CY1126110T1 - Παραγωγα βενζοϋδροξαμικου οξεος ως εκλεκτικοι αναστολε1σ του hdac6 - Google Patents
Παραγωγα βενζοϋδροξαμικου οξεος ως εκλεκτικοι αναστολε1σ του hdac6Info
- Publication number
- CY1126110T1 CY1126110T1 CY20231100364T CY231100364T CY1126110T1 CY 1126110 T1 CY1126110 T1 CY 1126110T1 CY 20231100364 T CY20231100364 T CY 20231100364T CY 231100364 T CY231100364 T CY 231100364T CY 1126110 T1 CY1126110 T1 CY 1126110T1
- Authority
- CY
- Cyprus
- Prior art keywords
- hdac6
- acid derivatives
- selective inhibitors
- benzohydroxamic acid
- benzohydroxamic
- Prior art date
Links
- VDEUYMSGMPQMIK-UHFFFAOYSA-N benzhydroxamic acid Chemical class ONC(=O)C1=CC=CC=C1 VDEUYMSGMPQMIK-UHFFFAOYSA-N 0.000 title abstract 2
- 102100022537 Histone deacetylase 6 Human genes 0.000 title 1
- 101000899330 Homo sapiens Histone deacetylase 6 Proteins 0.000 title 1
- 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 title 1
- 229940124639 Selective inhibitor Drugs 0.000 title 1
- 102000011427 Histone Deacetylase 6 Human genes 0.000 abstract 2
- 108010023925 Histone Deacetylase 6 Proteins 0.000 abstract 2
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- A61K31/425—Thiazoles
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- A61K31/4365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
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- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A61K31/5375—1,4-Oxazines, e.g. morpholine
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- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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- 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
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Abstract
Η παρούσα εφεύρεση αφορά νέες ενώσεις βενζοϋδροξαμικού του τύπου (Ι) και (II) και φαρμακευτικά αποδεκτά άλατα, ισομερή και προφάρμακα αυτών, που παρουσιάζουν υψηλή εκλεκτική ανασταλτική δραστικότητα έναντι του ενζύμου αποακετυλάσης ιστονών 6 (HDAC6).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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IT102017000041723A IT201700041723A1 (it) | 2017-04-14 | 2017-04-14 | Nuovi inibitori selettivi di HDAC6 |
PCT/EP2018/059468 WO2018189340A1 (en) | 2017-04-14 | 2018-04-12 | Selective hdac6 inhibitors |
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CY1126110T1 true CY1126110T1 (el) | 2023-11-15 |
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CY20231100364T CY1126110T1 (el) | 2017-04-14 | 2023-07-26 | Παραγωγα βενζοϋδροξαμικου οξεος ως εκλεκτικοι αναστολε1σ του hdac6 |
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Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
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US10357493B2 (en) | 2017-03-10 | 2019-07-23 | Selenity Therapeutics (Bermuda), Ltd. | Metalloenzyme inhibitor compounds |
CN109942564A (zh) * | 2019-04-16 | 2019-06-28 | 四川大学华西医院 | 一种组蛋白去乙酰化酶抑制剂及其制备方法和用途 |
TWI807201B (zh) * | 2019-07-23 | 2023-07-01 | 臺北醫學大學 | 組蛋白去乙醯化酶6抑制劑及治療神經病變性疼痛的方法 |
US20230286970A1 (en) | 2020-08-07 | 2023-09-14 | Italfarmaco S.P.A. | Novel oxadiazole-based selective hdac6 inhibitors |
CN112250638B (zh) * | 2020-11-13 | 2022-05-03 | 郑州大学 | 一种1,3-二芳基-1,2,4-三氮唑类化合物及其制备方法和应用 |
IT202100009926A1 (it) | 2021-04-20 | 2022-10-20 | Italfarmaco Spa | Una combinazione comprendente un inibitore di hdac6 specifico e almeno un inibitore del checkpoint ctla4 |
TW202340480A (zh) | 2021-11-23 | 2023-10-16 | 義大利商義大利藥品股份有限公司 | 檢測rna生物標記之方法 |
WO2023219456A1 (ko) * | 2022-05-12 | 2023-11-16 | 숙명여자대학교 산학협력단 | 퀴놀린 계열 히스톤디아세틸화 효소 저해활성물질, 이의 제조방법 및 이를 유효성분으로 포함하는 약학적 조성물 |
WO2024071935A1 (ko) * | 2022-09-27 | 2024-04-04 | 사회복지법인 삼성생명공익재단 | 히스톤 탈아세틸화효소 억제제를 포함하는 암 치료용 조성물, 및 암 면역치료용 항암 보조제 |
CN115611823A (zh) * | 2022-10-27 | 2023-01-17 | 新天地医药技术研究院(郑州)有限公司 | 一种1,2,4-三氮唑-苯基异羟肟酸类化合物、制备方法和应用 |
CN115737549A (zh) * | 2022-11-24 | 2023-03-07 | 北京鑫开元医药科技有限公司 | 一种具有hdac抑制活性的注射液及其制备方法和用途 |
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JP4469179B2 (ja) | 2002-01-23 | 2010-05-26 | バイエル ファーマセチカル コーポレーション | Rhoキナーゼ阻害剤としてのピリミジン誘導体 |
JP2008504345A (ja) | 2004-07-02 | 2008-02-14 | ノボ ノルディスク アクティーゼルスカブ | コンデンスチオフェン誘導体(condensedthiophenederivatives)およびそれらのサイクリックGLP−1アゴニストとしての使用 |
GB0607899D0 (en) | 2006-04-03 | 2006-05-31 | Glaxo Group Ltd | Process for preparing heterocyclic derivatives |
WO2009002534A1 (en) | 2007-06-26 | 2008-12-31 | Gilead Colorado, Inc. | Imidazopyridinyl thiazolyl histone deacetylase inhibitors |
JP5798115B2 (ja) | 2009-06-22 | 2015-10-21 | ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. | 置換ヒドロキサム酸およびその使用 |
US20120101099A1 (en) * | 2009-07-07 | 2012-04-26 | Anthem Biosciences Private Limited | Histone deacetylase inhibitors |
JP5518397B2 (ja) | 2009-08-12 | 2014-06-11 | 富士フイルム株式会社 | 水性インク組成物、複合粒子の製造方法、インクセット、及び、画像形成方法 |
WO2011106650A2 (en) | 2010-02-27 | 2011-09-01 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Novel p53-mdm2/p53-mdm4 antagonists to treat proliferative disease |
PL2640709T3 (pl) * | 2010-11-16 | 2016-10-31 | Związki pirymidynohydroksyamidowe jako inhibitory deacetylazy białkowej oraz sposoby ich stosowania” | |
USRE47009E1 (en) * | 2011-02-01 | 2018-08-28 | The Children's Hospital Of Philadelphia | HDAC inhibitors and therapeutic methods using the same |
EP2487159A1 (en) | 2011-02-11 | 2012-08-15 | MSD Oss B.V. | RorgammaT inhibitors |
EP2723338A2 (en) * | 2011-06-24 | 2014-04-30 | The Trustees of Stevens Institute of Technology | Selective inhibitors of histone deacetylase isoform 6 and methods thereof |
TR201900057T4 (tr) | 2013-12-12 | 2019-01-21 | Chong Kun Dang Pharmaceutical Corp | Selektif histon deasetilaz (HDAC) inhibitörleri olarak yeni azaindol deriveleri ve bunları içeren farmasötik bileşimler. |
KR101685639B1 (ko) | 2014-01-03 | 2016-12-12 | 주식회사 종근당 | 신규한 인돌 유도체 화합물 및 이를 포함하는 약제학적 조성물 |
RU2016148863A (ru) * | 2014-05-14 | 2018-06-18 | Дзе Риджентс Оф Дзе Юниверсити Оф Колорадо, Э Боди Корпорейт | Гетероциклические гидроксамовые кислоты в качестве ингибиторов протеин-деацетилазы и двойных ингибиторов протеин-деацетилазы-протеин-киназы и способы их применения |
JP6663863B2 (ja) | 2014-06-12 | 2020-03-13 | シーダーズ−サイナイ メディカル センター | がん治療のための組成物及び方法 |
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