengesellschaft | Arylcykloalkylové deriváty, spôsob ich prípravy, f |
| US5733920A (en) * | 1995-10-31 | 1998-03-31 | Mitotix, Inc. | Inhibitors of cyclin dependent kinases |
| US20060241173A1 (en) * | 1996-02-16 | 2006-10-26 | Sterix Ltd. | Compound |
| US6506792B1 (en) | 1997-03-04 | 2003-01-14 | Sterix Limited | Compounds that inhibit oestrone sulphatase and/or aromatase and methods for making and using |
| US6087366A (en) * | 1996-03-07 | 2000-07-11 | The Trustees Of Columbia University In The City Of New York | Use of flavopiridol or a pharmaceutically acceptable salt thereof for inhibiting cell damage or cell death |
| US5849733A (en) * | 1996-05-10 | 1998-12-15 | Bristol-Myers Squibb Co. | 2-thio or 2-oxo flavopiridol analogs |
| US5908934A (en) * | 1996-09-26 | 1999-06-01 | Bristol-Myers Squibb Company | Process for the preparation of chiral ketone intermediates useful for the preparation of flavopiridol and analogs |
| DE19802449A1 (de) * | 1998-01-23 | 1999-07-29 | Hoechst Marion Roussel De Gmbh | Verfahren zur Herstellung von (-)cis-3-Hydroxy-1-methyl-4-(2,4,6-trimethoxypyhenyl)-piperidin |
| GB9807779D0 (en) * | 1998-04-09 | 1998-06-10 | Ciba Geigy Ag | Organic compounds |
| US6399633B1 (en) * | 1999-02-01 | 2002-06-04 | Aventis Pharmaceuticals Inc. | Use of 4-H-1-benzopryan-4-one derivatives as inhibitors of smooth muscle cell proliferation |
| DE19959546A1 (de) * | 1999-12-09 | 2001-06-21 | Rhone Poulenc Rorer Gmbh | Pharmazeutische Zubereitung zur Behandlung von Tumorerkrankungen |
| US7335650B2 (en) | 2000-01-14 | 2008-02-26 | Sterix Limited | Composition |
| US6821990B2 (en) | 2000-01-18 | 2004-11-23 | Aventis Pharma Deutschland Gmbh | Ethanol solvate of (-)-cis-2-(2-chlorophenyl)-5, 7-dihydroxy-8 [4R-(3S-hydroxy-1-M ethyl) piperidinyl]-4H-1-benzopyran-4-one |
| AU2001226346A1 (en) * | 2000-01-18 | 2001-07-31 | Aventis Pharmaceuticals Inc. | Pseudopolymorph of |
| DK1252155T3 (da) * | 2000-01-18 | 2005-04-04 | Aventis Pharma Inc | Ethanolsolvat af (-)-cis-2-(2-chlorphenyl)-5,7-dihydroxy-8-[4R-(3S-hydroxy-1-methyl)piperidinyl]-4H-1-benzopyran-4-on |
| US6576647B2 (en) | 2000-01-18 | 2003-06-10 | Aventis Pharmaceuticals Inc. | Pseudopolymorph of (—)-cis-2-(2-chlorophenyl)-5,7-dihydroxy-8[4R-(3S-hydroxy -1-methyl)piperidinyl]-4H-1-benzopyran-4-one |
| FR2805538B1 (fr) * | 2000-02-29 | 2006-08-04 | Hoechst Marion Roussel Inc | Nouveaux derives de flavones, leur procede de preparation, leur application a titre de medicaments, compositions pharmaceutiques et nouvelle utilisation |
| KR100423899B1 (ko) | 2000-05-10 | 2004-03-24 | 주식회사 엘지생명과학 | 세포 증식 억제제로 유용한 1,1-디옥소이소티아졸리딘을갖는 인다졸 |
| CN100381437C (zh) | 2002-04-17 | 2008-04-16 | 赛特凯恩蒂克公司 | 化合物、组合物和方法 |
| US7884127B2 (en) * | 2002-07-08 | 2011-02-08 | Pirimal Life Sciences Ltd. | Inhibitors of cyclin dependent kinases and their use |
| US7915301B2 (en) | 2002-07-08 | 2011-03-29 | Piramal Life Science Limited | Inhibitors of cyclin dependent kinases and their use |
| US7271193B2 (en) * | 2002-07-08 | 2007-09-18 | Nicholas Piramal India, Ltd. | Inhibitors of cyclin-dependent kinases and their use |
| DE60326248D1 (de) * | 2002-07-17 | 2009-04-02 | Cytokinetics Inc | Verbindungen, zusammensetzungen und verfahren zur behandlung von zellulären proliferativen erkrankungen |
| WO2004024086A2 (en) * | 2002-09-13 | 2004-03-25 | Cytokinetics, Inc. | Compounds, compositions and methods |
| US20050165089A1 (en) * | 2003-10-06 | 2005-07-28 | Gustave Bergnes | Compounds, compositions and methods |
| US8044057B2 (en) * | 2003-12-09 | 2011-10-25 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Methods for suppressing an immune response or treating a proliferative disorder |
| US20050171182A1 (en) * | 2003-12-11 | 2005-08-04 | Roger Briesewitz | Methods and compositions for use in the treatment of mutant receptor tyrosine kinase driven cellular proliferative diseases |
| KR101346886B1 (ko) | 2005-01-21 | 2014-01-02 | 아스텍스 테라퓨틱스 리미티드 | 제약 화합물 |
| WO2007148158A1 (en) | 2006-06-21 | 2007-12-27 | Piramal Life Sciences Limited | Enantiomerically pure flavone derivatives for the treatment of poliferative disorders and processes for their preparation |
| EP2073807A1 (en) | 2006-10-12 | 2009-07-01 | Astex Therapeutics Limited | Pharmaceutical combinations |
| JP5528806B2 (ja) | 2006-10-12 | 2014-06-25 | アステックス、セラピューティックス、リミテッド | 複合薬剤 |
| TWI461194B (zh) | 2009-05-05 | 2014-11-21 | Piramal Entpr Ltd | 吡咯啶取代黃酮作為輻射致敏劑 |
| CA2790993A1 (en) | 2010-02-26 | 2011-09-01 | Piramal Enterprises Limited | Pyrrolidine substituted flavones for the treatment of inflammatory disorders |
| EP3399026B1 (en) | 2010-06-14 | 2024-06-26 | The Scripps Research Institute | Reprogramming of cells to a new fate |
| TW201300105A (zh) | 2011-05-31 | 2013-01-01 | Piramal Life Sciences Ltd | 治療頭頸鱗狀細胞癌之相乘藥物組合物 |
| EP2984078B1 (en) | 2013-04-10 | 2017-11-15 | Council of Scientific & Industrial Research | Novel chromone alkaloid dysoline for the treatment of cancer and inflammatory disorders |
| US9932327B2 (en) | 2013-04-17 | 2018-04-03 | The Council Of Scientific & Industrial Research | Rohitukine analogs as cyclin-dependent kinase inhibitors and a process for the preparation thereof |
| ES2733929T3 (es) | 2013-07-12 | 2019-12-03 | Piramal Entpr Ltd | Una combinación farmacéutica para el tratamiento del melanoma |
| IL278574B2 (en) | 2014-11-12 | 2024-11-01 | Seagen Inc | Glycan-interacting compounds and methods of use |
| JP6851978B2 (ja) | 2015-04-20 | 2021-03-31 | スミトモ ダイニッポン ファーマ オンコロジー, インコーポレイテッド | ミトコンドリアプロファイリングによるアルボシジブ応答の予測 |
| JP6510075B2 (ja) | 2015-05-18 | 2019-05-08 | トレロ ファーマシューティカルズ, インコーポレイテッド | バイオアベイラビリティが高いアルボシジブプロドラッグ |
| EP3331510A4 (en) | 2015-08-03 | 2019-04-03 | Tolero Pharmaceuticals, Inc. | COMBINATION THERAPIES FOR THE TREATMENT OF CANCER |
| WO2017083582A1 (en) | 2015-11-12 | 2017-05-18 | Siamab Therapeutics, Inc. | Glycan-interacting compounds and methods of use |
| WO2018094143A1 (en) | 2016-11-17 | 2018-05-24 | Siamab Therapeutics, Inc. | Glycan-interacting compounds and methods of use |
| US11279694B2 (en) | 2016-11-18 | 2022-03-22 | Sumitomo Dainippon Pharma Oncology, Inc. | Alvocidib prodrugs and their use as protein kinase inhibitors |
| CA3047557A1 (en) | 2016-12-19 | 2018-06-28 | Tolero Pharmaceuticals, Inc. | Profiling peptides and methods for sensitivity profiling |
| KR20240044544A (ko) | 2017-03-03 | 2024-04-04 | 씨젠 인크. | 글리칸-상호작용 화합물 및 사용 방법 |
| WO2019055579A1 (en) | 2017-09-12 | 2019-03-21 | Tolero Pharmaceuticals, Inc. | TREATMENT REGIME FOR CANCERS THAT ARE INSENSITIVE TO BCL-2 INHIBITORS USING THE MCL-1 ALVOCIDIB INHIBITOR |
| US11034710B2 (en) | 2018-12-04 | 2021-06-15 | Sumitomo Dainippon Pharma Oncology, Inc. | CDK9 inhibitors and polymorphs thereof for use as agents for treatment of cancer |
| US11793802B2 (en) | 2019-03-20 | 2023-10-24 | Sumitomo Pharma Oncology, Inc. | Treatment of acute myeloid leukemia (AML) with venetoclax failure |
| US12304889B2 (en) * | 2019-04-18 | 2025-05-20 | Sumitomo Pharma Co., Ltd. | Method for producing cis-(-)-flocino piperidol |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1223690A (en) * | 1967-10-17 | 1971-03-03 | Fisons Pharmaceuticals Ltd | Substituted chromon-2-carboxylic acids |
| DE2731566A1 (de) * | 1977-07-13 | 1979-02-01 | Bayer Ag | Verfahren zur herstellung von neuen chromon-derivaten, sowie ihre verwendung als pflanzenschutzmittel |
| GB2101115A (en) * | 1980-10-23 | 1983-01-12 | Pfizer Ltd | Thromboxane synthetase inhibitors |
| DE3311005A1 (de) * | 1983-03-25 | 1984-09-27 | Bayer Ag, 5090 Leverkusen | Chromon- und thiochromonsubstituierte 1,4-dihydropyridinderivate, mehrere verfahren zu ihrer herstellung sowie ihre verwendung in arzneimitteln |
| DE3329186A1 (de) * | 1983-08-12 | 1985-02-21 | Hoechst Ag, 6230 Frankfurt | Chromonalkaloid, verfahren zu seiner isolierung aus dysoxylum binectariferum, und seine verwendung als arzneimittel |
| DE3445852A1 (de) * | 1984-12-15 | 1986-06-19 | Bayer Ag, 5090 Leverkusen | Dihydropyridin-carbonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln |
-
1985
- 1985-10-31 IN IN300/BOM/85A patent/IN164232B/en unknown
-
1986
- 1986-04-11 DE DE19863612337 patent/DE3612337A1/de not_active Withdrawn
-
1987
- 1987-04-08 DE DE87105180T patent/DE3787661D1/de not_active Expired - Lifetime
- 1987-04-08 AT AT87105180T patent/ATE95519T1/de not_active IP Right Cessation
- 1987-04-08 ES ES87105180T patent/ES2060582T3/es not_active Expired - Lifetime
- 1987-04-08 EP EP87105180A patent/EP0241003B1/de not_active Expired - Lifetime
- 1987-04-09 ZA ZA872555A patent/ZA872555B/xx unknown
- 1987-04-09 IL IL8214987A patent/IL82149A/en not_active IP Right Cessation
- 1987-04-10 CA CA000534430A patent/CA1332238C/en not_active Expired - Lifetime
- 1987-04-10 JP JP62087252A patent/JPH0686446B2/ja not_active Expired - Lifetime
- 1987-04-10 AU AU71397/87A patent/AU602891B2/en not_active Expired
- 1987-04-10 DK DK185287A patent/DK169760B1/da not_active IP Right Cessation
- 1987-04-10 PT PT84654A patent/PT84654B/pt unknown
- 1987-04-10 IE IE94187A patent/IE62244B1/en not_active IP Right Cessation
- 1987-04-10 KR KR87003427A patent/KR950009861B1/ko not_active Expired - Lifetime
- 1987-10-08 AT AT0260587A patent/AT389875B/de active
-
1989
- 1989-01-26 US US07/302,084 patent/US4900727A/en not_active Expired - Lifetime
-
1998
- 1998-06-11 HK HK98105203A patent/HK1006021A1/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DK185287D0 (da) | 1987-04-10 |
| CA1332238C (en) | 1994-10-04 |
| KR870010045A (ko) | 1987-11-30 |
| DK169760B1 (da) | 1995-02-20 |
| IL82149A0 (en) | 1987-10-30 |
| ATE95519T1 (de) | 1993-10-15 |
| DE3787661D1 (de) | 1993-11-11 |
| IE62244B1 (en) | 1995-01-11 |
| AU602891B2 (en) | 1990-11-01 |
| EP0241003B1 (de) | 1993-10-06 |
| AT389875B (de) | 1990-02-12 |
| KR950009861B1 (en) | 1995-08-29 |
| EP0241003A2 (de) | 1987-10-14 |
| ATA260587A (de) | 1989-07-15 |
| IN164232B (enExample) | 1989-02-04 |
| JPH0686446B2 (ja) | 1994-11-02 |
| US4900727A (en) | 1990-02-13 |
| IL82149A (en) | 1994-01-25 |
| DK185287A (da) | 1987-10-12 |
| EP0241003A3 (en) | 1988-10-12 |
| DE3612337A1 (de) | 1987-10-15 |
| AU7139787A (en) | 1987-10-15 |
| JPS62242680A (ja) | 1987-10-23 |
| PT84654B (pt) | 1989-12-29 |
| PT84654A (de) | 1987-05-01 |
| ZA872555B (en) | 1987-11-25 |
| ES2060582T3 (es) | 1994-12-01 |
| IE870941L (en) | 1987-10-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PF | Patent in force | ||
| PE | Patent expired |
Effective date: 20070407 |