NO20083836L - N-hydroksyakrylamidforbindelser - Google Patents
N-hydroksyakrylamidforbindelserInfo
- Publication number
- NO20083836L NO20083836L NO20083836A NO20083836A NO20083836L NO 20083836 L NO20083836 L NO 20083836L NO 20083836 A NO20083836 A NO 20083836A NO 20083836 A NO20083836 A NO 20083836A NO 20083836 L NO20083836 L NO 20083836L
- Authority
- NO
- Norway
- Prior art keywords
- novel
- pharmaceutically acceptable
- acceptable salts
- same
- hdac
- Prior art date
Links
- HQVFKSDWNYVAQD-UHFFFAOYSA-N n-hydroxyprop-2-enamide Chemical class ONC(=O)C=C HQVFKSDWNYVAQD-UHFFFAOYSA-N 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 102000003964 Histone deacetylase Human genes 0.000 abstract 1
- 108090000353 Histone deacetylase Proteins 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229940121372 histone deacetylase inhibitor Drugs 0.000 abstract 1
- 239000003276 histone deacetylase inhibitor Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
Classifications
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- 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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene
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- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2006900588A AU2006900588A0 (en) | 2006-02-07 | HDAC inhibitor | |
PCT/JP2007/052447 WO2007091703A1 (en) | 2006-02-07 | 2007-02-06 | N-hydroxyacrylamide compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
NO20083836L true NO20083836L (no) | 2008-11-05 |
Family
ID=38038616
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20083836A NO20083836L (no) | 2006-02-07 | 2008-09-05 | N-hydroksyakrylamidforbindelser |
Country Status (19)
Country | Link |
---|---|
US (1) | US7750155B2 (es) |
EP (1) | EP1981877B1 (es) |
JP (1) | JP5218057B2 (es) |
KR (1) | KR20080091297A (es) |
CN (1) | CN101379059A (es) |
AT (1) | ATE554084T1 (es) |
AU (1) | AU2007213018A1 (es) |
BR (1) | BRPI0707693A2 (es) |
CA (1) | CA2641579A1 (es) |
ES (1) | ES2384121T3 (es) |
IL (1) | IL193252A0 (es) |
MX (1) | MX2008010035A (es) |
NO (1) | NO20083836L (es) |
PL (1) | PL1981877T3 (es) |
PT (1) | PT1981877E (es) |
RU (1) | RU2008135979A (es) |
TW (1) | TW200806652A (es) |
WO (1) | WO2007091703A1 (es) |
ZA (1) | ZA200806778B (es) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2628726A1 (en) * | 2008-03-26 | 2013-08-21 | Novartis AG | Hydroxamate-based inhibitors of deacetylases b |
WO2009118370A1 (en) | 2008-03-27 | 2009-10-01 | Janssen Pharmaceutica Nv | Aza-bicyclohexyl substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase |
WO2011017448A1 (en) * | 2009-08-05 | 2011-02-10 | The Trustees Of The University Of Pennsylvania | Use of histone deacetylase inhibitors for treatment of autoimmune diseases |
US8614223B2 (en) * | 2010-11-16 | 2013-12-24 | Acetylon Pharmaceuticals, Inc. | Pyrimidine hydroxy amide compounds as protein deacetylase inhibitors and methods of use thereof |
ES2929576T3 (es) | 2013-10-08 | 2022-11-30 | Acetylon Pharmaceuticals Inc | Combinaciones de inhibidores de histona deacetilasa 6 y el inhibidor de Her2 lapatinib para el uso en el tratamiento del cáncer de mama |
EP3055299B1 (en) | 2013-10-10 | 2021-01-06 | Acetylon Pharmaceuticals, Inc. | Pyrimidine hydroxy amide compounds as histone deacetylase inhibitors |
JP2016534069A (ja) | 2013-10-24 | 2016-11-04 | メイヨ・ファウンデーション・フォー・メディカル・エデュケーション・アンド・リサーチ | Hdac6阻害剤での多嚢胞性疾患の治療 |
PE20161030A1 (es) | 2013-12-03 | 2016-11-06 | Acetylon Pharmaceuticals Inc | Combinaciones de inhibidores de histona deacetilasa y farmacos inmunomoduladores |
US9464073B2 (en) | 2014-02-26 | 2016-10-11 | Acetylon Pharmaceuticals, Inc. | Pyrimidine hydroxy amide compounds as HDAC6 selective inhibitors |
EP3166603B1 (en) | 2014-07-07 | 2020-02-12 | Acetylon Pharmaceuticals, Inc. | Treatment of leukemia with histone deacetylase inhibitors |
CA2969790A1 (en) | 2014-12-05 | 2016-06-09 | University of Modena and Reggio Emilia | Combinations of histone deacetylase inhibitors and bendamustine |
US10272084B2 (en) | 2015-06-01 | 2019-04-30 | Regenacy Pharmaceuticals, Llc | Histone deacetylase 6 selective inhibitors for the treatment of cisplatin-induced peripheral neuropathy |
JP2019515909A (ja) | 2016-04-19 | 2019-06-13 | アセチロン ファーマシューティカルズ インコーポレイテッドAcetylon Pharmaceuticals,Inc. | 慢性リンパ性白血病の治療を目的とするhdac阻害剤単独またはbtk阻害剤との配合物 |
MX2020006587A (es) | 2017-12-22 | 2020-12-10 | Ravenna Pharmaceuticals Inc | Derivados de aminopiridina como inhibidores de fosfatidilinositol fosfato cinasa. |
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DK0570594T3 (es) | 1991-12-10 | 1997-08-25 | Shionogi & Co | |
WO1995013264A1 (fr) | 1993-11-08 | 1995-05-18 | Terumo Kabushiki Kaisha | Derive d'acide hydroxamique et preparation medicamenteuse contenant ledit derive |
ES2217386T3 (es) | 1996-01-02 | 2004-11-01 | Aventis Pharmaceuticals Inc. | Compuestos de acido(aril, heteroaril, arilmetil o heteroarilmetil) hidroxamico sustituido. |
US6593322B1 (en) | 1999-03-17 | 2003-07-15 | Signal Pharmaceuticals, Inc. | Compounds and methods for modulation of estrogen receptors |
UA74345C2 (uk) | 1999-09-08 | 2005-12-15 | Слоан-Кеттерінг Інстітьют Фо Кансер Рісерч | Засоби клітинної диференціації і інгібітори гістонової деацетилази та способи їх використання |
KR20100035666A (ko) | 1999-11-23 | 2010-04-05 | 메틸진 인크. | 히스톤 디아세틸라제의 억제제 |
EP1314721A1 (en) | 2000-08-31 | 2003-05-28 | Wakunaga Pharmaceutical Co., Ltd. | Novel propenohydroxamic acid derivatives |
PE20020354A1 (es) * | 2000-09-01 | 2002-06-12 | Novartis Ag | Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda) |
WO2002030872A1 (fr) | 2000-10-12 | 2002-04-18 | Maruha Corporation | Nouveaux composes aliphatiques, procede de preparation et utilisation associes |
BR0007130A (pt) * | 2000-12-22 | 2002-08-13 | Olivier Marie Marcel Autran | Método de envio e coleta de dados através de sistema de comunicação móvel |
WO2002074298A1 (fr) | 2001-03-21 | 2002-09-26 | Ono Pharmaceutical Co., Ltd. | Inhibiteurs de production d'il-6 |
US7148257B2 (en) | 2002-03-04 | 2006-12-12 | Merck Hdac Research, Llc | Methods of treating mesothelioma with suberoylanilide hydroxamic acid |
AU2003229883B2 (en) | 2002-04-03 | 2009-06-11 | Topotarget Uk Limited | Carbamic acid compounds comprising a piperazine linkage as HDAC inhibitors |
US7495022B2 (en) | 2002-04-11 | 2009-02-24 | Sk Chemicals Co., Ltd. | α,β-unsaturated hydroxamic acid derivatives and their use as histone deacetylase inhibitors |
EP1553948B1 (en) | 2002-09-13 | 2011-08-24 | Virginia Commonwealth University | Combination of imatnib and a histone deacetylase inhibitor for the treatment of leukemia |
WO2004043352A2 (en) | 2002-11-12 | 2004-05-27 | Alcon, Inc. | Histone deacetylase inhibitors for the treatment of ocular neovascular or edematous disorders and diseases |
US7135493B2 (en) | 2003-01-13 | 2006-11-14 | Astellas Pharma Inc. | HDAC inhibitor |
US20050159470A1 (en) * | 2003-12-19 | 2005-07-21 | Syrrx, Inc. | Histone deacetylase inhibitors |
US20050197336A1 (en) | 2004-03-08 | 2005-09-08 | Miikana Therapeutics Corporation | Inhibitors of histone deacetylase |
MX2007001550A (es) | 2004-08-09 | 2007-04-10 | Astellas Pharma Inc | Compuestos de hidroxiamida que tienen actividad como inhibidores de histona desacetilasa (hdac). |
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2007
- 2007-02-06 RU RU2008135979/04A patent/RU2008135979A/ru not_active Application Discontinuation
- 2007-02-06 AU AU2007213018A patent/AU2007213018A1/en not_active Abandoned
- 2007-02-06 JP JP2008533306A patent/JP5218057B2/ja not_active Expired - Fee Related
- 2007-02-06 PL PL07708338T patent/PL1981877T3/pl unknown
- 2007-02-06 AT AT07708338T patent/ATE554084T1/de active
- 2007-02-06 CN CNA2007800047171A patent/CN101379059A/zh active Pending
- 2007-02-06 KR KR1020087021783A patent/KR20080091297A/ko not_active Application Discontinuation
- 2007-02-06 WO PCT/JP2007/052447 patent/WO2007091703A1/en active Application Filing
- 2007-02-06 EP EP07708338A patent/EP1981877B1/en not_active Not-in-force
- 2007-02-06 ES ES07708338T patent/ES2384121T3/es active Active
- 2007-02-06 ZA ZA200806778A patent/ZA200806778B/xx unknown
- 2007-02-06 PT PT07708338T patent/PT1981877E/pt unknown
- 2007-02-06 CA CA002641579A patent/CA2641579A1/en not_active Abandoned
- 2007-02-06 MX MX2008010035A patent/MX2008010035A/es not_active Application Discontinuation
- 2007-02-06 BR BRPI0707693-2A patent/BRPI0707693A2/pt not_active IP Right Cessation
- 2007-02-06 US US12/278,580 patent/US7750155B2/en not_active Expired - Fee Related
- 2007-02-07 TW TW096104449A patent/TW200806652A/zh unknown
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2008
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MX2008010035A (es) | 2008-10-17 |
PT1981877E (pt) | 2012-05-24 |
RU2008135979A (ru) | 2010-03-20 |
BRPI0707693A2 (pt) | 2011-05-10 |
EP1981877A1 (en) | 2008-10-22 |
ATE554084T1 (de) | 2012-05-15 |
WO2007091703A1 (en) | 2007-08-16 |
EP1981877B1 (en) | 2012-04-18 |
ZA200806778B (en) | 2009-11-25 |
AU2007213018A1 (en) | 2007-08-16 |
US20090054465A1 (en) | 2009-02-26 |
JP5218057B2 (ja) | 2013-06-26 |
PL1981877T3 (pl) | 2012-12-31 |
ES2384121T3 (es) | 2012-06-29 |
KR20080091297A (ko) | 2008-10-09 |
JP2009525945A (ja) | 2009-07-16 |
US7750155B2 (en) | 2010-07-06 |
IL193252A0 (en) | 2009-02-11 |
TW200806652A (en) | 2008-02-01 |
CN101379059A (zh) | 2009-03-04 |
CA2641579A1 (en) | 2007-08-16 |
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