JP2011528662A - ホジキン病の治療のためのhdac阻害剤の使用 - Google Patents
ホジキン病の治療のためのhdac阻害剤の使用 Download PDFInfo
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- JP2011528662A JP2011528662A JP2011518898A JP2011518898A JP2011528662A JP 2011528662 A JP2011528662 A JP 2011528662A JP 2011518898 A JP2011518898 A JP 2011518898A JP 2011518898 A JP2011518898 A JP 2011518898A JP 2011528662 A JP2011528662 A JP 2011528662A
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- aryl
- alkyl
- heteroaryl
- cycloalkyl
- heterocycloalkyl
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- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
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- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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| US8180508P | 2008-07-18 | 2008-07-18 | |
| US61/081,805 | 2008-07-18 | ||
| PCT/US2009/050768 WO2010009280A1 (en) | 2008-07-18 | 2009-07-16 | Use of hdac inhibitors for the treatment of hodgkin's disease |
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| KR102020939B1 (ko) * | 2011-07-07 | 2019-09-11 | 리서치 캔서 인스티튜트 오브 아메리카 | 암 치료 시스템, 방법 및 제형 |
| US8933078B2 (en) | 2011-07-14 | 2015-01-13 | Research Cancer Institute Of America | Method of treating cancer with combinations of histone deacetylase inhibitors (HDAC1) substances |
| WO2018157081A1 (en) | 2017-02-27 | 2018-08-30 | Research Cancer Institute Of America | Compositions, methods, systems and/or kits for preventing and/or treating neoplasms |
| US11369585B2 (en) | 2017-03-17 | 2022-06-28 | Research Cancer Institute Of America | Compositions, methods, systems and/or kits for preventing and/or treating neoplasms |
| CN109705057B (zh) * | 2017-10-25 | 2023-05-30 | 成都先导药物开发股份有限公司 | 组蛋白去乙酰化酶抑制剂及其制备方法与用途 |
| EP3710434A4 (en) | 2017-11-17 | 2021-07-28 | Research Cancer Institute of America | COMPOSITIONS, METHODS, SYSTEMS AND / OR KITS FOR THE PREVENTION AND / OR TREATMENT OF NEOPLASMS |
| US20220387604A1 (en) * | 2019-11-06 | 2022-12-08 | Dana-Farber Cancer Institute, Inc. | Selective dual histone deacetylase 6/8 (hdac6/8) degraders and methods of use thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004509105A (ja) * | 2000-09-01 | 2004-03-25 | ノバルティス アクチエンゲゼルシャフト | デアセチラーゼ阻害剤として有用なヒドロキサム酸誘導体 |
| WO2008002862A1 (en) * | 2006-06-26 | 2008-01-03 | Novartis Ag | Organic compounds |
| WO2008070011A2 (en) * | 2006-12-04 | 2008-06-12 | Novartis Ag | Combination of an hdac inhibitor and an antimetabolite |
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- 2009-07-16 CA CA2730738A patent/CA2730738A1/en not_active Abandoned
- 2009-07-16 AU AU2009270886A patent/AU2009270886A1/en not_active Abandoned
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Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004509105A (ja) * | 2000-09-01 | 2004-03-25 | ノバルティス アクチエンゲゼルシャフト | デアセチラーゼ阻害剤として有用なヒドロキサム酸誘導体 |
| WO2008002862A1 (en) * | 2006-06-26 | 2008-01-03 | Novartis Ag | Organic compounds |
| WO2008070011A2 (en) * | 2006-12-04 | 2008-06-12 | Novartis Ag | Combination of an hdac inhibitor and an antimetabolite |
Non-Patent Citations (6)
| Title |
|---|
| JPN5011009432; REVILL P: 'PANOBINOSTAT: HISTONE DEACETYLASE (HDAC) INHIBITOR APOPTOSIS INDUCER ONCOLYTIC' DRUGS OF THE FUTURE V32 N4, 20070101, P315-322, PROUS SCIENCE * |
| JPN6013046733; Bhalla S, et al.: 'The Broad Spectrum HDAC Inhibitor PCI-24781 Induces Caspase- and ROS-Dependent Apoptosis and is Syne' Nature precedings, [online] , 20080712 * |
| JPN6013046735; O'Connor, OA: 'Clinical experience with the novel histone deacetylase inhibitor vorinostat (suberoylanilide hydroxa' British Journla of Cancer Vol.95, 2006, p.S7-S12 * |
| JPN6013046736; Viviani S, et al.: 'Phase II study of the histone-deacetylase inhibitor ITF2357 in relapsed/refractory Hodgkin's lympho' Journal of Clinical Oncology, 2008 ASCO Annual Meeting Proceedings (Post-Meeting Edition), [online] Vol.26, No.15S, 20080520, 8532 * |
| JPN6013046738; Bociek RG, et al.: 'Isotype-selective histone deacetylase (HDAC) inhibitor MGCD0103 demonstrates clinical activity and s' Journal of Clinical Oncology, 2008 ASCO Annual Meeting Proceedings (Post-Meeting Edition), [online] Vol.26, No.15S, 20080520, 8507 * |
| JPN7013003503; Spencer, A, et al.: 'ORAL PANOBINOSTAT (LBH589), A NOVEL DEACETYLASEINHIBITOR (DACI), DEMONSTRATES CLINICAL ACTIVITY INRE' Annuals of Oncology Vol.19, Suppl.4, 200806, p.iv128 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102099021A (zh) | 2011-06-15 |
| CL2011000100A1 (es) | 2011-07-01 |
| WO2010009280A1 (en) | 2010-01-21 |
| AU2009270886A1 (en) | 2010-01-21 |
| TW201006470A (en) | 2010-02-16 |
| ZA201100165B (en) | 2011-09-28 |
| US20110118309A1 (en) | 2011-05-19 |
| MX2011000719A (es) | 2011-03-01 |
| IL210489A0 (en) | 2011-03-31 |
| KR20110031980A (ko) | 2011-03-29 |
| EP2306996A1 (en) | 2011-04-13 |
| MA32482B1 (fr) | 2011-07-03 |
| BRPI0915927A2 (pt) | 2016-06-07 |
| CA2730738A1 (en) | 2010-01-21 |
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