MX2017013248A - Compuesto del inhibidor fgfr4 cristalino y usos del mismo. - Google Patents

Compuesto del inhibidor fgfr4 cristalino y usos del mismo.

Info

Publication number
MX2017013248A
MX2017013248A MX2017013248A MX2017013248A MX2017013248A MX 2017013248 A MX2017013248 A MX 2017013248A MX 2017013248 A MX2017013248 A MX 2017013248A MX 2017013248 A MX2017013248 A MX 2017013248A MX 2017013248 A MX2017013248 A MX 2017013248A
Authority
MX
Mexico
Prior art keywords
crystalline
inhibitor compound
fgfr4 inhibitor
salt form
fgfr4
Prior art date
Application number
MX2017013248A
Other languages
English (en)
Inventor
Sanders Kristen
Yoshida Kenshi
Chanda Arani
Moniz George
Original Assignee
Eisai R&D Man 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 Eisai R&D Man Co Ltd filed Critical Eisai R&D Man Co Ltd
Publication of MX2017013248A publication Critical patent/MX2017013248A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48Two nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Abstract

Se una serie de formas cristalinas de N-(2-((6-(3-(2,6-dicloro-3,5 -dimetoxifenil)-1-metilureido) pirimidin-4-il)amino)-5-(4-etilpipe razin-1-il)fenil)acrilamida. í‰stas incluyen una forma cristalina de base libre, una forma cristalina en sal monoclorhidrata, una forma cristalina de sal diclorhidrata, y una forma cristalina de sal etansulfonato. Tambión se proporcionan los métodos para elaborar y utilizar los compuestos cristalinos.
MX2017013248A 2015-04-14 2016-04-13 Compuesto del inhibidor fgfr4 cristalino y usos del mismo. MX2017013248A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201562147313P 2015-04-14 2015-04-14
PCT/US2016/027334 WO2016168331A1 (en) 2015-04-14 2016-04-13 Crystalline fgfr4 inhibitor compound and uses thereof

Publications (1)

Publication Number Publication Date
MX2017013248A true MX2017013248A (es) 2018-07-06

Family

ID=55806857

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2017013248A MX2017013248A (es) 2015-04-14 2016-04-13 Compuesto del inhibidor fgfr4 cristalino y usos del mismo.

Country Status (13)

Country Link
US (2) US10562888B2 (es)
EP (1) EP3283465B1 (es)
JP (3) JP6431622B2 (es)
KR (1) KR102548229B1 (es)
CN (1) CN107660200B (es)
AU (2) AU2016248056B2 (es)
CA (1) CA2982562C (es)
ES (1) ES2864712T3 (es)
IL (1) IL254974B (es)
MX (1) MX2017013248A (es)
RU (1) RU2763328C2 (es)
SG (2) SG11201708472WA (es)
WO (1) WO2016168331A1 (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10562888B2 (en) 2015-04-14 2020-02-18 Eisai R&D Management Co., Ltd. Crystalline FGFR4 inhibitor compound and uses thereof
WO2017196854A1 (en) 2016-05-10 2017-11-16 Eisai R&D Management Co., Ltd. Drug combinations for reducing cell viability and/or cell proliferation
CA3034875A1 (en) * 2016-08-23 2018-03-01 Eisai R&D Management Co., Ltd. Combination therapies for the treatment of hepatocellular carcinoma
JP7063899B2 (ja) * 2016-11-17 2022-05-09 グアンドン ジョンシェン ファーマシューティカル カンパニー リミテッド Fgfr4阻害剤、その製造方法及び使用
CN109422760B (zh) * 2017-09-01 2022-05-27 南京圣和药物研发有限公司 Fgfr4抑制剂及其应用
US11833119B2 (en) 2018-01-10 2023-12-05 Eisai R&D Management Co., Ltd. Combination therapies for the treatment of hepatocellular carcinoma
WO2021231928A1 (en) * 2020-05-15 2021-11-18 Eisai R&D Management Co., Ltd. A method for treating cancer with an oral dosage form of an fgfr4 inhibitor
JP2023533903A (ja) 2020-05-15 2023-08-07 エーザイ・アール・アンド・ディー・マネジメント株式会社 Fgfr4阻害剤の経口製剤によるがんの治療方法

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WO1999061444A2 (en) 1998-05-26 1999-12-02 Warner-Lambert Company Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation
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Also Published As

Publication number Publication date
RU2017139246A (ru) 2019-05-14
CA2982562C (en) 2023-06-13
AU2016248056A1 (en) 2017-11-02
CA2982562A1 (en) 2016-10-20
KR20180003559A (ko) 2018-01-09
US10562888B2 (en) 2020-02-18
AU2016248056B2 (en) 2020-07-23
US20180093972A1 (en) 2018-04-05
ES2864712T3 (es) 2021-10-14
WO2016168331A1 (en) 2016-10-20
BR112017022243A2 (pt) 2018-07-10
IL254974B (en) 2021-06-30
CN107660200B (zh) 2022-01-11
US11498916B2 (en) 2022-11-15
EP3283465A1 (en) 2018-02-21
US20200317645A1 (en) 2020-10-08
JP6431622B2 (ja) 2018-11-28
RU2763328C2 (ru) 2021-12-28
JP2021050231A (ja) 2021-04-01
SG11201708472WA (en) 2017-11-29
RU2017139246A3 (es) 2019-10-22
SG10201810057UA (en) 2018-12-28
IL254974A0 (en) 2017-12-31
JP2018188465A (ja) 2018-11-29
KR102548229B1 (ko) 2023-06-27
EP3283465B1 (en) 2021-01-06
AU2020257131A1 (en) 2020-11-19
JP2018511635A (ja) 2018-04-26
CN107660200A (zh) 2018-02-02

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