MX2017003782A - 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
MX2017003782A
MX2017003782A MX2017003782A MX2017003782A MX2017003782A MX 2017003782 A MX2017003782 A MX 2017003782A MX 2017003782 A MX2017003782 A MX 2017003782A MX 2017003782 A MX2017003782 A MX 2017003782A MX 2017003782 A MX2017003782 A MX 2017003782A
Authority
MX
Mexico
Prior art keywords
inhibitor
isocitrate dehydrogenase
isoxazole derivative
mutated
mutated isocitrate
Prior art date
Application number
MX2017003782A
Other languages
English (en)
Inventor
Kagoshima Yoshiko
Saito Shoichi
Itoh Masao
Fujisawa Tetsunori
Saito Hironao
KIYOTSUKA Yohei
Watanabe Hideaki
Matsunaga Hironori
Suzuki Tetsuya
OGAWARA Yoko
KITABAYASHI Kazuo
Original Assignee
Daiichi Sankyo Co Ltd
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 filed Critical Daiichi Sankyo Co Ltd
Publication of MX2017003782A publication Critical patent/MX2017003782A/es

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    • 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
    • A61K31/41Heterocyclic 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
    • C07D413/02Heterocyclic 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
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (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.
MX2017003782A 2014-10-01 2015-10-01 Derivado de isoxazol como inhibidor de isocitrato deshidrogenasa 1 mutante. MX2017003782A (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
MX2017003782A true MX2017003782A (es) 2017-08-10

Family

ID=55630718

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2017003782A MX2017003782A (es) 2014-10-01 2015-10-01 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) PH12017500530A1 (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
ES2764523T3 (es) * 2015-07-27 2020-06-03 Lilly Co Eli Compuestos de 7-feniletilamino-4H-pirimido[4,5-D][1,3]oxazin-2-ona y su uso como inhibidores de IDH1 mutantes
WO2017213910A1 (en) 2016-06-06 2017-12-14 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
CA3070878A1 (en) * 2017-08-01 2019-02-07 Deutsches Krebsforschungszentrum Combination of midh1 inhibitors and dna hypomethylating agents (hma)
WO2019146129A1 (ja) * 2018-01-29 2019-08-01 富士フイルム株式会社 イソクエン酸デヒドロゲナーゼ変異を有する腫瘍に対する医薬組成物および抗腫瘍剤ならびにその利用
WO2021176098A1 (en) 2020-03-05 2021-09-10 Université de Lausanne Modulators of aralar for treating neurological disorders
JP2022021331A (ja) 2020-07-21 2022-02-02 第一三共株式会社 テモゾロミドと変異型idh1酵素阻害剤の組み合わせ医薬
TW202233576A (zh) 2020-10-30 2022-09-01 日商第一三共股份有限公司 3-甲基-鹵-吲哚衍生物之製造方法

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
EP0665833B1 (en) 1992-10-23 1999-07-14 MERCK SHARP & DOHME LTD. 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
EA009919B1 (ru) 2003-02-11 2008-04-28 Вернэлис (Кембридж) Лимитед Соединения изоксазола
RU2392273C2 (ru) * 2004-09-10 2010-06-20 Синджента Лимитед Замещенные изоксазолы в качестве фунгицидов
BR112013001122B1 (pt) * 2010-07-16 2021-06-08 Agios Pharmaceuticals, Inc composto de fórmula ii, uso do composto e composição farmacêutica compreendendo dito composto
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
MX342326B (es) * 2011-09-27 2016-09-26 Novartis Ag 3-pirimidin-4-il-oxazolidin-2-onas como inhibidoras de idh mutante.
US20150087600A1 (en) 2012-01-19 2015-03-26 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
EP3202766B1 (en) 2019-12-25
IL251305A0 (en) 2017-05-29
US20170313696A1 (en) 2017-11-02
ZA201703013B (en) 2018-08-29
AU2015325279B2 (en) 2020-02-27
CA2963359C (en) 2020-03-31
HUE048997T2 (hu) 2020-09-28
JP6087033B2 (ja) 2017-03-01
IL251305B (en) 2020-06-30
RU2017114005A (ru) 2018-11-07
LT3202766T (lt) 2020-05-11
RU2692782C2 (ru) 2019-06-27
SI3202766T1 (sl) 2020-07-31
PH12017500530B1 (en) 2017-08-07
KR102440429B1 (ko) 2022-09-05
CO2017003969A2 (es) 2017-07-11
AU2015325279A1 (en) 2017-04-27
CY1122891T1 (el) 2021-05-05
CN106795146B (zh) 2020-06-26
DK3202766T3 (da) 2020-03-23
RS60064B1 (sr) 2020-04-30
JPWO2016052697A1 (ja) 2017-04-27
BR112017006425A2 (pt) 2017-12-12
CN106795146A (zh) 2017-05-31
EP3202766A1 (en) 2017-08-09
US10040791B2 (en) 2018-08-07
BR112017006425B8 (pt) 2023-05-16
WO2016052697A1 (ja) 2016-04-07
RU2017114005A3 (es) 2018-11-21
EP3202766A4 (en) 2018-04-04
HRP20200395T1 (hr) 2020-06-12
BR112017006425B1 (pt) 2023-02-23
SG11201702389XA (en) 2017-04-27
ES2779305T3 (es) 2020-08-14
PT3202766T (pt) 2020-03-25
NZ730855A (en) 2021-06-25
PL3202766T3 (pl) 2020-07-13
KR20170068501A (ko) 2017-06-19
PH12017500530A1 (en) 2017-08-07
CA2963359A1 (en) 2016-04-07

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