MX2019006830A - Compuestos de 7-feniletilamino-4h-pirimido[4,5-d] [1,3] -oxazin-2-ona como mutantes idh1 e inhibidores de idh2. - Google Patents

Compuestos de 7-feniletilamino-4h-pirimido[4,5-d] [1,3] -oxazin-2-ona como mutantes idh1 e inhibidores de idh2.

Info

Publication number
MX2019006830A
MX2019006830A MX2019006830A MX2019006830A MX2019006830A MX 2019006830 A MX2019006830 A MX 2019006830A MX 2019006830 A MX2019006830 A MX 2019006830A MX 2019006830 A MX2019006830 A MX 2019006830A MX 2019006830 A MX2019006830 A MX 2019006830A
Authority
MX
Mexico
Prior art keywords
phenylethylamino
pyrimido
oxazin
compounds
mutant idh1
Prior art date
Application number
MX2019006830A
Other languages
English (en)
Other versions
MX385562B (es
Inventor
Paul Burkholder Timothy
Alejandro Bauer Renato
Louis Boulet Serge
Gilmour Raymond
James Hahn Patric
Rankovic Zoran
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of MX2019006830A publication Critical patent/MX2019006830A/es
Publication of MX385562B publication Critical patent/MX385562B/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems
    • 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
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines ortho- or peri-condensed with heterocyclic ring systems
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Un compuesto, como se define en la presente, o composición farmacéutica que contiene el compuesto, para usar en el tratamiento del cáncer mutante de IDH1 o IDH2 y que tiene la estructura: (formula).
MX2019006830A 2016-12-16 2017-12-08 Compuestos de 7-feniletilamino-4h-pirimido[4,5-d] [1,3] -oxazin-2-ona como mutantes idh1 e inhibidores de idh2. MX385562B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201662435283P 2016-12-16 2016-12-16
PCT/US2017/065246 WO2018111707A1 (en) 2016-12-16 2017-12-08 7-phenylethylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant idh1 and idh2 inhibitors

Publications (2)

Publication Number Publication Date
MX2019006830A true MX2019006830A (es) 2019-08-22
MX385562B MX385562B (es) 2025-03-18

Family

ID=60888651

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2019006830A MX385562B (es) 2016-12-16 2017-12-08 Compuestos de 7-feniletilamino-4h-pirimido[4,5-d] [1,3] -oxazin-2-ona como mutantes idh1 e inhibidores de idh2.

Country Status (37)

Country Link
US (3) US11001596B2 (es)
EP (2) EP3763717B1 (es)
JP (1) JP6793836B2 (es)
KR (1) KR102276022B1 (es)
CN (2) CN115109075B (es)
AU (2) AU2017378060B2 (es)
CA (1) CA3045303C (es)
CL (1) CL2019001551A1 (es)
CO (1) CO2019005287A2 (es)
CR (1) CR20190252A (es)
CY (1) CY1123577T1 (es)
DK (1) DK3555105T3 (es)
DO (1) DOP2019000163A (es)
EA (1) EA036112B1 (es)
EC (1) ECSP19042682A (es)
ES (2) ES2835281T3 (es)
HR (1) HRP20201882T1 (es)
HU (1) HUE052067T2 (es)
IL (1) IL267236B (es)
JO (1) JOP20190142B1 (es)
LT (1) LT3555105T (es)
MA (2) MA47399B1 (es)
MD (1) MD3555105T2 (es)
MX (1) MX385562B (es)
MY (1) MY197313A (es)
NZ (1) NZ754115A (es)
PE (1) PE20190977A1 (es)
PH (1) PH12019501328B1 (es)
PL (1) PL3555105T3 (es)
PT (1) PT3555105T (es)
RS (1) RS61108B1 (es)
SA (1) SA519401897B1 (es)
SI (1) SI3555105T1 (es)
TN (1) TN2019000158A1 (es)
UA (1) UA123640C2 (es)
WO (1) WO2018111707A1 (es)
ZA (1) ZA201903125B (es)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102209667B1 (ko) 2014-09-19 2021-01-29 포르마 세라퓨틱스 인크. 돌연변이-아이소시트레이트 탈수소효소 저해제로서의 피리딘-2(1h)-온 퀴놀린 유도체
MX372964B (es) 2014-09-19 2020-03-27 Forma Therapeutics Inc Derivados de fenil quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh)
AU2015317321B2 (en) 2014-09-19 2020-03-12 Forma Therapeutics, Inc. Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors
EP3201185B1 (en) 2014-09-19 2018-11-21 Forma Therapeutics, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2016171755A1 (en) 2015-04-21 2016-10-27 Forma Therapeutics, 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
JOP20190090B1 (ar) 2016-10-24 2023-03-28 Astrazeneca Ab مشتقات 9،8،7،6-رابع هيدرو-3h-بيرازولو [4،3-f]أيزوكينولين مفيدة في علاج السرطان
JOP20190144A1 (ar) 2016-12-16 2019-06-16 Janssen Pharmaceutica Nv إيميدازو بيرولو بيريدين كمثبطات لعائلة jak الخاصة بإنزيمات الكيناز
PH12019501328B1 (en) * 2016-12-16 2023-05-12 Lilly Co Eli 7-phenylethlamino-4h-pyrimido][4,5-d][1,3] oxazin-2-one compounds as mutant 1dh1 and 1dh2 inhibitors
JP7291077B2 (ja) 2016-12-16 2023-06-14 ヤンセン ファーマシューティカ エヌ.ベー. Jakファミリーのキナーゼの低分子阻害物質
EP3689873B1 (en) 2017-01-30 2022-09-14 Astrazeneca AB Estrogen receptor modulators
US20210196701A1 (en) 2018-05-16 2021-07-01 Forma Therapeutics, Inc. Inhibiting mutant idh-1
US11497743B2 (en) 2018-05-16 2022-11-15 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase 1 (IDH-1) mutation
US11013733B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-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
US11013734B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation
US11738018B2 (en) 2018-05-16 2023-08-29 FORMA Therapeuetics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
US11311527B2 (en) 2018-05-16 2022-04-26 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
TW202016110A (zh) 2018-06-15 2020-05-01 比利時商健生藥品公司 Jak激酶家族之小分子抑制劑
ES3033669T3 (en) 2019-11-08 2025-08-06 Nerviano Medical Sciences Srl Gem-disubstituted heterocyclic compounds and their use as idh inhibitors
AU2021241470B2 (en) * 2020-03-23 2023-12-14 Board Of Regents, The University Of Texas System Combination therapy with a mutant IDH inhibitor and a Bcl-2 inhibitor
ES2981250T3 (es) * 2020-03-23 2024-10-08 Lilly Co Eli Terapia combinada con un inhibidor de IDH mutante
IL296094A (en) * 2020-03-23 2022-11-01 Lilly Co Eli Method for treating idh1 inhibitor-resistant subjects
JP7712955B2 (ja) 2020-04-24 2025-07-24 アストラゼネカ・アクチエボラーグ 癌の治療のための投薬レジメン
MX2022013258A (es) 2020-04-24 2022-11-14 Astrazeneca Ab Formulaciones farmaceuticas.
CN115768775B (zh) * 2020-06-28 2024-10-25 微境生物医药科技(上海)有限公司 Idh突变体抑制剂及其用途
JP2023534991A (ja) * 2020-07-20 2023-08-15 イーライ リリー アンド カンパニー 変異型idh1阻害剤、デオキシアデノシン類似体、及び白金剤を用いた併用療法
AU2022233254A1 (en) 2021-03-11 2023-10-26 Janssen Pharmaceutica Nv Lorpucitinib for use in the treatment of jak mediated disorders
CN113588768B (zh) * 2021-05-18 2022-07-05 国家卫生健康委科学技术研究所 一种以分子图像方式定量组织内内源性代谢物的质谱方法
CN117460514A (zh) * 2021-06-09 2024-01-26 伊莱利利公司 用于治疗idh抑制剂耐药的对象的方法
US20240208978A1 (en) * 2021-06-15 2024-06-27 Wigen Biomedicine Technology (shanghai) Co., Ltd. Idh mutant inhibitor and use thereof
CA3224704A1 (en) 2021-08-13 2023-02-16 David Andrew Coates Solid forms of 7-[[(1s)-1-[4-[(1s)-2-cyclopropyl-1-(4-prop-2-enoylpiper azin-1-yl)ethyl]phenyl]ethyl]amino]-1-ethyl-4h- pyrimido[4,5-d] [1,3]oxazin-2-one
WO2023141087A1 (en) 2022-01-19 2023-07-27 Eli Lilly And Company Combination therapy with a mutant idh inhibitor

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2012313888B2 (en) * 2011-09-27 2016-03-31 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant IDH
BR112015022483A2 (pt) * 2013-03-14 2017-07-18 Novartis Ag 3-pirimidin-4-il-oxazolidin-2-onas como inibidores de idh mutante
WO2014147586A1 (en) * 2013-03-22 2014-09-25 Novartis Ag 1-(2-(ethylamino)pyrimidin-4-yl)pyrrolidin-2-ones as inhibitors of mutant idh
WO2016171755A1 (en) * 2015-04-21 2016-10-27 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2016171715A1 (en) * 2015-04-24 2016-10-27 Halliburton Energy Services, Inc. Methods of fabricating ceramic or intermetallic parts
JP6473270B2 (ja) * 2015-07-27 2019-02-20 イーライ リリー アンド カンパニー 7−フェニルエチルアミノ−4h−ピリミド[4,5−d][1,3]オキサジン−2−オン化合物及び変異体idh1阻害剤としてのそれらの使用
ES2814290T3 (es) * 2016-06-06 2021-03-26 Lilly Co Eli Inhibidores de IDH1 mutante
PH12019501328B1 (en) * 2016-12-16 2023-05-12 Lilly Co Eli 7-phenylethlamino-4h-pyrimido][4,5-d][1,3] oxazin-2-one compounds as mutant 1dh1 and 1dh2 inhibitors

Also Published As

Publication number Publication date
US11629156B2 (en) 2023-04-18
EA036112B1 (ru) 2020-09-29
CL2019001551A1 (es) 2019-10-25
KR102276022B1 (ko) 2021-07-13
MD3555105T2 (ro) 2021-01-31
AU2020260493B2 (en) 2021-09-09
JP2020502157A (ja) 2020-01-23
RS61108B1 (sr) 2020-12-31
JOP20190142B1 (ar) 2023-03-28
PL3555105T3 (pl) 2021-05-17
CN110072867A (zh) 2019-07-30
WO2018111707A1 (en) 2018-06-21
US11649247B2 (en) 2023-05-16
CR20190252A (es) 2019-08-26
ES2835281T3 (es) 2021-06-22
CN115109075A (zh) 2022-09-27
CN110072867B (zh) 2022-07-08
IL267236A (en) 2019-08-29
SA519401897B1 (ar) 2022-07-28
ES2941631T3 (es) 2023-05-24
MY197313A (en) 2023-06-13
EP3763717A1 (en) 2021-01-13
AU2020260493A1 (en) 2020-11-26
US11001596B2 (en) 2021-05-11
US20210206780A1 (en) 2021-07-08
SI3555105T1 (sl) 2020-12-31
UA123640C2 (uk) 2021-05-05
DK3555105T3 (da) 2020-11-09
CY1123577T1 (el) 2022-03-24
MA47399B1 (fr) 2021-02-26
PE20190977A1 (es) 2019-07-09
BR112019009648A2 (pt) 2019-09-10
MX385562B (es) 2025-03-18
TN2019000158A1 (en) 2020-10-05
KR20190077539A (ko) 2019-07-03
IL267236B (en) 2020-08-31
MA53881A (fr) 2022-04-27
AU2017378060A1 (en) 2019-05-30
US20200079791A1 (en) 2020-03-12
HUE052067T2 (hu) 2021-04-28
EP3555105A1 (en) 2019-10-23
CN115109075B (zh) 2024-09-20
EP3555105B1 (en) 2020-10-28
CO2019005287A2 (es) 2019-05-31
PT3555105T (pt) 2020-12-21
CA3045303C (en) 2022-05-17
DOP2019000163A (es) 2019-07-15
LT3555105T (lt) 2021-01-11
ZA201903125B (en) 2024-08-28
CA3045303A1 (en) 2018-06-21
PH12019501328B1 (en) 2023-05-12
HRP20201882T1 (hr) 2021-01-22
EA201991161A1 (ru) 2019-11-29
JP6793836B2 (ja) 2020-12-02
PH12019501328A1 (en) 2020-02-24
ECSP19042682A (es) 2019-06-30
JOP20190142A1 (ar) 2019-06-13
EP3763717B1 (en) 2023-03-08
US20210230185A1 (en) 2021-07-29
AU2017378060B2 (en) 2020-09-03
MA47399A (fr) 2019-10-23
NZ754115A (en) 2021-07-30

Similar Documents

Publication Publication Date Title
CO2019005287A2 (es) Compuestos de 7-feniletilamino-4h-pirimido[4,5-d][1,3]-oxazin-2-ona como inhibidores de idh1 e idh2 mutantes
ECSP18094983A (es) Derivados de pirazol como inhibidores de la calicreína plasmática
GEP20237506B (en) Pcsk9 antagonist compounds
MX2018011992A (es) Compuestos de aminopurina sustituida, composiciones de estos y metodos de tratamiento con estos.
CL2009000483A1 (es) Compuestos derivados de n-(piridin-3-il)-1,3-tiazol-5-amino-4-carboxamida, inhibidores de cinasa pim; composicion farmaceutica; y uso para el tratamiento del cancer.
BR112018004620A2 (pt) moduladores da expressão de kras
SV2017005461A (es) Benzamidas sustituidas con 1,3-tiazol-2-ilo
MX2020011104A (es) Composiciones farmaceuticas de compuestos terapeuticamente activos y sus metodos de uso.
CL2011000454A1 (es) Compuestos derivados de picolinamida, inhibidores de quinasa pim, asociada a tumorigenesis; composicion farmaceutica que los comprende; y su uso en el tratamiento del cancer.
NI200900184A (es) Uso de compuestos inhibidores de quinaxolina de pi3k-alfa para el tratamiento del cáncer.
DOP2016000208A (es) Benzimidazol-2-aminas como inhibidores de midh1
CL2014001793A1 (es) Compuestos derivados de 1,3,5-triazinas sustituidas y sus sales, como inhibidores de la idh2 mutante; composicion farmaceutica que los comprende; y su uso para el tratamiento del cancer.
BR112015026297A2 (pt) terapia combinada composta por um inibidor tor quinase e um composto de 5-quinazolinona substituído para o tratamento de câncer
MX2017004600A (es) Compuestos de aminopurina sustituida, composiciones del mismo, y metodos de tratamiento con los mismos.
MX2018006674A (es) Tratamiento de cancer usando 2-desoxi-2-fluoro-l-fucosa en combinacion con un inhibidor del punto de control.
AR096892A1 (es) Una combinación farmacéutica para el tratamiento del melanoma
CO2022000481A2 (es) Inhibidores de enzimas
NZ758177A (en) Modulators of pcsk9 expression
DOP2020000100A (es) Novedosos derivados de pirazolo-pirrolo-pirimidina como inhibidores de p2x3
CR20160047A (es) Inhibidores de rorc2 y sus métodos de uso
MX2016015437A (es) Combinacion que comprende un glucocorticoide y edo-s101.
CO2022000270A2 (es) Inhibidores de enzimas
MX2016010524A (es) Derivados de piridazina para uso en la prevencion o tratamiento de trastorno ataxico.
CR20150148A (es) Azaindolinas
CL2011000168A1 (es) Compuestos derivados de narciclasina y pancratistatina; procedimiento de preparación; composición farmacéutica; combinación farmacéutica; y su uso para el tratamiento del cáncer.