MA43823A - Inhibiteurs bicycliques pontés de ménine-mll et méthodes d'utilisation - Google Patents
Inhibiteurs bicycliques pontés de ménine-mll et méthodes d'utilisationInfo
- Publication number
- MA43823A MA43823A MA043823A MA43823A MA43823A MA 43823 A MA43823 A MA 43823A MA 043823 A MA043823 A MA 043823A MA 43823 A MA43823 A MA 43823A MA 43823 A MA43823 A MA 43823A
- Authority
- MA
- Morocco
- Prior art keywords
- menin
- mll
- methods
- bridged bicyclic
- bicyclic inhibitors
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
Classifications
-
- 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
- A61K31/435—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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662309362P | 2016-03-16 | 2016-03-16 | |
| US201662431387P | 2016-12-07 | 2016-12-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA43823A true MA43823A (fr) | 2018-11-28 |
Family
ID=59851929
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA043823A MA43823A (fr) | 2016-03-16 | 2017-03-15 | Inhibiteurs bicycliques pontés de ménine-mll et méthodes d'utilisation |
Country Status (17)
| Country | Link |
|---|---|
| US (3) | US10752639B2 (fr) |
| EP (1) | EP3429585B1 (fr) |
| JP (1) | JP7000333B2 (fr) |
| KR (1) | KR102419524B1 (fr) |
| CN (1) | CN109640987B (fr) |
| AU (1) | AU2017235462B2 (fr) |
| BR (1) | BR112018068702A2 (fr) |
| CA (1) | CA3015845A1 (fr) |
| IL (1) | IL261625B (fr) |
| MA (1) | MA43823A (fr) |
| MX (1) | MX387806B (fr) |
| MY (1) | MY199965A (fr) |
| PH (1) | PH12018501955B1 (fr) |
| SG (1) | SG11201807834WA (fr) |
| TW (1) | TWI743096B (fr) |
| WO (1) | WO2017161002A1 (fr) |
| ZA (1) | ZA201805845B (fr) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE49687E1 (en) | 2014-09-09 | 2023-10-10 | The Regents Of The University Of Michigan | Thienopyrimidine and thienopyridine compounds and methods of use thereof |
| WO2016197027A1 (fr) | 2015-06-04 | 2016-12-08 | Kura Oncology, Inc. | Méthodes et compositions d'inhibition de l'interaction de la ménine avec les protéines mll |
| 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 |
| WO2017161028A1 (fr) | 2016-03-16 | 2017-09-21 | Kura Oncology, Inc. | Inhibiteurs substitués de ménine-mll et méthodes d'utilisation |
| US10752639B2 (en) | 2016-03-16 | 2020-08-25 | Kura Oncology, Inc. | Bridged bicyclic inhibitors of menin-MLL and methods of use |
| CN109415337B (zh) | 2016-05-02 | 2022-01-18 | 密执安大学评议会 | 作为多发性内分泌腺瘤蛋白抑制剂的哌啶 |
| ES2831084T3 (es) | 2016-06-10 | 2021-06-07 | Vitae Pharmaceuticals Inc | Inhibidores de la interacción menina-MLL |
| TWI753016B (zh) | 2016-09-14 | 2022-01-21 | 比利時商健生藥品公司 | Menin-mll相互作用之稠合二環抑制劑 |
| US12084462B2 (en) | 2016-09-14 | 2024-09-10 | Janssen Pharmaceutica Nv | Spiro bicyclic inhibitors of menin-MLL interaction |
| AU2017326487B2 (en) | 2016-09-14 | 2021-08-05 | Janssen Pharmaceutica Nv | Spiro bicyclic inhibitors of menin-MLL interaction |
| KR102513564B1 (ko) | 2016-12-15 | 2023-03-22 | 얀센 파마슈티카 엔.브이. | 메닌-mll 상호작용의 아제판 억제제 |
| EA201991448A1 (ru) | 2017-01-06 | 2019-12-30 | Янссен Фармацевтика Нв | Азепановые ингибиторы взаимодействия менин-mll |
| 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 |
| EP3600313A4 (fr) | 2017-03-31 | 2020-09-23 | The Regents of The University of Michigan | Pipéridines en tant qu'inhibiteurs covalents de la ménine |
| US11542248B2 (en) | 2017-06-08 | 2023-01-03 | Kura Oncology, Inc. | Methods and compositions for inhibiting the interaction of menin with MLL proteins |
| TW201920170A (zh) * | 2017-09-20 | 2019-06-01 | 美商庫拉腫瘤技術股份有限公司 | 經取代之menin-mll 抑制劑及使用方法 |
| JP7307729B2 (ja) | 2017-12-20 | 2023-07-12 | ヤンセン ファーマシューティカ エヌ．ベー． | メニン－ｍｌｌ相互作用のエキソ－アザスピロ阻害剤 |
| US11396517B1 (en) | 2017-12-20 | 2022-07-26 | Janssen Pharmaceutica Nv | Exo-aza spiro inhibitors of menin-MLL interaction |
| CN110204552B (zh) * | 2018-02-28 | 2021-08-17 | 中国科学院上海药物研究所 | 一类噻吩并[3,2-d]嘧啶衍生物、其制备方法、药物组合物与用途 |
| 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 |
| JP2022503792A (ja) * | 2018-09-26 | 2022-01-12 | クラ オンコロジー，インク． | メニン阻害剤を用いた血液悪性腫瘍の処置 |
| CN110964016B (zh) * | 2018-09-29 | 2021-05-28 | 南京药捷安康生物科技有限公司 | 氨基降茨烷衍生物及其制备方法与应用 |
| CA3116141C (fr) | 2018-12-06 | 2023-09-05 | Daiichi Sankyo Company, Limited | Derive de cycloalcane-1,3-diamine |
| TW202043205A (zh) | 2018-12-31 | 2020-12-01 | 美商拜歐米富士恩有限公司 | Menin-mll相互作用之抑制劑 |
| WO2020142557A1 (fr) | 2018-12-31 | 2020-07-09 | Biomea Fusion, Llc | Inhibiteurs irréversibles de l'interaction ménine-mll |
| US12319676B2 (en) | 2019-02-15 | 2025-06-03 | Bristol-Myers Squibb Company | Substituted amide compounds useful as farnesoid X receptor modulators |
| JP7449300B2 (ja) | 2019-02-15 | 2024-03-13 | ブリストル－マイヤーズ スクイブ カンパニー | ファルネソイドｘ受容体モジュレータとして有用な置換アミド化合物 |
| JP7465883B2 (ja) | 2019-02-15 | 2024-04-11 | ブリストル－マイヤーズ スクイブ カンパニー | ファルネソイドｘ受容体モジュレータとしての置換二環式化合物 |
| UY38988A (es) | 2019-12-19 | 2021-06-30 | Janssen Pharmaceutica Nv | Derivados espiráncos sustituidos de cadena lineal |
| 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 |
| IL297039A (en) * | 2020-04-07 | 2022-12-01 | Syndax Pharmaceuticals Inc | Combinations of menin inhibitors and cyp3a4 inhibitors and methods of use thereof |
| EP4232020A4 (fr) * | 2020-10-21 | 2024-08-07 | Kura Oncology, Inc. | Traitement de malignités hématologiques par des inhibiteurs de ménine |
| BR112023021040A2 (pt) | 2021-05-08 | 2024-02-06 | Janssen Pharmaceutica Nv | Derivados espiro substituídos |
| EP4334310A1 (fr) | 2021-05-08 | 2024-03-13 | JANSSEN Pharmaceutica NV | Dérivés spiro substitués |
| AR125866A1 (es) | 2021-05-14 | 2023-08-23 | Syndax Pharmaceuticals Inc | Inhibidores de la interacción de menina-mll |
| CA3218479A1 (fr) | 2021-06-01 | 2022-12-08 | Wei Cai | Derives de phenyl-1h-pyrrolo [2, 3-c] pyridine substitues |
| WO2022253289A1 (fr) | 2021-06-03 | 2022-12-08 | Janssen Pharmaceutica Nv | Pyridazines ou 1,2,4-triazines substituées par des amines spirocycliques |
| AU2022292697A1 (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 |
| JP7891524B2 (ja) | 2021-08-11 | 2026-07-16 | バイオメア フュージョン，インコーポレイテッド | 真性糖尿病に対するメニン－ｍｌｌ相互作用の共有結合性阻害剤 |
| MX2024002189A (es) | 2021-08-20 | 2024-06-11 | Biomea Fusion Inc | Forma cristalina de n-[4-[4-(4-morfolinil)-7h-pirrolo[2,3-d]pirimi din-6-il]fenil]-4-[[3(r)-[(1-oxo)-2-propen-1-il)amino]-1-piperidi nil]metil]-2-piridinacarboxamida, un inhibidor irreversible de menina-mll para el tratamiento del cancer. |
| MX2024007201A (es) * | 2021-12-15 | 2024-08-06 | Dana Farber Cancer Inst Inc | Direccionamiento terapeutico del tumor del estroma gastrointestinal (gist) mediante la alteracion del complejo epigenetico de menina-mll. |
| CN120514709A (zh) * | 2022-05-09 | 2025-08-22 | 赛达克斯制药股份有限公司 | 用于治疗癌症的menin-mll抑制剂 |
| US20260151399A1 (en) | 2022-11-24 | 2026-06-04 | Oryzon Genomics, S.A. | Combinations of lsd1 inhibitors and menin inhibitors for treating cancer |
| WO2024155719A1 (fr) | 2023-01-18 | 2024-07-25 | Biomea Fusion, Inc. | Formes cristallines de n-[4-[4-(4-morpholinyl)-7h-pyrrolo[2,3-d]pyrimidin-6-yl]phényl]-4-[[3(r)-[(l-oxo-2-propen-l-yl)amino]-l-pipéridinyl]méthyl]-2- pyridinecarboxamide en tant qu'inhibiteur covalent de l'interaction ménine-mll |
| AR132185A1 (es) | 2023-03-24 | 2025-06-04 | Acerta Pharma Bv | COMPUESTOS DE 1-H-PIRROLO[2,3-c]PIRIDINA |
Family Cites Families (92)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US510A (en) | 1837-12-07 | soeel | ||
| US5863A (en) | 1848-10-17 | Matthias p | ||
| US949A (en) | 1838-09-27 | Improvement in roller cotton-gins for ginning long-staple and other kinds of cotton | ||
| US5861A (en) | 1848-10-17 | Locking umbrella and parasol | ||
| US1007727A (en) | 1908-02-17 | 1911-11-07 | Oscar F Onken | Auxiliary table-top. |
| US5033252A (en) | 1987-12-23 | 1991-07-23 | Entravision, Inc. | Method of packaging and sterilizing a pharmaceutical product |
| US5052558A (en) | 1987-12-23 | 1991-10-01 | Entravision, Inc. | Packaged pharmaceutical product |
| GB8827305D0 (en) | 1988-11-23 | 1988-12-29 | British Bio Technology | Compounds |
| US5323907A (en) | 1992-06-23 | 1994-06-28 | Multi-Comp, Inc. | Child resistant package assembly for dispensing pharmaceutical medications |
| DE4239169A1 (de) | 1992-11-21 | 1994-05-26 | Merck Patent Gmbh | Cyclobutan - Benzol - Derivate |
| US5455258A (en) | 1993-01-06 | 1995-10-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
| US5863949A (en) | 1995-03-08 | 1999-01-26 | Pfizer Inc | Arylsulfonylamino hydroxamic acid derivatives |
| CA2218503C (fr) | 1995-04-20 | 2001-07-24 | Pfizer Inc. | Derives d'acide hydroxamique arylsufonyle en tant qu'inhibiteurs de mmp et de tnf |
| DK0780386T3 (da) | 1995-12-20 | 2003-02-03 | Hoffmann La Roche | Matrixmetalloproteaseinhibitorer |
| JP3195756B2 (ja) | 1996-07-04 | 2001-08-06 | 公子 吉水 | 潤滑補助体 |
| EP0923585B1 (fr) | 1996-07-18 | 2002-05-08 | Pfizer Inc. | Composes a base de phosphinate inhibiteurs des metalloproteases matricielles |
| JP3333870B2 (ja) | 1996-07-26 | 2002-10-15 | 国土交通省北陸地方整備局長 | 草刈機 |
| EP0922030A1 (fr) | 1996-08-23 | 1999-06-16 | Pfizer Inc. | Derives de l'acide arylsulfonylamino hydroxamique |
| US5866562A (en) | 1996-10-25 | 1999-02-02 | Bayer Aktiengesellschaft | Ring-bridged bis-quinolines |
| US6077864A (en) | 1997-01-06 | 2000-06-20 | Pfizer Inc. | Cyclic sulfone derivatives |
| HUP0000852A2 (hu) | 1997-02-03 | 2001-05-28 | Pfizer Products Inc. | Aril-szulfonil-amino-hidroxámsav-származékok, valamint e vegyületeket tartalmazó gyógyászati készítmények |
| JP2000507975A (ja) | 1997-02-07 | 2000-06-27 | ファイザー・インク | Ｎ−ヒドロキシ−β−スルホニルプロピオンアミド誘導体類及びそれらのマトリックスメタロプロテイナーゼ阻害薬としての使用 |
| NZ336836A (en) | 1997-02-11 | 2001-02-23 | Pfizer | Arylsulfonyl hydroxamic acid derivatives suitable for a broad range of medicinal treatments |
| JPH10330377A (ja) | 1997-06-02 | 1998-12-15 | Kyowa Hakko Kogyo Co Ltd | ピペリジン誘導体 |
| GB9725782D0 (en) | 1997-12-05 | 1998-02-04 | Pfizer Ltd | Therapeutic agents |
| GB9801690D0 (en) | 1998-01-27 | 1998-03-25 | Pfizer Ltd | Therapeutic agents |
| US6479487B1 (en) | 1998-02-26 | 2002-11-12 | Aventis Pharmaceuticals Inc. | 6, 9-disubstituted 2-[trans-(4-aminocyclohexyl)amino] purines |
| PA8469401A1 (es) | 1998-04-10 | 2000-05-24 | Pfizer Prod Inc | Derivados biciclicos del acido hidroxamico |
| PA8469501A1 (es) | 1998-04-10 | 2000-09-29 | Pfizer Prod Inc | Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico |
| PA8474101A1 (es) | 1998-06-19 | 2000-09-29 | Pfizer Prod Inc | Compuestos de pirrolo [2,3-d] pirimidina |
| EP2048142A3 (fr) | 2001-04-26 | 2009-04-22 | Eisai R&D Management Co., Ltd. | Composé cyclique condensé contenant de l'azote disposant d'un groupe pyrazolyl en tant que groupe substituant et sa composition pharmaceutique |
| CN101100472A (zh) | 2001-04-30 | 2008-01-09 | 美国拜尔公司 | 4-氨基-5,6-取代的噻吩并[2,3-d]嘧啶化合物及其应用 |
| WO2003022214A2 (fr) | 2001-09-06 | 2003-03-20 | Millennium Pharmaceuticals, Inc. | Composes a base de piperazine et d'homopiperazine |
| AU2003255482A1 (en) | 2002-10-02 | 2004-04-23 | Merck Patent Gmbh | Use of 4 amino-quinazolines as anti cancer agents |
| WO2004030671A2 (fr) | 2002-10-02 | 2004-04-15 | Merck Patent Gmbh | Utilisation de 4-amino-quinazolines comme agents anticancereux |
| US20050222175A1 (en) | 2004-03-31 | 2005-10-06 | Dhanoa Dale S | New piperidinylamino-thieno[2,3-D] pyrimidine compounds |
| US7612078B2 (en) | 2003-03-31 | 2009-11-03 | Epix Delaware, Inc. | Piperidinylamino-thieno[2,3-D] pyrimidine compounds |
| BRPI0408988A (pt) | 2003-03-31 | 2006-03-28 | Predix Pharmaceuticals Holding | composto de piperidinilamino-tieno[2,3-d]pirimidina |
| EP1663962A4 (fr) | 2003-08-22 | 2007-08-22 | Dendreon Corp | Compositions et methodes permettant de traiter une maladie associee a l'expression de trp-p8 |
| US20050123906A1 (en) | 2003-11-06 | 2005-06-09 | Rana Tariq M. | Protein modulation |
| WO2006014420A1 (fr) | 2004-07-06 | 2006-02-09 | Angion Biomedica Corporation | Modulateurs quinazoline d'activite de facteur de croissance hepatocyte/c-met permettant de traiter le cancer |
| ES2371774T3 (es) | 2005-06-03 | 2012-01-10 | Abbott Laboratories | Derivados de ciclobutilamina. |
| US20060281769A1 (en) | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using thienopyrimidine and thienopyridine kinase modulators |
| US20060281771A1 (en) | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using aminoquinoline and aminoquinazoline kinase modulators |
| US20090221559A1 (en) | 2005-09-02 | 2009-09-03 | Jean-Francois Bonfanti | Benzodiazepines as hcv inhibitors |
| JP5456315B2 (ja) | 2005-09-19 | 2014-03-26 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | シクロブタンおよびスピロ［３．３］ヘプタン化合物類 |
| FR2891829A1 (fr) | 2005-10-12 | 2007-04-13 | Sanofi Aventis Sa | Derives de la 4-amino-quinazoline, leur preparation et leur application en therapeutique |
| ATE541844T1 (de) | 2005-12-21 | 2012-02-15 | Abbott Lab | Antivirale verbindungen |
| CA2651898A1 (fr) | 2006-04-07 | 2007-10-18 | Develogen Aktiengesellschaft | Thienopyrimidines ayant une activite inhibitrice mnk1/mnk2 utilisees dans des compositions pharmaceutiques |
| EP1903044A1 (fr) * | 2006-09-14 | 2008-03-26 | Novartis AG | Derivés de l'adénosine en tant qu' agonistes du récepteur A2A |
| WO2008070303A2 (fr) | 2006-10-19 | 2008-06-12 | The University Of Chicago | Agents thérapeutiques permettant d'inhiber l'interaction mll-ménine pour traiter une leucémie |
| EP1947103A1 (fr) | 2007-01-22 | 2008-07-23 | 4Sc Ag | Aryloxypropanolamines, procédés de préparation correspondant et utilisation d'aryloxypropanolamines en tant que médicaments |
| WO2008099019A1 (fr) | 2007-02-16 | 2008-08-21 | Tibotec Pharmaceuticals Ltd. | 6-hydroxy-dibenzodiazépinones utiles comme inhibiteurs du virus de l'hépatite c |
| FR2913017A1 (fr) | 2007-02-23 | 2008-08-29 | Cerep Sa | Derives de piperidine et piperazine comme agents anti-neoplasiques ou inhibiteurs de proliferation cellulaire |
| ATE496022T1 (de) | 2007-03-19 | 2011-02-15 | Council Scient Ind Res | Anthranilsäure-derivat als antikrebswirkstoff und verfahren zur herstellung davon |
| WO2008135232A1 (fr) | 2007-05-02 | 2008-11-13 | Riccardo Cortese | Utilisation et compositions de dérivés de purine pour le traitement de troubles prolifératifs |
| EP2148944A1 (fr) | 2007-05-25 | 2010-02-03 | Burnham Institute for Medical Research | Inhibiteurs de mort cellulaire induite par la thapsigargine |
| WO2009017838A2 (fr) | 2007-08-01 | 2009-02-05 | Exelixis, Inc. | Combinaisons d'inhibiteurs jak-2 et d'autres agents |
| WO2009064388A2 (fr) | 2007-11-09 | 2009-05-22 | Liu Jun O | Inhibiteurs de la méthionine aminopeptidase humaine 1 et procédés de traitement de troubles |
| AU2008345225A1 (en) | 2007-12-21 | 2009-07-09 | University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| JP2011523420A (ja) | 2008-05-22 | 2011-08-11 | アラーガン インコーポレイテッド | Ｃｘｃｒ４受容体において活性を有する二環式化合物 |
| DE102008027574A1 (de) * | 2008-06-10 | 2009-12-17 | Merck Patent Gmbh | Neue Pyrrolidinderivate als MetAP-2 Inhibitoren |
| CN102203067B (zh) | 2008-08-25 | 2014-01-15 | Irm责任有限公司 | Hedgehog通路调节剂 |
| AR073739A1 (es) | 2008-09-10 | 2010-12-01 | Kalypsys Inc | Aminopirimidinas como inhibidores de los receptores de histamina |
| JP5690823B2 (ja) | 2009-07-08 | 2015-03-25 | レオ ファーマ アクティーゼルスカブ | Ｊａｋ受容体およびタンパク質チロシンキナーゼ阻害薬としての複素環化合物 |
| WO2011014128A1 (fr) | 2009-07-30 | 2011-02-03 | National University Of Singapore | Inhibiteurs à petite molécule d'isoprénylcystéine carboxyl méthyltranférase avec une activité anticancer potentielle |
| AU2010289321A1 (en) | 2009-09-04 | 2012-04-05 | The Regents Of The University Of Michigan | Compositions and methods for treatment of leukemia |
| BR112012019561A2 (pt) | 2010-02-22 | 2019-09-24 | Merck Patent Gmbh | hetarilamino naftiridinas |
| BR112013003864B1 (pt) | 2010-08-20 | 2021-08-31 | Hutchison Medipharma Limited | Compostos de pirrolpirimidina, composição e uso dos mesmos |
| WO2013019966A1 (fr) * | 2011-08-04 | 2013-02-07 | Allergan, Inc. | Dérivés bicycliques aromatiques utiles en tant que modulateurs du récepteur cxcr4 |
| GB201114212D0 (en) | 2011-08-18 | 2011-10-05 | Ucb Pharma Sa | Therapeutic agents |
| AR090037A1 (es) | 2011-11-15 | 2014-10-15 | Xention Ltd | Derivados de tieno y/o furo-pirimidinas y piridinas inhibidores de los canales de potasio |
| CN103833759A (zh) * | 2012-11-23 | 2014-06-04 | 华东理工大学 | 作为blk、flt3抑制剂的蝶啶酮衍生物及其应用 |
| AU2014249233A1 (en) * | 2013-03-13 | 2015-09-24 | The Regents Of The University Of Michigan | Compositions comprising thienopyrimidine and thienopyridine compounds and methods of use thereof |
| EP2968285A4 (fr) | 2013-03-13 | 2016-12-21 | Flatley Discovery Lab | Composés et procédés pour le traitement de fibrose kystique |
| US9212180B2 (en) * | 2013-06-12 | 2015-12-15 | The Regents Of The University Of Michigan | Menin-MLL inhibitors and methods of use thereof |
| MX358346B (es) * | 2014-04-04 | 2018-08-15 | Syros Pharmaceuticals Inc | Inhibidores de la quinasa dependiente de ciclina 7 (cdk7). |
| US20170119769A1 (en) | 2014-06-10 | 2017-05-04 | The Trustees Of The University Of Pennsylvania | Scaffolds for inhibitors of menin-mll interactions |
| USRE49687E1 (en) | 2014-09-09 | 2023-10-10 | The Regents Of The University Of Michigan | Thienopyrimidine and thienopyridine compounds and methods of use thereof |
| 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 |
| WO2016197027A1 (fr) | 2015-06-04 | 2016-12-08 | Kura Oncology, Inc. | Méthodes et compositions d'inhibition de l'interaction de la ménine avec les protéines mll |
| BR112018012707A2 (pt) | 2015-12-22 | 2019-01-29 | Vitae Pharmaceuticals Inc | inibidores da interação de menin-mll |
| AU2017212572A1 (en) | 2016-01-26 | 2018-08-23 | Memorial Sloan-Kettering Cancer Center | Targeting chromatin regulators inhibits leukemogenic gene expression in NPM1 mutant leukemia |
| US10752639B2 (en) | 2016-03-16 | 2020-08-25 | Kura Oncology, Inc. | Bridged bicyclic inhibitors of menin-MLL and methods of use |
| WO2017161028A1 (fr) | 2016-03-16 | 2017-09-21 | Kura Oncology, Inc. | Inhibiteurs substitués de ménine-mll et méthodes d'utilisation |
| CN109415337B (zh) | 2016-05-02 | 2022-01-18 | 密执安大学评议会 | 作为多发性内分泌腺瘤蛋白抑制剂的哌啶 |
| WO2017207387A1 (fr) | 2016-05-31 | 2017-12-07 | Bayer Pharma Aktiengesellschaft | Dérivés d'azétidine spiro condensés en tant qu'inhibiteurs de l'interaction ménine-mml1 |
| ES2831084T3 (es) | 2016-06-10 | 2021-06-07 | Vitae Pharmaceuticals Inc | Inhibidores de la interacción menina-MLL |
| WO2018024602A1 (fr) | 2016-08-04 | 2018-02-08 | Bayer Aktiengesellschaft | 2,7-diazaspiro [4,4] nonanes |
| CA3033239A1 (fr) | 2016-09-14 | 2018-03-22 | Janssen Pharmaceutica Nv | Inhibiteurs spiro bicycliques de l'interaction menine-mll |
| TWI753016B (zh) | 2016-09-14 | 2022-01-21 | 比利時商健生藥品公司 | Menin-mll相互作用之稠合二環抑制劑 |
| CN118359610A (zh) | 2016-09-16 | 2024-07-19 | 生命医药有限责任公司 | Menin-mll相互作用的抑制剂 |
-
2017
- 2017-03-15 US US16/082,645 patent/US10752639B2/en active Active
- 2017-03-15 BR BR112018068702A patent/BR112018068702A2/pt not_active Application Discontinuation
- 2017-03-15 MY MYPI2018001516A patent/MY199965A/en unknown
- 2017-03-15 CA CA3015845A patent/CA3015845A1/fr active Pending
- 2017-03-15 EP EP17767444.7A patent/EP3429585B1/fr active Active
- 2017-03-15 JP JP2018544323A patent/JP7000333B2/ja active Active
- 2017-03-15 WO PCT/US2017/022535 patent/WO2017161002A1/fr not_active Ceased
- 2017-03-15 SG SG11201807834WA patent/SG11201807834WA/en unknown
- 2017-03-15 TW TW106108619A patent/TWI743096B/zh active
- 2017-03-15 PH PH1/2018/501955A patent/PH12018501955B1/en unknown
- 2017-03-15 KR KR1020187029700A patent/KR102419524B1/ko active Active
- 2017-03-15 MX MX2018011092A patent/MX387806B/es unknown
- 2017-03-15 AU AU2017235462A patent/AU2017235462B2/en active Active
- 2017-03-15 MA MA043823A patent/MA43823A/fr unknown
- 2017-03-15 CN CN201780030449.4A patent/CN109640987B/zh active Active
-
2018
- 2018-08-30 ZA ZA2018/05845A patent/ZA201805845B/en unknown
- 2018-09-05 IL IL261625A patent/IL261625B/en unknown
-
2020
- 2020-07-13 US US16/927,844 patent/US11555041B2/en active Active
-
2025
- 2025-01-10 US US19/017,093 patent/US20250340566A1/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| AU2017235462A1 (en) | 2018-09-27 |
| MX387806B (es) | 2025-03-19 |
| CN109640987B (zh) | 2022-12-02 |
| IL261625B (en) | 2021-08-31 |
| ZA201805845B (en) | 2023-03-29 |
| US11555041B2 (en) | 2023-01-17 |
| US10752639B2 (en) | 2020-08-25 |
| CA3015845A1 (fr) | 2017-09-21 |
| KR20180127406A (ko) | 2018-11-28 |
| EP3429585A4 (fr) | 2019-10-09 |
| EP3429585A1 (fr) | 2019-01-23 |
| PH12018501955A1 (en) | 2019-06-17 |
| SG11201807834WA (en) | 2018-10-30 |
| EP3429585B1 (fr) | 2021-11-24 |
| US20250340566A1 (en) | 2025-11-06 |
| TW201742870A (zh) | 2017-12-16 |
| JP7000333B2 (ja) | 2022-02-10 |
| MX2018011092A (es) | 2018-11-22 |
| US20190092783A1 (en) | 2019-03-28 |
| US20210107917A1 (en) | 2021-04-15 |
| IL261625A (en) | 2018-10-31 |
| PH12018501955B1 (en) | 2024-01-24 |
| AU2017235462B2 (en) | 2021-07-01 |
| MY199965A (en) | 2023-11-30 |
| CN109640987A (zh) | 2019-04-16 |
| WO2017161002A1 (fr) | 2017-09-21 |
| BR112018068702A2 (pt) | 2019-01-15 |
| TWI743096B (zh) | 2021-10-21 |
| KR102419524B1 (ko) | 2022-07-08 |
| HK1258821A1 (en) | 2019-11-22 |
| JP2019508426A (ja) | 2019-03-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP3429585A4 (fr) | Inhibiteurs bicycliques pontés de ménine-mll et méthodes d'utilisation | |
| EP3429591A4 (fr) | Inhibiteurs substitués de ménine-mll et méthodes d'utilisation | |
| EP3684361A4 (fr) | Inhibiteurs substitués de ménine-mll et méthodes d'utilisation | |
| EP3317273A4 (fr) | Inhibiteurs d'egfr et méthodes d'utilisation de ceux-ci | |
| EP3700527A4 (fr) | Inhibiteurs de papd5 et leurs méthodes d'utilisation | |
| MA42925A (fr) | Anticorps anti-tigit et méthodes d'utilisation | |
| EP3634430A4 (fr) | Agents multibiotiques et procédés d'utilisation de ceux-ci | |
| EP3337517A4 (fr) | Conjugués anticorps-médicaments anti-dll3 et méthodes d'utilisation | |
| EP3393382A4 (fr) | Couteau ophtalmique et méthodes d'utilisation | |
| EP3377612A4 (fr) | Expression fonctionnelle de monooxygénases et procédés d'utilisation | |
| MA42243A (fr) | Anticorps de facteur xi et méthodes d'utilisation | |
| EP3402549A4 (fr) | Compositions pour micro-aiguilles et méthodes d'utilisation de celles-ci | |
| PT3548033T (pt) | Compostos e respectivos métodos de utilização | |
| HRP20251095T1 (hr) | Neoantigeni i metode njihove uporabe | |
| MA44990A (fr) | Polythérapies d'inhibiteurs de hdac et d'inhibiteurs de pd-l1 | |
| MA48579A (fr) | Anticorps anti-pd1 et méthodes d'utilisation de ceux-ci | |
| EP3394065A4 (fr) | Tétrahydropyranyl-amino-pyrrolopyrimidinone et procédés d'utilisation associés | |
| EP3303435A4 (fr) | Hydrofluoroléfines et procédés d'utilisation associés | |
| MA40921A (fr) | Récepteurs antigéniques chimériques anti-cldn et procédés d'utilisation | |
| EP3373969A4 (fr) | Composés interagissant avec le glycane et méthodes d'utilisation | |
| IL283782A (en) | Anellosomes and methods of use | |
| EP3635000A4 (fr) | Manabodies et procédés d'utilisation | |
| MA46422A (fr) | Oligonucléotides modifiés et méthodes d'utilisation | |
| IL280655A (en) | Particles containing coloring agents and methods of using the same | |
| EP3543240A4 (fr) | Inhibiteur de l'urat1 et son utilisation |