PT3468966T - Inibidores da interação menina-mll - Google Patents
Inibidores da interação menina-mllInfo
- Publication number
- PT3468966T PT3468966T PT177393832T PT17739383T PT3468966T PT 3468966 T PT3468966 T PT 3468966T PT 177393832 T PT177393832 T PT 177393832T PT 17739383 T PT17739383 T PT 17739383T PT 3468966 T PT3468966 T PT 3468966T
- Authority
- PT
- Portugal
- Prior art keywords
- menin
- inhibitors
- mll interaction
- mll
- interaction
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/10—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—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
- 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
-
- 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
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—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
- 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
- C07D491/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—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
- 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
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Diabetes (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Endocrinology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Obesity (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662348496P | 2016-06-10 | 2016-06-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PT3468966T true PT3468966T (pt) | 2020-11-10 |
Family
ID=59325631
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PT177393832T PT3468966T (pt) | 2016-06-10 | 2017-06-08 | Inibidores da interação menina-mll |
Country Status (21)
| Country | Link |
|---|---|
| US (4) | US10683302B2 (enExample) |
| EP (2) | EP3468966B1 (enExample) |
| JP (4) | JP7007302B2 (enExample) |
| KR (3) | KR20220123727A (enExample) |
| CN (1) | CN109743875B (enExample) |
| AU (3) | AU2017278950B2 (enExample) |
| BR (1) | BR122024002146A2 (enExample) |
| CA (1) | CA3024180A1 (enExample) |
| CY (1) | CY1124834T1 (enExample) |
| DK (1) | DK3468966T3 (enExample) |
| ES (1) | ES2831084T3 (enExample) |
| HR (1) | HRP20201771T1 (enExample) |
| HU (1) | HUE051451T2 (enExample) |
| IL (4) | IL263586B (enExample) |
| LT (1) | LT3468966T (enExample) |
| MX (3) | MX381228B (enExample) |
| PL (1) | PL3468966T3 (enExample) |
| PT (1) | PT3468966T (enExample) |
| SI (1) | SI3468966T1 (enExample) |
| WO (1) | WO2017214367A1 (enExample) |
| ZA (1) | ZA201900150B (enExample) |
Families Citing this family (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016040330A1 (en) | 2014-09-09 | 2016-03-17 | The Regents Of The University Of Michigan | Thienopyrimidine and thienopyridine compounds and methods of use thereof |
| US10588907B2 (en) | 2015-06-04 | 2020-03-17 | Kura Oncology, Inc. | Methods and compositions for inhibiting the interaction of menin with MLL proteins |
| TWI703150B (zh) | 2015-06-04 | 2020-09-01 | 美商庫拉腫瘤技術股份有限公司 | 用於抑制ｍｅｎｉｎ及ｍｌｌ蛋白之交互作用的方法及組合物 |
| SI3429591T1 (sl) | 2016-03-16 | 2023-07-31 | Kura Oncology, Inc. | Substituirani tieno(2,3-d)pirimidinski derivati kot inhibitorji menin-MLL in postopki uporabe |
| PH12018501955B1 (en) | 2016-03-16 | 2024-01-24 | Kura Oncology Inc | Bridged bicyclic inhibitors of menin-mll and methods of use |
| WO2017192543A1 (en) | 2016-05-02 | 2017-11-09 | Regents Of The University Of Michigan | Piperidines as menin inhibitors |
| JP7007302B2 (ja) | 2016-06-10 | 2022-01-24 | ヴァイティー ファーマシューティカルズ，エルエルシー | メニン－ｍｌｌ相互作用の阻害剤 |
| MX392051B (es) | 2016-09-14 | 2025-03-21 | Janssen Pharmaceutica Nv | Inhibidores espirobiciclicos de la interaccion de menina-mll |
| US12084462B2 (en) | 2016-09-14 | 2024-09-10 | Janssen Pharmaceutica Nv | Spiro bicyclic inhibitors of menin-MLL interaction |
| CA3033020A1 (en) | 2016-09-14 | 2018-03-22 | Janssen Pharmaceutica Nv | Fused bicyclic inhibitors of menin-mll interaction |
| JP7142010B2 (ja) | 2016-12-15 | 2022-09-26 | ヤンセン ファーマシューティカ エヌ．ベー． | メニン－ｍｌｌ相互作用のアゼパン阻害剤 |
| CN110691779B (zh) | 2017-03-24 | 2023-10-10 | 库拉肿瘤学公司 | 治疗血液系统恶性肿瘤和尤因肉瘤的方法 |
| AU2018243586A1 (en) | 2017-03-31 | 2019-10-17 | The Regents Of The University Of Michigan | Piperidines as covalent menin inhibitors |
| WO2018190350A1 (ja) * | 2017-04-10 | 2018-10-18 | 三井化学アグロ株式会社 | ピリドン化合物およびそれを有効成分とする農園芸用殺菌剤 |
| US11542248B2 (en) | 2017-06-08 | 2023-01-03 | Kura Oncology, Inc. | Methods and compositions for inhibiting the interaction of menin with MLL proteins |
| WO2019060365A1 (en) | 2017-09-20 | 2019-03-28 | Kura Oncology, Inc. | SUBSTITUTED MÉNINE-MLL INHIBITORS AND METHODS OF USE |
| US11396517B1 (en) | 2017-12-20 | 2022-07-26 | Janssen Pharmaceutica Nv | Exo-aza spiro inhibitors of menin-MLL interaction |
| EP3728260A4 (en) * | 2017-12-20 | 2021-08-11 | Janssen Pharmaceutica NV | SPIRO EXO-AZA INHIBITORS OF MENIN-MLL INTERACTION |
| CN112105621B (zh) | 2018-03-30 | 2024-02-20 | 住友制药株式会社 | 光学活性桥型环状仲胺衍生物 |
| US10815241B2 (en) | 2018-08-27 | 2020-10-27 | Sumitomo Dainippon Pharma Co., Ltd. | Optically active azabicyclo ring derivative |
| KR102779601B1 (ko) * | 2018-08-27 | 2025-03-12 | 스미토모 파마 가부시키가이샤 | 광학 활성인 아자비시클로환 유도체 |
| US20230030720A1 (en) | 2018-12-06 | 2023-02-02 | Daiichi Sankyo Company, Limited | Cycloalkane-1,3-diamine derivative |
| WO2020114474A1 (zh) * | 2018-12-06 | 2020-06-11 | 苏州信诺维医药科技有限公司 | 一种杂环化合物、其应用及含其的药物组合物 |
| US11174263B2 (en) * | 2018-12-31 | 2021-11-16 | Biomea Fusion, Inc. | Inhibitors of menin-MLL interaction |
| JP7536767B2 (ja) | 2018-12-31 | 2024-08-20 | バイオメア フュージョン，インコーポレイテッド | メニン－ｍｌｌ相互作用の不可逆的阻害剤 |
| CN119390705A (zh) * | 2019-10-09 | 2025-02-07 | 诺华股份有限公司 | 作为m4激动剂的5-氧杂-2-氮杂螺[3.4]辛烷衍生物 |
| AU2020361735B2 (en) | 2019-10-09 | 2024-04-18 | Novartis Ag | 2-azaspiro(3.4)octane derivatives as M4 agonists |
| UA129208C2 (uk) * | 2019-12-19 | 2025-02-05 | Янссен Фармацевтика Нв | Заміщені спіропохідні з прямим ланцюгом |
| JP7454520B2 (ja) * | 2020-02-26 | 2024-03-22 | 住友ファーマ株式会社 | 光学活性なアザビシクロ環誘導体からなる医薬 |
| CN111297863B (zh) * | 2020-03-30 | 2021-06-25 | 四川大学华西医院 | menin-MLL抑制剂在制备治疗子宫内膜癌的药物中的应用 |
| AU2021252552A1 (en) * | 2020-04-07 | 2022-10-27 | Syndax Pharmaceuticals, Inc. | Combinations of menin inhibitors and CYP3A4 inhibitors and methods of use thereof |
| EP4232020A4 (en) * | 2020-10-21 | 2024-08-07 | Kura Oncology, Inc. | Treatment of hematological malignancies with inhibitors of menin |
| CN114516873A (zh) * | 2020-11-18 | 2022-05-20 | 苏州优理生物医药科技有限公司 | 一种螺环类化合物、包含其药物组合物及其应用 |
| RU2752079C1 (ru) * | 2020-12-01 | 2021-07-22 | Федеральное государственное автономное образовательное учреждение высшего образования "Пермский государственный национальный исследовательский университет" | (Е)-(6-(2-гидроксифенил)-2-иминио-4,7,8-триоксо-1,3-дифенил-1,3,6-триазаспиро[4.4]нонан-9-илиден)(4-метоксифенил)метаноат, обладающий противомикробной активностью, и способ его получения |
| EP4334320A1 (en) | 2021-05-08 | 2024-03-13 | JANSSEN Pharmaceutica NV | Substituted spiro derivatives |
| KR20240006542A (ko) | 2021-05-08 | 2024-01-15 | 얀센 파마슈티카 엔브이 | 치환된 스피로 유도체 |
| AU2022274071A1 (en) * | 2021-05-11 | 2024-01-04 | Janssen Pharmaceutica Nv | Combination therapies |
| CN117337180A (zh) * | 2021-05-11 | 2024-01-02 | 詹森药业有限公司 | 组合疗法 |
| MX2023013515A (es) * | 2021-05-14 | 2024-02-29 | Syndax Pharmaceuticals Inc | Inhibidores de la interaccion de menina-mll. |
| CR20230605A (es) | 2021-06-01 | 2024-05-24 | Janssen Pharmaceutica Nv | Derivados de fenil-1h-pirrolo[2,3-c]piridina sustituidos |
| US20250333421A1 (en) | 2021-06-03 | 2025-10-30 | Janssen Pharmaceutica Nv | Pyridazines or 1,2,4-triazines substituted by spirocyclic amines |
| CN117412964A (zh) * | 2021-06-03 | 2024-01-16 | 首药控股(北京)股份有限公司 | 取代的杂环化合物及其应用 |
| WO2022257047A1 (en) * | 2021-06-09 | 2022-12-15 | Acerand Therapeutics (Hong Kong) Limited | Diazaspirobicylic compounds as protein-protein interaction inhibitors and applications thereof |
| IL309359A (en) * | 2021-06-17 | 2024-02-01 | Janssen Pharmaceutica Nv | (r)-n-ethyl-5-fluoro-n-isopropyl-2-((5-(2-(6-((2-methoxyethyl)(methyl)amino)-2-methylhexan-3-yl)-2,6-diazaspiro[3.4]octan-6-yl)-1,2,4-triazin-6-yl)oxy)benzamide besylate salt for the treatment of diseases such as cancer |
| WO2023011446A1 (zh) * | 2021-08-04 | 2023-02-09 | 成都苑东生物制药股份有限公司 | 一种新型磺酰胺类menin-MLL相互作用抑制剂、其制备方法及医药用途 |
| CN115515958B (zh) * | 2021-08-04 | 2023-09-29 | 成都苑东生物制药股份有限公司 | 一种新型磺酰胺类menin-MLL相互作用抑制剂、其制备方法及医药用途 |
| TW202320796A (zh) | 2021-08-11 | 2023-06-01 | 美商拜歐米富士恩股份有限公司 | 用於糖尿病的menin-mll相互作用之共價抑制劑 |
| TW202313004A (zh) | 2021-08-20 | 2023-04-01 | 美商拜歐米富士恩股份有限公司 | Ｍｅｎｉｎ－ｍｌｌ相互作用之不可逆抑制劑的結晶形式 |
| CN113769098B (zh) * | 2021-09-22 | 2022-09-30 | 中国医学科学院肿瘤医院深圳医院 | MLL-menin抑制剂组合物在制备抗肝癌药物中的应用 |
| JP7681116B6 (ja) * | 2021-12-03 | 2025-06-19 | バイオノバ ファーマシューティカルズ リミティド | カルボニル置換ジアザスピロ化合物及びその使用 |
| KR20240131421A (ko) * | 2021-12-31 | 2024-08-30 | 히트젠 주식회사 | 메닌 저해제 및 이의 용도 |
| US20250214980A1 (en) | 2022-03-14 | 2025-07-03 | Slap Pharmaceuticals Llc | Multicyclic compounds |
| CN117069719A (zh) * | 2022-08-17 | 2023-11-17 | 烨辉医药科技(上海)有限公司 | 二氮杂螺环-哒嗪化合物及其用途 |
| CA3266114A1 (en) * | 2022-09-02 | 2024-03-07 | Hutchmed Limited | TRIAZINE COMPOUNDS AND THEIR USES |
| KR20250109775A (ko) | 2022-11-24 | 2025-07-17 | 오리존 지노믹스 에스.에이. | 암 치료를 위한 lsd1 억제제 및 메닌 억제제의 조합 |
| WO2024140798A1 (zh) * | 2022-12-30 | 2024-07-04 | 成都先导药物开发股份有限公司 | Menin抑制剂及其用途 |
| TW202430528A (zh) | 2023-01-18 | 2024-08-01 | 美商拜歐米富士恩股份有限公司 | Ｎ－［４－［４－（４－嗎啉基）－７ｈ－吡咯並［２，３－ｄ］嘧啶－６－基］苯基］－４－［［３（ｒ）－［（１－氧代－２－丙烯－１－基）氨基］－１－哌啶基］甲基］－２－吡啶甲醯胺的結晶形式作為ｍｅｎｉｎ－ｍｌｌ相互作用的共價抑制劑 |
| WO2024213101A1 (zh) * | 2023-04-13 | 2024-10-17 | 首药控股(北京)股份有限公司 | 取代的杂环化合物 |
| CN118994033B (zh) * | 2023-05-17 | 2025-09-16 | 成都先导药物开发股份有限公司 | 一种sdnx-5613的合成方法及其中间体化合物 |
| CN116969891A (zh) * | 2023-07-28 | 2023-10-31 | 杭州国瑞生物科技有限公司 | 一种7-甲基-5-醛基-1h-吲唑的合成方法 |
| TW202525797A (zh) * | 2023-08-28 | 2025-07-01 | 美商錫達斯醫藥股份有限公司 | 作為ｍｅｎｉｎ－ｍｌｌ交互作用之抑制劑的芳基醚類似物 |
| WO2025059366A1 (en) * | 2023-09-13 | 2025-03-20 | Kumquat Biosciences Inc. | Ras inhibitors |
| WO2025097148A2 (en) | 2023-11-04 | 2025-05-08 | Syndax Pharmaceuticals, Inc. | Salts and polymorphic forms of menin inhibitors and pharmaceutical compositions thereof |
| WO2025188611A1 (en) * | 2024-03-04 | 2025-09-12 | Dana-Farber Cancer Institute, Inc. | Chemical matters for targeting leukemic complex proteins |
Family Cites Families (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2086544C1 (ru) | 1991-06-13 | 1997-08-10 | Хоффманн-Ля Рош АГ | Бензолсульфонамидные производные пиримидина или их соли, фармацевтическая композиция для лечения заболеваний, связанных с активностью эндотелина |
| US5820915A (en) | 1996-06-27 | 1998-10-13 | Bioavailability Systems, L.L.C. | Method for the preparation of a first-pass effective citrus-derived substance and product thereof |
| US6124477A (en) | 1996-06-27 | 2000-09-26 | Bioavailability Systems, Llc | Anti-first-pass effect compounds |
| US5990154A (en) | 1997-05-30 | 1999-11-23 | Bioavailability Systems, L.L.C. | Anti-first-pass effect compounds and citrus extract |
| US6063809A (en) | 1997-08-26 | 2000-05-16 | Bioavailability Systems, Llc | Anti-first-pass effect compounds |
| US20040058982A1 (en) | 1999-02-17 | 2004-03-25 | Bioavailability System, Llc | Pharmaceutical compositions |
| US6248776B1 (en) | 1997-08-26 | 2001-06-19 | Bioavailability Systems, L.L.C. | Anti-first-pass effect compounds |
| US5993887A (en) | 1998-06-29 | 1999-11-30 | Bioavailability Systems, L.L.C. | Safe citrus juice and process for preparation |
| WO2004037827A1 (en) | 2000-10-20 | 2004-05-06 | Bioavailability Systems, Llc | Synthesis of spiro ortho esters, spiro ortho carbonates, and intermediates |
| US7968569B2 (en) | 2002-05-17 | 2011-06-28 | Celgene Corporation | Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione |
| EP1732891A4 (en) | 2004-03-11 | 2009-05-06 | Sequoia Pharmaceuticals Inc | RESISTANT PREVENTIVE INHIBITORS FOR RETROVIRAL PROTEASES |
| JP5073480B2 (ja) | 2004-05-07 | 2012-11-14 | セコイア、ファーマシューティカルズ、インコーポレイテッド | 耐性防止レトロウイルスプロテアーゼ阻害薬 |
| US20090281114A1 (en) * | 2008-05-08 | 2009-11-12 | Fabre-Kramer Pharmaceuticals, Inc. | Indolylalkyl derivatives of pyrimidinylpiperazine and metabolites thereof for treatment of anxiety, depression, and sexual dysfunction |
| AR071717A1 (es) | 2008-05-13 | 2010-07-07 | Array Biopharma Inc | Pirrolo[2,3-b]piridinas inhibidoras de quinasas chk1 y chk2,composiciones farmaceuticas que las contienen,proceso para prepararlas y uso de las mismas en el tratamiento y prevencion del cancer. |
| US9073947B2 (en) | 2011-06-10 | 2015-07-07 | Merck Patent Gmbh | Compositions and methods for the production of pyrimidine and pyridine compounds with BTK inhibitory activity |
| US8466159B2 (en) | 2011-10-21 | 2013-06-18 | Abbvie Inc. | Methods for treating HCV |
| KR20140040594A (ko) | 2012-09-26 | 2014-04-03 | 아로그 파마슈티칼스, 엘엘씨 | 돌연변이체 c-kit의 억제 방법 |
| BR112015022602A2 (pt) * | 2013-03-13 | 2017-07-18 | Univ Michigan Regents | composições compreendendo compostos de tienopirimidina e tienopiridina e métodos de uso dos mesmos |
| WO2015108940A2 (en) | 2014-01-14 | 2015-07-23 | The Trustees Of The University Of Pennsylvania | Tailored combinatorial epigenetic therapies for p53 gain-of-function tumors |
| WO2015191701A1 (en) * | 2014-06-10 | 2015-12-17 | The Trustees Of The University Of Pennsylvania | Scaffolds for inhibitors of menin-mll interactions |
| US20170232030A1 (en) | 2014-08-13 | 2017-08-17 | Epizyme, Inc. | Combination therapy for treating cancer |
| CN105732636B (zh) * | 2014-12-30 | 2020-04-21 | 广东东阳光药业有限公司 | 杂芳化合物及其在药物中的应用 |
| US10588907B2 (en) | 2015-06-04 | 2020-03-17 | Kura Oncology, Inc. | Methods and compositions for inhibiting the interaction of menin with MLL proteins |
| EP3394064A1 (en) * | 2015-12-22 | 2018-10-31 | Vitae Pharmaceuticals, Inc. | Inhibitors of the menin-mll interaction |
| US10869868B2 (en) | 2016-01-26 | 2020-12-22 | Memorial Sloan Kettering Cancer Center | Targeting chromatin regulators inhibits leukemogenic gene expression in NPM1 mutant leukemia |
| PH12018501955B1 (en) | 2016-03-16 | 2024-01-24 | Kura Oncology Inc | Bridged bicyclic inhibitors of menin-mll and methods of use |
| WO2017192543A1 (en) | 2016-05-02 | 2017-11-09 | Regents Of The University Of Michigan | Piperidines as menin inhibitors |
| EP3454862B1 (en) | 2016-05-10 | 2024-09-11 | C4 Therapeutics, Inc. | Spirocyclic degronimers for target protein degradation |
| JP7007302B2 (ja) | 2016-06-10 | 2022-01-24 | ヴァイティー ファーマシューティカルズ，エルエルシー | メニン－ｍｌｌ相互作用の阻害剤 |
| JP2019529421A (ja) | 2016-09-16 | 2019-10-17 | ヴァイティー ファーマシューティカルズ，エルエルシー | ｍｅｎｉｎ−ＭＬＬ相互作用の阻害剤 |
| CN110691779B (zh) | 2017-03-24 | 2023-10-10 | 库拉肿瘤学公司 | 治疗血液系统恶性肿瘤和尤因肉瘤的方法 |
| EP3728260A4 (en) | 2017-12-20 | 2021-08-11 | Janssen Pharmaceutica NV | SPIRO EXO-AZA INHIBITORS OF MENIN-MLL INTERACTION |
| EP3740491A1 (en) | 2018-01-18 | 2020-11-25 | Array Biopharma, Inc. | Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors |
| CN111936465A (zh) | 2018-03-30 | 2020-11-13 | 密歇根大学董事会 | 作为共价menin抑制剂的哌啶化合物 |
| EP3849606A4 (en) | 2018-09-13 | 2022-06-29 | Merck Sharp & Dohme Corp. | Combination of pd-1 antagonist and lag3 antagonist for treating non-microsatellite instablity-high/proficient mismatch repair colorectal cancer |
| EP3856173A4 (en) | 2018-09-26 | 2022-07-06 | Kura Oncology, Inc. | TREATMENT OF HEMOPATHY MALIGNANCE WITH MENIN INHIBITORS |
| JP7536767B2 (ja) | 2018-12-31 | 2024-08-20 | バイオメア フュージョン，インコーポレイテッド | メニン－ｍｌｌ相互作用の不可逆的阻害剤 |
| AU2021252552A1 (en) | 2020-04-07 | 2022-10-27 | Syndax Pharmaceuticals, Inc. | Combinations of menin inhibitors and CYP3A4 inhibitors and methods of use thereof |
| EP4337329A4 (en) | 2021-05-12 | 2025-01-01 | Syndax Pharmaceuticals, Inc. | COMBINATIONS FOR CANCER TREATMENT |
| MX2023013515A (es) | 2021-05-14 | 2024-02-29 | Syndax Pharmaceuticals Inc | Inhibidores de la interaccion de menina-mll. |
| TW202320796A (zh) | 2021-08-11 | 2023-06-01 | 美商拜歐米富士恩股份有限公司 | 用於糖尿病的menin-mll相互作用之共價抑制劑 |
| CN118234497A (zh) | 2021-12-15 | 2024-06-21 | 丹娜-法伯癌症研究所 | 通过破坏menin-mll表观遗传复合体靶向治疗胃肠道间质瘤(gist) |
-
2017
- 2017-06-08 JP JP2018564288A patent/JP7007302B2/ja active Active
- 2017-06-08 MX MX2018015252A patent/MX381228B/es unknown
- 2017-06-08 DK DK17739383.2T patent/DK3468966T3/da active
- 2017-06-08 WO PCT/US2017/036506 patent/WO2017214367A1/en not_active Ceased
- 2017-06-08 EP EP17739383.2A patent/EP3468966B1/en active Active
- 2017-06-08 ES ES17739383T patent/ES2831084T3/es active Active
- 2017-06-08 US US16/308,739 patent/US10683302B2/en active Active
- 2017-06-08 BR BR122024002146-3A patent/BR122024002146A2/pt not_active Application Discontinuation
- 2017-06-08 AU AU2017278950A patent/AU2017278950B2/en active Active
- 2017-06-08 KR KR1020227028964A patent/KR20220123727A/ko active Pending
- 2017-06-08 EP EP20189251.0A patent/EP3805215A1/en active Pending
- 2017-06-08 KR KR1020197000269A patent/KR102436430B1/ko active Active
- 2017-06-08 CA CA3024180A patent/CA3024180A1/en active Pending
- 2017-06-08 KR KR1020257017598A patent/KR20250079083A/ko active Pending
- 2017-06-08 HR HRP20201771TT patent/HRP20201771T1/hr unknown
- 2017-06-08 SI SI201730492T patent/SI3468966T1/sl unknown
- 2017-06-08 CN CN201780035865.3A patent/CN109743875B/zh active Active
- 2017-06-08 HU HUE17739383A patent/HUE051451T2/hu unknown
- 2017-06-08 PT PT177393832T patent/PT3468966T/pt unknown
- 2017-06-08 LT LTEP17739383.2T patent/LT3468966T/lt unknown
- 2017-06-08 PL PL17739383T patent/PL3468966T3/pl unknown
-
2018
- 2018-12-07 MX MX2021003939A patent/MX2021003939A/es unknown
- 2018-12-07 MX MX2023002982A patent/MX2023002982A/es unknown
- 2018-12-09 IL IL263586A patent/IL263586B/en active IP Right Grant
-
2019
- 2019-01-09 ZA ZA2019/00150A patent/ZA201900150B/en unknown
-
2020
- 2020-04-01 US US16/837,421 patent/US11479557B2/en active Active
- 2020-11-03 CY CY20201101035T patent/CY1124834T1/el unknown
-
2021
- 2021-05-19 IL IL283267A patent/IL283267B2/en unknown
- 2021-10-29 AU AU2021258089A patent/AU2021258089B2/en active Active
-
2022
- 2022-01-06 JP JP2022000946A patent/JP7461390B2/ja active Active
- 2022-09-02 US US17/902,432 patent/US12312359B2/en active Active
- 2022-11-20 IL IL298381A patent/IL298381B2/en unknown
-
2024
- 2024-01-04 JP JP2024000278A patent/JP2024045176A/ja active Pending
- 2024-04-24 AU AU2024202700A patent/AU2024202700A1/en active Pending
-
2025
- 2025-04-16 US US19/180,560 patent/US20250326764A1/en active Pending
- 2025-05-19 JP JP2025083421A patent/JP2025113339A/ja active Pending
- 2025-06-30 IL IL321844A patent/IL321844A/en unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IL321844A (en) | Menin–MLL interaction inhibitors | |
| IL259560A (en) | Inhibitors of the menin-mll interaction | |
| PL3512850T3 (pl) | Inhibitory interakcji menina-mll | |
| IL251584B (en) | Dihydropyrrolopyridines ror–gamma inhibitors | |
| IL250891A0 (en) | smyd inhibitors | |
| IL246902A0 (en) | Dihydropyrrolopyridine ror–gamma inhibitors | |
| AU364417S (en) | Back of the case | |
| IL248895A0 (en) | Phosphatidylinositol 3-kinase inhibitors | |
| ZA201907136B (en) | Ip6k inhibitors | |
| GB201513481D0 (en) | Inhibitor compounds | |
| GB201403536D0 (en) | Inhibitor compounds | |
| GB201521059D0 (en) | Inhibitors of metallo-beta-lactamases | |
| IL265139B (en) | Dopamine-b-hydroxylase inhibitors | |
| GB201505658D0 (en) | Inhibitor compounds | |
| GB201612860D0 (en) | Inhibitors | |
| GB201501004D0 (en) | Inhibitors | |
| IL274550A (en) | Dopamine-B-hydroxylase inhibitors | |
| IL262111B1 (en) | Monovalent inhibitors of hutnfr1 interaction | |
| GB201520949D0 (en) | Inhibitors | |
| GB201401005D0 (en) | Inhibitor | |
| GB201721465D0 (en) | Inhibitors | |
| GB201720189D0 (en) | Dopamine-B-hydroxylase inhibitors | |
| GB201621619D0 (en) | Inhibitor compounds | |
| GB201616201D0 (en) | Blood-brain barrier-penetrant dopamine-B-hydroxylase inhibitors | |
| GB201522453D0 (en) | Inhibitor compounds |