MX2023011779A - Combinaciones de inhibidores de lsd1 para el tratamiento de canceres mieloides. - Google Patents

Combinaciones de inhibidores de lsd1 para el tratamiento de canceres mieloides.

Info

Publication number
MX2023011779A
MX2023011779A MX2023011779A MX2023011779A MX2023011779A MX 2023011779 A MX2023011779 A MX 2023011779A MX 2023011779 A MX2023011779 A MX 2023011779A MX 2023011779 A MX2023011779 A MX 2023011779A MX 2023011779 A MX2023011779 A MX 2023011779A
Authority
MX
Mexico
Prior art keywords
combinations
lsd1 inhibitors
treating myeloid
myeloid cancers
cancers
Prior art date
Application number
MX2023011779A
Other languages
English (en)
Inventor
Tamara Maes
Natalia Sacilotto
Original Assignee
Oryzon Genomics Sa
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 Oryzon Genomics Sa filed Critical Oryzon Genomics Sa
Publication of MX2023011779A publication Critical patent/MX2023011779A/es

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
    • A61K31/13—Amines
    • A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
    • A61K31/137—Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine or methadone
    • 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
    • A61K31/4965—Non-condensed pyrazines
    • A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
    • 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
    • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • 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)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

La presente invención se refiere a combinaciones de inhibidores de LSD1 (o sales farmacéuticamente aceptables de los mismos) y gilteritinib (o una sal farmacéuticamente aceptable del mismo). Las combinaciones son particularmente útiles para el tratamiento de cánceres mieloides, tal como leucemia mieloide aguda o síndrome mielodisplásico.
MX2023011779A 2021-04-08 2022-03-21 Combinaciones de inhibidores de lsd1 para el tratamiento de canceres mieloides. MX2023011779A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP21382301 2021-04-08
EP21382676 2021-07-23
PCT/EP2022/057386 WO2022214303A1 (en) 2021-04-08 2022-03-21 Combinations of lsd1 inhibitors for treating myeloid cancers

Publications (1)

Publication Number Publication Date
MX2023011779A true MX2023011779A (es) 2023-11-22

Family

ID=81327652

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2023011779A MX2023011779A (es) 2021-04-08 2022-03-21 Combinaciones de inhibidores de lsd1 para el tratamiento de canceres mieloides.

Country Status (9)

Country Link
EP (1) EP4319732A1 (es)
JP (1) JP2024513260A (es)
KR (1) KR20230167102A (es)
AU (1) AU2022254484A1 (es)
BR (1) BR112023020554A2 (es)
CA (1) CA3231846A1 (es)
MX (1) MX2023011779A (es)
TW (1) TW202304416A (es)
WO (1) WO2022214303A1 (es)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024110649A1 (en) * 2022-11-24 2024-05-30 Oryzon Genomics, S.A. Combinations of lsd1 inhibitors and menin inhibitors for treating cancer

Family Cites Families (122)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2361242B1 (en) 2008-10-17 2018-08-01 Oryzon Genomics, S.A. Oxidase inhibitors and their use
WO2010084160A1 (en) 2009-01-21 2010-07-29 Oryzon Genomics S.A. Phenylcyclopropylamine derivatives and their medical use
WO2010143582A1 (ja) 2009-06-11 2010-12-16 公立大学法人名古屋市立大学 フェニルシクロプロピルアミン誘導体及びlsd1阻害剤
MX338041B (es) 2009-09-25 2016-03-30 Oryzon Genomics Sa Inhibidores de demetilasa-1 especificos de lisina y su uso.
EP2486002B1 (en) 2009-10-09 2019-03-27 Oryzon Genomics, S.A. Substituted heteroaryl- and aryl- cyclopropylamine acetamides and their use
MX2012012111A (es) 2010-04-19 2013-05-30 Oryzon Genomics Sa Inhibidores de demetilasa-1 especifica de lisina y su uso.
BR112012027062B8 (pt) 2010-04-20 2021-05-25 Fond Ieo composto, processo para a preparação de um composto e usos do mesmo
RS57331B1 (sr) 2010-07-29 2018-08-31 Oryzon Genomics Sa Inhibitori demetilaze za lsd1 zasnovani na arilciklopropilaminu i njihova medicinska upotreba
US9006449B2 (en) 2010-07-29 2015-04-14 Oryzon Genomics, S.A. Cyclopropylamine derivatives useful as LSD1 inhibitors
US9061966B2 (en) 2010-10-08 2015-06-23 Oryzon Genomics S.A. Cyclopropylamine inhibitors of oxidases
JP5813855B2 (ja) 2011-03-25 2015-11-17 グラクソスミスクライン、インテレクチュアル、プロパティー、ナンバー２、リミテッドＧｌａｘｏｓｍｉｔｈｋｌｉｎｅ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ Ｎｏ．２ Ｌｉｍｉｔｅｄ Ｌｓｄ１阻害剤としてのシクロプロピルアミン
EP2743256B1 (en) 2011-08-09 2018-06-27 Takeda Pharmaceutical Company Limited Cyclopropaneamine compound
EA026389B1 (ru) 2011-08-15 2017-04-28 Юниверсити Оф Юта Рисерч Фаундейшн Замещенные аналоги (e)-n'-(1-фенилэтилиден)бензогидразида в качестве ингибиторов деметилазы гистонов
PE20141692A1 (es) 2011-10-20 2014-11-08 Oryzon Genomics Sa Compuestos de (hetero) aril ciclopropilamina como inhibidores de lsd1
CN107266345B (zh) 2011-10-20 2021-08-17 奥瑞泽恩基因组学股份有限公司 作为lsd1抑制剂的(杂)芳基环丙胺化合物
WO2014058071A1 (ja) 2012-10-12 2014-04-17 武田薬品工業株式会社 シクロプロパンアミン化合物およびその用途
US9388123B2 (en) 2012-11-28 2016-07-12 Kyoto University LSD1-selective inhibitor having lysine structure
EP2740474A1 (en) 2012-12-05 2014-06-11 Instituto Europeo di Oncologia S.r.l. Cyclopropylamine derivatives useful as inhibitors of histone demethylases kdm1a
CN103054869A (zh) 2013-01-18 2013-04-24 郑州大学 含***基的氨基二硫代甲酸酯化合物在制备以lsd1为靶标药物中的应用
WO2014164867A1 (en) 2013-03-11 2014-10-09 Imago Biosciences Kdm1a inhibitors for the treatment of disease
EP3003301B1 (en) 2013-05-30 2021-02-24 Board Of Regents Of The Nevada System Of Higher Education On Behalf Of The University Of Nevada, Las Vegas Novel suicidal lsd1 inhibitors targeting sox2-expressing cancer cells
EP3010915B1 (en) 2013-06-19 2019-05-08 University of Utah Research Foundation Substituted (3-(5-chloro-2-hydroxyphenyl)-1-benzoyl-1h-pyrazole compounds as histone demethylase inhibitors
CN103319466B (zh) 2013-07-04 2016-03-16 郑州大学 含香豆素母核的1,2,3-***-氨基二硫代甲酸酯化合物、制备方法及其应用
ES2734209T3 (es) 2013-08-06 2019-12-04 Imago Biosciences Inc Inhibidores de KDM1A para el tratamiento de enfermedades
WO2015031564A2 (en) 2013-08-30 2015-03-05 University Of Utah Substituted-1h-benzo[d]imidazole series compounds as lysine-specfic demethylase 1 (lsd1) inhibitors
ES2935746T3 (es) 2013-12-11 2023-03-09 Celgene Quanticel Res Inc Inhibidores de desmetilasa-1 específica de lisina
WO2015120281A1 (en) 2014-02-07 2015-08-13 Musc Foundation For Research Development Aminotriazole- and aminotetrazole-based kdm1a inhibitors as epigenetic modulators
PL3105218T3 (pl) 2014-02-13 2020-03-31 Incyte Corporation Cyklopropyloaminy jako inhibitory lsd1
LT3105226T (lt) 2014-02-13 2019-11-11 Incyte Corp Ciklopropilaminai, kaip lsd1 inhibitoriai
US9493442B2 (en) 2014-02-13 2016-11-15 Incyte Corporation Cyclopropylamines as LSD1 inhibitors
WO2015123437A1 (en) 2014-02-13 2015-08-20 Incyte Corporation Cyclopropylamines as lsd1 inhibitors
CN106458856A (zh) 2014-03-07 2017-02-22 约翰霍普金斯大学 组蛋白赖氨酸特异性的脱甲基酶(lsd1)和组蛋白脱乙酰基酶(hdac)的抑制剂
DK3137169T3 (da) 2014-05-01 2022-02-14 Celgene Quanticel Res Inc Hæmmere af lysin-specifik demethylase-1
DK3148974T3 (en) 2014-05-30 2018-10-29 St Europeo Di Oncologia S R L CYCLOPROPYLAMINE COMPOUNDS AS HYDONDEMETHYLASE INHIBITORS
CN104119280B (zh) 2014-06-27 2016-03-16 郑州大学 含氨基类脲与端炔结构单元的嘧啶衍生物、制备方法及应用
PL3160956T3 (pl) 2014-06-27 2020-11-30 Celgene Quanticel Research, Inc. Inhibitory demetylazy-1 specyficznej dla lizyny
WO2016003917A1 (en) 2014-07-03 2016-01-07 Quanticel Pharmaceuticals, Inc. Inhibitors of lysine specific demethylase-1
CA2954060A1 (en) 2014-07-03 2016-01-07 Celgene Quanticel Research, Inc. Inhibitors of lysine specific demethylase-1
WO2016007731A1 (en) 2014-07-10 2016-01-14 Incyte Corporation Imidazopyridines and imidazopyrazines as lsd1 inhibitors
WO2016007727A1 (en) 2014-07-10 2016-01-14 Incyte Corporation Triazolopyridines and triazolopyrazines as lsd1 inhibitors
WO2016007722A1 (en) 2014-07-10 2016-01-14 Incyte Corporation Triazolopyridines and triazolopyrazines as lsd1 inhibitors
TW201613925A (en) 2014-07-10 2016-04-16 Incyte Corp Imidazopyrazines as LSD1 inhibitors
EP2993175A1 (en) 2014-09-05 2016-03-09 IEO - Istituto Europeo di Oncologia Srl Thienopyrroles as histone demethylase inhibitors
ES2935114T3 (es) 2014-09-05 2023-03-01 Celgene Quanticel Res Inc Inhibidores de la desmetilasa 1 específica de lisina
JP6636031B2 (ja) 2015-01-30 2020-01-29 ジェネンテック， インコーポレイテッド 治療用化合物およびその使用
CN107427699B (zh) 2015-02-12 2021-10-19 伊美格生物科学公司 用于治疗疾病的kdm1a抑制剂
CN106146361A (zh) 2015-03-16 2016-11-23 四川大学 茚-1-亚基磺酰基苯甲酰肼衍生物及其制备方法和用途
EP3277689B1 (en) 2015-04-03 2019-09-04 Incyte Corporation Heterocyclic compounds as lsd1 inhibitors
CN106045862B (zh) 2015-04-10 2019-04-23 上海迪诺医药科技有限公司 环丙胺类螺(杂)环化合物、其药物组合物及应用
WO2016172496A1 (en) 2015-04-23 2016-10-27 Constellation Pharmaceuticals, Inc. Lsd1 inhibitors and uses thereof
EP3090998A1 (en) 2015-05-06 2016-11-09 F. Hoffmann-La Roche AG Solid forms
US20170001970A1 (en) 2015-07-02 2017-01-05 University Of Utah Research Foundation Substituted benzohydrazide analogs as histone demethylase inhibitors
SG10202001219UA (en) 2015-08-12 2020-03-30 Incyte Corp Salts of an lsd1 inhibitor
CN108473442B (zh) 2015-11-05 2022-03-25 赛尔基因昆蒂赛尔研究公司 包含赖氨酸特异性脱甲基酶-1的抑制剂的组合物
US10059668B2 (en) 2015-11-05 2018-08-28 Mirati Therapeutics, Inc. LSD1 inhibitors
FI3381896T3 (fi) 2015-11-27 2023-04-21 Taiho Pharmaceutical Co Ltd Bifenyyliyhdiste tai sen suola
WO2017109061A1 (en) 2015-12-23 2017-06-29 Ieo - Istituto Europeo Di Oncologia S.R.L. Spirocyclopropylamine derivatives useful as inhibitors of histone demethylases kdm1a
CN105541806A (zh) 2015-12-25 2016-05-04 中国药科大学 巴比妥酸类化合物、制备方法及其应用
CA3009805C (en) 2015-12-29 2023-10-17 Mirati Therapeutics, Inc. Lsd1 inhibitors
CN105924362B (zh) 2016-02-05 2018-08-17 上海龙翔生物医药开发有限公司 芳香环丙基胺类化合物、其药学上可接受的盐、其制备方法及其用途
CN110267945A (zh) 2016-03-01 2019-09-20 诺华股份有限公司 氰基取代的吲哚化合物及其作为lsd1抑制剂的用途
CN107174584B (zh) 2016-03-12 2020-09-01 福建金乐医药科技有限公司 含哌嗪结构化合物在制备lsd1抑制剂中的应用
CN107176927B (zh) 2016-03-12 2020-02-18 福建金乐医药科技有限公司 组蛋白去甲基化酶lsd1抑制剂
SG11201807972YA (en) * 2016-03-15 2018-10-30 Oryzon Genomics Sa Combinations of lsd1 inhibitors for the treatment of hematological malignancies
CN107200706A (zh) 2016-03-16 2017-09-26 中国科学院上海药物研究所 一类氟取代的环丙胺类化合物及其制备方法、药物组合物和用途
US20170283397A1 (en) 2016-03-31 2017-10-05 University Of Utah Research Foundation Substituted 1-h-indol-3-yl-benzamide and 1, 1'-biphenyl analogs as histone demethylase inhibitors
PE20190377A1 (es) 2016-04-22 2019-03-08 Incyte Corp Formulaciones de un inhibidor de lsd 1
AU2017263361B2 (en) 2016-05-09 2021-08-05 Jubilant Epicore LLC Cyclopropyl-amide compounds as dual LSD1/HDAC inhibitors
EP3246330A1 (en) 2016-05-18 2017-11-22 Istituto Europeo di Oncologia S.r.l. Imidazoles as histone demethylase inhibitors
CN106045881B (zh) 2016-05-26 2017-10-31 新乡医学院 一类白藜芦醇衍生物、其制备方法及作为lsd1抑制剂的应用
CN107459476B (zh) 2016-06-03 2022-06-24 中国科学院上海药物研究所 反吲哚啉环丙胺类化合物及其制备方法、药物组合物和用途
CN107513068A (zh) 2016-06-16 2017-12-26 中国科学院上海药物研究所 一种具有fgfr抑制活性的新型化合物及其制备和应用
WO2018035259A1 (en) 2016-08-16 2018-02-22 Imago Biosciences, Inc. Methods and processes for the preparation of kdm1a inhibitors
CN106478639B (zh) 2016-09-05 2018-09-18 郑州大学 嘧啶并1,2,4–三氮唑类的lsd1抑制剂、其制备方法及应用
CN106432248B (zh) 2016-09-27 2018-11-27 郑州大学 含嘧啶并三氮唑类lsd1抑制剂、其制备方法及应用
WO2018081342A1 (en) 2016-10-26 2018-05-03 Constellation Pharmaceuticals, Inc. Lsd1 inhibitors and uses thereof
FI3532459T3 (fi) 2016-10-26 2023-10-23 Constellation Pharmaceuticals Inc Lsd1-estäjiä ja niiden lääkinnällisiä käyttöjä
US11433053B2 (en) 2017-01-24 2022-09-06 Medshine Discovery Inc. LSD1 inhibitor and preparation method and application thereof
CN108530302A (zh) 2017-03-06 2018-09-14 华东师范大学 2`,3`-二氢螺[环丙烷-1,1`-茚]-2-胺衍生物及其制备方法和应用
CN106831489B (zh) 2017-03-23 2018-04-17 郑州大学 苯环丙胺酰腙类化合物、制备方法及其应用
CN107033148B (zh) 2017-05-03 2018-10-26 郑州大学 含嘧啶并三氮唑—巯基四氮唑类lsd1抑制剂、其制备方法及应用
CN106928235A (zh) 2017-05-03 2017-07-07 郑州大学 含嘧啶并三氮唑类lsd1抑制剂、其制备方法及应用
EP3628044B1 (en) 2017-05-15 2023-11-22 The Regents of The University of Michigan Pyrrolo[2,3-c]pyridines and related analogs as lsd-1 inhibitors
BR112019024785A2 (pt) 2017-05-26 2020-06-09 Taiho Pharmaceutical Co Ltd composto de bifenila ou sal do mesmo, composição farmacêutica, agente antineoplásico e uso
KR20180134675A (ko) 2017-06-09 2018-12-19 한미약품 주식회사 시클로프로필아민 유도체 화합물 및 이의 용도
UY37774A (es) 2017-06-19 2019-01-31 Novartis Ag Compuestos 5-cianoindol sustituidos y usos de los mismos
JP2020152641A (ja) 2017-07-07 2020-09-24 国立研究開発法人理化学研究所 リジン特異的脱メチル化酵素１阻害活性を有する新規化合物、その製造方法及びその用途
EP3668877B1 (en) 2017-08-18 2024-05-01 Istituto Europeo di Oncologia S.r.l. Indole derivatives as histone demethylase inhibitors
CN107474011B (zh) 2017-08-25 2020-03-27 新乡医学院 一类2-苯基-4-苯乙烯基吡啶类lsd1抑制剂、其制备方法及应用
CN107501169B (zh) 2017-08-25 2020-03-27 新乡医学院 一类反式二芳基乙烯类lsd1抑制剂、其制备方法及应用
TWI794294B (zh) 2017-09-13 2023-03-01 南韓商韓美藥品股份有限公司 吡唑衍生化合物及其用途
CN109535019B (zh) 2017-09-21 2021-08-20 华东师范大学 1,1a,6,6a-四氢环丙并[a]茚-1-胺衍生物及其制备方法与应用
KR20190040763A (ko) 2017-10-11 2019-04-19 한미약품 주식회사 피라졸로피리딘 유도체 화합물 및 이의 용도
KR20190040783A (ko) 2017-10-11 2019-04-19 한미약품 주식회사 라이신 특이적 데메틸라제-1 억제제로서의 피라졸 유도체
CN107936022A (zh) 2017-11-30 2018-04-20 郑州大学 黄嘌呤类lsd1抑制剂及其制备方法和应用
CN110204551B (zh) 2018-02-28 2021-08-17 中国科学院上海药物研究所 一类含环丙胺结构的噻吩并[3,2-d]嘧啶衍生物、其制备方法与用途
JP2021522305A (ja) 2018-05-04 2021-08-30 オリソン ヘノミクス，ソシエダ アノニマ 安定した医薬製剤
EP3790867B1 (en) 2018-05-11 2024-03-27 Imago Biosciences Inc. Kdm1a inhibitors for the treatment of disease
EP3794003A1 (en) 2018-05-15 2021-03-24 The Regents Of The University Of Michigan Imidazo[4,5-c]pyridine compounds as lsd-1 inhibitors
EP3825309B1 (en) 2018-07-20 2023-09-06 CSPC Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. Salt of lsd1 inhibitor and a polymorph thereof
WO2020047198A1 (en) 2018-08-31 2020-03-05 Incyte Corporation Salts of an lsd1 inhibitor and processes for preparing the same
WO2020052649A1 (zh) 2018-09-13 2020-03-19 南京明德新药研发有限公司 作为lsd1抑制剂的环丙胺类化合物及其应用
WO2020052647A1 (zh) 2018-09-13 2020-03-19 南京明德新药研发有限公司 作为lsd1抑制剂的杂螺环类化合物及其应用
CN109265462B (zh) 2018-10-31 2020-06-02 郑州大学 嘧啶并1,2,4-三氮唑类化合物及其制备方法和应用
CN109293664B (zh) 2018-11-14 2020-06-02 郑州大学 嘧啶并1,2,4-三氮唑肼类化合物及其制备方法和应用
WO2020138398A1 (ja) 2018-12-28 2020-07-02 国立研究開発法人理化学研究所 リジン特異的脱メチル化酵素１を阻害する新規化合物、その製造方法及びその用途
AU2020216034A1 (en) 2019-02-01 2021-08-19 Hanmi Pharm. Co., Ltd. Imidazopyridine derivative compounds and use of same
JP2022518959A (ja) 2019-02-01 2022-03-17 ハンミ ファーマシューティカルズ カンパニー リミテッド イミダゾピリジン誘導体化合物及びその用途
CN112110936B (zh) 2019-06-20 2021-12-07 沈阳药科大学 四氢喹啉类衍生物及其制备方法和应用
CN110478352A (zh) 2019-08-30 2019-11-22 郑州大学 含***基的5-氰基-6-苯基-嘧啶类化合物在抑制lsd1中的应用及lsd1抑制剂
WO2021058024A1 (zh) 2019-09-29 2021-04-01 南京明德新药研发有限公司 Lsd1抑制剂
EP4058018A4 (en) 2019-11-13 2023-06-21 Taiho Pharmaceutical Co., Ltd. METHODS OF TREATMENT OF LSD1-RELATED DISEASES AND DISORDERS USING LSD1 INHIBITORS
CN111072610B (zh) 2019-12-16 2022-08-30 杭州师范大学 一类取代的苯并呋喃2-甲酰腙类lsd1抑制剂的制备和应用
CN113354622B (zh) 2020-03-06 2022-11-01 沈阳药科大学 对苯二胺类lsd1抑制剂及其制备方法
CN111454252B (zh) 2020-05-13 2021-06-11 郑州大学 含芳环/芳杂环-三氮唑-亚甲基-tcp衍生物及其制备方法和应用
CN114105950B (zh) 2020-08-31 2022-09-06 南京明德新药研发有限公司 吡唑类化合物及其应用
CN112409310B (zh) 2020-12-18 2023-04-21 许昌学院 一种具有lsd1抑制活性的化合物、制备方法及应用
CN113105479B (zh) 2021-04-12 2022-07-01 郑州大学 胶霉毒素6-芳香环羧酸酯系列衍生物及其制备方法
CN113087712B (zh) 2021-04-12 2022-02-22 郑州大学 L-氨基酸-6-胶霉毒素酯三氟乙酸盐及其制备方法
CN113264903A (zh) 2021-05-27 2021-08-17 郑州大学 一种吩噻嗪类化合物及其制备方法和应用
CN113599380A (zh) 2021-08-24 2021-11-05 郑州大学 小檗碱类化合物在制备抗肿瘤药物中的应用
CN113582906B (zh) 2021-08-24 2023-05-16 郑州大学 二氟苯环丙胺类化合物及其制备方法和应用

Also Published As

Publication number Publication date
KR20230167102A (ko) 2023-12-07
BR112023020554A2 (pt) 2023-12-05
AU2022254484A1 (en) 2023-11-09
JP2024513260A (ja) 2024-03-22
CA3231846A1 (en) 2022-10-13
EP4319732A1 (en) 2024-02-14
TW202304416A (zh) 2023-02-01
WO2022214303A1 (en) 2022-10-13

Similar Documents

Publication Publication Date Title
PH12019502138A1 (en) Compounds and compositions for treating hematological disorders
NZ763551A (en) Compounds useful for inhibiting cdk7
MX2021014177A (es) Inhibidores de kras con la mutacion de glicina a cisteina en el codon 12 (g12c) y usos de los mismos.
MX2023000025A (es) Inhibidores de la quinasa progenitora hematopoyética 1 y usos de estos.
EA202193015A1 (ru) Ингибиторы cdk
CR20220251A (es) Nuevos derivados de metilquinazolinona
MX2021012423A (es) Métodos y composiciones para degradación de proteínas específicas.
MX2022005298A (es) Compuestos intermediarios de sintesis de inhibidores de a2a.
MX2022013081A (es) Compuestos para el tratamiento de sars.
PH12017500881A1 (en) Aurora a kinase inhibitor
MX2023011779A (es) Combinaciones de inhibidores de lsd1 para el tratamiento de canceres mieloides.
MX2020010697A (es) Kit, composicion y terapia de combinacion para el sindrome del cromosoma x fragil.
MX2021006011A (es) Un inhibidor de la quinasa aurora a para su uso en el tratamiento del neuroblastoma.
CR20220029A (es) Compuestos macrocíclicos como agonistas de sting y métodos y usos de los mismos
PH12019500875A1 (en) Pyridone compound as c-met inhibitor
MX2021009863A (es) Una molecula dbait en combinacion con inhibidor de quinasa para el tratamiento del cancer.
MX2019002430A (es) Agente antitumoral, mejorador del efecto antitumoral, y kit antitumoral.
MX2023009212A (es) Proceso novedoso.
MX2023000333A (es) Sales y formas de un inhibidor wee1.
EP4069246A4 (en) TREATMENT FOR ACUTE MYELOID LEUKEMIA OR MYELODYSPLASTIC SYNDROME
MX2021008009A (es) Inhibidores del receptor de crecimiento transformante beta 1 (alk5) para tratar el sindrome mielodisplasico.
MX2022000782A (es) Inhibidores de la ferroportina para el uso en el tratamiento de la beta-talasemia dependiente de transfusiones (tdt).
MX2022001467A (es) Derivados quinolina como inhibidores de proteína quinasa.
MX2018002611A (es) Agente antitumoral para cancer del tracto biliar y metodo para tratar cancer del tracto biliar.
MX2022001044A (es) Inhibidor de sglt2/dpp4 y su aplicacion.