JP2015510886A5 - - Google Patents
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- Publication number
- JP2015510886A5 JP2015510886A5 JP2014561101A JP2014561101A JP2015510886A5 JP 2015510886 A5 JP2015510886 A5 JP 2015510886A5 JP 2014561101 A JP2014561101 A JP 2014561101A JP 2014561101 A JP2014561101 A JP 2014561101A JP 2015510886 A5 JP2015510886 A5 JP 2015510886A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- hydroxy
- substituted
- compound according
- aryl
- 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
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- 150000001875 compounds Chemical class 0.000 claims 24
- -1 C 1 -C 5 alkyl Chemical group 0.000 claims 17
- 125000003118 aryl group Chemical group 0.000 claims 16
- 125000001072 heteroaryl group Chemical group 0.000 claims 15
- 229910052739 hydrogen Inorganic materials 0.000 claims 13
- 125000001475 halogen functional group Chemical group 0.000 claims 12
- 239000001257 hydrogen Substances 0.000 claims 12
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 12
- 125000000217 alkyl group Chemical group 0.000 claims 11
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims 8
- 150000002431 hydrogen Chemical class 0.000 claims 8
- 125000003396 thiol group Chemical class [H]S* 0.000 claims 8
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 6
- 239000003112 inhibitor Substances 0.000 claims 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 125000004650 C1-C8 alkynyl group Chemical group 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 125000001188 haloalkyl group Chemical group 0.000 claims 3
- 125000004464 hydroxyphenyl group Chemical group 0.000 claims 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 3
- 125000004076 pyridyl group Chemical group 0.000 claims 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 125000005189 alkyl hydroxy group Chemical group 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 claims 2
- GOVYBPLHWIEHEJ-UHFFFAOYSA-N tubastatin A Chemical group C1N(C)CCC2=C1C1=CC=CC=C1N2CC1=CC=C(C(=O)NO)C=C1 GOVYBPLHWIEHEJ-UHFFFAOYSA-N 0.000 claims 2
- 229940122617 Histone deacetylase 6 inhibitor Drugs 0.000 claims 1
- 208000025205 Mantle-Cell Lymphoma Diseases 0.000 claims 1
- BHUZLJOUHMBZQY-YXQOSMAKSA-N N-[4-[(2R,4R,6S)-4-[[(4,5-diphenyl-2-oxazolyl)thio]methyl]-6-[4-(hydroxymethyl)phenyl]-1,3-dioxan-2-yl]phenyl]-N'-hydroxyoctanediamide Chemical compound C1=CC(CO)=CC=C1[C@H]1O[C@@H](C=2C=CC(NC(=O)CCCCCCC(=O)NO)=CC=2)O[C@@H](CSC=2OC(=C(N=2)C=2C=CC=CC=2)C=2C=CC=CC=2)C1 BHUZLJOUHMBZQY-YXQOSMAKSA-N 0.000 claims 1
- 102000004495 STAT3 Transcription Factor Human genes 0.000 claims 1
- 108010017324 STAT3 Transcription Factor Proteins 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- GXJABQQUPOEUTA-RDJZCZTQSA-N bortezomib Chemical compound C([C@@H](C(=O)N[C@@H](CC(C)C)B(O)O)NC(=O)C=1N=CC=NC=1)C1=CC=CC=C1 GXJABQQUPOEUTA-RDJZCZTQSA-N 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 229940121372 histone deacetylase inhibitor Drugs 0.000 claims 1
- 239000003276 histone deacetylase inhibitor Substances 0.000 claims 1
- 229960005386 ipilimumab Drugs 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 201000001441 melanoma Diseases 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 229940099039 velcade Drugs 0.000 claims 1
- GPXBXXGIAQBQNI-UHFFFAOYSA-N vemurafenib Chemical compound CCCS(=O)(=O)NC1=CC=C(F)C(C(=O)C=2C3=CC(=CN=C3NC=2)C=2C=CC(Cl)=CC=2)=C1F GPXBXXGIAQBQNI-UHFFFAOYSA-N 0.000 claims 1
- 229960003862 vemurafenib Drugs 0.000 claims 1
Applications Claiming Priority (15)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261607803P | 2012-03-07 | 2012-03-07 | |
| US61/607,803 | 2012-03-07 | ||
| US201261618150P | 2012-03-30 | 2012-03-30 | |
| US61/618,150 | 2012-03-30 | ||
| US201261648946P | 2012-05-18 | 2012-05-18 | |
| US61/648,946 | 2012-05-18 | ||
| US201261651595P | 2012-05-25 | 2012-05-25 | |
| US201261651896P | 2012-05-25 | 2012-05-25 | |
| US61/651,896 | 2012-05-25 | ||
| US61/651,595 | 2012-05-25 | ||
| US201261674942P | 2012-07-24 | 2012-07-24 | |
| US61/674,942 | 2012-07-24 | ||
| US201261715379P | 2012-10-18 | 2012-10-18 | |
| US61/715,379 | 2012-10-18 | ||
| PCT/US2013/029521 WO2013134467A1 (en) | 2012-03-07 | 2013-03-07 | Selective histone deactylase 6 inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015510886A JP2015510886A (ja) | 2015-04-13 |
| JP2015510886A5 true JP2015510886A5 (enExample) | 2016-05-19 |
| JP6233812B2 JP6233812B2 (ja) | 2017-11-22 |
Family
ID=49117326
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014561101A Expired - Fee Related JP6233812B2 (ja) | 2012-03-07 | 2013-03-07 | 選択的ヒストンデアセチラーゼ6阻害剤 |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP2822926A4 (enExample) |
| JP (1) | JP6233812B2 (enExample) |
| AU (1) | AU2013230881A1 (enExample) |
| CA (1) | CA2866707A1 (enExample) |
| WO (1) | WO2013134467A1 (enExample) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ724030A (en) | 2014-03-12 | 2017-09-29 | Chong Kun Dang Pharmaceutical Corp | Novel compounds as histone deacetylase 6 inhibitors and pharmaceutical compositions comprising the same |
| US10016421B2 (en) | 2014-04-05 | 2018-07-10 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Histone deacetylase 6 inhibition for enhancing T-cell function during anti-tumor response and tumor-peptide vaccination |
| AU2015289922A1 (en) | 2014-07-15 | 2017-02-16 | The Johns Hopkins University | Suppression of myeloid derived suppressor cells and immune checkpoint blockade |
| WO2016020288A1 (en) | 2014-08-04 | 2016-02-11 | Nuevolution A/S | Optionally fused heterocyclyl-substituted derivatives of pyrimidine useful for the treatment of inflammatory, metabolic, oncologic and autoimmune diseases |
| AU2015335029B2 (en) * | 2014-10-24 | 2021-09-23 | Astrazeneca Ab | Combination |
| WO2016110541A1 (en) | 2015-01-08 | 2016-07-14 | Universiteit Gent | Selective hdac6 inhibitors and uses thereof |
| SG11201708622UA (en) | 2015-02-02 | 2017-11-29 | Forma Therapeutics Inc | 3-aryl-4-amido-bicyclic [4,5,0] hydroxamic acids as hdac inhibitors |
| US10183934B2 (en) | 2015-02-02 | 2019-01-22 | Forma Therapeutics, Inc. | Bicyclic [4,6,0] hydroxamic acids as HDAC inhibitors |
| ES2935932T3 (es) | 2015-07-27 | 2023-03-13 | Chong Kun Dang Pharmaceutical Corp | Compuestos de derivados de 1,3,4-oxadiazolsulfonamida como inhibidor de histona desacetilasa 6, y la composición farmacéutica que comprende los mismos |
| AU2016299485B2 (en) | 2015-07-27 | 2019-02-07 | Chong Kun Dang Pharmaceutical Corp. | 1,3,4-oxadiazole amide derivative compound as histone deacetylase 6 inhibitor, and pharmaceutical composition containing same |
| MX376585B (es) | 2015-07-27 | 2025-03-07 | Chong Kun Dang Pharmaceutical Corp | Compuestos derivados de sulfamida de 1,3,4-oxadiazol como inhibidor de histona desacetilasa 6, y la composición farmacéutica que comprende los mismos. |
| AU2016303891B2 (en) | 2015-08-04 | 2019-08-01 | Chong Kun Dang Pharmaceutical Corp. | 1,3,4-oxadiazole derivative compounds as histone deacetylase 6 inhibitor, and the pharmaceutical composition comprising the same |
| WO2017218950A1 (en) | 2016-06-17 | 2017-12-21 | Forma Therapeutics, Inc. | 2-spiro-5- and 6-hydroxamic acid indanes as hdac inhibitors |
| JP7300394B2 (ja) | 2017-01-17 | 2023-06-29 | ヘパリジェニックス ゲーエムベーハー | 肝再生の促進又は肝細胞死の低減もしくは予防のためのプロテインキナーゼ阻害 |
| EP3615025A4 (en) * | 2017-04-26 | 2020-11-25 | The Board of Trustees of the University of Illionis | NRF AND HIF ACTIVATORS / HDAC INHIBITORS AND THERAPEUTIC METHODS USING THEM |
| NL2019548B1 (en) * | 2017-09-14 | 2019-03-27 | Academisch Ziekenhuis Leiden | T-cell based immunotherapy |
| WO2019054865A1 (en) * | 2017-09-14 | 2019-03-21 | ACADEMISCH ZIEKENHUIS LEIDEN (h.o.d.n. LUMC) | T-cell based immunotherapy |
| CN108191748A (zh) * | 2018-01-24 | 2018-06-22 | 齐鲁师范学院 | 一种含芳杂环氨基肟类化合物、制备方法及其用途 |
| KR102316234B1 (ko) | 2018-07-26 | 2021-10-22 | 주식회사 종근당 | 히스톤 탈아세틸화효소 6 억제제로서의 1,3,4-옥사다이아졸 유도체 화합물 및 이를 포함하는 약제학적 조성물 |
| PH12021552905A1 (en) | 2019-05-31 | 2022-04-04 | Chong Kun Dang Pharmaceutical Corp | 1,3,4-oxadiazole homophthalimide derivative compounds as histone deacetylase 6 inhibitor, and the pharmaceutical composition comprising the same |
| KR102476818B1 (ko) | 2019-05-31 | 2022-12-13 | 주식회사 종근당 | 히스톤 탈아세틸화효소 6 억제제로서의 1,3,4-옥사다이아졸 유도체 화합물 및 이를 포함하는 약제학적 조성물 |
| KR102331206B1 (ko) * | 2019-12-09 | 2021-11-25 | 계명대학교 산학협력단 | 히스톤 탈아세틸효소 억제 활성을 갖는 신규 화합물 및 이의 의학적 용도 |
| JOP20220160A1 (ar) | 2019-12-20 | 2023-01-30 | Nuevolution As | مركبات فعّالة نحو مستقبلات نووية |
| EP4076657A1 (en) | 2019-12-20 | 2022-10-26 | Nuevolution A/S | Compounds active towards nuclear receptors |
| KR102537616B1 (ko) | 2020-02-25 | 2023-05-26 | 주식회사 종근당 | 히스톤 탈아세틸화 효소 6 억제제로서의 1,3,4-옥사다이아졸 유도체 화합물 및 이를 포함하는 약제학적 조성물 |
| KR102537615B1 (ko) | 2020-02-25 | 2023-05-30 | 주식회사 종근당 | 히스톤 탈아세틸화효소 6 억제제로서의 1,3,4-옥사다이아졸 유도체 화합물 및 이를 포함하는 약제학적 조성물 |
| MX2022012260A (es) | 2020-03-31 | 2022-11-30 | Nuevolution As | Compuestos activos frente a receptores nucleares. |
| MX2022012259A (es) | 2020-03-31 | 2022-12-08 | Nuevolution As | Compuestos activos frente a receptores nucleares. |
| KR102576148B1 (ko) | 2020-04-13 | 2023-09-07 | 주식회사 종근당 | 히스톤 탈아세틸화효소 6 억제제로서의 1,3,4-옥사다이아졸 유도체 화합물 및 이를 포함하는 약제학적 조성물 |
| WO2021252475A1 (en) * | 2020-06-08 | 2021-12-16 | Annji Pharmaceutical Co., Ltd. | Quinazoline derivatives useful as selective hdac6 inhibitors |
| JP7691716B2 (ja) * | 2020-06-26 | 2025-06-12 | ザ ボード オブ トラスティーズ オブ ザ ユニバーシティ オブ イリノイ | 選択的ヒストンデアセチラーゼ6阻害剤 |
| KR102504830B1 (ko) | 2020-07-14 | 2023-03-02 | 주식회사 종근당 | 히스톤 탈아세틸화효소 6 억제제로서의 새로운 구조의 화합물 및 이를 포함하는 약제학적 조성물 |
| KR102685058B1 (ko) | 2020-09-02 | 2024-07-15 | 주식회사 종근당 | 히스톤 탈아세틸화효소 6 억제제로서의 새로운 구조의 화합물 및 이를 포함하는 약제학적 조성물 |
| CA3260663A1 (en) | 2022-07-15 | 2024-01-18 | Chong Kun Dang Pharmaceutical Corp. | 1,3,4-OXADIAZOLE TRIAZOLE COMPOUNDS USED AS HISTONE DEACETYLASE 6 INHIBITORS, AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM |
| KR20240035172A (ko) | 2022-09-08 | 2024-03-15 | 주식회사 종근당 | 히스톤 탈아세틸화효소 6 억제제로서의 1,3,4-옥사다이아졸 유도체 화합물 및 이의 용도 |
| WO2024079682A1 (en) | 2022-10-14 | 2024-04-18 | Chong Kun Dang Pharmaceutical Corp. | Sulfoximine compounds as histone deacetylase 6 inhibitor, and pharmaceutical composition comprising the same |
| KR20240133645A (ko) | 2023-02-28 | 2024-09-04 | 주식회사 종근당 | 옥사다이아졸 유도체 화합물 및 이를 포함하는 약제학적 조성물 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1133317A1 (de) | 1998-11-26 | 2001-09-19 | Pentapharm AG | Transportsystemkonjugate |
| US20030070691A1 (en) * | 2000-08-03 | 2003-04-17 | Anthony Giletto | Biocide formation via ozonation |
| US7033597B2 (en) | 2000-10-13 | 2006-04-25 | Université de Lausanne | Intracellular delivery of biological effectors |
| AU2002220979A1 (en) | 2000-10-13 | 2002-04-22 | Xigen Sa | Intracellular delivery of biological effectors by novel transporter peptide sequences |
| AU2003211362A1 (en) * | 2002-02-21 | 2003-09-09 | Osaka Industrial Promotion Organization | N-hydroxycarboxamide derivative |
| TW200530166A (en) * | 2003-10-27 | 2005-09-16 | S Bio Pte Ltd | Acylurea connected and sulfonylurea connected hydroxamates |
| CN1997627A (zh) * | 2004-07-12 | 2007-07-11 | 默克公司 | 组蛋白脱乙酰基酶抑制剂 |
| EP1796681A2 (en) * | 2004-08-02 | 2007-06-20 | Genmedica Therapeutics SL | Compounds for inhibiting copper-containing amine oxidases and uses thereof |
| US20070066646A1 (en) * | 2005-08-02 | 2007-03-22 | Genmedica Therapeutics Sl | Compounds for Inhibiting Copper-Containing Amine Oxidases and Uses Thereof |
| WO2011106632A1 (en) * | 2010-02-26 | 2011-09-01 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
| WO2012178208A2 (en) * | 2011-06-24 | 2012-12-27 | The Trustees Of The Stevens Institute Of Technology | Selective inhibitors of histone deacetylase isoform 6 and methods thereof |
-
2013
- 2013-03-07 JP JP2014561101A patent/JP6233812B2/ja not_active Expired - Fee Related
- 2013-03-07 CA CA2866707A patent/CA2866707A1/en not_active Abandoned
- 2013-03-07 EP EP13758416.5A patent/EP2822926A4/en not_active Withdrawn
- 2013-03-07 WO PCT/US2013/029521 patent/WO2013134467A1/en not_active Ceased
- 2013-03-07 AU AU2013230881A patent/AU2013230881A1/en not_active Abandoned
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