ZA200906609B - Inhibitors of histone deacetylase - Google Patents
Inhibitors of histone deacetylaseInfo
- Publication number
- ZA200906609B ZA200906609B ZA200906609A ZA200906609A ZA200906609B ZA 200906609 B ZA200906609 B ZA 200906609B ZA 200906609 A ZA200906609 A ZA 200906609A ZA 200906609 A ZA200906609 A ZA 200906609A ZA 200906609 B ZA200906609 B ZA 200906609B
- Authority
- ZA
- South Africa
- Prior art keywords
- inhibitors
- histone deacetylase
- deacetylase
- histone
- Prior art date
Links
- 102000003964 Histone deacetylase Human genes 0.000 title 1
- 108090000353 Histone deacetylase Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
Classifications
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
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- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07C235/32—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
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- C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
- C07C259/06—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
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- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/52—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
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- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
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- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
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- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
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- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
-
- 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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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Virology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Immunology (AREA)
- Endocrinology (AREA)
- Rheumatology (AREA)
- Emergency Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Furan Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
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| US92250507P | 2007-04-09 | 2007-04-09 |
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| EP (1) | EP2139850B1 (fr) |
| JP (1) | JP5746860B2 (fr) |
| KR (1) | KR101561292B1 (fr) |
| CN (1) | CN101679220A (fr) |
| AU (1) | AU2008235212B2 (fr) |
| CA (1) | CA2683557C (fr) |
| TW (1) | TWI539947B (fr) |
| WO (1) | WO2008122115A1 (fr) |
| ZA (1) | ZA200906609B (fr) |
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| US20070207950A1 (en) * | 2005-12-21 | 2007-09-06 | Duke University | Methods and compositions for regulating HDAC6 activity |
| US7737175B2 (en) * | 2007-06-01 | 2010-06-15 | Duke University | Methods and compositions for regulating HDAC4 activity |
| AU2009289649B2 (en) | 2008-09-03 | 2016-05-05 | Biomarin Pharmaceutical Inc. | Compositions including 6-aminohexanoic acid derivatives as HDAC inhibitors |
| ES2736200T3 (es) | 2009-07-22 | 2019-12-26 | Univ Illinois | Inhibidores de HDAC y métodos terapéuticos que utilizan los mismos |
| WO2011153359A1 (fr) | 2010-06-04 | 2011-12-08 | Albany Molecular Research, Inc. | Inhibiteurs du transporteur 1 de la glycine, procédés de fabrication associés, et utilisations associées |
| TW201245115A (en) | 2011-01-24 | 2012-11-16 | Chdi Foundation Inc | Histone deacetylase inhibitors and compositions and methods of use thereof |
| US8957066B2 (en) | 2011-02-28 | 2015-02-17 | Biomarin Pharmaceutical Inc. | Histone deacetylase inhibitors |
| US9540395B2 (en) | 2011-02-28 | 2017-01-10 | Biomarin Pharmaceutical Inc. | Histone deacetylase inhibitors |
| US10059723B2 (en) | 2011-02-28 | 2018-08-28 | Biomarin Pharmaceutical Inc. | Histone deacetylase inhibitors |
| EP2785690B1 (fr) * | 2011-12-02 | 2016-07-13 | Boehringer Ingelheim International GmbH | Dérivés de pipéridine, leurs compositions pharmaceutiques et leurs utilisations |
| WO2013138568A1 (fr) | 2012-03-16 | 2013-09-19 | Vitae Pharmaceuticals, Inc. | Modulateurs du récepteur x du foie |
| CN104203951B (zh) | 2012-03-16 | 2016-11-02 | 生命医药公司 | 肝x受体调节剂 |
| TW201408628A (zh) * | 2012-07-16 | 2014-03-01 | Chdi Foundation Inc | 組蛋白去乙醯酶抑制劑及組成物,暨其使用之方法 |
| WO2014089296A2 (fr) * | 2012-12-06 | 2014-06-12 | Institute For Hepatitis And Virus Research | Dérivés fonctionnalisés de benzamide en tant qu'agents antiviraux contre une infection à vhb |
| WO2014116962A1 (fr) * | 2013-01-24 | 2014-07-31 | Trustees Of Boston University | Inhibiteurs sélectifs de l'histone désacétylase 8 |
| JP6363164B2 (ja) * | 2013-03-14 | 2018-07-25 | シーエイチディーアイ ファウンデーション,インコーポレーテッド | ヒストンデアセチラーゼ阻害剤及びその組成物と使用方法 |
| US9617259B2 (en) | 2013-03-14 | 2017-04-11 | Chdi Foundation, Inc. | Histone deacetylase inhibitors and compositions and methods of use thereof |
| HK1220407A1 (zh) * | 2013-03-14 | 2017-05-05 | Chdi Foundation, Inc. | 组蛋白去乙酰酶抑制剂,其组合物及其使用方法 |
| DK2970139T3 (en) | 2013-03-15 | 2018-08-13 | Biomarin Pharm Inc | HDAC inhibitors |
| PT2994465T (pt) | 2013-05-10 | 2018-10-25 | Karus Therapeutics Ltd | Novos inibidores de histona desacetilase |
| KR20170012404A (ko) * | 2014-06-02 | 2017-02-02 | 씨에이치디아이 파운데이션, 인코포레이티드 | 히스톤 데아세틸라제 억제제 및 그것의 조성물 및 사용 방법 |
| GB201419228D0 (en) * | 2014-10-29 | 2014-12-10 | Karus Therapeutics Ltd | Compounds |
| US10723705B2 (en) | 2015-08-14 | 2020-07-28 | Incyte Corporation | Heterocyclic compounds and uses thereof |
| CN109096272B (zh) * | 2018-09-27 | 2021-04-02 | 沈阳药科大学 | 一种具有抗肿瘤活性的吲哚异羟肟酸类化合物及其应用 |
| CN110003102B (zh) * | 2019-05-16 | 2022-03-22 | 河南师范大学 | (R)-2-(α-氘-α-烷基-α-芳香)氮杂芳基化合物及其制备方法和应用 |
| CN116710448B (zh) * | 2021-01-20 | 2025-05-16 | 莱托克斯有限公司 | 被保护的hdac(组蛋白脱乙酰酶)抑制剂 |
| CN113045550A (zh) * | 2021-03-12 | 2021-06-29 | 深圳济康医药科技有限公司 | 一种三氮唑类衍生物及其制备方法和应用 |
| US20250074907A1 (en) * | 2021-12-22 | 2025-03-06 | The Texas A&M University System | Inhibitors of sars-cov-2 |
| CN116535343B (zh) * | 2022-03-08 | 2026-02-17 | 温州医科大学 | 异羟肟酸类化合物及其应用 |
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| DD242802A1 (de) * | 1983-02-28 | 1987-02-11 | Univ Berlin Humboldt | Verfahren zur herstellung neuer w(2'-naphthoxy)-hydroxamsaeuren enthaltende pharmazeutische zubereitungen und ihren salzen |
| FR2677984B1 (fr) * | 1991-06-21 | 1994-02-25 | Elf Sanofi | Derives d'imidazoline n-substitues, leur preparation, les compositions pharmaceutiques en contenant. |
| US6376506B1 (en) | 1997-01-23 | 2002-04-23 | Syntex (U.S.A.) Llc | Sulfamide-metalloprotease inhibitors |
| US6197791B1 (en) * | 1997-02-27 | 2001-03-06 | American Cyanamid Company | N-hdroxy-2-(alkyl, aryl, or heteroaryl, sulfanyl, sulfinyl or sulfonyl)-3-substituted alkyl, aryl or heteroarylamides as matrix metalloproteinase inhibitors |
| US6403632B1 (en) * | 2000-03-01 | 2002-06-11 | Bristol Myers Squibb Pharma Co | Lactam metalloprotease inhibitors |
| ZA988967B (en) | 1997-10-03 | 2000-04-03 | Du Pont Pharm Co | Lactam metalloprotease inhibitors. |
| EP1165546A2 (fr) * | 1999-04-02 | 2002-01-02 | Du Pont Pharmaceuticals Company | Nouveaux inhibiteurs de lactame de metalloproteases matricielles, de tnf-alpha, et de l'aggrecanase |
| AU4249700A (en) | 1999-04-19 | 2000-11-02 | Sumitomo Pharmaceuticals Company, Limited | Hydroxamic acid derivative |
| EP1748046A3 (fr) * | 1999-11-23 | 2007-08-22 | Methylgene, Inc. | Inhibiteurs d'histone déacetylase |
| JP2003519119A (ja) * | 1999-12-24 | 2003-06-17 | スミスクライン ビーチャム パブリック リミテッド カンパニー | (ヘテロ)ビシクリルメタンスルホニルアミノ置換ヒドロキサム酸誘導体 |
| ES2228906T3 (es) * | 2000-07-18 | 2005-04-16 | Leo Pharma A/S | Inhibidores de la metaloproteinasas de matriz. |
| PE20020354A1 (es) * | 2000-09-01 | 2002-06-12 | Novartis Ag | Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda) |
| NZ532463A (en) | 2001-11-13 | 2007-02-23 | Dimensional Pharm Inc | Substituted 1,4-benzodiazepines and uses thereof for the treatment of cancer |
| US20030225054A1 (en) * | 2002-06-03 | 2003-12-04 | Jingwu Duan | Combined use of tace inhibitors and COX2 inhibitors as anti-inflammatory agents |
| US8022092B2 (en) * | 2005-12-14 | 2011-09-20 | Medivir Ab | (2,5-dioxoimidazolidin-1-yl)-N-hydroxy-acetamides as metalloproteinase inhibitors |
| CN105481788A (zh) | 2006-10-28 | 2016-04-13 | 梅特希尔基因公司 | 组蛋白脱乙酰酶抑制剂 |
| MX2009006542A (es) * | 2006-12-19 | 2009-06-30 | Methylgene Inc | Inhibidores de histona desacetilasa y sus profarmacos. |
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2008
- 2008-04-09 WO PCT/CA2008/000631 patent/WO2008122115A1/fr not_active Ceased
- 2008-04-09 AU AU2008235212A patent/AU2008235212B2/en not_active Ceased
- 2008-04-09 TW TW097112879A patent/TWI539947B/zh not_active IP Right Cessation
- 2008-04-09 US US12/100,200 patent/US9096565B2/en active Active
- 2008-04-09 CA CA2683557A patent/CA2683557C/fr not_active Expired - Fee Related
- 2008-04-09 EP EP08748100.8A patent/EP2139850B1/fr active Active
- 2008-04-09 JP JP2010502392A patent/JP5746860B2/ja active Active
- 2008-04-09 KR KR1020097023348A patent/KR101561292B1/ko not_active Expired - Fee Related
- 2008-04-09 CN CN200880019410A patent/CN101679220A/zh active Pending
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2009
- 2009-09-22 ZA ZA200906609A patent/ZA200906609B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2139850A4 (fr) | 2011-07-20 |
| WO2008122115A1 (fr) | 2008-10-16 |
| JP2010523601A (ja) | 2010-07-15 |
| KR20100016351A (ko) | 2010-02-12 |
| US20090181943A1 (en) | 2009-07-16 |
| CA2683557A1 (fr) | 2008-10-16 |
| AU2008235212B2 (en) | 2014-01-16 |
| JP5746860B2 (ja) | 2015-07-08 |
| EP2139850B1 (fr) | 2018-09-12 |
| CN101679220A (zh) | 2010-03-24 |
| EP2139850A1 (fr) | 2010-01-06 |
| TWI539947B (zh) | 2016-07-01 |
| US9096565B2 (en) | 2015-08-04 |
| AU2008235212A1 (en) | 2008-10-16 |
| CA2683557C (fr) | 2016-10-18 |
| TW200845966A (en) | 2008-12-01 |
| KR101561292B1 (ko) | 2015-10-19 |
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