MX383928B - Derivado de piridona que tiene un grupo tetrahidropiranilmetilo. - Google Patents

Derivado de piridona que tiene un grupo tetrahidropiranilmetilo.

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Publication number
MX383928B
MX383928B MX2017000330A MX2017000330A MX383928B MX 383928 B MX383928 B MX 383928B MX 2017000330 A MX2017000330 A MX 2017000330A MX 2017000330 A MX2017000330 A MX 2017000330A MX 383928 B MX383928 B MX 383928B
Authority
MX
Mexico
Prior art keywords
sub
salt
derivative
treatment
hyperfunction
Prior art date
Application number
MX2017000330A
Other languages
English (en)
Other versions
MX2017000330A (es
Inventor
Noriyasu Haginoya
Takeshi Jimbo
Katsuhiro Kobayashi
Miho Hayakawa
Koichi Nakamura
Masahiro Ota
Takashi Suzuki
Tomoharu Tsukada
Yosuke Ando
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 MX2017000330A publication Critical patent/MX2017000330A/es
Publication of MX383928B publication Critical patent/MX383928B/es

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    • 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
    • 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
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • AHUMAN NECESSITIES
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • 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
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    • 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
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
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    • 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
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    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
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    • C07C309/02Sulfonic acids having sulfo groups bound to acyclic carbon atoms
    • C07C309/03Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
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    • C07C309/28Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/33Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton of six-membered aromatic rings being part of condensed ring systems
    • C07C309/34Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton of six-membered aromatic rings being part of condensed ring systems formed by two rings
    • C07C309/35Naphthalene sulfonic acids
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  • Health & Medical Sciences (AREA)
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  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
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  • Physical Education & Sports Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Endocrinology (AREA)
  • Oncology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Hematology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Dermatology (AREA)
  • Reproductive Health (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Diabetes (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Se pretende proporcionar un compuesto novedoso o una sal del mismo, o cristales del compuesto o la sal, que inhiben AxI y son útiles en el tratamiento de una enfermedad causada por la hiperfunción de AxI, el tratamiento de una enfermedad asociada con la hiperfunción de Axl, y/o el tratamiento de una enfermedad que implica la hiperfunción de Axl; [solución] la presente invención proporciona un derivado de piridona que tiene un grupo tetrahidropiranilmetilo representado por la siguiente fórmula (I) (ver Fórmula) que tiene varios sustituyentes, o una sal del mismo, o cristales del compuesto o la sal (en donde R1, R2, R3, R4, R5, W, X, Y y Z cada uno como se definen en la especificación).
MX2017000330A 2014-07-07 2015-07-06 Derivado de piridona que tiene un grupo tetrahidropiranilmetilo. MX383928B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2014139628 2014-07-07
PCT/JP2015/069976 WO2016006706A1 (ja) 2014-07-07 2015-07-06 テトラヒドロピラ二ルメチル基を有するピリドン誘導体

Publications (2)

Publication Number Publication Date
MX2017000330A MX2017000330A (es) 2017-08-25
MX383928B true MX383928B (es) 2025-03-14

Family

ID=55064330

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2017000330A MX383928B (es) 2014-07-07 2015-07-06 Derivado de piridona que tiene un grupo tetrahidropiranilmetilo.

Country Status (28)

Country Link
US (3) US10442797B2 (es)
EP (2) EP3868757A1 (es)
JP (2) JP6086516B2 (es)
KR (1) KR102348190B1 (es)
CN (2) CN106604920B (es)
AU (1) AU2015288648B2 (es)
CA (1) CA2954488C (es)
CO (1) CO2017001178A2 (es)
CY (1) CY1124537T1 (es)
DK (1) DK3168219T3 (es)
ES (1) ES2875360T3 (es)
HR (1) HRP20210899T1 (es)
HU (1) HUE054534T2 (es)
IL (2) IL249948B (es)
LT (1) LT3168219T (es)
MX (1) MX383928B (es)
MY (1) MY194307A (es)
PH (2) PH12022552034A1 (es)
PL (1) PL3168219T3 (es)
PT (1) PT3168219T (es)
RS (1) RS61941B1 (es)
RU (1) RU2707953C2 (es)
SG (2) SG10201900144TA (es)
SI (1) SI3168219T1 (es)
SM (1) SMT202100303T1 (es)
TW (2) TWI690525B (es)
WO (1) WO2016006706A1 (es)
ZA (1) ZA201700139B (es)

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TWI690525B (zh) 2014-07-07 2020-04-11 日商第一三共股份有限公司 具有四氫吡喃基甲基之吡啶酮衍生物及其用途
WO2017146236A1 (ja) 2016-02-26 2017-08-31 小野薬品工業株式会社 Axl阻害剤と免疫チェックポイント阻害剤とを組み合わせて投与することを特徴とする癌治療のための医薬
CN108250200A (zh) * 2016-12-28 2018-07-06 中国科学院上海药物研究所 一种具有Axl抑制活性的化合物及其制备和应用
TWI796326B (zh) 2017-03-24 2023-03-21 日商第一三共股份有限公司 含有axl抑制劑與egfr酪胺酸激酶抑制藥的醫藥品及其用途
WO2019039525A1 (ja) 2017-08-23 2019-02-28 小野薬品工業株式会社 Axl阻害剤を有効成分として含むがん治療剤
JP7223998B2 (ja) 2017-10-13 2023-02-17 小野薬品工業株式会社 Axl阻害剤を有効成分として含む固形がん治療剤
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JP2021512160A (ja) * 2018-01-29 2021-05-13 カピュラス セラピューティクス リミテッド ライアビリティ カンパニー 6員の中央環を含むsrebp阻害剤
TWI840378B (zh) * 2018-07-04 2024-05-01 日商第一三共股份有限公司 二芳基吡啶衍生物之製造方法
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
CA3159348A1 (en) 2019-11-08 2021-05-14 Inserm (Institut National De La Sante Et De La Recherche Medicale) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
WO2022220227A1 (ja) * 2021-04-14 2022-10-20 エーザイ・アール・アンド・ディー・マネジメント株式会社 テトラヒドロピリドピリミジン化合物
WO2024217587A1 (zh) * 2023-04-21 2024-10-24 南京正大天晴制药有限公司 具有axl抑制活性的取代吡嗪化合物

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