DE60316686D1 - Bisarylsulfonamid-derivate und ihre verwendung für krebs therapie - Google Patents
Bisarylsulfonamid-derivate und ihre verwendung für krebs therapieInfo
- Publication number
- DE60316686D1 DE60316686D1 DE60316686T DE60316686T DE60316686D1 DE 60316686 D1 DE60316686 D1 DE 60316686D1 DE 60316686 T DE60316686 T DE 60316686T DE 60316686 T DE60316686 T DE 60316686T DE 60316686 D1 DE60316686 D1 DE 60316686D1
- Authority
- DE
- Germany
- Prior art keywords
- sub
- sup
- group
- bisaryl
- cancer therapy
- 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 - Fee Related
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/70—Sulfur atoms
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/429—Thiazoles condensed with heterocyclic ring systems
- A61K31/43—Compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula, e.g. penicillins, penems
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- A61K31/5375—1,4-Oxazines, e.g. morpholine
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- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07C311/44—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/62—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes 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 carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
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- Chemical & Material Sciences (AREA)
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- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Epidemiology (AREA)
- Urology & Nephrology (AREA)
- Dermatology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Pyridine Compounds (AREA)
- Pyrrole Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0215650.3A GB0215650D0 (en) | 2002-07-05 | 2002-07-05 | Bisarylsufonamide compounds |
| GB0215650 | 2002-07-05 | ||
| PCT/GB2003/002923 WO2004005278A1 (en) | 2002-07-05 | 2003-07-07 | Bisarylsulfonamide compounds and their use in cancer therapy |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60316686D1 true DE60316686D1 (de) | 2007-11-15 |
| DE60316686T2 DE60316686T2 (de) | 2008-01-24 |
Family
ID=9939950
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60316686T Expired - Fee Related DE60316686T2 (de) | 2002-07-05 | 2003-07-07 | Bisarylsulfonamid-derivate und ihre verwendung für krebs therapie |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20050215548A1 (de) |
| EP (1) | EP1519932B1 (de) |
| JP (1) | JP2006508906A (de) |
| CN (1) | CN1665802A (de) |
| AT (1) | ATE374763T1 (de) |
| AU (1) | AU2003244847A1 (de) |
| CA (1) | CA2488816A1 (de) |
| DE (1) | DE60316686T2 (de) |
| GB (1) | GB0215650D0 (de) |
| IL (1) | IL166027A0 (de) |
| NZ (1) | NZ536494A (de) |
| WO (1) | WO2004005278A1 (de) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0012528D0 (en) * | 2000-05-23 | 2000-07-12 | Univ Palackeho | Triterpenoid derivatives |
| KR101022977B1 (ko) | 2002-03-26 | 2011-03-18 | 베링거 인겔하임 파마슈티칼즈, 인코포레이티드 | 글루코코르티코이드 모사체, 이의 제조방법, 약제학적조성물 및 이의 용도 |
| CN1678306A (zh) * | 2002-08-29 | 2005-10-05 | 贝林格尔·英格海姆药物公司 | 在炎性、变应性和增生性疾病中用作糖皮质激素模拟物的3-(磺酰氨基乙基)-吲哚衍生物 |
| EP1651595A2 (de) * | 2003-05-30 | 2006-05-03 | Rigel Pharmaceuticals, Inc. | Ubiquitinligaseinhibitoren |
| UY28526A1 (es) | 2003-09-24 | 2005-04-29 | Boehringer Ingelheim Pharma | Miméticos de glucocorticoides, métodos de preparación composiciones farmacéuticas y usos de los mismos |
| US7795272B2 (en) | 2004-03-13 | 2010-09-14 | Boehringer Ingelheim Pharmaceutical, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions and uses thereof |
| MXPA06010520A (es) * | 2004-03-30 | 2007-03-26 | Chiron Corp | Derivados de tiofeno sustituidos como agentes anticancerosos. |
| EP1758873A1 (de) * | 2004-06-22 | 2007-03-07 | Rigel Pharmaceuticals, Inc. | Ubiquitinligasehemmer |
| JP5156378B2 (ja) | 2004-09-22 | 2013-03-06 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | MDM2とp53の間の相互作用の阻害剤 |
| ES2326907T3 (es) | 2004-12-27 | 2009-10-21 | Boehringer Ingelheim Pharmaceuticals Inc. | Mimeticos de glucocorticoides, metodos para su preparacion, composiciones farmaceuticas y su uso. |
| EP1879881A2 (de) * | 2005-04-14 | 2008-01-23 | Bristol-Myers Squibb Company | Inhibitoren der 11-beta-hydroxysteroiddehydrogenase vom typ i |
| US20090156611A1 (en) * | 2005-11-11 | 2009-06-18 | Licentia Ltd. | Mammalian hedgehog signaling modulators |
| DE602007007065D1 (de) | 2006-03-22 | 2010-07-22 | Janssen Pharmaceutica Nv | Cycloalkylaminderivate als inhibitoren der wechselwirkung zwischen mdm2 und p53 |
| RU2434863C2 (ru) * | 2006-03-22 | 2011-11-27 | Янссен Фармацевтика Н.В. | Производные циклических алкиламинов в качестве ингибиторов взаимодействия между mdm2 и р53 |
| US8232298B2 (en) | 2006-03-22 | 2012-07-31 | Janssen Pharmaceutica N.V. | Inhibitors of the interaction between MDM2 and P53 |
| US8614192B2 (en) | 2006-07-28 | 2013-12-24 | Leiden University Medical Center | Method for treating ocular cancer |
| US8470785B2 (en) | 2006-07-28 | 2013-06-25 | St. Jude Children's Research Hospital | Method for treating ocular cancer |
| RU2009125614A (ru) | 2006-12-06 | 2011-01-20 | Бёрингер Ингельхайм Интернациональ Гмбх (De) | Глюкокортикоидные миметики, способы их получения, фармацевтические композиции и их применения |
| CN101605798A (zh) * | 2006-12-14 | 2009-12-16 | 第一三共株式会社 | 咪唑并噻唑衍生物 |
| WO2008112164A2 (en) * | 2007-03-08 | 2008-09-18 | The Board Of Trustees Of The Leland Stanford Junior University | Mitochondrial aldehyde dehydrogenase-2 modulators and methods of use thereof |
| US8263588B2 (en) * | 2007-04-06 | 2012-09-11 | Neurocrine Biosciences, Inc. | Gonadotropin-releasing hormone receptor antagonists and methods relating thereto |
| NZ580457A (en) | 2007-04-06 | 2012-03-30 | Neurocrine Biosciences Inc | Gonadotropin-releasing hormone receptor antagonists and methods relating thereto |
| PA8792401A1 (es) | 2007-08-06 | 2009-03-31 | Janssen Pharmaceutica Nv | Fenilendiaminas |
| US8039493B2 (en) * | 2007-09-27 | 2011-10-18 | Hoffmann-La Roche Inc. | Biaryl sulfonamide derivatives |
| EP2224961A1 (de) * | 2007-11-26 | 2010-09-08 | The Research Foundation of the State University of New York | Kleinmolekülige krebsbehandlungen, die nekrose in krebszellen verursachen, aber normale zellen nicht angreifen |
| EP2116547A1 (de) * | 2008-05-09 | 2009-11-11 | Laboratorios Del. Dr. Esteve, S.A. | Substituierte n-Imidazo[2,1-b]thiazol-5-sulfonamid-Derivative als 5-TH6-Liganden |
| BRPI0915680A2 (pt) | 2008-06-06 | 2019-09-24 | Boehringer Ingelheim Int | miméticos de glicocorticoide, métodos de prepará-los, composições farmacêuticas, e usos dos mesmos |
| JPWO2009151069A1 (ja) * | 2008-06-12 | 2011-11-17 | 第一三共株式会社 | 4,7−ジアザスピロ[2.5]オクタン環構造を有するイミダゾチアゾール誘導体 |
| EP2337563B1 (de) | 2008-09-08 | 2014-04-09 | The Board of Trustees of The Leland Stanford Junior University | Modulatoren der aldehyddehydrogenase-aktivität und anwendungsverfahren für diese |
| WO2010062308A1 (en) | 2008-10-28 | 2010-06-03 | The Board Of Trustees Of The Leland Stanford Junior University | Modulators of aldehyde dehydrogenase and methods of use thereof |
| MY152018A (en) | 2009-02-04 | 2014-08-15 | Janssen Pharmaceutica Nv | Indole derivatives as anticancer agents |
| KR101920202B1 (ko) * | 2009-05-26 | 2018-11-21 | 애브비 아일랜드 언리미티드 컴퍼니 | 암,면역 질환 및 자가면역 질환의 치료를 위한 아폽토시스-유도제 |
| EP2563761A1 (de) * | 2010-04-29 | 2013-03-06 | The U.S.A. As Represented By The Secretary, Department Of Health And Human Services | Aktivatoren der menschlichen pyruvatkinase |
| WO2012149106A1 (en) | 2011-04-29 | 2012-11-01 | The Board Of Trustees Of The Leland Stanford Junior University | Compositions and methods for increasing proliferation of adult salivary stem cells |
| EP3447046A1 (de) | 2012-11-30 | 2019-02-27 | Novomedix, LLC | Substituierte biarylsulfonamide und verwendung davon |
| KR102196882B1 (ko) | 2012-12-20 | 2020-12-30 | 머크 샤프 앤드 돔 코포레이션 | Hdm2 억제제로서의 치환된 이미다조피리딘 |
| CN105358531B (zh) * | 2013-03-14 | 2017-11-14 | 利兰-斯坦福大学初级学院的董事会 | 线粒体醛脱氢酶‑2调节剂和其使用方法 |
| US10448637B2 (en) * | 2014-10-03 | 2019-10-22 | Arizona Board Of Regents On Behalf Of The University Of Arizona | Inhibitors of GRB2-associated binding protein 1 (GAB1) and methods of treating cancer using the same |
| WO2016112177A1 (en) * | 2015-01-08 | 2016-07-14 | Yale University | Novel Compositions Useful for Killing DNA Repair-Deficient Cancer Cells, and Methods Using Same |
| EP3412652A1 (de) * | 2017-06-06 | 2018-12-12 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Inhibitoren von rac1 und verwendungen zur behandlung von krebs |
| WO2019139869A1 (en) | 2018-01-10 | 2019-07-18 | Cura Therapeutics Llc | Pharmaceutical compositions comprising phenylsulfonamides, and their therapeutic applications |
| CA3096978A1 (en) | 2018-04-06 | 2019-10-10 | Oncolyze, Inc. | Compositions for use in lysis of selective cancer cells |
| US12485169B2 (en) | 2018-11-23 | 2025-12-02 | Grey Wolf Therapeutics Limited | Compounds |
| EP4051283A4 (de) * | 2019-11-01 | 2024-03-27 | The Regents of the University of California | P53-modulatoren und verwendungen davon |
| CN117050053A (zh) * | 2023-08-11 | 2023-11-14 | 北京中医药大学 | 一种新型噻吩类抗肿瘤化合物及其制备方法与应用 |
| CN119462567B (zh) * | 2024-11-12 | 2025-11-07 | 中国药科大学 | N-苯基苯磺酰胺类化合物、制备方法和用途 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2402623A (en) * | 1943-06-24 | 1946-06-25 | Rohm & Haas | Nu-nitroaryl haloarylsulphonamides |
| CH361275A (de) * | 1957-09-10 | 1962-04-15 | Geigy Ag J R | Verfahren zur Herstellung von neuen Arylsulfonarylamiden |
| US3991081A (en) * | 1975-05-19 | 1976-11-09 | Chevron Research Company | Fungicidal 2-(N-haloalkylthiosulfonamido)thiophenes |
| JP3545461B2 (ja) * | 1993-09-10 | 2004-07-21 | エーザイ株式会社 | 二環式ヘテロ環含有スルホンアミド誘導体 |
| GB9819860D0 (en) * | 1998-09-12 | 1998-11-04 | Zeneca Ltd | Chemical compounds |
| WO2001012593A1 (en) * | 1999-08-17 | 2001-02-22 | Tularik Inc. | Arylsulfonanilide derivatives |
| RU2240826C2 (ru) * | 2000-02-03 | 2004-11-27 | Эйсай Ко., Лтд. | Ингибитор экспрессии интегрина |
| US7491718B2 (en) * | 2002-10-08 | 2009-02-17 | Abbott Laboratories | Sulfonamides having antiangiogenic and anticancer activity |
-
2002
- 2002-07-05 GB GBGB0215650.3A patent/GB0215650D0/en not_active Ceased
-
2003
- 2003-07-07 WO PCT/GB2003/002923 patent/WO2004005278A1/en not_active Ceased
- 2003-07-07 AU AU2003244847A patent/AU2003244847A1/en not_active Abandoned
- 2003-07-07 DE DE60316686T patent/DE60316686T2/de not_active Expired - Fee Related
- 2003-07-07 EP EP03738323A patent/EP1519932B1/de not_active Expired - Lifetime
- 2003-07-07 AT AT03738323T patent/ATE374763T1/de not_active IP Right Cessation
- 2003-07-07 NZ NZ536494A patent/NZ536494A/en unknown
- 2003-07-07 CN CN038159481A patent/CN1665802A/zh active Pending
- 2003-07-07 JP JP2004518989A patent/JP2006508906A/ja not_active Withdrawn
- 2003-07-07 CA CA002488816A patent/CA2488816A1/en not_active Abandoned
-
2004
- 2004-11-12 US US10/988,388 patent/US20050215548A1/en not_active Abandoned
- 2004-12-02 IL IL16602704A patent/IL166027A0/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2488816A1 (en) | 2004-01-15 |
| CN1665802A (zh) | 2005-09-07 |
| EP1519932B1 (de) | 2007-10-03 |
| WO2004005278A1 (en) | 2004-01-15 |
| ATE374763T1 (de) | 2007-10-15 |
| AU2003244847A1 (en) | 2004-01-23 |
| EP1519932A1 (de) | 2005-04-06 |
| GB0215650D0 (en) | 2002-08-14 |
| US20050215548A1 (en) | 2005-09-29 |
| JP2006508906A (ja) | 2006-03-16 |
| IL166027A0 (en) | 2006-01-15 |
| DE60316686T2 (de) | 2008-01-24 |
| NZ536494A (en) | 2006-10-27 |
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