PE20171056A1 - Derivados de piridin-2(1h)-on quinolinona como inhibidores de isocitrato deshidrogenasa - Google Patents

Derivados de piridin-2(1h)-on quinolinona como inhibidores de isocitrato deshidrogenasa

Info

Publication number
PE20171056A1
PE20171056A1 PE2017000471A PE2017000471A PE20171056A1 PE 20171056 A1 PE20171056 A1 PE 20171056A1 PE 2017000471 A PE2017000471 A PE 2017000471A PE 2017000471 A PE2017000471 A PE 2017000471A PE 20171056 A1 PE20171056 A1 PE 20171056A1
Authority
PE
Peru
Prior art keywords
pyridin
inhibitors
oxo
methyl
quinolinone
Prior art date
Application number
PE2017000471A
Other languages
English (en)
Spanish (es)
Inventor
Susan Ashwell
Ann-Marie Campbell
Justin Andrew Caravella
R Bruce Diebold
Anna Ericsson
Gary Gustafson
David R Lancia
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 PE20171056A1 publication Critical patent/PE20171056A1/es

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)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicinal Preparation (AREA)
PE2017000471A 2014-09-19 2015-09-18 Derivados de piridin-2(1h)-on quinolinona como inhibidores de isocitrato deshidrogenasa PE20171056A1 (es)

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
PE20171056A1 true PE20171056A1 (es) 2017-07-21

Family

ID=54291606

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2017000471A PE20171056A1 (es) 2014-09-19 2015-09-18 Derivados de piridin-2(1h)-on quinolinona como inhibidores de isocitrato deshidrogenasa

Country Status (37)

Country Link
US (8) US9834539B2 (enExample)
EP (4) EP4257131A3 (enExample)
JP (1) JP6648115B2 (enExample)
KR (1) KR102209667B1 (enExample)
CN (3) CN117695280A (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) DK3194376T3 (enExample)
EA (1) EA034336B1 (enExample)
EC (1) ECSP17022933A (enExample)
ES (3) ES2953347T3 (enExample)
FI (1) FI3733662T3 (enExample)
HR (1) HRP20200666T1 (enExample)
HU (2) HUE062424T2 (enExample)
IL (3) IL292608B2 (enExample)
LT (2) LT3447050T (enExample)
MA (2) MA53352A (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) PL3447050T3 (enExample)
PT (3) PT3733662T (enExample)
RS (2) RS60140B1 (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
JP6067226B2 (ja) 2009-03-13 2017-01-25 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 細胞増殖関連疾患のための方法および組成物
ES2594402T3 (es) * 2009-10-21 2016-12-20 Agios Pharmaceuticals, Inc. Métodos y composiciones para trastornos relacionados con la proliferación celular
HRP20241145T1 (hr) 2014-02-06 2024-11-22 Nxera Pharma Uk Limited Biciklički aza spojevi kao agonisti muskarinskih receptora
EP3194383B1 (en) 2014-09-19 2019-11-06 Forma Therapeutics, Inc. Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors
AU2015316796A1 (en) 2014-09-19 2017-03-30 Bayer Pharma Aktiengesellschaft Benzyl substituted indazoles as Bub1 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
HUE062424T2 (hu) 2014-09-19 2023-11-28 Forma Therapeutics Inc Piridin-2(1H)-on kinolinon származékok mint mutáns izocitrát dehidrogenáz inhibitorok
EP3237385B1 (en) * 2014-12-22 2021-11-24 The United States of America, as represented by The Secretary, Department of Health and Human Services Mutant idh1 inhibitors useful for treating cancer
WO2016171756A1 (en) 2015-04-21 2016-10-27 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
EP3619196B1 (de) 2017-05-04 2022-03-30 Bayer CropScience Aktiengesellschaft 2-{[2-(phenyloxymethyl)pyridin-5-yl]oxy}-ethanamin-derivate und verwandte verbindungen als schädlingsbekämpfungsmittel z.b. für den pflanzenschutz
SI3720442T1 (sl) 2018-05-16 2023-06-30 Forma Therapeutics, Inc. Zaviranje mutantnega IDF-1
WO2020232381A1 (en) 2019-05-16 2020-11-19 Forma Therapeutics, Inc. INHIBITING MUTANT ISOCITRATE DEHYDROGENASE 1 (mIDH-1)
WO2019222553A1 (en) 2018-05-16 2019-11-21 Forma Therapeutics, Inc. Inhibiting mutant idh-1
US11311527B2 (en) 2018-05-16 2022-04-26 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
US11013733B2 (en) * 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1)
US11013734B2 (en) * 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation
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
WO2003106452A2 (en) 2002-06-12 2003-12-24 Millennium Pharmaceuticals, Inc. 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
JPWO2005095382A1 (ja) 2004-03-30 2007-08-16 協和醗酵工業株式会社 抗腫瘍剤
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
EP2044068A4 (en) * 2006-07-17 2010-07-21 Merck Sharp & Dohme 1-HYDROXY Naphthyridine Compounds as Anti- HIV Drugs
JP2010043004A (ja) 2006-12-06 2010-02-25 Dainippon Sumitomo Pharma Co Ltd 新規2環性複素環化合物
WO2008131547A1 (en) 2007-04-30 2008-11-06 Prometic Biosciences Inc. 'triazine derivatives, compositions containing such derivatives, and methods of treatment of cancer and autoimmune diseases using such derivatives'
WO2010144338A1 (en) 2009-06-08 2010-12-16 Abraxis Bioscience, Llc 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
US20120184548A1 (en) 2011-01-19 2012-07-19 Romyr Dominique Carboxylic acid aryl amides
US20120184562A1 (en) 2011-01-19 2012-07-19 Kin-Chun Luk 1,6- and 1,8-naphthyridines
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
CA2860623A1 (en) 2012-01-06 2013-07-11 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
MX2015012822A (es) * 2013-03-14 2016-05-31 Novartis Ag 3-pirimidin-4-il-oxazolidin-2-onas- como inhibidores del idh mutante.
WO2015003146A1 (en) 2013-07-03 2015-01-08 Georgetown University Boronic acid derivatives of resveratrol for activating deacetylase enzymes
WO2015121210A1 (en) 2014-02-11 2015-08-20 Bayer Pharma Aktiengesellschaft 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
EP3194383B1 (en) 2014-09-19 2019-11-06 Forma Therapeutics, Inc. Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors
HUE062424T2 (hu) 2014-09-19 2023-11-28 Forma Therapeutics Inc Piridin-2(1H)-on kinolinon származékok mint mutáns izocitrát dehidrogenáz inhibitorok
EP3237385B1 (en) 2014-12-22 2021-11-24 The United States of America, as represented by The Secretary, Department of Health and Human Services Mutant idh1 inhibitors useful for treating cancer
GB2533925A (en) 2014-12-31 2016-07-13 Univ Bath Antimicrobial compounds, compositions and methods
WO2016171756A1 (en) 2015-04-21 2016-10-27 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
US10253041B2 (en) 2015-07-27 2019-04-09 Eli Lilly And Company 7-phenylethylamino-4H-pyrimido[4,5-d][1,3]oxazin-2-one compounds and their 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
CN109311863B (zh) 2016-06-06 2021-10-29 伊莱利利公司 突变型idh1抑制剂
JP6987798B2 (ja) 2016-06-22 2022-01-05 ザ ユナイテッド ステイツ オブ アメリカ, アズ リプレゼンテッド バイ ザ セクレタリー, デパートメント オブ ヘルス アンド ヒューマン サービシーズ 癌の治療に変異体idh1阻害剤として有用なチアゾール誘導体
TN2019000158A1 (en) 2016-12-16 2020-10-05 Lilly Co Eli 7-phenylethylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant idh1 and idh2 inhibitors

Also Published As

Publication number Publication date
KR102209667B1 (ko) 2021-01-29
CN111909130A (zh) 2020-11-10
EP3447050B1 (en) 2020-02-19
PL3194376T3 (pl) 2019-05-31
EP3447050A1 (en) 2019-02-27
BR112017005238A2 (pt) 2017-12-19
EP4257131A2 (en) 2023-10-11
HUE041460T2 (hu) 2019-05-28
CN107001328A (zh) 2017-08-01
US20170174658A1 (en) 2017-06-22
SI3194376T1 (sl) 2019-03-29
US20240150319A1 (en) 2024-05-09
US20160083366A1 (en) 2016-03-24
US9834539B2 (en) 2017-12-05
CY1122865T1 (el) 2021-05-05
PT3733662T (pt) 2023-08-18
SMT201900018T1 (it) 2019-02-28
PL3733662T3 (pl) 2024-01-22
EA034336B1 (ru) 2020-01-29
US20180312487A1 (en) 2018-11-01
ES2953347T3 (es) 2023-11-10
TW201617335A (zh) 2016-05-16
AU2019283765B2 (en) 2021-05-13
EP3733662A1 (en) 2020-11-04
IL292608B1 (en) 2024-06-01
US10414752B2 (en) 2019-09-17
IL251163A0 (en) 2017-04-30
US10889567B2 (en) 2021-01-12
NZ730373A (en) 2019-11-29
SMT202000212T1 (it) 2020-05-08
AU2019283765A1 (en) 2020-01-16
MY197533A (en) 2023-06-21
ME03776B (me) 2021-04-20
PH12017500517A1 (en) 2017-08-07
SG11201702194SA (en) 2017-04-27
LT3194376T (lt) 2019-02-25
PL3447050T3 (pl) 2020-07-27
MA40481A (fr) 2017-07-26
AU2015317329A1 (en) 2017-04-27
CL2017000658A1 (es) 2017-12-22
PH12017500517B1 (en) 2022-08-03
DK3194376T3 (en) 2019-01-21
JP6648115B2 (ja) 2020-02-14
US11498913B2 (en) 2022-11-15
MX385512B (es) 2025-03-18
AU2015317329B2 (en) 2019-10-31
RS58184B1 (sr) 2019-03-29
MX2017003404A (es) 2017-07-28
US20200223822A1 (en) 2020-07-16
US20210078973A1 (en) 2021-03-18
EP4257131A3 (en) 2024-01-10
NZ758641A (en) 2023-12-22
ES2704897T3 (es) 2019-03-20
SI3447050T1 (sl) 2020-08-31
HUE062424T2 (hu) 2023-11-28
HRP20200666T1 (hr) 2020-07-24
CA2961817A1 (en) 2016-03-24
AU2021215141A1 (en) 2021-09-02
MY176250A (en) 2020-07-24
US20190263778A1 (en) 2019-08-29
TWI686390B (zh) 2020-03-01
DK3447050T3 (da) 2020-03-09
EP3194376A1 (en) 2017-07-26
IL282363A (en) 2021-06-30
AU2021215141B2 (en) 2023-10-19
FI3733662T3 (fi) 2023-08-09
ZA202304409B (en) 2024-08-28
ZA201902446B (en) 2023-12-20
US20230125739A1 (en) 2023-04-27
MX2019013203A (es) 2020-01-20
MA53352A (fr) 2021-09-15
ES2790640T3 (es) 2020-10-28
PT3194376T (pt) 2019-02-04
SA517381129B1 (ar) 2021-04-26
IL251163B (en) 2021-05-31
EP3194376B1 (en) 2018-10-24
LT3447050T (lt) 2020-05-11
RS60140B1 (sr) 2020-05-29
EA201790657A8 (ru) 2018-02-28
EP3733662B1 (en) 2023-06-07
IL292608A (en) 2022-07-01
JP2017528487A (ja) 2017-09-28
EA201790657A1 (ru) 2017-08-31
IL292608B2 (en) 2024-10-01
CA2961817C (en) 2024-03-12
IL282363B (en) 2022-06-01
CN107001328B (zh) 2020-06-05
PT3447050T (pt) 2020-09-17
WO2016044789A1 (en) 2016-03-24
CO2017003241A2 (es) 2017-09-20
US10550098B2 (en) 2020-02-04
US12275715B2 (en) 2025-04-15
CN111909130B (zh) 2023-10-31
BR112017005238B1 (pt) 2023-01-17
CN117695280A (zh) 2024-03-15
ECSP17022933A (es) 2017-08-31
KR20170063742A (ko) 2017-06-08
CY1121149T1 (el) 2020-05-29
ZA201702127B (en) 2019-06-26

Similar Documents

Publication Publication Date Title
PE20171056A1 (es) Derivados de piridin-2(1h)-on quinolinona como inhibidores de isocitrato deshidrogenasa
MX2017003626A (es) Derivados de piridinil quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh).
MX2017003627A (es) Composiciones de pirimidin quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh).
PE20150734A1 (es) Inhibidores de glucosilceramida sintasa
EA201591745A1 (ru) 3-пиримидин-4-ил-оксазолидин-2-оны в качестве ингибиторов мутантого idh
PE20160934A1 (es) (aza) piridopirazolopirimidinonas e indazolopirimidinonas como inhibidores de fibrinolisis
MX2017003637A (es) Derivados de fenil quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh).
EA201892151A1 (ru) Способ синтеза 2-гидрокси-6-((2-(1-изопропил-1h-пиразол-5-ил)пиридин-3-ил)метокси)бензальдегида
AR082799A1 (es) Derivados de quinolina y quinoxalina como inhibidores de quinasa
EA201400333A1 (ru) Бензонитрильные производные в качестве ингибиторов киназ
MX387984B (es) Inhibidor del egfr y preparación y aplicación del mismo.
CA2919397C (en) Aryl ethers as hif-2.alpha. inhibitors for the treatment of cancer
MX2016001037A (es) Inhibidores de factores de transcripción y usos.
EA201891917A1 (ru) Бициклические гетероциклические производные в качестве ингибиторов irak4
PE20170666A1 (es) 2-(morfolin-4-il)-1,7-naftiridinas
EA201391236A1 (ru) Новые циклические производные азабензимидазола, используемые в качестве антидиабетических агентов
PE20170143A1 (es) Benzimidazol-2-aminas como inhibidores de midh1
PE20141283A1 (es) Nuevos derivados biciclicos de dihidroisoquinolin-1-ona
EA201592082A1 (ru) 3,4-дигидроизохинолин-2(1h)-ильные соединения
PE20160050A1 (es) Inhibidores/ antiandrogenos novedosos de cyp17
PE20170640A1 (es) Derivados de quinolizinona como inhibidores de pi3k
PE20081893A1 (es) Subtipo de amidas selectivas de diazabicicloalcanos
BR112014005864A2 (pt) compostos de beta-lactama para tratar diabetes
PE20171736A1 (es) Derivados de 3-(4'-sustituido)-bencil-eter de pregnenolona
EA201992489A2 (ru) Хинолиноновые производные пиридин-2(1h)-она как ингибиторы мутантной изоцитратдегидрогеназы