IL161580A0 - Pyrrole, pyrazole, imidazole, triazole and tetrazole derivatives and their use - Google Patents
Pyrrole, pyrazole, imidazole, triazole and tetrazole derivatives and their useInfo
- Publication number
- IL161580A0 IL161580A0 IL16158002A IL16158002A IL161580A0 IL 161580 A0 IL161580 A0 IL 161580A0 IL 16158002 A IL16158002 A IL 16158002A IL 16158002 A IL16158002 A IL 16158002A IL 161580 A0 IL161580 A0 IL 161580A0
- Authority
- IL
- Israel
- Prior art keywords
- pyrazole
- pyrrole
- triazole
- imidazole
- tetrazole derivatives
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C07D233/60—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with hydrocarbon radicals, substituted by oxygen or sulfur atoms, attached to ring nitrogen atoms
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- 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
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- 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
- A61K31/4164—1,3-Diazoles
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- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- 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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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- C07D233/61—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms not forming part of a nitro radical, attached to ring nitrogen atoms
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- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US33604001P | 2001-10-23 | 2001-10-23 | |
PCT/US2002/033963 WO2003035626A2 (fr) | 2001-10-23 | 2002-10-23 | Composes a activite pharmaceutique et leurs methodes d'utilisation |
Publications (1)
Publication Number | Publication Date |
---|---|
IL161580A0 true IL161580A0 (en) | 2004-09-27 |
Family
ID=23314305
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL16158002A IL161580A0 (en) | 2001-10-23 | 2002-10-23 | Pyrrole, pyrazole, imidazole, triazole and tetrazole derivatives and their use |
Country Status (8)
Country | Link |
---|---|
US (2) | US7253199B2 (fr) |
EP (2) | EP1438295B1 (fr) |
JP (1) | JP4602667B2 (fr) |
AU (2) | AU2002359291C1 (fr) |
CA (1) | CA2463101A1 (fr) |
ES (1) | ES2393186T3 (fr) |
IL (1) | IL161580A0 (fr) |
WO (1) | WO2003035626A2 (fr) |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003035626A2 (fr) * | 2001-10-23 | 2003-05-01 | Applied Research Systems Ars Holding N.V. | Composes a activite pharmaceutique et leurs methodes d'utilisation |
SI1802579T1 (sl) | 2004-10-20 | 2014-03-31 | Merck Serono Sa | Derivati 3-arilaminopiridina |
US8546404B2 (en) | 2005-12-13 | 2013-10-01 | Merck Sharp & Dohme | Compounds that are ERK inhibitors |
CN101415674A (zh) | 2006-02-16 | 2009-04-22 | 先灵公司 | 作为erk抑制剂的吡咯烷衍生物 |
CN102015693B (zh) | 2008-02-21 | 2014-10-29 | 默沙东公司 | 作为erk抑制剂的化合物 |
US8951979B2 (en) * | 2008-06-13 | 2015-02-10 | Cornell University | Pain treatment using ERK2 inhibitors |
WO2010051933A2 (fr) | 2008-11-10 | 2010-05-14 | Bayer Schering Pharma Aktiengesellschaft | Sulfonamido phénoxybenzamides substitués |
EP2370568B1 (fr) | 2008-12-10 | 2017-07-19 | Dana-Farber Cancer Institute, Inc. | Mutations de mek conférant une résistance aux inhibiteurs de mek |
JP2013508318A (ja) | 2009-10-21 | 2013-03-07 | バイエル・ファルマ・アクチェンゲゼルシャフト | 置換されたベンゾスルホンアミド誘導体 |
WO2011047796A1 (fr) | 2009-10-21 | 2011-04-28 | Bayer Schering Pharma Aktiengesellschaft | Dérivés d'halogénophénoxybenzamide substitués |
CA2777430A1 (fr) | 2009-10-21 | 2011-04-28 | Bayer Pharma Aktiengesellschaft | Benzosulfonamides substitues |
EP3028699B1 (fr) | 2010-02-25 | 2018-03-21 | Dana-Farber Cancer Institute, Inc. | Mutations braf conférant une résistance aux inhibiteurs de braf |
AU2011224410B2 (en) | 2010-03-09 | 2015-05-28 | Dana-Farber Cancer Institute, Inc. | Methods of diagnosing and treating cancer in patients having or developing resistance to a first cancer therapy |
WO2012055953A1 (fr) | 2010-10-29 | 2012-05-03 | Bayer Pharma Aktiengesellschaft | Phénoxypyridines substituées |
WO2013109142A1 (fr) | 2012-01-16 | 2013-07-25 | Stichting Het Nederlands Kanker Instituut | Inhibition de la voie des mapk/erk et pdk combinée dans des cas de néoplasie |
WO2013169858A1 (fr) | 2012-05-08 | 2013-11-14 | The Broad Institute, Inc. | Méthodes de diagnostic et de traitement chez des patients ayant ou présentant un risque de développer une résistance à une thérapie anticancéreuse |
WO2015041533A1 (fr) | 2013-09-20 | 2015-03-26 | Stichting Het Nederlands Kanker Instituut | Association de rock et de la voie mapk |
WO2015041534A1 (fr) | 2013-09-20 | 2015-03-26 | Stichting Het Nederlands Kanker Instituut | P90rsk en combinaison avec raf/erk/mek |
WO2015156674A2 (fr) | 2014-04-10 | 2015-10-15 | Stichting Het Nederlands Kanker Instituut | Méthode de traitement du cancer |
WO2015178770A1 (fr) | 2014-05-19 | 2015-11-26 | Stichting Het Nederlands Kanker Instituut | Compositions pour le traitement du cancer |
US10864179B2 (en) | 2015-10-01 | 2020-12-15 | Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | Histone deacetylase inhibitors for the use in the treatment of drug resistant melanoma |
WO2017099591A1 (fr) | 2015-12-07 | 2017-06-15 | Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | Traitement de cancers à mutation braf résistants aux inhibiteurs |
WO2017204626A1 (fr) | 2016-05-24 | 2017-11-30 | Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | Polythérapie combinant map2k4/map3k1 et une inhibition de mek/erk |
CN110845703A (zh) * | 2019-10-28 | 2020-02-28 | 上海瀚岱化学有限公司 | 一种水性环氧树脂及其制备方法 |
CN110903735A (zh) * | 2019-11-11 | 2020-03-24 | 上海瀚岱化学有限公司 | 一种水性环氧涂料及其制备方法与应用 |
WO2021221953A1 (fr) | 2020-04-28 | 2021-11-04 | The Regents Of The University Of Michigan | Inhibiteurs pyridine de la glucosylcéramide synthase et procédés thérapeutiques les utilisant |
CN112794989A (zh) * | 2020-12-18 | 2021-05-14 | 江西瀚泰新材料科技有限公司 | 一种增韧阻燃水性环氧树脂及其制备方法 |
CN112759742A (zh) * | 2020-12-18 | 2021-05-07 | 江西瀚泰新材料科技有限公司 | 一种增韧型水性环氧树脂及其制备方法 |
CN112646123A (zh) * | 2020-12-18 | 2021-04-13 | 江西瀚泰新材料科技有限公司 | 一种低粘度水性环氧树脂及其制备方法 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1271477A (fr) * | 1983-11-18 | 1990-07-10 | John F. Gerster | 1h-imidazo[4,5-c]quinoleine-4-amines |
BR9910474A (pt) * | 1998-05-15 | 2001-01-02 | Astrazeneca Ab | Composto derivado de amida, processo para preparação do mesmo, composição farmacêutica, e, uso de um composto derivado de amida |
ES2221426T3 (es) * | 1998-08-20 | 2004-12-16 | Smithkline Beecham Corporation | Nuevos compuestos de triazol sustituidos. |
CA2355374A1 (fr) * | 1999-01-13 | 2000-07-20 | Warner-Lambert Company | Diarylamines a substitution 1-heterocyclique |
WO2003035626A2 (fr) * | 2001-10-23 | 2003-05-01 | Applied Research Systems Ars Holding N.V. | Composes a activite pharmaceutique et leurs methodes d'utilisation |
-
2002
- 2002-10-23 WO PCT/US2002/033963 patent/WO2003035626A2/fr active Application Filing
- 2002-10-23 JP JP2003538142A patent/JP4602667B2/ja not_active Expired - Fee Related
- 2002-10-23 ES ES02793814T patent/ES2393186T3/es not_active Expired - Lifetime
- 2002-10-23 EP EP02793814A patent/EP1438295B1/fr not_active Expired - Lifetime
- 2002-10-23 US US10/491,902 patent/US7253199B2/en not_active Expired - Fee Related
- 2002-10-23 CA CA002463101A patent/CA2463101A1/fr not_active Abandoned
- 2002-10-23 EP EP10075495A patent/EP2332922A1/fr not_active Withdrawn
- 2002-10-23 IL IL16158002A patent/IL161580A0/xx unknown
- 2002-10-23 AU AU2002359291A patent/AU2002359291C1/en not_active Ceased
-
2007
- 2007-07-24 US US11/782,251 patent/US7541375B2/en not_active Expired - Fee Related
-
2008
- 2008-06-20 AU AU2008202731A patent/AU2008202731A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
AU2002359291B8 (en) | 2008-04-17 |
CA2463101A1 (fr) | 2003-05-01 |
ES2393186T3 (es) | 2012-12-19 |
JP2005508972A (ja) | 2005-04-07 |
US7253199B2 (en) | 2007-08-07 |
WO2003035626A2 (fr) | 2003-05-01 |
JP4602667B2 (ja) | 2010-12-22 |
AU2008202731A1 (en) | 2008-07-17 |
WO2003035626A3 (fr) | 2003-11-06 |
EP1438295B1 (fr) | 2012-08-15 |
US20070293555A1 (en) | 2007-12-20 |
AU2002359291C1 (en) | 2008-11-20 |
US20050054706A1 (en) | 2005-03-10 |
US7541375B2 (en) | 2009-06-02 |
EP2332922A1 (fr) | 2011-06-15 |
AU2002359291B2 (en) | 2008-04-03 |
EP1438295A2 (fr) | 2004-07-21 |
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