DK3447050T3 - Pyridin-2(1h)-on-quinolinderivater som mutant-isocitrat dehydrogenaseinhibitorer - Google Patents

Pyridin-2(1h)-on-quinolinderivater som mutant-isocitrat dehydrogenaseinhibitorer Download PDF

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Publication number
DK3447050T3
DK3447050T3 DK18198969.0T DK18198969T DK3447050T3 DK 3447050 T3 DK3447050 T3 DK 3447050T3 DK 18198969 T DK18198969 T DK 18198969T DK 3447050 T3 DK3447050 T3 DK 3447050T3
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Prior art keywords
pyridin
quinoline derivatives
isocitrate dehydrogenase
dehydrogenase inhibitors
mutant isocitrate
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DK18198969.0T
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English (en)
Inventor
Susan Ashwell
Ann-Marie Campbell
Justin Andrew Caravella
R Bruce Diebold
Anna Ericsson
Gary Gustafson
David R Lancia Jr
Jian Lin
Wei Lu
Zhongguo Wang
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Forma Therapeutics Inc
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Publication of DK3447050T3 publication Critical patent/DK3447050T3/da

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicinal Preparation (AREA)
DK18198969.0T 2014-09-19 2015-09-18 Pyridin-2(1h)-on-quinolinderivater som mutant-isocitrat dehydrogenaseinhibitorer DK3447050T3 (da)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201462053006P 2014-09-19 2014-09-19
US201562128089P 2015-03-04 2015-03-04
US201562150812P 2015-04-21 2015-04-21
EP15778433.1A EP3194376B1 (en) 2014-09-19 2015-09-18 Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors

Publications (1)

Publication Number Publication Date
DK3447050T3 true DK3447050T3 (da) 2020-03-09

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DK15778433.1T DK3194376T3 (da) 2014-09-19 2015-09-18 Pyridin-2(1h)-on quinolinon-derivater som mutant-isocitratdehydrogenase inhibitorer
DK18198969.0T DK3447050T3 (da) 2014-09-19 2015-09-18 Pyridin-2(1h)-on-quinolinderivater som mutant-isocitrat dehydrogenaseinhibitorer

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DK15778433.1T DK3194376T3 (da) 2014-09-19 2015-09-18 Pyridin-2(1h)-on quinolinon-derivater som mutant-isocitratdehydrogenase inhibitorer

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US (8) US9834539B2 (da)
EP (4) EP4257131A3 (da)
JP (1) JP6648115B2 (da)
KR (1) KR102209667B1 (da)
CN (3) CN107001328B (da)
AU (3) AU2015317329B2 (da)
BR (1) BR112017005238B1 (da)
CA (1) CA2961817C (da)
CL (1) CL2017000658A1 (da)
CO (1) CO2017003241A2 (da)
CY (2) CY1121149T1 (da)
DK (2) DK3194376T3 (da)
EA (1) EA034336B1 (da)
EC (1) ECSP17022933A (da)
ES (3) ES2704897T3 (da)
FI (1) FI3733662T3 (da)
HR (1) HRP20200666T1 (da)
HU (2) HUE041460T2 (da)
IL (3) IL292608B2 (da)
LT (2) LT3194376T (da)
MA (2) MA40481A (da)
ME (1) ME03776B (da)
MX (2) MX2017003404A (da)
MY (2) MY176250A (da)
NZ (1) NZ730373A (da)
PE (1) PE20171056A1 (da)
PH (1) PH12017500517A1 (da)
PL (3) PL3733662T3 (da)
PT (3) PT3447050T (da)
RS (2) RS60140B1 (da)
SA (1) SA517381129B1 (da)
SG (1) SG11201702194SA (da)
SI (2) SI3447050T1 (da)
TW (1) TWI686390B (da)
WO (1) WO2016044789A1 (da)
ZA (3) ZA201702127B (da)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010105243A1 (en) 2009-03-13 2010-09-16 Agios Pharmaceuticals, Inc. Methods and compositions for cell-proliferation-related disorders
EP3561077B1 (en) 2009-10-21 2022-12-21 Les Laboratoires Servier Methods for cell-proliferation-related disorders
RS65894B1 (sr) 2014-02-06 2024-09-30 Nxera Pharma Uk Ltd Biciklična aza jedinjenja kao agonisti muskarinskog receptora
WO2016042084A1 (en) 2014-09-19 2016-03-24 Bayer Pharma Aktiengesellschaft Benzyl substituted indazoles as bub1 inhibitors
MX2017003627A (es) 2014-09-19 2018-01-24 Forma Therapeutics Inc Composiciones de pirimidin quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh).
EP4257131A3 (en) 2014-09-19 2024-01-10 Forma Therapeutics, Inc. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US10005734B2 (en) 2014-09-19 2018-06-26 Forma Therapeutics, Inc. Pyridin-2(1H)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
JP6751081B2 (ja) 2014-09-19 2020-09-02 フォーマ セラピューティクス,インコーポレイテッド 変異イソクエン酸デヒドロゲナーゼ阻害剤としてのピリジニルキノリノン誘導体
ES2905564T3 (es) 2014-12-22 2022-04-11 Us Health Inhibidores mutantes de IDH1 útiles para tratar el cáncer
US10407419B2 (en) 2015-04-21 2019-09-10 Forma Therapeutics, Inc. Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors
US10294206B2 (en) 2015-04-21 2019-05-21 Forma Tm2, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2018202524A1 (de) 2017-05-04 2018-11-08 Bayer Cropscience Aktiengesellschaft 2-{[2-(phenyloxymethyl)pyridin-5-yl]oxy}-ethanamin-derivate und verwandte verbindungen als schädlingsbekämpfungsmittel z.b. für den pflanzenschutz
US11013733B2 (en) * 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1)
WO2019222553A1 (en) 2018-05-16 2019-11-21 Forma Therapeutics, Inc. Inhibiting mutant idh-1
WO2019222551A1 (en) 2018-05-16 2019-11-21 Forma Therapeutics, Inc. Solid forms of ((s)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile
WO2020232381A1 (en) 2019-05-16 2020-11-19 Forma Therapeutics, Inc. INHIBITING MUTANT ISOCITRATE DEHYDROGENASE 1 (mIDH-1)
US11013734B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation
SI3720442T1 (sl) 2018-05-16 2023-06-30 Forma Therapeutics, Inc. Zaviranje mutantnega IDF-1
US11311527B2 (en) 2018-05-16 2022-04-26 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
TW202104207A (zh) * 2019-04-17 2021-02-01 美商健生生物科技公司 二氫乳清酸脫氫酶抑制劑
US11566013B1 (en) * 2019-11-20 2023-01-31 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH1)
CN112321571B (zh) * 2020-10-27 2022-06-03 浙江工业大学 2-呋喃-喹啉-4-甲酰胺类化合物及其应用
CN112341389B (zh) * 2020-10-27 2022-07-29 浙江工业大学 一种含氮芳杂环取代的喹啉甲酰胺类衍生物及其应用
CN115850240B (zh) * 2022-12-28 2023-09-19 北京康立生医药技术开发有限公司 一种治疗急性髓系白血病药物奥卢他西尼的合成方法

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL99731A0 (en) 1990-10-18 1992-08-18 Merck & Co Inc Hydroxylated pyridine derivatives,their preparation and pharmaceutical compositions containing them
US5262564A (en) 1992-10-30 1993-11-16 Octamer, Inc. Sulfinic acid adducts of organo nitroso compounds useful as retroviral inactivating agents anti-retroviral agents and anti-tumor agents
US20030105124A1 (en) 2000-04-27 2003-06-05 Susan Beth Sobolov-Jaynes Substituted benzolactam compounds
JP2005532368A (ja) 2002-06-12 2005-10-27 アボット・ラボラトリーズ メラニン濃縮ホルモン受容体の拮抗薬
JPWO2004043936A1 (ja) 2002-11-14 2006-03-09 協和醗酵工業株式会社 Plk阻害剤
RU2284325C2 (ru) 2003-12-17 2006-09-27 Общество С Ограниченной Ответственностью "Асинэкс Медхим" Производные фенил-3-аминометил-хинолона-2 в качестве ингибиторов no-синтетазы, способ их получения, биологически активные соединения и фармацевтическая композиция на их основе
EP1749827A4 (en) 2004-03-30 2010-04-21 Kyowa Hakko Kirin Co Ltd ANTITUMOR AGENTS
WO2006054912A1 (fr) * 2004-11-18 2006-05-26 Obchestvo S Ogranichennoy Otvetstvennost'u 'asineks Medhim' Derives d'aryl(hetaryl)-3-aminomethylchinolone-2 utilises en tant qu'inhibiteurs de no-synthetase et de cyclo-oxygenase-2, procedes de leur fabrication et compositions pharmaceutiques sur leur base
TW200803855A (en) 2006-02-24 2008-01-16 Kalypsys Inc Quinolones useful as inducible nitric oxide synthase inhibitors
US20100056516A1 (en) * 2006-07-17 2010-03-04 Williams Peter D 1-hydroxy naphthyridine compounds as anti-hiv agents
JP2010043004A (ja) 2006-12-06 2010-02-25 Dainippon Sumitomo Pharma Co Ltd 新規2環性複素環化合物
PT2152676E (pt) 2007-04-30 2013-06-25 Prometic Biosciences Inc Derivados de triazina, composições contendo tais derivados, e métodos de tratamento do cancro e de doenças autoimunes usando tais derivados
AU2010259002B2 (en) 2009-06-08 2014-03-20 Nantbio, Inc. Triazine derivatives and their therapeutical applications
JP5967827B2 (ja) * 2009-12-09 2016-08-10 アジオス ファーマシューティカルズ, インコーポレイテッド Idh変異体をもつことを特徴とする癌治療用の治療的活性化合物
WO2012006104A2 (en) 2010-06-28 2012-01-12 Academia Sinica, Taiwan Compounds and methods for treating tuberculosis infection
CN102558049B (zh) 2010-12-17 2015-02-04 中国科学院上海药物研究所 一类双香豆素类化合物及其制备方法和用途
US20120184562A1 (en) 2011-01-19 2012-07-19 Kin-Chun Luk 1,6- and 1,8-naphthyridines
US20120184548A1 (en) 2011-01-19 2012-07-19 Romyr Dominique Carboxylic acid aryl amides
WO2012129562A2 (en) 2011-03-24 2012-09-27 The Scripps Research Institute Compounds and methods for inducing chondrogenesis
CN102827170A (zh) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
CN103814020B (zh) * 2011-06-17 2017-07-14 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
EP2771337B1 (en) 2011-09-27 2017-08-02 Novartis AG 3-(pyrimidin-4-yl)-oxazolidin-2-ones as inhibitors of mutant idh
JP6473330B2 (ja) 2011-12-21 2019-02-20 ザ リージェンツ オブ ザ ユニヴァーシティ オブ コロラド,ア ボディ コーポレイト RalGTPアーゼを標的とする抗がん化合物及びその使用方法
SI2800743T1 (en) 2012-01-06 2018-08-31 Agios Pharmaceuticals, Inc. Therapeutically active compounds and methods for their use
EP2970242B1 (en) * 2013-03-14 2017-09-06 Novartis AG 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
US10478445B2 (en) 2013-07-03 2019-11-19 Georgetown University Boronic acid derivatives of resveratrol for activating deacetylase enzymes
SG11201605810WA (en) 2014-02-11 2016-08-30 Bayer Pharma AG Benzimidazol-2-amines as midh1 inhibitors
US10005734B2 (en) 2014-09-19 2018-06-26 Forma Therapeutics, Inc. Pyridin-2(1H)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
JP6751081B2 (ja) 2014-09-19 2020-09-02 フォーマ セラピューティクス,インコーポレイテッド 変異イソクエン酸デヒドロゲナーゼ阻害剤としてのピリジニルキノリノン誘導体
EP4257131A3 (en) 2014-09-19 2024-01-10 Forma Therapeutics, Inc. Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
MX2017003627A (es) 2014-09-19 2018-01-24 Forma Therapeutics Inc Composiciones de pirimidin quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh).
ES2905564T3 (es) 2014-12-22 2022-04-11 Us Health Inhibidores mutantes de IDH1 útiles para tratar el cáncer
GB2533925A (en) 2014-12-31 2016-07-13 Univ Bath Antimicrobial compounds, compositions and methods
US10407419B2 (en) 2015-04-21 2019-09-10 Forma Therapeutics, Inc. Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors
US10294206B2 (en) 2015-04-21 2019-05-21 Forma Tm2, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2017019429A1 (en) 2015-07-27 2017-02-02 Eli Lilly And Company 7-phenylethylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one compounds and theit use as mutant idh1 inhibitors
ES2912909T3 (es) 2016-02-26 2022-05-30 Celgene Corp Enasidenib para su uso en el tratamiento de la leucemia mieloide aguda recidivante o refractaria
ES2814290T3 (es) 2016-06-06 2021-03-26 Lilly Co Eli Inhibidores de IDH1 mutante
EP3475276B1 (en) 2016-06-22 2021-03-31 The United States of America, as represented by the Secretary, Department of Health and Human Services Thiazole derivatives useful as mutant idh1 inhibitors for treating cancer
CR20190252A (es) 2016-12-16 2019-08-26 Lilly Co Eli Compuestos de 7-feniletilamino-4h-pirimido[4,5-d][1,3]-oxazin-2-ona como inhibidores de idh1 e idh2 mutantes

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CY1122865T1 (el) 2021-05-05
EP3733662A1 (en) 2020-11-04
MY197533A (en) 2023-06-21
PT3194376T (pt) 2019-02-04
US20240150319A1 (en) 2024-05-09
US10889567B2 (en) 2021-01-12
EA201790657A1 (ru) 2017-08-31
LT3447050T (lt) 2020-05-11
SG11201702194SA (en) 2017-04-27
PL3447050T3 (pl) 2020-07-27
DK3194376T3 (da) 2019-01-21
AU2021215141A1 (en) 2021-09-02
TWI686390B (zh) 2020-03-01
MX2019013203A (es) 2020-01-20
CA2961817C (en) 2024-03-12
PL3194376T3 (pl) 2019-05-31
RS60140B1 (sr) 2020-05-29
PT3447050T (pt) 2020-09-17
ZA201902446B (en) 2023-12-20
EP3194376A1 (en) 2017-07-26
ES2790640T3 (es) 2020-10-28
SI3194376T1 (sl) 2019-03-29
IL282363A (en) 2021-06-30
EP4257131A2 (en) 2023-10-11
FI3733662T3 (fi) 2023-08-09
ES2953347T3 (es) 2023-11-10
AU2021215141B2 (en) 2023-10-19
PE20171056A1 (es) 2017-07-21
CN107001328A (zh) 2017-08-01
IL292608B1 (en) 2024-06-01
EP4257131A3 (en) 2024-01-10
MA53352A (fr) 2021-09-15
MY176250A (en) 2020-07-24
HUE041460T2 (hu) 2019-05-28
WO2016044789A1 (en) 2016-03-24
PT3733662T (pt) 2023-08-18
US20160083366A1 (en) 2016-03-24
US20170174658A1 (en) 2017-06-22
JP6648115B2 (ja) 2020-02-14
AU2015317329A1 (en) 2017-04-27
PH12017500517A1 (en) 2017-08-07
EA201790657A8 (ru) 2018-02-28
MA40481A (fr) 2017-07-26
ZA201702127B (en) 2019-06-26
US20230125739A1 (en) 2023-04-27
IL251163B (en) 2021-05-31
IL282363B (en) 2022-06-01
ME03776B (me) 2021-04-20
US11498913B2 (en) 2022-11-15
CY1121149T1 (el) 2020-05-29
EP3733662B1 (en) 2023-06-07
EP3194376B1 (en) 2018-10-24
HUE062424T2 (hu) 2023-11-28
LT3194376T (lt) 2019-02-25
CL2017000658A1 (es) 2017-12-22
HRP20200666T1 (hr) 2020-07-24
ZA202304409B (en) 2024-08-28
US10414752B2 (en) 2019-09-17
CO2017003241A2 (es) 2017-09-20
IL251163A0 (en) 2017-04-30
IL292608A (en) 2022-07-01
BR112017005238A2 (pt) 2017-12-19
US20180312487A1 (en) 2018-11-01
US20210078973A1 (en) 2021-03-18
CN107001328B (zh) 2020-06-05
ECSP17022933A (es) 2017-08-31
EP3447050B1 (en) 2020-02-19
AU2015317329B2 (en) 2019-10-31
BR112017005238B1 (pt) 2023-01-17
MX2017003404A (es) 2017-07-28
US20200223822A1 (en) 2020-07-16
CN111909130B (zh) 2023-10-31
CN117695280A (zh) 2024-03-15
US20190263778A1 (en) 2019-08-29
NZ730373A (en) 2019-11-29
US9834539B2 (en) 2017-12-05
JP2017528487A (ja) 2017-09-28
NZ758641A (en) 2023-12-22
SI3447050T1 (sl) 2020-08-31
US10550098B2 (en) 2020-02-04
CA2961817A1 (en) 2016-03-24
CN111909130A (zh) 2020-11-10
RS58184B1 (sr) 2019-03-29
IL292608B2 (en) 2024-10-01
KR102209667B1 (ko) 2021-01-29
ES2704897T3 (es) 2019-03-20
EP3447050A1 (en) 2019-02-27
EA034336B1 (ru) 2020-01-29
KR20170063742A (ko) 2017-06-08
TW201617335A (zh) 2016-05-16
AU2019283765B2 (en) 2021-05-13
AU2019283765A1 (en) 2020-01-16
PL3733662T3 (pl) 2024-01-22
SA517381129B1 (ar) 2021-04-26

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