MA43823A - Inhibiteurs bicycliques pontés de ménine-mll et méthodes d'utilisation - Google Patents

Inhibiteurs bicycliques pontés de ménine-mll et méthodes d'utilisation

Info

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
Application number
MA043823A
Other languages
English (en)
Inventor
Dmitry Borkin
Tomasz Cierpicki
Jolanta Grembecka
Szymon Klossowski
Liansheng Li
Jonathan Pollock
Pingda Ren
Yi Wang
Tao Wu
Original Assignee
Kura Oncology Inc
Univ Michigan Regents
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kura Oncology Inc, Univ Michigan Regents filed Critical Kura Oncology Inc
Publication of MA43823A publication Critical patent/MA43823A/fr

Links

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
MA043823A 2016-03-16 2017-03-15 Inhibiteurs bicycliques pontés de ménine-mll et méthodes d'utilisation MA43823A (fr)

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 (2) 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)
HK (1) HK1258821A1 (fr)
IL (1) IL261625B (fr)
MA (1) MA43823A (fr)
MX (1) MX2018011092A (fr)
PH (1) PH12018501955A1 (fr)
SG (1) SG11201807834WA (fr)
TW (1) TWI743096B (fr)
WO (1) WO2017161002A1 (fr)
ZA (1) ZA201805845B (fr)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10246464B2 (en) 2014-09-09 2019-04-02 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
PT3429591T (pt) 2016-03-16 2023-06-21 Univ Michigan Regents Derivados de tieno[2,3-d]pirimidina substituídos como inibidores de menina-llm e métodos de utilização
TWI743096B (zh) 2016-03-16 2021-10-21 美商庫拉腫瘤技術股份有限公司 Menin-mll之橋聯雙環抑制劑及使用方法
CA3022868A1 (fr) 2016-05-02 2017-11-09 Shaomeng Wang Piperidines en tant qu'inhibiteurs de menine
MX2019002959A (es) 2016-09-14 2019-07-04 Janssen Pharmaceutica Nv Inhibidores biciclicos condensados de la interaccion de menina-mll.
EP3512857B1 (fr) 2016-09-14 2021-02-24 Janssen Pharmaceutica NV Inhibiteurs spiro-bicyclique de menin-mll-interaction
EP3555103B1 (fr) 2016-12-15 2021-09-22 Janssen Pharmaceutica NV Dérivés d'azépane en tant qu'inhibiteurs de l'interaction ménine-mll
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
SG11201909083UA (en) 2017-03-31 2019-10-30 Univ Michigan Regents Piperidines as covalent menin inhibitors
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
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
WO2019189732A1 (fr) 2018-03-30 2019-10-03 大日本住友製薬株式会社 Dérivé d'amine secondaire cyclique réticulé optiquement actif
CN113164443A (zh) * 2018-09-26 2021-07-23 库拉肿瘤学公司 用多发性内分泌抑癌蛋白抑制剂治疗血液系统恶性肿瘤
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
TW202039512A (zh) 2018-12-06 2020-11-01 日商第一三共股份有限公司 環烷-1,3-二胺化合物
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
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
KR20230007359A (ko) * 2020-04-07 2023-01-12 신닥스 파마슈티컬스, 인크. 메닌 억제제 및 cyp3a4 억제제의 조합물 및 그의 사용 방법
BR112023023154A2 (pt) 2021-05-08 2024-01-23 Janssen Pharmaceutica Nv Derivados espiro substituídos
CN117730081A (zh) 2021-05-08 2024-03-19 詹森药业有限公司 取代的螺环衍生物
EP4337203A1 (fr) 2021-05-14 2024-03-20 Syndax Pharmaceuticals, Inc. Inhibiteurs de l'interaction ménine-mll
AU2022286467A1 (en) 2021-06-01 2024-01-25 Janssen Pharmaceutica Nv SUBSTITUTED PHENYL-1H-PYRROLO[2, 3-c]PYRIDINE DERIVATIVES
CA3218340A1 (fr) 2021-06-03 2022-12-08 Janssen Pharmaceutica Nv Pyridazines ou 1,2,4-triazines substituees par des amines spirocycliques
CN117597348A (zh) 2021-06-17 2024-02-23 詹森药业有限公司 用于治疗诸如癌症的疾病的(r)-n-乙基-5-氟-n-异丙基-2-((5-(2-(6-((2-甲氧基乙基)(甲基)氨基)-2-甲基己-3-基)-2,6-二氮杂螺[3.4]辛-6-基)-1,2,4-三嗪-6-基)氧基)苯甲酰胺苯磺酸盐
WO2023220098A1 (fr) * 2022-05-09 2023-11-16 Syndax Pharmaceuticals, Inc. Inhibiteurs de ménine-mll pour le traitement du cancer

Family Cites Families (92)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US949A (en) 1838-09-27 Improvement in roller cotton-gins for ginning long-staple and other kinds of cotton
US5863A (en) 1848-10-17 Matthias p
US510A (en) 1837-12-07 soeel
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
PT821671E (pt) 1995-04-20 2001-04-30 Pfizer Derivados do acido arilsulfonil hidroxamico como inibidores de mmp e tnf
DE69624081T2 (de) 1995-12-20 2003-06-12 Hoffmann La Roche Matrix-metalloprotease Inhibitoren
JP3195756B2 (ja) 1996-07-04 2001-08-06 公子 吉水 潤滑補助体
KR20000067904A (ko) 1996-07-18 2000-11-25 디. 제이. 우드, 스피겔 알렌 제이 매트릭스 메탈로프로테아제의 포스피네이트계 억제제
JP3333870B2 (ja) 1996-07-26 2002-10-15 国土交通省北陸地方整備局長 草刈機
PL331895A1 (en) 1996-08-23 1999-08-16 Pfizer Arylosulphonylamino derivatives of hydroxamic acid
US5866562A (en) 1996-10-25 1999-02-02 Bayer Aktiengesellschaft Ring-bridged bis-quinolines
CA2277100C (fr) 1997-01-06 2005-11-22 Pfizer Inc. Derives de sulfone cyclique
CN1113862C (zh) 1997-02-03 2003-07-09 辉瑞产品公司 芳基磺酰氨基异羟肟酸衍生物
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
DE60227794D1 (de) 2001-04-26 2008-09-04 Eisai R&D Man Co Ltd Stickstoffhaltige verbindung mit kondensiertem ring und pyrazolylgruppe als substituent und medizinische zusammensetzung davon
US6849638B2 (en) 2001-04-30 2005-02-01 Bayer Pharmaceuticals Corporation 4-amino-5,6-substituted thiopheno [2,3-d] pyrimidines, pharmaceutical compositions containing the same, and their use in the treatment or prevention of pde7b-mediated diseases and conditions
WO2003022214A2 (fr) 2001-09-06 2003-03-20 Millennium Pharmaceuticals, Inc. Composes a base de piperazine et d'homopiperazine
WO2004030671A2 (fr) 2002-10-02 2004-04-15 Merck Patent Gmbh Utilisation de 4-amino-quinazolines comme agents anticancereux
AU2003255482A1 (en) 2002-10-02 2004-04-23 Merck Patent Gmbh Use of 4 amino-quinazolines as anti cancer agents
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
MXPA05009818A (es) 2003-03-31 2006-03-13 Predix Pharmaceuticals Holding Nuevos compuestos de piperidinilamino-tieno[2,3-d] pirimidina.
US8362264B2 (en) 2003-08-22 2013-01-29 Dendreon Corporation Compositions and methods for the treatment of disease associated with Trp-p8 expression
US20050123906A1 (en) 2003-11-06 2005-06-09 Rana Tariq M. Protein modulation
CA2573103A1 (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
ATE530519T1 (de) * 2005-06-03 2011-11-15 Abbott Lab Cyclobutylaminderivate
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
AU2006286441A1 (en) 2005-09-02 2007-03-08 Janssen R&D Ireland Benzodiazepines as HCV inhibitors
KR101359093B1 (ko) 2005-09-19 2014-02-05 메르크 파텐트 게엠베하 시클로부테인 및 스피로［3.3］헵테인 화합물
FR2891829A1 (fr) 2005-10-12 2007-04-13 Sanofi Aventis Sa Derives de la 4-amino-quinazoline, leur preparation et leur application en therapeutique
WO2007076034A2 (fr) 2005-12-21 2007-07-05 Abbott Laboratories Composes antiviraux
EP2004656B1 (fr) 2006-04-07 2013-07-10 Boehringer Ingelheim International GmbH Thiénopyrimidines ayant une activité inhibitrice mnk1/mnk2 utilisées 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
US8242078B2 (en) * 2006-10-19 2012-08-14 The University Of Chicago Therapeutics to inhibit MLL-menin interaction for treating leukemia
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
WO2008114275A2 (fr) 2007-03-19 2008-09-25 Council Of Scientific & Industrial Research Nouveau dérivé de l'acide anthranilique comme anticancéreux potentiel et procédé de préparation de celui-ci
WO2008135232A1 (fr) 2007-05-02 2008-11-13 Riccardo Cortese Utilisation et compositions de dérivés de purine pour le traitement de troubles prolifératifs
JP2010530736A (ja) 2007-05-25 2010-09-16 バーンハム インスティトゥート フォー メディカル リサーチ タプシガルジンにより誘導される細胞死の阻害剤
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
US8642660B2 (en) 2007-12-21 2014-02-04 The University Of Rochester Method for altering the lifespan of eukaryotic organisms
RU2010152290A (ru) 2008-05-22 2012-06-27 Аллерган, Инк. (Us) Бициклические соединения, обладающие активностью при рецепторе сxcr4
DE102008027574A1 (de) 2008-06-10 2009-12-17 Merck Patent Gmbh Neue Pyrrolidinderivate als MetAP-2 Inhibitoren
US8507491B2 (en) 2008-08-25 2013-08-13 Irm Llc Compounds and compositions as hedgehog pathway inhibitors
AU2009291783A1 (en) 2008-09-10 2010-03-18 Alcon Research, Ltd Aminopyrimidine inhibitors of histamine receptors for the treatment of disease
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
US8742100B2 (en) 2009-07-30 2014-06-03 National University Of Singapore Small molecule inhibitors of isoprenylcysteine carboxyl methyltransferase with potential anticancer activity
EP2473054B1 (fr) 2009-09-04 2017-06-14 The Regents of the University of Michigan Compositions et méthodes de traitement de la leucémie
EA022064B1 (ru) 2010-02-22 2015-10-30 Мерк Патент Гмбх Гетариламинонафтиридины в качестве ингибиторов атф-связывающих белков
CA2808543C (fr) 2010-08-20 2016-01-26 Hutchison Medipharma Limited Composes de pyrrolopyrimidine et leurs utilisations
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
US20140371238A1 (en) 2013-03-13 2014-12-18 Flatley Discovery Lab Compounds and methods for the treatment of cystic fibrosis
CN105188705A (zh) 2013-03-13 2015-12-23 密歇根大学董事会 包含噻吩并嘧啶和噻吩并吡啶化合物的组合物及其使用方法
US9212180B2 (en) * 2013-06-12 2015-12-15 The Regents Of The University Of Michigan Menin-MLL inhibitors and methods of use thereof
SG10201809260XA (en) * 2014-04-04 2018-11-29 Syros Pharmaceuticals Inc Inhibitors of cyclin-dependent kinase 7 (cdk7)
WO2015191701A1 (fr) * 2014-06-10 2015-12-17 The Trustees Of The University Of Pennsylvania Échafaudages pour inhibiteurs d'interactions ménine-mll
US10246464B2 (en) 2014-09-09 2019-04-02 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
US20190010167A1 (en) 2015-12-22 2019-01-10 Vitae Pharmaceuticals, Inc. Inhibitors of the menin-mll interaction
AU2017212572A1 (en) 2016-01-26 2018-08-23 Memorial Sloan-Kettering Cancer Center Targeting chromatin regulators inhibits leukemogenic gene expression in NPM1 mutant leukemia
TWI743096B (zh) 2016-03-16 2021-10-21 美商庫拉腫瘤技術股份有限公司 Menin-mll之橋聯雙環抑制劑及使用方法
PT3429591T (pt) 2016-03-16 2023-06-21 Univ Michigan Regents Derivados de tieno[2,3-d]pirimidina substituídos como inibidores de menina-llm e métodos de utilização
CA3022868A1 (fr) 2016-05-02 2017-11-09 Shaomeng Wang Piperidines en tant qu'inhibiteurs de menine
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
BR122024002146A2 (pt) 2016-06-10 2024-03-05 Vitae Pharmaceuticals, Inc. Compostos inibidores da interação de menina-llm e forma cristalina destes
WO2018024602A1 (fr) 2016-08-04 2018-02-08 Bayer Aktiengesellschaft 2,7-diazaspiro [4,4] nonanes
MX2019002959A (es) 2016-09-14 2019-07-04 Janssen Pharmaceutica Nv Inhibidores biciclicos condensados de la interaccion de menina-mll.
WO2018050686A1 (fr) 2016-09-14 2018-03-22 Janssen Pharmaceutica Nv Inhibiteurs spiro bicycliques de l'interaction ménine-mll
AR109658A1 (es) 2016-09-16 2019-01-09 Vitae Pharmaceuticals Inc Inhibidores de la interacción de menina-mll

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Publication number Publication date
AU2017235462A1 (en) 2018-09-27
CN109640987A (zh) 2019-04-16
BR112018068702A2 (pt) 2019-01-15
ZA201805845B (en) 2023-03-29
CA3015845A1 (fr) 2017-09-21
IL261625B (en) 2021-08-31
PH12018501955A1 (en) 2019-06-17
AU2017235462B2 (en) 2021-07-01
US20210107917A1 (en) 2021-04-15
HK1258821A1 (zh) 2019-11-22
KR20180127406A (ko) 2018-11-28
MX2018011092A (es) 2018-11-22
EP3429585B1 (fr) 2021-11-24
US10752639B2 (en) 2020-08-25
JP2019508426A (ja) 2019-03-28
SG11201807834WA (en) 2018-10-30
US11555041B2 (en) 2023-01-17
TWI743096B (zh) 2021-10-21
EP3429585A4 (fr) 2019-10-09
CN109640987B (zh) 2022-12-02
WO2017161002A1 (fr) 2017-09-21
EP3429585A1 (fr) 2019-01-23
JP7000333B2 (ja) 2022-02-10
TW201742870A (zh) 2017-12-16
KR102419524B1 (ko) 2022-07-08
US20190092783A1 (en) 2019-03-28
IL261625A (en) 2018-10-31

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