HUE041460T2 - Piridin-2(1H)-on kinolinon származékok mint a mutáns iizocitrát-dehidrogenáz inhibitorai - Google Patents

Piridin-2(1H)-on kinolinon származékok mint a mutáns iizocitrát-dehidrogenáz inhibitorai

Info

Publication number
HUE041460T2
HUE041460T2 HUE15778433A HUE15778433A HUE041460T2 HU E041460 T2 HUE041460 T2 HU E041460T2 HU E15778433 A HUE15778433 A HU E15778433A HU E15778433 A HUE15778433 A HU E15778433A HU E041460 T2 HUE041460 T2 HU E041460T2
Authority
HU
Hungary
Prior art keywords
lysocitrate
pyridin
dehydrogenase
mutant
inhibitors
Prior art date
Application number
HUE15778433A
Other languages
English (en)
Hungarian (hu)
Inventor
Susan Ashwell
Ann-Marie Campbell
Justin Andrew Caravella
R Bruce Diebold
Anna Ericsson
Gary Gustafson
Lancia, Jr
Jian Lin
Wei Lu
Zhongguo Wang
Original Assignee
Forma Therapeutics Inc
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 Forma Therapeutics Inc filed Critical Forma Therapeutics Inc
Publication of HUE041460T2 publication Critical patent/HUE041460T2/hu

Links

Classifications

    • 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

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)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
HUE15778433A 2014-09-19 2015-09-18 Piridin-2(1H)-on kinolinon származékok mint a mutáns iizocitrát-dehidrogenáz inhibitorai HUE041460T2 (hu)

Applications Claiming Priority (3)

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

Publications (1)

Publication Number Publication Date
HUE041460T2 true HUE041460T2 (hu) 2019-05-28

Family

ID=54291606

Family Applications (2)

Application Number Title Priority Date Filing Date
HUE15778433A HUE041460T2 (hu) 2014-09-19 2015-09-18 Piridin-2(1H)-on kinolinon származékok mint a mutáns iizocitrát-dehidrogenáz inhibitorai
HUE20157755A HUE062424T2 (hu) 2014-09-19 2015-09-18 Piridin-2(1H)-on kinolinon származékok mint mutáns izocitrát dehidrogenáz inhibitorok

Family Applications After (1)

Application Number Title Priority Date Filing Date
HUE20157755A HUE062424T2 (hu) 2014-09-19 2015-09-18 Piridin-2(1H)-on kinolinon származékok mint mutáns izocitrát dehidrogenáz inhibitorok

Country Status (37)

Country Link
US (8) US9834539B2 (enExample)
EP (4) EP4257131A3 (enExample)
JP (1) JP6648115B2 (enExample)
KR (1) KR102209667B1 (enExample)
CN (3) CN107001328B (enExample)
AU (3) AU2015317329B2 (enExample)
BR (1) BR112017005238B1 (enExample)
CA (1) CA2961817C (enExample)
CL (1) CL2017000658A1 (enExample)
CO (1) CO2017003241A2 (enExample)
CY (2) CY1121149T1 (enExample)
DK (2) DK3447050T3 (enExample)
EA (1) EA034336B1 (enExample)
EC (1) ECSP17022933A (enExample)
ES (3) ES2704897T3 (enExample)
FI (1) FI3733662T3 (enExample)
HR (1) HRP20200666T1 (enExample)
HU (2) HUE041460T2 (enExample)
IL (3) IL292608B2 (enExample)
LT (2) LT3194376T (enExample)
MA (2) MA40481A (enExample)
ME (1) ME03776B (enExample)
MX (2) MX385512B (enExample)
MY (2) MY197533A (enExample)
NZ (1) NZ730373A (enExample)
PE (1) PE20171056A1 (enExample)
PH (1) PH12017500517B1 (enExample)
PL (3) PL3194376T3 (enExample)
PT (3) PT3733662T (enExample)
RS (2) RS58184B1 (enExample)
SA (1) SA517381129B1 (enExample)
SG (1) SG11201702194SA (enExample)
SI (2) SI3194376T1 (enExample)
SM (2) SMT202000212T1 (enExample)
TW (1) TWI686390B (enExample)
WO (1) WO2016044789A1 (enExample)
ZA (3) ZA201702127B (enExample)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2406389B1 (en) 2009-03-13 2019-05-08 Agios Pharmaceuticals, Inc. Methods and compositions for cell-proliferation-related disorders
CA2793835C (en) 2009-10-21 2021-07-20 Agios Pharmaceuticals, Inc. Methods and compositions for cell-proliferation-related disorders
SMT202400446T1 (it) 2014-02-06 2024-11-15 Nxera Pharma Uk Ltd Composti aza biciclici come agonisti del recettore muscarinico
PT3733662T (pt) 2014-09-19 2023-08-18 Forma Therapeutics Inc Derivados piridin-2(1h)-ona-quinolinona como inibidores de isocitrato desidrogenase mutante
EP3194375B1 (en) 2014-09-19 2018-11-21 Forma Therapeutics, Inc. Phenyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
ES2768694T3 (es) 2014-09-19 2020-06-23 Forma Therapeutics Inc Composiciones de quinolinona pirimidinas como inhibidores de isocitrato dehidrogenasa mutante
US9771349B2 (en) 2014-09-19 2017-09-26 Forma Therapeutics, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US10350206B2 (en) 2014-09-19 2019-07-16 Bayer Pharma Aktiengesellschaft Benzyl substituted indazoles as BUB1 inhibitors
WO2016106331A1 (en) 2014-12-22 2016-06-30 The United States Of America Mutant idh1 inhibitors useful for treating cancer
US10294206B2 (en) 2015-04-21 2019-05-21 Forma Tm2, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US9624216B2 (en) 2015-04-21 2017-04-18 Forma Therapeutics, Inc. Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors
BR112019023152B1 (pt) 2017-05-04 2023-10-03 Discovery Purchaser Corporation Compostos heterocíclicos derivados de 2-{[2-(feniloximetil) piridina-5-il] oxi}-etanamina, seus usos e seus intermediários, formulações, e método para controle de pragas
EP3720442B1 (en) 2018-05-16 2022-12-28 Forma Therapeutics, Inc. Inhibiting mutant idh-1
US11013733B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1)
US11311527B2 (en) 2018-05-16 2022-04-26 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
LT3720442T (lt) 2018-05-16 2023-04-25 Forma Therapeutics, Inc. Mutantinės idh-1 slopinimas
US11013734B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation
WO2020232381A1 (en) 2019-05-16 2020-11-19 Forma Therapeutics, Inc. INHIBITING MUTANT ISOCITRATE DEHYDROGENASE 1 (mIDH-1)
US10532047B2 (en) 2018-05-16 2020-01-14 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
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
US6921821B2 (en) 2002-06-12 2005-07-26 Abbott Laboratories Antagonists of melanin concentrating hormone receptor
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
US7956060B2 (en) 2004-03-30 2011-06-07 Kyowa Hakko Kirin Co., Ltd. Pyrimidine derivative compound
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
BRPI0810921A2 (pt) 2007-04-30 2014-10-29 Prometic Biosciences Inc Derivados de triazina, composições contendo tais derivados e métodos de tratamento de câncer e doenças autoimunes usando tais compostos
AU2010259002B2 (en) 2009-06-08 2014-03-20 Nantbio, Inc. Triazine derivatives and their therapeutical applications
ES2642109T3 (es) * 2009-12-09 2017-11-15 Agios Pharmaceuticals, Inc. Compuestos terapéuticamente activos para su uso en el tratamiento de cáncer caracterizados por tener una mutación de IDH
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
US9464065B2 (en) 2011-03-24 2016-10-11 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
JP6026544B2 (ja) 2011-09-27 2016-11-16 ノバルティス アーゲー 変異体idhの阻害剤としての3−ピリミジン−4−イル−オキサゾリジン−2−オン類
EP2793881B1 (en) 2011-12-21 2018-10-31 The Regents of the University of Colorado Anti-cancer compounds targeting ral gtpase
SG11201403878QA (en) * 2012-01-06 2014-08-28 Agios Pharmaceuticals Inc Therapeutically active compounds and their methods of use
KR20150127197A (ko) * 2013-03-14 2015-11-16 노파르티스 아게 돌연변이 idh의 억제제로서의 3-피리미딘-4-일-옥사졸리딘-2-온
WO2015003146A1 (en) 2013-07-03 2015-01-08 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
PT3733662T (pt) 2014-09-19 2023-08-18 Forma Therapeutics Inc Derivados piridin-2(1h)-ona-quinolinona como inibidores de isocitrato desidrogenase mutante
EP3194375B1 (en) 2014-09-19 2018-11-21 Forma Therapeutics, Inc. Phenyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US9771349B2 (en) 2014-09-19 2017-09-26 Forma Therapeutics, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
ES2768694T3 (es) 2014-09-19 2020-06-23 Forma Therapeutics Inc Composiciones de quinolinona pirimidinas como inhibidores de isocitrato dehidrogenasa mutante
WO2016106331A1 (en) 2014-12-22 2016-06-30 The United States Of America Mutant idh1 inhibitors useful for treating cancer
GB2533925A (en) 2014-12-31 2016-07-13 Univ Bath Antimicrobial compounds, compositions and methods
US9624216B2 (en) 2015-04-21 2017-04-18 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
EP3419593B1 (en) 2016-02-26 2022-03-23 Celgene Corporation Enasidenib for use in the treatment of relapsed or refractory acute myeloid leukaemia
ES2814290T3 (es) 2016-06-06 2021-03-26 Lilly Co Eli Inhibidores de IDH1 mutante
WO2017223202A1 (en) 2016-06-22 2017-12-28 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
CN110072867B (zh) 2016-12-16 2022-07-08 伊莱利利公司 作为突变体idh1和idh2抑制剂的7-苯基乙基氨基-4h-嘧啶并[4,5-d][1,3]噁嗪-2-酮化合物

Also Published As

Publication number Publication date
CY1122865T1 (el) 2021-05-05
EP3733662A1 (en) 2020-11-04
CN111909130A (zh) 2020-11-10
EP3194376B1 (en) 2018-10-24
PH12017500517B1 (en) 2022-08-03
AU2021215141A1 (en) 2021-09-02
ZA202304409B (en) 2024-08-28
CN117695280A (zh) 2024-03-15
MA53352A (fr) 2021-09-15
US20170174658A1 (en) 2017-06-22
SI3447050T1 (sl) 2020-08-31
NZ730373A (en) 2019-11-29
FI3733662T3 (fi) 2023-08-09
IL282363A (en) 2021-06-30
IL292608B1 (en) 2024-06-01
US11498913B2 (en) 2022-11-15
AU2021215141B2 (en) 2023-10-19
SG11201702194SA (en) 2017-04-27
CN107001328A (zh) 2017-08-01
BR112017005238A2 (pt) 2017-12-19
JP6648115B2 (ja) 2020-02-14
US12275715B2 (en) 2025-04-15
TWI686390B (zh) 2020-03-01
US20160083366A1 (en) 2016-03-24
PH12017500517A1 (en) 2017-08-07
ZA201702127B (en) 2019-06-26
US10414752B2 (en) 2019-09-17
ES2953347T3 (es) 2023-11-10
SA517381129B1 (ar) 2021-04-26
EA201790657A8 (ru) 2018-02-28
BR112017005238B1 (pt) 2023-01-17
IL251163A0 (en) 2017-04-30
IL292608B2 (en) 2024-10-01
IL282363B (en) 2022-06-01
NZ758641A (en) 2023-12-22
EP3733662B1 (en) 2023-06-07
HRP20200666T1 (hr) 2020-07-24
EP3447050A1 (en) 2019-02-27
MX385512B (es) 2025-03-18
US20180312487A1 (en) 2018-11-01
PT3447050T (pt) 2020-09-17
ECSP17022933A (es) 2017-08-31
LT3194376T (lt) 2019-02-25
ES2704897T3 (es) 2019-03-20
CA2961817C (en) 2024-03-12
PT3194376T (pt) 2019-02-04
RS58184B1 (sr) 2019-03-29
SMT202000212T1 (it) 2020-05-08
US20210078973A1 (en) 2021-03-18
EP4257131A3 (en) 2024-01-10
CL2017000658A1 (es) 2017-12-22
HUE062424T2 (hu) 2023-11-28
JP2017528487A (ja) 2017-09-28
US20190263778A1 (en) 2019-08-29
EP3447050B1 (en) 2020-02-19
TW201617335A (zh) 2016-05-16
AU2015317329A1 (en) 2017-04-27
US9834539B2 (en) 2017-12-05
KR20170063742A (ko) 2017-06-08
MY176250A (en) 2020-07-24
PL3194376T3 (pl) 2019-05-31
PL3447050T3 (pl) 2020-07-27
IL251163B (en) 2021-05-31
ES2790640T3 (es) 2020-10-28
ZA201902446B (en) 2023-12-20
SMT201900018T1 (it) 2019-02-28
MX2019013203A (es) 2020-01-20
MX2017003404A (es) 2017-07-28
AU2019283765A1 (en) 2020-01-16
LT3447050T (lt) 2020-05-11
CN107001328B (zh) 2020-06-05
IL292608A (en) 2022-07-01
US20240150319A1 (en) 2024-05-09
DK3194376T3 (en) 2019-01-21
CN111909130B (zh) 2023-10-31
CY1121149T1 (el) 2020-05-29
US20200223822A1 (en) 2020-07-16
CA2961817A1 (en) 2016-03-24
EP4257131A2 (en) 2023-10-11
US10889567B2 (en) 2021-01-12
EA201790657A1 (ru) 2017-08-31
PL3733662T3 (pl) 2024-01-22
MY197533A (en) 2023-06-21
AU2015317329B2 (en) 2019-10-31
PT3733662T (pt) 2023-08-18
EA034336B1 (ru) 2020-01-29
SI3194376T1 (sl) 2019-03-29
PE20171056A1 (es) 2017-07-21
US10550098B2 (en) 2020-02-04
DK3447050T3 (da) 2020-03-09
EP3194376A1 (en) 2017-07-26
CO2017003241A2 (es) 2017-09-20
AU2019283765B2 (en) 2021-05-13
MA40481A (fr) 2017-07-26
KR102209667B1 (ko) 2021-01-29
WO2016044789A1 (en) 2016-03-24
US20230125739A1 (en) 2023-04-27
ME03776B (me) 2021-04-20
RS60140B1 (sr) 2020-05-29

Similar Documents

Publication Publication Date Title
HUE041460T2 (hu) Piridin-2(1H)-on kinolinon származékok mint a mutáns iizocitrát-dehidrogenáz inhibitorai
IL247970A0 (en) Quinoline history as smo inhibitors
IL263163A (en) Pyridines are converted as inhibitors of dnmt1
IL246140A0 (en) History of bicyclic heterocyclics as bromodomain repressors
IL244438A0 (en) Modified quinolizine derivatives for use in inhibiting human immunodeficiency virus integrase
IL279949A (en) Heterocyclic MCT4 inhibitors
EP3188731A4 (en) Isoquinoline derivatives useful as inhibitors of diacylglyceride o-acyltransferase 2
EP3138843A4 (en) Isoquinolinesulfonyl derivative as rho kinase inhibitor
PL3200786T3 (pl) Zastosowanie pochodnych pirydylowych o skondensowanym układzie bicyklicznym jako inhibitorów fgfr4
EP3107540A4 (en) Polymorphs of lomitapide and its salts
EP3049087A4 (en) Benzoquinolone inhibitors of vmat2
LT3263106T (lt) Chinolino darinių kartumo sumažinimo būdas
PL3191491T3 (pl) Pochodne pirydazynonu jako inhibitory kinaz 3-fosfoinozytolu
HRP20182176T1 (hr) Derivati piridin-2(1h)-on kinolinona kao inhibitori mutirane izocitrat dehidrogenaze
IL266121A (en) A history of metamorphosed quinoxaline as an inhibitor of pfkfb
IL252162A0 (en) Crystal forms of poly(adenosine diphosphate) ribose polymerase inhibitors
TH1601000368A (th) อนุพันธ์ควินอลีน
TH1501005718A (th) อนุพันธ์ 6-(5-ไฮดรอกซี-1เอช-ไพราซอล-1-อิล)นิโคตินเอไมด์และการใช้เป็นสารยับยั้ง phd
UA26905S (uk) Коробок із сірниками - комплект засобів для отримання відкритого вогню
UA30226S (uk) Комплект засобів для отримання відкритого вогню