SA519401897B1 - [4، 5-d][1،3] 4h مركبات 7-فينيل إيثيل أمينو--بيريميدو أكسازين-2-ون كمثبطات أيزو سيترات ديهيدروجيناز 1 وأيزو سيترات ديهيدروجيناز 2 الطافر - Google Patents

[4، 5-d][1،3] 4h مركبات 7-فينيل إيثيل أمينو--بيريميدو أكسازين-2-ون كمثبطات أيزو سيترات ديهيدروجيناز 1 وأيزو سيترات ديهيدروجيناز 2 الطافر

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Publication number
SA519401897B1
SA519401897B1 SA519401897A SA519401897A SA519401897B1 SA 519401897 B1 SA519401897 B1 SA 519401897B1 SA 519401897 A SA519401897 A SA 519401897A SA 519401897 A SA519401897 A SA 519401897A SA 519401897 B1 SA519401897 B1 SA 519401897B1
Authority
SA
Saudi Arabia
Prior art keywords
phenylethlamino
pyrimido
oxazin
compounds
mutant idh1
Prior art date
Application number
SA519401897A
Other languages
English (en)
Inventor
جيمس هان باتريك
بول بوركهولدير تيموثى
جيلمور رايموند
اليجاندرو باوير ريناتو
رانكوفيس زوران
لويس بوليت سيرج
Original Assignee
ايلاي ليلى اند كومباني
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.)
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Publication date
Application filed by ايلاي ليلى اند كومباني filed Critical ايلاي ليلى اند كومباني
Publication of SA519401897B1 publication Critical patent/SA519401897B1/ar

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic 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
    • C07D498/04Ortho-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
    • A61K31/535Heterocyclic 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
    • A61K31/5365Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia

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  • 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

يتعلق الاختراع الحالي بمركب، وفقًا لتعريفه هنا، أو تركيبة صيدلية pharmaceutical composition تشتمل على المركب، للاستخدام في علاج سرطان يعبر عن أيزو سيترات ديهيدروجيناز 1 isocitrate dehydrogenase 1 (IDH1) أو أيزو سيترات ديهيدروجيناز 2 isocitrate dehydrogenase 2 (IDH2) الطافر له الصيغة البنائية التالية:
SA519401897A 2016-12-16 2019-05-30 [4، 5-d][1،3] 4h مركبات 7-فينيل إيثيل أمينو--بيريميدو أكسازين-2-ون كمثبطات أيزو سيترات ديهيدروجيناز 1 وأيزو سيترات ديهيدروجيناز 2 الطافر SA519401897B1 (ar)

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 (1)

Publication Number Publication Date
SA519401897B1 true SA519401897B1 (ar) 2022-07-28

Family

ID=60888651

Family Applications (1)

Application Number Title Priority Date Filing Date
SA519401897A SA519401897B1 (ar) 2016-12-16 2019-05-30 [4، 5-d][1،3] 4h مركبات 7-فينيل إيثيل أمينو--بيريميدو أكسازين-2-ون كمثبطات أيزو سيترات ديهيدروجيناز 1 وأيزو سيترات ديهيدروجيناز 2 الطافر

Country Status (36)

Country Link
US (3) US11001596B2 (ar)
EP (2) EP3555105B1 (ar)
JP (1) JP6793836B2 (ar)
KR (1) KR102276022B1 (ar)
CN (2) CN115109075A (ar)
AU (2) AU2017378060B2 (ar)
CA (1) CA3045303C (ar)
CL (1) CL2019001551A1 (ar)
CO (1) CO2019005287A2 (ar)
CR (1) CR20190252A (ar)
CY (1) CY1123577T1 (ar)
DK (1) DK3555105T3 (ar)
DO (1) DOP2019000163A (ar)
EA (1) EA036112B1 (ar)
EC (1) ECSP19042682A (ar)
ES (2) ES2941631T3 (ar)
HR (1) HRP20201882T1 (ar)
HU (1) HUE052067T2 (ar)
IL (1) IL267236B (ar)
JO (1) JOP20190142B1 (ar)
LT (1) LT3555105T (ar)
MA (2) MA47399B1 (ar)
MD (1) MD3555105T2 (ar)
MX (1) MX2019006830A (ar)
MY (1) MY197313A (ar)
NZ (1) NZ754115A (ar)
PE (1) PE20190977A1 (ar)
PH (1) PH12019501328A1 (ar)
PL (1) PL3555105T3 (ar)
PT (1) PT3555105T (ar)
RS (1) RS61108B1 (ar)
SA (1) SA519401897B1 (ar)
SI (1) SI3555105T1 (ar)
TN (1) TN2019000158A1 (ar)
UA (1) UA123640C2 (ar)
WO (1) WO2018111707A1 (ar)

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AU2015317322B2 (en) 2014-09-19 2020-09-17 Forma Therapeutics, Inc. Phenyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
CA2961793C (en) 2014-09-19 2021-03-16 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
SG11201702194SA (en) 2014-09-19 2017-04-27 Forma Therapeutics Inc Pyridin-2(1h)-one 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
US9624175B2 (en) 2015-04-21 2017-04-18 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
MX2019004685A (es) 2016-10-24 2019-08-21 Astrazeneca Ab Derivados de 6,7,8,9-tetrahidro-3h-pirazolo[4,3f] isoquinolina utiles en el tratamiento del cancer.
MA47399B1 (fr) * 2016-12-16 2021-02-26 Lilly Co Eli Dérivés de 7-phényléthylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one en tant qu'inhibiteurs de la forme mutée des protéines idh1 et idh2
ES2922379T3 (es) 2016-12-16 2022-09-14 Janssen Pharmaceutica Nv Compuestos de imidazo[4,5,D]pirrolo[2,3,B]piridina como inhibidores de Janus quinasas
JOP20190144A1 (ar) 2016-12-16 2019-06-16 Janssen Pharmaceutica Nv إيميدازو بيرولو بيريدين كمثبطات لعائلة jak الخاصة بإنزيمات الكيناز
TWI794205B (zh) 2017-01-30 2023-03-01 瑞典商阿斯特捷利康公司 化合物
US11013734B2 (en) 2018-05-16 2021-05-25 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)
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
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
US20230000871A1 (en) * 2019-11-08 2023-01-05 Nerviano Medical Sciences S.R.L. Gem-disubstituted heterocyclic compounds and their use as idh inhibitors
CN115443137B (zh) * 2020-03-23 2024-05-31 伊莱利利公司 使用突变idh抑制剂和bcl-2抑制剂的组合疗法
US20230071978A1 (en) * 2020-03-23 2023-03-09 Eli Lilly And Company Method for treating idh1 inhibitor-resistant subjects
CA3172669A1 (en) 2020-03-23 2021-09-30 Nathan Arthur BROOKS Combination therapy with a mutant idh inhibitor
WO2022001916A1 (zh) * 2020-06-28 2022-01-06 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
EP4181927A1 (en) 2020-07-20 2023-05-24 Eli Lilly and Company Combination therapy with a mutant idh1 inhibitor, a deoxyadenosine analog, and a platinum agent
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
WO2022262784A1 (zh) * 2021-06-15 2022-12-22 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
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

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CA2849995A1 (en) 2011-09-27 2013-04-04 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
US9624175B2 (en) * 2015-04-21 2017-04-18 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
CN107849059B (zh) * 2015-07-27 2020-04-28 伊莱利利公司 7-苯基乙基氨基-4h-嘧啶并[4,5-d][1,3]噁嗪-2-酮化合物及其作为突变体idh1抑制剂的用途
US10696665B2 (en) 2016-06-06 2020-06-30 Eli Lilly And Company Mutant IDH1 inhibitors
MA47399B1 (fr) * 2016-12-16 2021-02-26 Lilly Co Eli Dérivés de 7-phényléthylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one en tant qu'inhibiteurs de la forme mutée des protéines idh1 et idh2

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BR112019009648A2 (pt) 2019-09-10
MD3555105T2 (ro) 2021-01-31
MA47399A (fr) 2019-10-23
IL267236A (en) 2019-08-29
DOP2019000163A (es) 2019-07-15
CO2019005287A2 (es) 2019-05-31
MX2019006830A (es) 2019-08-22
JP2020502157A (ja) 2020-01-23
PH12019501328A1 (en) 2020-02-24
EA201991161A1 (ru) 2019-11-29
US11629156B2 (en) 2023-04-18
LT3555105T (lt) 2021-01-11
JOP20190142A1 (ar) 2019-06-13
ES2941631T3 (es) 2023-05-24
KR102276022B1 (ko) 2021-07-13
US20210230185A1 (en) 2021-07-29
EP3763717B1 (en) 2023-03-08
AU2020260493B2 (en) 2021-09-09
US11649247B2 (en) 2023-05-16
PT3555105T (pt) 2020-12-21
CN110072867B (zh) 2022-07-08
JOP20190142B1 (ar) 2023-03-28
NZ754115A (en) 2021-07-30
CA3045303A1 (en) 2018-06-21
UA123640C2 (uk) 2021-05-05
EP3763717A1 (en) 2021-01-13
MY197313A (en) 2023-06-13
EP3555105A1 (en) 2019-10-23
CL2019001551A1 (es) 2019-10-25
WO2018111707A1 (en) 2018-06-21
US11001596B2 (en) 2021-05-11
US20210206780A1 (en) 2021-07-08
CA3045303C (en) 2022-05-17
CN115109075A (zh) 2022-09-27
MA53881A (fr) 2022-04-27
PL3555105T3 (pl) 2021-05-17
PE20190977A1 (es) 2019-07-09
MA47399B1 (fr) 2021-02-26
AU2020260493A1 (en) 2020-11-26
KR20190077539A (ko) 2019-07-03
ES2835281T3 (es) 2021-06-22
RS61108B1 (sr) 2020-12-31
HUE052067T2 (hu) 2021-04-28
AU2017378060A1 (en) 2019-05-30
CR20190252A (es) 2019-08-26
TN2019000158A1 (en) 2020-10-05
DK3555105T3 (da) 2020-11-09
HRP20201882T1 (hr) 2021-01-22
US20200079791A1 (en) 2020-03-12
ECSP19042682A (es) 2019-06-30
AU2017378060B2 (en) 2020-09-03
EA036112B1 (ru) 2020-09-29
EP3555105B1 (en) 2020-10-28
JP6793836B2 (ja) 2020-12-02
CY1123577T1 (el) 2022-03-24
SI3555105T1 (sl) 2020-12-31
IL267236B (en) 2020-08-31
CN110072867A (zh) 2019-07-30

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