JP2013518050A5 - - Google Patents
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- JP2013518050A5 JP2013518050A5 JP2012550137A JP2012550137A JP2013518050A5 JP 2013518050 A5 JP2013518050 A5 JP 2013518050A5 JP 2012550137 A JP2012550137 A JP 2012550137A JP 2012550137 A JP2012550137 A JP 2012550137A JP 2013518050 A5 JP2013518050 A5 JP 2013518050A5
- Authority
- JP
- Japan
- Prior art keywords
- optionally substituted
- heteroaryl
- aryl
- ring
- alkyl
- 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.)
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- 125000001072 heteroaryl group Chemical group 0.000 claims description 120
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 60
- 125000003107 substituted aryl group Chemical group 0.000 claims description 60
- 125000003118 aryl group Chemical group 0.000 claims description 45
- 125000000623 heterocyclic group Chemical group 0.000 claims description 45
- 125000000217 alkyl group Chemical group 0.000 claims description 30
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 30
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 30
- 125000002252 acyl group Chemical group 0.000 claims description 15
- 125000003342 alkenyl group Chemical group 0.000 claims description 15
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 15
- 125000002619 bicyclic group Chemical group 0.000 claims description 15
- 125000002837 carbocyclic group Chemical group 0.000 claims description 15
- 125000001188 haloalkyl group Chemical group 0.000 claims description 15
- 125000005309 thioalkoxy group Chemical group 0.000 claims description 15
- 150000002148 esters Chemical class 0.000 claims description 12
- 229940002612 prodrug Drugs 0.000 claims description 12
- 239000000651 prodrug Substances 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 12
- 208000034578 Multiple myelomas Diseases 0.000 claims description 7
- 206010035226 Plasma cell myeloma Diseases 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- 102000003964 Histone deacetylase Human genes 0.000 claims description 6
- 108090000353 Histone deacetylase Proteins 0.000 claims description 6
- 230000002401 inhibitory effect Effects 0.000 claims description 5
- 102100022537 Histone deacetylase 6 Human genes 0.000 claims description 2
- 101000899330 Homo sapiens Histone deacetylase 6 Proteins 0.000 claims description 2
- WWGBHDIHIVGYLZ-UHFFFAOYSA-N N-[4-[3-[[[7-(hydroxyamino)-7-oxoheptyl]amino]-oxomethyl]-5-isoxazolyl]phenyl]carbamic acid tert-butyl ester Chemical compound C1=CC(NC(=O)OC(C)(C)C)=CC=C1C1=CC(C(=O)NCCCCCCC(=O)NO)=NO1 WWGBHDIHIVGYLZ-UHFFFAOYSA-N 0.000 claims description 2
- 201000010099 disease Diseases 0.000 claims description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 2
- 230000000694 effects Effects 0.000 claims description 2
- 230000001404 mediated effect Effects 0.000 claims description 2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US33646010P | 2010-01-22 | 2010-01-22 | |
| US61/336,460 | 2010-01-22 | ||
| PCT/US2011/021982 WO2011091213A2 (en) | 2010-01-22 | 2011-01-21 | Reverse amide compounds as protein deacetylase inhibitors and methods of use thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016100346A Division JP2016153425A (ja) | 2010-01-22 | 2016-05-19 | タンパク質デアセチラーゼ阻害剤としてのリバースアミド化合物とその使用方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013518050A JP2013518050A (ja) | 2013-05-20 |
| JP2013518050A5 true JP2013518050A5 (OSRAM) | 2016-05-12 |
| JP5940984B2 JP5940984B2 (ja) | 2016-06-29 |
Family
ID=44307593
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012550137A Active JP5940984B2 (ja) | 2010-01-22 | 2011-01-21 | タンパク質デアセチラーゼ阻害剤としてのリバースアミド化合物とその使用方法 |
| JP2016100346A Pending JP2016153425A (ja) | 2010-01-22 | 2016-05-19 | タンパク質デアセチラーゼ阻害剤としてのリバースアミド化合物とその使用方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016100346A Pending JP2016153425A (ja) | 2010-01-22 | 2016-05-19 | タンパク質デアセチラーゼ阻害剤としてのリバースアミド化合物とその使用方法 |
Country Status (28)
| Country | Link |
|---|---|
| US (7) | US8394810B2 (OSRAM) |
| EP (2) | EP3091004B1 (OSRAM) |
| JP (2) | JP5940984B2 (OSRAM) |
| KR (1) | KR101808874B1 (OSRAM) |
| CN (3) | CN102933558B (OSRAM) |
| AU (1) | AU2016213729A1 (OSRAM) |
| BR (1) | BR112012018246B1 (OSRAM) |
| CA (1) | CA2787756C (OSRAM) |
| CL (1) | CL2012002026A1 (OSRAM) |
| CY (1) | CY1118156T1 (OSRAM) |
| DK (1) | DK2526093T3 (OSRAM) |
| EA (1) | EA026514B1 (OSRAM) |
| ES (1) | ES2592278T3 (OSRAM) |
| HR (1) | HRP20161367T1 (OSRAM) |
| HU (1) | HUE030679T2 (OSRAM) |
| LT (1) | LT2526093T (OSRAM) |
| MX (1) | MX2012008553A (OSRAM) |
| NZ (1) | NZ601655A (OSRAM) |
| PH (1) | PH12012501492B1 (OSRAM) |
| PL (1) | PL2526093T3 (OSRAM) |
| PT (1) | PT2526093T (OSRAM) |
| RS (1) | RS55227B1 (OSRAM) |
| SG (2) | SG10201500444TA (OSRAM) |
| SI (1) | SI2526093T1 (OSRAM) |
| SM (1) | SMT201600382B (OSRAM) |
| TW (3) | TWI600638B (OSRAM) |
| WO (1) | WO2011091213A2 (OSRAM) |
| ZA (1) | ZA201206063B (OSRAM) |
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| EP3067346A1 (en) | 2010-11-16 | 2016-09-14 | Acetylon Pharmaceuticals, Inc. | Pyrimidine hydroxy amide compounds as protein deacetylase inhibitors and methods of use thereof |
| WO2012117421A1 (en) | 2011-03-02 | 2012-09-07 | Orchid Research Laboratories Ltd | Histone deacetylase inhibitors |
| FR2975911A1 (fr) * | 2011-06-06 | 2012-12-07 | Univ Strasbourg | Bisacodyl et analogues comme medicaments destines au traitement du cancer |
| WO2013013113A2 (en) * | 2011-07-20 | 2013-01-24 | The General Hospital Corporation | Histone deacetylase 6 selective inhibitors for the treatment of bone disease |
| KR101359571B1 (ko) | 2011-10-06 | 2014-02-10 | 서울대학교산학협력단 | Ｈｄａｃ 저해제와 알파칼슘설페이트를 유효성분으로 함유하는 치주질환 예방 및 치료용 약학적 조성물 |
| EP2827869A4 (en) | 2012-03-23 | 2015-09-23 | Dennis Brown | COMPOSITIONS AND METHODS FOR IMPROVING THE THERAPEUTIC BENEFIT OF INDIRUBIN AND ANALOGUE THEREOF, WITH MEISOINDIGO |
| HK1207403A1 (en) * | 2012-04-19 | 2016-01-29 | Acetylon Pharmaceuticals, Inc. | Biomarkers to identify patients that will respond to treatment and treating such patients |
| US9145412B2 (en) | 2012-11-02 | 2015-09-29 | Acetylon Pharmaceuticals, Inc. | Selective HDAC1 and HDAC2 inhibitors |
| 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 |
| ES2818933T3 (es) * | 2013-10-10 | 2021-04-14 | Acetylon Pharmaceuticals Inc | Inhibidores de la HDAC en combinación con los inhibidores de la pi3k, para el tratamiento del linfoma no Hodgkin |
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| JP2016536354A (ja) * | 2013-10-10 | 2016-11-24 | 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． | 非ホジキンリンパ腫を治療するための、ｈｄａｃ阻害剤単独またはｂｔｋ阻害剤との組み合わせ |
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| US9464073B2 (en) | 2014-02-26 | 2016-10-11 | Acetylon Pharmaceuticals, Inc. | Pyrimidine hydroxy amide compounds as HDAC6 selective inhibitors |
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| US9840520B2 (en) * | 2014-05-14 | 2017-12-12 | The Regents Of The University Of Colorado, A Body Corporate | Heterocyclic hydroxamic acids as protein deacetylase inhibitors and dual protein deacetylase-protein kinase inhibitors and methods of use thereof |
| EA201790142A1 (ru) * | 2014-07-07 | 2017-07-31 | Эситайлон Фармасьютикалз, Инк. | Лечение лейкоза ингибиторами гистондеацетилазы |
| AU2015356779A1 (en) * | 2014-12-05 | 2017-07-13 | University of Modena and Reggio Emilia | Combinations of histone deacetylase inhibitors and bendamustine for use in the treatment of lymphoma |
| EP3292113B1 (en) | 2014-12-12 | 2020-07-08 | Regenacy Pharmaceuticals, LLC | Piperidine derivatives as hdac1/2 inhibitors |
| US10183934B2 (en) | 2015-02-02 | 2019-01-22 | Forma Therapeutics, Inc. | Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors |
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| US10421778B2 (en) | 2015-05-05 | 2019-09-24 | Washington University | Isoform-selective lysine deacetylase inhibitors |
| HUE049645T2 (hu) | 2015-05-22 | 2020-09-28 | Chong Kun Dang Pharmaceutical Corp | Heterocikloalkil-származékok vegyületek mint szelektív hiszton deacetiláz inhibitorok és ezeket tartalmazó gyógyszerkészítmények |
| US10272084B2 (en) | 2015-06-01 | 2019-04-30 | Regenacy Pharmaceuticals, Llc | Histone deacetylase 6 selective inhibitors for the treatment of cisplatin-induced peripheral neuropathy |
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| CN105017135A (zh) * | 2015-07-19 | 2015-11-04 | 佛山市赛维斯医药科技有限公司 | 一类二吡啶叔醇结构的11β-HSD1抑制剂、制备方法及其用途 |
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| KR102685058B1 (ko) | 2020-09-02 | 2024-07-15 | 주식회사 종근당 | 히스톤 탈아세틸화효소 6 억제제로서의 새로운 구조의 화합물 및 이를 포함하는 약제학적 조성물 |
| CN114621754A (zh) * | 2022-04-18 | 2022-06-14 | 武汉轻工大学 | 一种荧光探针的制备及其在组蛋白去乙酰化酶中的应用 |
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| KR20240035172A (ko) | 2022-09-08 | 2024-03-15 | 주식회사 종근당 | 히스톤 탈아세틸화효소 6 억제제로서의 1,3,4-옥사다이아졸 유도체 화합물 및 이의 용도 |
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| KR20240133645A (ko) | 2023-02-28 | 2024-09-04 | 주식회사 종근당 | 옥사다이아졸 유도체 화합물 및 이를 포함하는 약제학적 조성물 |
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