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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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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US (2) | US20210260040A1 (fr) |
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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JP7187449B2 (ja) * | 2016-09-30 | 2022-12-12 | エピザイム,インコーポレイティド | Ehmt2阻害剤としての置換された融合二環式または三環式複素環化合物 |
AU2018254577B2 (en) | 2017-04-21 | 2024-06-13 | Epizyme, Inc. | Combination therapies with EHMT2 inhibitors |
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 |
WO2020168197A1 (fr) | 2019-02-15 | 2020-08-20 | Incyte Corporation | Composés de pyrrolo[2,3-d]pyrimidinone en tant qu'inhibiteurs de cdk2 |
US11472791B2 (en) | 2019-03-05 | 2022-10-18 | Incyte Corporation | Pyrazolyl pyrimidinylamine compounds as CDK2 inhibitors |
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 |
US20220298140A1 (en) * | 2019-06-28 | 2022-09-22 | Chengdu Zenitar Biomedical Technology Co., Ltd. | 2,4-disubstituted pyrimidine derivative, preparation method therefor and use thereof |
WO2021030537A1 (fr) | 2019-08-14 | 2021-02-18 | Incyte Corporation | Composés imidazolyl-pyrimidinylamines utilisés comme inhibiteurs de la cdk2 |
PE20221905A1 (es) | 2019-10-11 | 2022-12-23 | Incyte Corp | Aminas biciclicas como inhibidoras de la cdk2 |
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 |
TW202128675A (zh) | 2019-12-06 | 2021-08-01 | 美商維泰克斯製藥公司 | 作為鈉通道調節劑之經取代四氫呋喃 |
JP2023511302A (ja) * | 2020-01-13 | 2023-03-17 | アプタバイオ セラピューティクス インコーポレイテッド | 新規なピラゾール誘導体 |
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 |
KR20230020983A (ko) | 2020-05-04 | 2023-02-13 | 암젠 인코포레이션 | 골수성 세포 2 작용제 상에서 발현되는 유발 수용체로서의 헤테로고리 화합물 및 사용 방법 |
AU2021267373A1 (en) | 2020-05-06 | 2022-12-08 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as JAK2 inhibitors |
WO2022140527A1 (fr) | 2020-12-23 | 2022-06-30 | Ajax Therapeutics, Inc. | 6-hétéroaryloxy benzimidazoles et azabenzimidazoles utilisés en tant qu'inhibiteurs de jak2 |
MX2023009682A (es) | 2021-02-19 | 2023-10-30 | Sudo Biosciences Ltd | Inhibidores de tyk2 y sus usos. |
WO2022175752A1 (fr) | 2021-02-19 | 2022-08-25 | 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 |
PE20241335A1 (es) | 2021-06-04 | 2024-07-03 | Vertex Pharma | N-(hidroxialquil (hetero)aril) tetrahidrofurano carboxamidas como moduladores de canales de sodio |
US11981671B2 (en) | 2021-06-21 | 2024-05-14 | Incyte Corporation | Bicyclic pyrazolyl amines as CDK2 inhibitors |
AU2022366869A1 (en) * | 2021-10-15 | 2024-05-02 | Tango Therapeutics, Inc. | Novel modulators of ehmt1 and ehmt2 and therapeutic use thereof |
WO2023078252A1 (fr) | 2021-11-02 | 2023-05-11 | Flare Therapeutics Inc. | Agonistes inverses de pparg et leurs utilisations |
EP4430042A1 (fr) | 2021-11-09 | 2024-09-18 | Ajax Therapeutics, Inc. | 6-hetero-aryloxy-benzimidazoles et azabenzimidazoles en tant qu'inhibiteurs de 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 |
IL313670A (en) | 2021-12-30 | 2024-08-01 | Biomea Fusion Inc | Pyrazine compounds as inhibitors of FLT3 |
WO2023159139A1 (fr) * | 2022-02-18 | 2023-08-24 | Ponce Therapeutics, Inc. | Compositions pharmaceutiques de multimérisation |
WO2024019541A1 (fr) * | 2022-07-20 | 2024-01-25 | 일동제약(주) | Composé dérivé d'hétéroaryle et son utilisation |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
CA2987978C (fr) * | 2014-06-16 | 2022-08-16 | Fundacion Para La Investigacion Medica Aplicada | Nouveaux composes utilises comme inhibiteurs doubles d'histone methyltransferases et d'adn methyltransferases |
US20170232030A1 (en) * | 2014-08-13 | 2017-08-17 | Epizyme, Inc. | Combination therapy for treating cancer |
BR112017009671A2 (pt) * | 2014-11-06 | 2017-12-26 | Dana Farber Cancer Inst Inc | inibidores de ezh2 e usos destes |
WO2017085053A1 (fr) * | 2015-11-16 | 2017-05-26 | Fundación Para La Investigación Médica Aplicada | Utilisation de nouveaux composés comme inhibiteurs d'adn méthyltransférases |
WO2017102677A1 (fr) * | 2015-12-14 | 2017-06-22 | Fundación Para La Investigación Médica Aplicada | Composés de quinoléine 2,4,6,7-tétrasubstitués utilisés en tant qu'inhibiteurs d'adn méthyltransférases |
BR112018071093A2 (pt) * | 2016-04-15 | 2019-01-29 | Epizyme Inc | composto de fórmula, composição farmacêutica, e método para prevenir ou tratar um distúrbio sanguíneo |
DK3555070T3 (da) * | 2016-12-19 | 2023-09-18 | Epizyme Inc | Aminsubstituerede, heterocykliske forbindelser som ehmt2-hæmmere og fremgangsmåder til anvendelse deraf |
WO2018119208A1 (fr) * | 2016-12-22 | 2018-06-28 | Global Blood Therapeutics, Inc. | Inhibiteurs de l'histone méthyltransférase |
AU2018254577B2 (en) * | 2017-04-21 | 2024-06-13 | Epizyme, Inc. | Combination therapies with EHMT2 inhibitors |
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2018
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- 2018-10-18 KR KR1020207014172A patent/KR20200101332A/ko not_active Application Discontinuation
- 2018-10-18 WO PCT/US2018/056530 patent/WO2019079607A1/fr unknown
- 2018-10-18 IL IL273824A patent/IL273824B2/en unknown
- 2018-10-18 US US16/756,304 patent/US20210260040A1/en not_active Abandoned
- 2018-10-18 BR BR112020007585-0A patent/BR112020007585A2/pt unknown
- 2018-10-18 MX MX2020007092A patent/MX2020007092A/es unknown
- 2018-10-18 AU AU2018353150A patent/AU2018353150B2/en active Active
- 2018-10-18 SG SG11202003162RA patent/SG11202003162RA/en unknown
- 2018-10-18 MA MA050417A patent/MA50417A/fr unknown
- 2018-10-18 CN CN201880071576.3A patent/CN111315371A/zh active Pending
- 2018-10-18 IL IL310625A patent/IL310625A/en unknown
- 2018-10-18 CA CA3081946A patent/CA3081946A1/fr active Pending
- 2018-10-18 JP JP2020520818A patent/JP2021500326A/ja active Pending
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2020
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- 2020-07-13 MX MX2024004332A patent/MX2024004332A/es unknown
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2023
- 2023-01-10 CL CL2023000095A patent/CL2023000095A1/es unknown
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- 2023-09-07 CL CL2023002682A patent/CL2023002682A1/es unknown
- 2023-09-19 JP JP2023151702A patent/JP2023164613A/ja active Pending
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CO2020006009A2 (es) | 2020-08-10 |
EP3697400A1 (fr) | 2020-08-26 |
JP2021500326A (ja) | 2021-01-07 |
AU2018353150A1 (en) | 2020-06-04 |
IL273824A (en) | 2020-05-31 |
IL273824B2 (en) | 2024-07-01 |
SG11202003162RA (en) | 2020-05-28 |
US20240180880A1 (en) | 2024-06-06 |
IL310625A (en) | 2024-04-01 |
MX2020007092A (es) | 2020-12-09 |
CL2020001019A1 (es) | 2020-11-27 |
US20210260040A1 (en) | 2021-08-26 |
WO2019079607A9 (fr) | 2020-05-28 |
IL273824B1 (en) | 2024-03-01 |
CA3081946A1 (fr) | 2019-04-25 |
WO2019079607A1 (fr) | 2019-04-25 |
KR20200101332A (ko) | 2020-08-27 |
CN111315371A (zh) | 2020-06-19 |
BR112020007585A2 (pt) | 2020-09-24 |
CL2023002682A1 (es) | 2024-03-01 |
CL2023000095A1 (es) | 2023-09-15 |
JP2023164613A (ja) | 2023-11-10 |
MX2024004332A (es) | 2024-06-19 |
AU2018353150B2 (en) | 2024-06-06 |
EP3697400A4 (fr) | 2021-08-11 |
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