JP2013528182A5 - - Google Patents
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- Publication number
- JP2013528182A5 JP2013528182A5 JP2013512261A JP2013512261A JP2013528182A5 JP 2013528182 A5 JP2013528182 A5 JP 2013528182A5 JP 2013512261 A JP2013512261 A JP 2013512261A JP 2013512261 A JP2013512261 A JP 2013512261A JP 2013528182 A5 JP2013528182 A5 JP 2013528182A5
- Authority
- JP
- Japan
- Prior art keywords
- cycloalkyl
- alkyl
- heterocycloalkyl
- independently
- heteroaryl
- 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.)
- Granted
Links
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 73
- 125000000217 alkyl group Chemical group 0.000 claims description 68
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 67
- 229910052739 hydrogen Inorganic materials 0.000 claims description 28
- 229910052799 carbon Inorganic materials 0.000 claims description 27
- 125000001072 heteroaryl group Chemical group 0.000 claims description 27
- 125000003118 aryl group Chemical group 0.000 claims description 26
- 125000001475 halogen functional group Chemical group 0.000 claims description 24
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 18
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 18
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 8
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 3
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 10
- 241000023320 Luma <angiosperm> Species 0.000 claims 7
- -1 cycloalkyl luma Chemical compound 0.000 claims 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 claims 1
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims 1
- 102000003964 Histone deacetylase Human genes 0.000 claims 1
- 108090000353 Histone deacetylase Proteins 0.000 claims 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 1
- 239000002246 antineoplastic agent Substances 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 125000005349 heteroarylcycloalkyl group Chemical group 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
- 0 *C(*)([C@@](C=C*)OC([C@](*)(N(*)C(C(*)(*)N(*)C(C1=CC=CC=CCC(C(*)(*)N2*)=C1)=O)=O)I)=O)C2=O Chemical compound *C(*)([C@@](C=C*)OC([C@](*)(N(*)C(C(*)(*)N(*)C(C1=CC=CC=CCC(C(*)(*)N2*)=C1)=O)=O)I)=O)C2=O 0.000 description 2
- 229940002612 prodrug Drugs 0.000 description 1
- 239000000651 prodrug Substances 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US34897810P | 2010-05-27 | 2010-05-27 | |
| US61/348,978 | 2010-05-27 | ||
| PCT/US2011/038246 WO2011150283A1 (en) | 2010-05-27 | 2011-05-26 | Macrocyclic compounds useful as inhibitors of histone deacetylases |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013528182A JP2013528182A (ja) | 2013-07-08 |
| JP2013528182A5 true JP2013528182A5 (OSRAM) | 2014-06-26 |
| JP5931850B2 JP5931850B2 (ja) | 2016-06-08 |
Family
ID=45004403
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013512261A Active JP5931850B2 (ja) | 2010-05-27 | 2011-05-26 | ヒストンデアセチラーゼの阻害剤として有用な大環状化合物 |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US8754050B2 (OSRAM) |
| EP (1) | EP2575467B1 (OSRAM) |
| JP (1) | JP5931850B2 (OSRAM) |
| KR (2) | KR102028850B1 (OSRAM) |
| CN (1) | CN102946732B (OSRAM) |
| AU (1) | AU2011258110B2 (OSRAM) |
| BR (1) | BR112012030193B1 (OSRAM) |
| CA (1) | CA2800958C (OSRAM) |
| DK (1) | DK2575467T3 (OSRAM) |
| ES (1) | ES2594500T3 (OSRAM) |
| HU (1) | HUE030812T2 (OSRAM) |
| LT (1) | LT2575467T (OSRAM) |
| MX (1) | MX2012013507A (OSRAM) |
| PL (1) | PL2575467T3 (OSRAM) |
| PT (1) | PT2575467T (OSRAM) |
| RU (1) | RU2565076C2 (OSRAM) |
| WO (1) | WO2011150283A1 (OSRAM) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102391359B (zh) * | 2011-11-17 | 2014-07-16 | 南京优科生物医药研究有限公司 | 组蛋白去乙酰化酶抑制剂及其合成方法和制药用途 |
| CN103232474A (zh) * | 2013-04-16 | 2013-08-07 | 中国药科大学 | 组蛋白去乙酰化酶抑制剂 |
| CN106800589B (zh) * | 2013-09-02 | 2021-01-12 | 李铁旦 | 一类环肽类化合物、其制备方法、药物组合物及用途 |
| PT3148540T (pt) * | 2014-05-27 | 2020-03-31 | Onkure Inc | PROCESSO PARA A PREPARAÇAÞO DE DEPSIPÉPTIDOS CIìCLICOS |
| JP6785801B2 (ja) * | 2015-03-06 | 2020-11-18 | コロラド ステート ユニバーシティー リサーチ ファウンデーション | 新しいキャップ基ラルガゾールの類似体の合成及び使用 |
| WO2016144665A1 (en) * | 2015-03-06 | 2016-09-15 | Colorado State University Research Foundation | Method for preparing largazole analogs and uses thereof |
| CN105131082A (zh) * | 2015-09-17 | 2015-12-09 | 广州康缔安生物科技有限公司 | 环肽类化合物及其应用 |
| CN106674252B (zh) * | 2015-11-11 | 2019-10-29 | 复旦大学 | 海洋天然产物环酯肽的氟代烯烃类似物、其制备方法和用途 |
| HK1250948A1 (zh) * | 2016-05-20 | 2019-01-18 | 恩库勒公司 | 作为组蛋白脱乙酰酶抑制剂的大环硫代酸酯前体药物 |
| CN107286223B (zh) * | 2017-07-17 | 2019-12-20 | 湖北大学 | 一种用于检测组蛋白位点乙酰化的重组蛋白及其应用 |
| CN111269245B (zh) * | 2018-12-04 | 2021-08-27 | 杭州百新生物医药科技有限公司 | 一种环状氨基嘧啶衍生物及其抑制激酶的活性和用途 |
| US20220017520A1 (en) * | 2018-12-19 | 2022-01-20 | Keythera (Suzhou) Pharmaceuticals Co. Ltd. | Macrocyclic compound as cdk inhibitor, preparation method therefor, and use thereof in medicine |
| WO2020190827A1 (en) * | 2019-03-21 | 2020-09-24 | Merck Sharp & Dohme Corp. | Inhibitors of histone deacetylase useful for the treatment or prevention of hiv infection |
| KR102436309B1 (ko) * | 2020-05-26 | 2022-08-25 | 연세대학교 산학협력단 | 암의 예방 또는 치료용 약학적 조성물 |
| US12227522B2 (en) | 2020-12-21 | 2025-02-18 | Colorado State University Research Foundation | Synthesis of structural analogs of largazole and associated compounds |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8920304D0 (en) | 1989-09-08 | 1989-10-25 | Fujisawa Pharmaceutical Co | Fr901375 substance and preparation thereof |
| WO2004020460A1 (ja) * | 2002-08-30 | 2004-03-11 | Yamanouchi Pharmaceutical Co., Ltd. | 新規なデプシペプチド化合物 |
| US20070088045A1 (en) * | 2002-11-12 | 2007-04-19 | Hellberg Peggy E | Histone deacetylase inhibitors for treating degenerative diseases of the eye |
| US20060128660A1 (en) * | 2004-12-10 | 2006-06-15 | Wisconsin Alumni Research Foundation | FK228 analogs and methods of making and using the same |
| JP5178731B2 (ja) * | 2006-11-22 | 2013-04-10 | カルス セラピューティクス リミテッド | デプシペプチドおよびその治療的使用 |
| GB0623388D0 (en) * | 2006-11-23 | 2007-01-03 | Univ Southampton | Chemical compounds |
| GB0715750D0 (en) * | 2007-08-13 | 2007-09-19 | Karus Therapeutics Ltd | Chemical compounds |
| WO2009126315A2 (en) | 2008-04-11 | 2009-10-15 | University Of Florida Research Foundation, Inc. | Macrocyclic compounds and methods of treatment |
| US8217076B2 (en) * | 2008-07-17 | 2012-07-10 | Colorado State University Research Foundation | Method for preparing largazole analogs and uses thereof |
| CN102391359B (zh) * | 2011-11-17 | 2014-07-16 | 南京优科生物医药研究有限公司 | 组蛋白去乙酰化酶抑制剂及其合成方法和制药用途 |
-
2011
- 2011-05-26 BR BR112012030193-4A patent/BR112012030193B1/pt active IP Right Grant
- 2011-05-26 PL PL11787462T patent/PL2575467T3/pl unknown
- 2011-05-26 MX MX2012013507A patent/MX2012013507A/es unknown
- 2011-05-26 HU HUE11787462A patent/HUE030812T2/en unknown
- 2011-05-26 LT LTEP11787462.8T patent/LT2575467T/lt unknown
- 2011-05-26 JP JP2013512261A patent/JP5931850B2/ja active Active
- 2011-05-26 KR KR1020187018653A patent/KR102028850B1/ko active Active
- 2011-05-26 CN CN201180030608.3A patent/CN102946732B/zh active Active
- 2011-05-26 US US13/700,373 patent/US8754050B2/en active Active
- 2011-05-26 AU AU2011258110A patent/AU2011258110B2/en active Active
- 2011-05-26 WO PCT/US2011/038246 patent/WO2011150283A1/en not_active Ceased
- 2011-05-26 CA CA2800958A patent/CA2800958C/en active Active
- 2011-05-26 PT PT117874628T patent/PT2575467T/pt unknown
- 2011-05-26 RU RU2012157293/04A patent/RU2565076C2/ru active
- 2011-05-26 DK DK11787462.8T patent/DK2575467T3/en active
- 2011-05-26 ES ES11787462.8T patent/ES2594500T3/es active Active
- 2011-05-26 KR KR1020127033908A patent/KR20130123301A/ko not_active Abandoned
- 2011-05-26 EP EP11787462.8A patent/EP2575467B1/en active Active
-
2014
- 2014-05-29 US US14/289,877 patent/US9422340B2/en active Active
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