BR112016008080A8 - sal de composto heterocíclico contendo nitrogênio ou cristal do mesmo, composição farmacêutica e inibidor de flt3 - Google Patents

sal de composto heterocíclico contendo nitrogênio ou cristal do mesmo, composição farmacêutica e inibidor de flt3 Download PDF

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Publication number
BR112016008080A8
BR112016008080A8 BR112016008080A BR112016008080A BR112016008080A8 BR 112016008080 A8 BR112016008080 A8 BR 112016008080A8 BR 112016008080 A BR112016008080 A BR 112016008080A BR 112016008080 A BR112016008080 A BR 112016008080A BR 112016008080 A8 BR112016008080 A8 BR 112016008080A8
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Brazil
Prior art keywords
crystal
pharmaceutical composition
flt3
salt
heterocyclic compound
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BR112016008080A
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BR112016008080B1 (pt
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Mizumoto Shinsuke
Matsumoto Takuya
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Fujifilm Corp
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Publication of BR112016008080A8 publication Critical patent/BR112016008080A8/pt
Publication of BR112016008080B1 publication Critical patent/BR112016008080B1/pt

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    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/18Sulfonamides
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/28Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/29Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton of non-condensed six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C55/00Saturated compounds having more than one carboxyl group bound to acyclic carbon atoms
    • C07C55/02Dicarboxylic acids
    • C07C55/10Succinic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/02Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
    • C07C57/13Dicarboxylic acids
    • C07C57/15Fumaric acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C65/00Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C65/01Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups
    • C07C65/105Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups polycyclic
    • C07C65/11Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups polycyclic with carboxyl groups on a condensed ring system containing two rings
    • 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
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

resumo “sal de composto heterocíclico contendo nitrogênio ou cristal do mesmo, composição farmacêutica e inibidor de flt3” a presente invenção refere-se a um composto e composição farmacêutica que mostram estabilidade e/ou solubilidade superior, etc. e têm atividade inibitória de flt3 superior. a presente invenção provê um sal de (s,e)-n-(1-((5-(2-((4-cianofenil)amino)-4-(propilamino)pirimidin-5-il)pent-4-in-1-il)amino)-1-oxopropan-2-il)-4-(dimetilamino)-n-metilbut-2-enamida ou um cristal do mesmo. uma vez que o sal ou um cristal do mesmo tenha atividade inibitória de flt3 superior e mostre pro-priedades físico-químicas superiores como fármacos, tais como estabilidade de ar-mazenamento, solubilidade e assim por diante, ele é útil para tratamentos de doen-ças ou condições relacionadas à flt3. a presente invenção também provê uma composição farmacêutica e inibidor de flt3 contendo o sal ou um cristal do mesmo.
BR112016008080-7A 2013-10-16 2014-10-15 sal de ácido carboxílico ou um sal de ácido mineral, cristal de succinato, cristal de fumarato e composição farmacêutica BR112016008080B1 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2013215755 2013-10-16
JP2013-215755 2013-10-16
PCT/JP2014/077368 WO2015056683A1 (ja) 2013-10-16 2014-10-15 含窒素複素環化合物の塩またはその結晶、医薬組成物およびflt3阻害剤

Publications (2)

Publication Number Publication Date
BR112016008080A8 true BR112016008080A8 (pt) 2020-03-17
BR112016008080B1 BR112016008080B1 (pt) 2021-02-23

Family

ID=52828126

Family Applications (1)

Application Number Title Priority Date Filing Date
BR112016008080-7A BR112016008080B1 (pt) 2013-10-16 2014-10-15 sal de ácido carboxílico ou um sal de ácido mineral, cristal de succinato, cristal de fumarato e composição farmacêutica

Country Status (14)

Country Link
US (1) US9701644B2 (pt)
EP (1) EP3059227B1 (pt)
JP (1) JP5887028B2 (pt)
KR (1) KR101744033B1 (pt)
CN (1) CN105683167B (pt)
AU (1) AU2014335312B9 (pt)
BR (1) BR112016008080B1 (pt)
CA (1) CA2927079C (pt)
DK (1) DK3059227T3 (pt)
ES (1) ES2738573T3 (pt)
HK (1) HK1219946A1 (pt)
PL (1) PL3059227T3 (pt)
RU (1) RU2641106C2 (pt)
WO (1) WO2015056683A1 (pt)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2727195C2 (ru) 2014-08-22 2020-07-21 Фуджифилм Корпорэйшн Фармацевтическая композиция для лечения злокачественной опухоли, положительной по мутации flt3, ингибитор мутантного flt3 и их применение
US11286670B2 (en) 2015-02-06 2022-03-29 Roofguard Manufacturing, Llc Roof drain cover
JP6412471B2 (ja) * 2015-07-15 2018-10-24 富士フイルム株式会社 含窒素複素環化合物の製造方法およびその中間体
TW202027749A (zh) * 2018-10-12 2020-08-01 日商富士軟片股份有限公司 急性骨髓性白血病用抗腫瘤劑
CN112996514A (zh) * 2018-10-31 2021-06-18 富士胶片株式会社 包含抗肿瘤剂的片剂
WO2020090969A1 (ja) 2018-10-31 2020-05-07 富士フイルム株式会社 抗腫瘍剤を含む医薬組成物の包装体
EP3875091A4 (en) * 2018-10-31 2021-12-29 FUJIFILM Corporation Pharmaceutical composition containing antitumor agent
JPWO2020090968A1 (ja) * 2018-10-31 2021-09-16 富士フイルム株式会社 抗腫瘍剤を含む造粒物
TW202045174A (zh) 2019-02-28 2020-12-16 日商富士軟片股份有限公司 組合醫藥
BR112021018168B1 (pt) 2019-03-21 2023-11-28 Onxeo Composição farmacêutica, combinação e kit compreendendo uma molécula dbait e um inibidor de quinase para o tratamento de câncer
KR20220098759A (ko) 2019-11-08 2022-07-12 인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) 키나제 억제제에 대해 내성을 획득한 암의 치료 방법
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
WO2023027966A1 (en) 2021-08-24 2023-03-02 Biomea Fusion, Inc. Pyrazine compounds as irreversible inhibitors of flt3
US11945785B2 (en) 2021-12-30 2024-04-02 Biomea Fusion, Inc. Pyrazine compounds as inhibitors of FLT3
WO2023225005A1 (en) 2022-05-17 2023-11-23 Biomea Fusion, Inc. Flt3 combination therapy for cancer and compositions therefor

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8928839D0 (en) 1989-12-21 1990-02-28 Beecham Group Plc Novel compounds
US5936399A (en) * 1997-09-16 1999-08-10 Mitutoyo Corporation Inductive position transducer having a multi-tap receiver winding
ATE407678T1 (de) * 2001-10-17 2008-09-15 Boehringer Ingelheim Pharma Pyrimidinderivate, arzneimittel enthaltend diese verbindungen, deren verwendung und verfahren zu ihrer herstellung
CN101282945A (zh) * 2005-06-08 2008-10-08 里格尔药品股份有限公司 抑制jak途径的组合物和方法
CN105348203B (zh) * 2005-06-08 2018-09-18 里格尔药品股份有限公司 抑制jak途径的组合物和方法
US8071768B2 (en) * 2005-06-10 2011-12-06 Janssen Pharmaceutica, N.V. Alkylquinoline and alkylquinazoline kinase modulators
US20060281755A1 (en) 2005-06-10 2006-12-14 Baumann Christian A Synergistic modulation of flt3 kinase using aminopyrimidines kinase modulators
US7825244B2 (en) * 2005-06-10 2010-11-02 Janssen Pharmaceutica Nv Intermediates useful in the synthesis of alkylquinoline and alkylquinazoline kinase modulators, and related methods of synthesis
CA2629244C (en) 2005-11-11 2014-08-05 Boehringer Ingelheim International Gmbh Quinazoline derivatives for the treatment of cancer diseases
CN101448843B (zh) 2006-03-17 2012-05-09 埃姆比特生物科学公司 用于疾病治疗的咪唑并噻唑化合物
EP2022785A1 (en) * 2007-06-20 2009-02-11 Bayer Schering Pharma Aktiengesellschaft Alkynylpyrimidines as Tie2 kinase inhibitors
CN101779250B (zh) * 2007-06-21 2014-01-08 桑迪士克科技股份有限公司 编程脉冲持续期的智能控制
RU2493152C2 (ru) 2008-02-01 2013-09-20 Акинион Фармасьютикалз Аб Новые соединения, применение и получение их
LT2300013T (lt) 2008-05-21 2017-12-27 Ariad Pharmaceuticals, Inc. Fosforo dariniai kaip kinazių inhibitoriai
WO2010129053A2 (en) 2009-05-05 2010-11-11 Dana Farber Cancer Institute Egfr inhibitors and methods of treating disorders
US9290485B2 (en) * 2010-08-04 2016-03-22 Novartis Ag N-((6-amino-pyridin-3-yl)methyl)-heteroaryl-carboxamides
US9238629B2 (en) 2010-11-01 2016-01-19 Celgene Avilomics Research, Inc. Heteroaryl compounds and uses thereof
JP5957003B2 (ja) 2010-11-10 2016-07-27 セルジーン アヴィロミクス リサーチ, インコーポレイテッド 変異体選択的egfr阻害剤およびその使用
EP2694486B1 (en) 2011-04-01 2018-01-10 University of Utah Research Foundation Substituted n-(3-(pyrimidin-4-yl)phenyl)acrylamide analogs as tyrosine receptor kinase btk inhibitors
RU2017112522A (ru) 2011-05-04 2019-01-24 ФОРМА ТиЭм, ЭлЭлСИ Новые соединения и композиции для ингибирования nampt
DK2840080T3 (da) 2012-04-17 2018-01-29 Fujifilm Corp Nitrogenholdig heterocyklisk forbindelse eller salt deraf

Also Published As

Publication number Publication date
DK3059227T3 (da) 2019-08-26
AU2014335312B9 (en) 2017-05-25
WO2015056683A1 (ja) 2015-04-23
EP3059227A4 (en) 2016-09-07
BR112016008080B1 (pt) 2021-02-23
CA2927079C (en) 2017-05-23
CN105683167A (zh) 2016-06-15
ES2738573T3 (es) 2020-01-23
HK1219946A1 (zh) 2017-04-21
CN105683167B (zh) 2018-10-23
CA2927079A1 (en) 2015-04-23
JPWO2015056683A1 (ja) 2017-03-09
EP3059227A1 (en) 2016-08-24
KR101744033B1 (ko) 2017-06-07
KR20160049009A (ko) 2016-05-04
RU2016114540A (ru) 2017-11-21
US20160229812A1 (en) 2016-08-11
PL3059227T3 (pl) 2019-11-29
US9701644B2 (en) 2017-07-11
EP3059227B1 (en) 2019-06-26
RU2641106C2 (ru) 2018-01-16
AU2014335312B2 (en) 2017-01-05
AU2014335312A1 (en) 2016-05-05
JP5887028B2 (ja) 2016-03-16

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