CO2017003969A2 - Derivado de isoxazol como inhibidor de isocitrato deshidrogenasa 1 mutante - Google Patents

Derivado de isoxazol como inhibidor de isocitrato deshidrogenasa 1 mutante

Info

Publication number
CO2017003969A2
CO2017003969A2 CONC2017/0003969A CO2017003969A CO2017003969A2 CO 2017003969 A2 CO2017003969 A2 CO 2017003969A2 CO 2017003969 A CO2017003969 A CO 2017003969A CO 2017003969 A2 CO2017003969 A2 CO 2017003969A2
Authority
CO
Colombia
Prior art keywords
inhibitor
isocitrate dehydrogenase
isoxazole derivative
mutant isocitrate
protein
Prior art date
Application number
CONC2017/0003969A
Other languages
English (en)
Inventor
Hironori Matsunaga
Hironao Saito
Hideaki Watanabe
Yoshiko Kagoshima
Shoichi Saito
Masao Itoh
Yohei Kiyotsuka
Tetsunori Fujisawa
Tetsuya Suzuki
Yoko Ogawara
Kazuo Kitabayashi
Original Assignee
Daiichi Sankyo Co Ltd
Nat Cancer Ct
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 Daiichi Sankyo Co Ltd, Nat Cancer Ct filed Critical Daiichi Sankyo Co Ltd
Publication of CO2017003969A2 publication Critical patent/CO2017003969A2/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
    • A61K31/422Oxazoles not condensed and containing further heterocyclic rings
    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms 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

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (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)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Se ha encontrado que un compuesto de la fórmula general (I) que tiene una estructura de isoxazol tiene excelente actividad inhibidora contra la proteína IDH1 mutante e inhibe la producción de 2-HG por esta proteína, mientras que el compuesto también es capaz de inhibir efectivamente el crecimiento de varios tumores que expresan la proteína. En la fórmula, R1, R2, R3, Y y Z son como se definen en la reivindicación 1.
CONC2017/0003969A 2014-10-01 2017-04-24 Derivado de isoxazol como inhibidor de isocitrato deshidrogenasa 1 mutante CO2017003969A2 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2014203475 2014-10-01
JP2015116774 2015-06-09
PCT/JP2015/077916 WO2016052697A1 (ja) 2014-10-01 2015-10-01 変異型イソクエン酸デヒドロゲナーゼ1阻害剤としてのイソキサゾール誘導体

Publications (1)

Publication Number Publication Date
CO2017003969A2 true CO2017003969A2 (es) 2017-07-11

Family

ID=55630718

Family Applications (1)

Application Number Title Priority Date Filing Date
CONC2017/0003969A CO2017003969A2 (es) 2014-10-01 2017-04-24 Derivado de isoxazol como inhibidor de isocitrato deshidrogenasa 1 mutante

Country Status (26)

Country Link
US (1) US10040791B2 (es)
EP (1) EP3202766B1 (es)
JP (1) JP6087033B2 (es)
KR (1) KR102440429B1 (es)
CN (1) CN106795146B (es)
AU (1) AU2015325279B2 (es)
BR (1) BR112017006425B8 (es)
CA (1) CA2963359C (es)
CO (1) CO2017003969A2 (es)
CY (1) CY1122891T1 (es)
DK (1) DK3202766T3 (es)
ES (1) ES2779305T3 (es)
HR (1) HRP20200395T1 (es)
HU (1) HUE048997T2 (es)
IL (1) IL251305B (es)
LT (1) LT3202766T (es)
MX (1) MX2017003782A (es)
PH (1) PH12017500530B1 (es)
PL (1) PL3202766T3 (es)
PT (1) PT3202766T (es)
RS (1) RS60064B1 (es)
RU (1) RU2692782C2 (es)
SG (1) SG11201702389XA (es)
SI (1) SI3202766T1 (es)
WO (1) WO2016052697A1 (es)
ZA (1) ZA201703013B (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
EP3464281B1 (en) 2016-06-06 2020-07-08 Eli Lilly and Company Mutant idh1 inhibitors
WO2018010142A1 (en) * 2016-07-14 2018-01-18 Shanghai Meton Pharmaceutical Co., Ltd Iso-citrate dehydrogenase (idh) inhibitor
WO2019025256A1 (en) * 2017-08-01 2019-02-07 Bayer Aktiengesellschaft COMBINATION OF MIDH1 INHIBITORS AND DNA HYPOMETHYLATION (AHM) AGENTS
MX2018002612A (es) * 2018-01-29 2019-07-30 Fujifilm Corp Composicion farmaceutica para tumor que tiene mutacion de isocitrato deshidrogenada, agente antitumoral y uso del mismo.
WO2021176098A1 (en) 2020-03-05 2021-09-10 Université de Lausanne Modulators of aralar for treating neurological disorders
AU2021311539A1 (en) 2020-07-21 2023-02-09 Daiichi Sankyo Company, Limited Combination drug of temozolomide and inhibitor of mutated IDH1 enzyme
AU2021371592A1 (en) * 2020-10-30 2023-06-15 Daiichi Sankyo Company, Limited Method of producing 3-methyl-4-halo-indole derivative

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3194811A (en) 1963-09-05 1965-07-13 Merck & Co Inc Aroyl-benzindolyl acids
WO1994010145A1 (en) 1992-10-23 1994-05-11 Merck Sharp & Dohme Limited Dopamine receptor subtype ligands
WO1994024095A1 (en) 1993-04-16 1994-10-27 Abbott Laboratories Immunosuppressive agents
GB2284600A (en) * 1994-01-21 1995-06-14 Shell Int Research Herbicidal 3-(hetero)aryl-4-acylisoxazole compositions and compounds
JP4921162B2 (ja) 2003-02-11 2012-04-25 ヴァーナリス(ケンブリッジ)リミテッド 熱ショックタンパク質の阻害剤としてのイソオキサゾール化合物類
RU2392273C2 (ru) * 2004-09-10 2010-06-20 Синджента Лимитед Замещенные изоксазолы в качестве фунгицидов
WO2012009678A1 (en) * 2010-07-16 2012-01-19 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their method of use
WO2012173682A2 (en) 2011-03-29 2012-12-20 The Broad Institute, Inc. Compounds and methods for the treatment of isocitrate dehydrognase related diseases
CN102827073A (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
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
CA2849995A1 (en) 2011-09-27 2013-04-04 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
WO2013107405A1 (en) 2012-01-19 2013-07-25 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US9474779B2 (en) 2012-01-19 2016-10-25 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use

Also Published As

Publication number Publication date
CY1122891T1 (el) 2021-05-05
PH12017500530A1 (en) 2017-08-07
KR102440429B1 (ko) 2022-09-05
RU2017114005A (ru) 2018-11-07
RU2017114005A3 (es) 2018-11-21
EP3202766B1 (en) 2019-12-25
JP6087033B2 (ja) 2017-03-01
BR112017006425B1 (pt) 2023-02-23
PH12017500530B1 (en) 2017-08-07
EP3202766A1 (en) 2017-08-09
CA2963359C (en) 2020-03-31
EP3202766A4 (en) 2018-04-04
MX2017003782A (es) 2017-08-10
BR112017006425A2 (pt) 2017-12-12
AU2015325279A1 (en) 2017-04-27
PL3202766T3 (pl) 2020-07-13
IL251305B (en) 2020-06-30
RS60064B1 (sr) 2020-04-30
IL251305A0 (en) 2017-05-29
US20170313696A1 (en) 2017-11-02
CA2963359A1 (en) 2016-04-07
CN106795146A (zh) 2017-05-31
ZA201703013B (en) 2018-08-29
ES2779305T3 (es) 2020-08-14
DK3202766T3 (da) 2020-03-23
PT3202766T (pt) 2020-03-25
CN106795146B (zh) 2020-06-26
AU2015325279B2 (en) 2020-02-27
RU2692782C2 (ru) 2019-06-27
SG11201702389XA (en) 2017-04-27
LT3202766T (lt) 2020-05-11
KR20170068501A (ko) 2017-06-19
SI3202766T1 (sl) 2020-07-31
HUE048997T2 (hu) 2020-09-28
BR112017006425B8 (pt) 2023-05-16
HRP20200395T1 (hr) 2020-06-12
JPWO2016052697A1 (ja) 2017-04-27
WO2016052697A1 (ja) 2016-04-07
NZ730855A (en) 2021-06-25
US10040791B2 (en) 2018-08-07

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