MA50417A - Procédés d'utilisation d'inhibiteurs de l'ehmt2 dans le traitement ou la prévention de troubles du sang - Google Patents
Procédés d'utilisation d'inhibiteurs de l'ehmt2 dans le traitement ou la prévention de troubles du sangInfo
- Publication number
- MA50417A MA50417A MA050417A MA50417A MA50417A MA 50417 A MA50417 A MA 50417A MA 050417 A MA050417 A MA 050417A MA 50417 A MA50417 A MA 50417A MA 50417 A MA50417 A MA 50417A
- Authority
- MA
- Morocco
- Prior art keywords
- prevention
- treatment
- methods
- blood disorders
- ehmt2 inhibitors
- Prior art date
Links
- 102100035042 Histone-lysine N-methyltransferase EHMT2 Human genes 0.000 title 1
- 101000877312 Homo sapiens Histone-lysine N-methyltransferase EHMT2 Proteins 0.000 title 1
- 239000008280 blood Substances 0.000 title 1
- 210000004369 blood Anatomy 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 230000002265 prevention Effects 0.000 title 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/33—Heterocyclic compounds
- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/404—Indoles, e.g. pindolol
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- A61K31/13—Amines
- A61K31/155—Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
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- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
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- A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
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- A61K31/19—Carboxylic acids, e.g. valproic acid
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- A61K31/437—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 containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/4406—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
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- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
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- C07D417/12—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 chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—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
- 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
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
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- Life Sciences & Earth Sciences (AREA)
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- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
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| US201762573876P | 2017-10-18 | 2017-10-18 | |
| US201762574128P | 2017-10-18 | 2017-10-18 |
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| MA50417A true MA50417A (fr) | 2020-08-26 |
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| MA050417A MA50417A (fr) | 2017-10-18 | 2018-10-18 | Procédés d'utilisation d'inhibiteurs de l'ehmt2 dans le traitement ou la prévention de troubles du sang |
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| EP (1) | EP3697400A4 (fr) |
| JP (2) | JP2021500326A (fr) |
| KR (1) | KR20200101332A (fr) |
| CN (1) | CN111315371A (fr) |
| AU (1) | AU2018353150B2 (fr) |
| BR (1) | BR112020007585A2 (fr) |
| CA (1) | CA3081946A1 (fr) |
| CL (3) | CL2020001019A1 (fr) |
| CO (1) | CO2020006009A2 (fr) |
| IL (2) | IL273824B2 (fr) |
| MA (1) | MA50417A (fr) |
| MX (2) | MX2020007092A (fr) |
| SG (1) | SG11202003162RA (fr) |
| WO (1) | WO2019079607A1 (fr) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CA3037587A1 (fr) * | 2016-09-30 | 2018-04-05 | Epizyme, Inc. | Composes bi-ou tri-heterocycliques fusionnes substitues en tant qu'inhibiteurs de l'ehmt2 |
| CN110621316B (zh) | 2017-04-21 | 2024-01-26 | Epizyme股份有限公司 | 用ehmt2抑制剂进行的组合疗法 |
| WO2019219805A1 (fr) * | 2018-05-16 | 2019-11-21 | Ctxone Pty Ltd | Polythérapie |
| US11066404B2 (en) | 2018-10-11 | 2021-07-20 | Incyte Corporation | Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors |
| EP3876939A4 (fr) | 2018-11-07 | 2022-08-10 | Dana-Farber Cancer Institute, Inc. | Dérivés benzothiazoles et dérivés 7-aza benzothiazoles comme inhibiteurs de la janus kinase 2 et leurs utilisations |
| EP3877371A4 (fr) | 2018-11-07 | 2022-07-27 | Dana-Farber Cancer Institute, Inc. | Dérivés d'imidazopyridine et dérivés d'aza-imidazopyridine utilisés comme inhibiteurs de la janus kinase 2 et utilisations associées |
| US12522583B2 (en) | 2018-11-07 | 2026-01-13 | Dana-Farber Cancer Institute, Inc. | Benzimidazole derivatives and aza-benzimidazole derivatives as Janus kinase 2 inhibitors and uses thereof |
| US11384083B2 (en) | 2019-02-15 | 2022-07-12 | Incyte Corporation | Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors |
| TW202100520A (zh) | 2019-03-05 | 2021-01-01 | 美商英塞特公司 | 作為cdk2 抑制劑之吡唑基嘧啶基胺化合物 |
| WO2020205560A1 (fr) | 2019-03-29 | 2020-10-08 | Incyte Corporation | Composés sulfonylamides utilisés comme inhibiteurs de la cdk2 |
| WO2020223469A1 (fr) | 2019-05-01 | 2020-11-05 | Incyte Corporation | Dérivés de n-(1-(méthylsulfonyl)pipéridin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine et composés apparentés utilisés en tant qu'inhibiteurs de kinase 2 dépendante des cyclines (cdk2) pour le traitement du cancer |
| US11447494B2 (en) | 2019-05-01 | 2022-09-20 | Incyte Corporation | Tricyclic amine compounds as CDK2 inhibitors |
| WO2020259683A1 (fr) * | 2019-06-28 | 2020-12-30 | 成都赜灵生物医药科技有限公司 | Dérivé de pyrimidine disubstitué en position 2 et 4, son procédé de préparation et ses utilisations |
| CA3150681A1 (fr) | 2019-08-14 | 2021-02-18 | Incyte Corporation | Composes imidazolyl-pyrimidinylamines utilises comme inhibiteurs de la cdk2 |
| US11851426B2 (en) | 2019-10-11 | 2023-12-26 | Incyte Corporation | Bicyclic amines as CDK2 inhibitors |
| CN110882274A (zh) * | 2019-10-21 | 2020-03-17 | 浙江生创精准医疗科技有限公司 | 间充质干细胞在降低地西他滨毒副作用的用途及相关药物 |
| CA3163206A1 (fr) * | 2019-11-27 | 2021-06-03 | Riken | Inhibiteur de g9a |
| BR112022010924A2 (pt) | 2019-12-06 | 2022-09-06 | Vertex Pharma | Tetra-hidrofuranos substituídos como moduladores de canais de sódio |
| US12509438B2 (en) * | 2020-01-13 | 2025-12-30 | Aptabio Therapeutics Inc. | Pyrazole derivative |
| TW202208355A (zh) | 2020-05-04 | 2022-03-01 | 美商安進公司 | 作為骨髓細胞觸發受體2促效劑之雜環化合物及使用方法 |
| JP7741100B2 (ja) | 2020-05-04 | 2025-09-17 | アムジェン インコーポレイテッド | ミエロイド細胞に発現するトリガー受容体2アゴニストとしての複素環化合物及び使用方法 |
| US11691963B2 (en) | 2020-05-06 | 2023-07-04 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as JAK2 inhibitors |
| US12043632B2 (en) | 2020-12-23 | 2024-07-23 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as JAK2 inhibitors |
| AU2022222470A1 (en) | 2021-02-19 | 2023-09-21 | Sudo Biosciences Limited | Tyk2 inhibitors and uses thereof |
| CA3208361A1 (fr) | 2021-02-19 | 2022-08-25 | Anjali Pandey | Inhibiteurs de tyk2 et leurs utilisations |
| EP4294806A1 (fr) | 2021-02-19 | 2023-12-27 | Sudo Biosciences Limited | Inhibiteurs de tyk2 et leurs utilisations |
| CN113289020B (zh) * | 2021-05-17 | 2023-04-18 | 福州大学 | 蛋白质二硫键异构酶小分子抑制剂及其应用 |
| SMT202500481T1 (it) | 2021-06-04 | 2026-01-12 | Vertex Pharma | N-(idrossialchil(etero)aril)tetraidrofuran carbossammidi come modulatori di canali del sodio |
| US11981671B2 (en) | 2021-06-21 | 2024-05-14 | Incyte Corporation | Bicyclic pyrazolyl amines as CDK2 inhibitors |
| JP2024538128A (ja) * | 2021-10-15 | 2024-10-18 | タンゴ セラピューティクス, インコーポレイテッド | Ehmt1及びehmt2の新規調節因子及びその治療用途 |
| PT4426434T (pt) | 2021-11-02 | 2025-11-24 | Flare Therapeutics Inc | Agonistas inversos de pparg e suas utilizações |
| WO2023086319A1 (fr) | 2021-11-09 | 2023-05-19 | Ajax Therapeutics, Inc. | 6-hetero-aryloxy-benzimidazoles et azabenzimidazoles en tant qu'inhibiteurs de jak2 |
| US12162881B2 (en) | 2021-11-09 | 2024-12-10 | Ajax Therapeutics, Inc. | Forms and compositions of inhibitors of JAK2 |
| US11976073B2 (en) | 2021-12-10 | 2024-05-07 | Incyte Corporation | Bicyclic amines as CDK2 inhibitors |
| US12084453B2 (en) | 2021-12-10 | 2024-09-10 | Incyte Corporation | Bicyclic amines as CDK12 inhibitors |
| MX2024008057A (es) | 2021-12-30 | 2024-08-28 | Biomea Fusion Inc | Compuestos de pirazina como inhibidores de flt3. |
| US20250161288A1 (en) * | 2022-02-18 | 2025-05-22 | Ponce Therapeutics, Inc. | Multimerizer pharmaceutical compositions |
| CN119585255A (zh) * | 2022-07-20 | 2025-03-07 | S2C生物株式会社 | 杂芳基衍生化合物及其用途 |
| WO2024216164A1 (fr) * | 2023-04-13 | 2024-10-17 | Tango Therapeutics, Inc. | Dérivés de n2-((5-hydroxy)-2-pyridyl)-pyridine-2,4-diamine utilisés comme modulateurs d'ehmt1/2 pour le traitement du cancer |
| WO2025064402A1 (fr) * | 2023-09-22 | 2025-03-27 | St. Jude Children's Research Hospital, Inc. | Méthode de traitement de la drépanocytose par ciblage des cellules sénescentes |
Family Cites Families (12)
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|---|---|---|---|---|
| AU2009279825A1 (en) * | 2008-08-05 | 2010-02-11 | Targegen, Inc. | Methods of treating thalassemia |
| WO2012023285A1 (fr) * | 2010-08-20 | 2012-02-23 | Oncotherapy Science, Inc. | Ehmt2 comme gène cible pour le traitement et le diagnostic du cancer |
| US20150250824A1 (en) * | 2014-03-07 | 2015-09-10 | The Research Foundation For The State University Of New York | Methods and compositions for expansion of stem cells and other cells |
| CN106536509B (zh) * | 2014-06-16 | 2020-06-09 | 基础应用医学研究基金会 | 作为组蛋白甲基转移酶和dna甲基转移酶的双重抑制剂的新型化合物 |
| AU2015301746A1 (en) * | 2014-08-13 | 2017-02-16 | Celgene Corporation | Combination therapy for treating cancer |
| WO2016073956A1 (fr) * | 2014-11-06 | 2016-05-12 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs d'ezh2 et leurs utilisations |
| AU2016356884A1 (en) * | 2015-11-16 | 2018-06-21 | Fundación Para La Investigación Médica Aplicada | Novel compounds as inhibitors of dna methyltransferases |
| US20190127354A1 (en) * | 2015-12-14 | 2019-05-02 | Fundación Para La Investigación Médica Aplicada | 2,4,6,7-tetrasubstituted quinoline compounds as inhibitors of dna methyltransferases |
| PL3442947T3 (pl) * | 2016-04-15 | 2023-10-02 | Epizyme, Inc. | Związki arylowe lub heteroarylowe podstawione aminą jako inhibitory ehmt1 i ehmt2 |
| US20200039998A1 (en) * | 2016-12-19 | 2020-02-06 | Epizyme, Inc. | Amine-substituted heterocyclic compounds as ehmt2 inhibitors and methods of use thereof |
| JP7091336B2 (ja) * | 2016-12-22 | 2022-06-27 | グローバル ブラッド セラピューティクス インコーポレイテッド | ヒストンメチルトランスフェラーゼ阻害剤 |
| CN110621316B (zh) * | 2017-04-21 | 2024-01-26 | Epizyme股份有限公司 | 用ehmt2抑制剂进行的组合疗法 |
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- 2018-10-18 MX MX2020007092A patent/MX2020007092A/es unknown
- 2018-10-18 CA CA3081946A patent/CA3081946A1/fr active Pending
- 2018-10-18 KR KR1020207014172A patent/KR20200101332A/ko not_active Ceased
- 2018-10-18 WO PCT/US2018/056530 patent/WO2019079607A1/fr not_active Ceased
- 2018-10-18 US US16/756,304 patent/US20210260040A1/en not_active Abandoned
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| CN111315371A (zh) | 2020-06-19 |
| IL273824B2 (en) | 2024-07-01 |
| CL2023002682A1 (es) | 2024-03-01 |
| CO2020006009A2 (es) | 2020-08-10 |
| CL2020001019A1 (es) | 2020-11-27 |
| BR112020007585A2 (pt) | 2020-09-24 |
| WO2019079607A9 (fr) | 2020-05-28 |
| EP3697400A1 (fr) | 2020-08-26 |
| EP3697400A4 (fr) | 2021-08-11 |
| IL310625A (en) | 2024-04-01 |
| SG11202003162RA (en) | 2020-05-28 |
| AU2018353150A1 (en) | 2020-06-04 |
| IL273824B1 (en) | 2024-03-01 |
| JP2023164613A (ja) | 2023-11-10 |
| US20210260040A1 (en) | 2021-08-26 |
| AU2018353150B2 (en) | 2024-06-06 |
| CA3081946A1 (fr) | 2019-04-25 |
| CL2023000095A1 (es) | 2023-09-15 |
| JP2021500326A (ja) | 2021-01-07 |
| MX2020007092A (es) | 2020-12-09 |
| KR20200101332A (ko) | 2020-08-27 |
| US20240180880A1 (en) | 2024-06-06 |
| MX2024004332A (es) | 2024-06-19 |
| IL273824A (en) | 2020-05-31 |
| WO2019079607A1 (fr) | 2019-04-25 |
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