BR112018076800A2 - derivado de guanidina, medicamento, inibidor da proteína 1 da translocação de linfoma de tecido linfóide associado com mucosa, e, agente terapêutico ou profilático. - Google Patents

derivado de guanidina, medicamento, inibidor da proteína 1 da translocação de linfoma de tecido linfóide associado com mucosa, e, agente terapêutico ou profilático.

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Publication number
BR112018076800A2
BR112018076800A2 BR112018076800-6A BR112018076800A BR112018076800A2 BR 112018076800 A2 BR112018076800 A2 BR 112018076800A2 BR 112018076800 A BR112018076800 A BR 112018076800A BR 112018076800 A2 BR112018076800 A2 BR 112018076800A2
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BR
Brazil
Prior art keywords
therapeutic
mucosal
medicament
inhibitor
protein
Prior art date
Application number
BR112018076800-6A
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English (en)
Inventor
Numajiri Yoshitaka
OKIMURA Keiichi
Matsumura Yuki
Asaba Kennunettsu
Masuda Tomohide
Tokumaru Kazuyuki
Goto Yasufumi
Fujii Shigeo
Original Assignee
Toray Industries, Inc.
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 Toray Industries, Inc. filed Critical Toray Industries, Inc.
Publication of BR112018076800A2 publication Critical patent/BR112018076800A2/pt

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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36Radicals substituted by singly-bound nitrogen atoms
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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
    • A61K31/435Heterocyclic 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
    • A61K31/4418Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
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    • 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
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    • 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
    • A61K31/4436Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom
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    • 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
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    • 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
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    • 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
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    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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Abstract

a presente invenção trata o problema de fornecer um composto tendo uma cadeia principal de guanidina, que pode inibir a atividade da protease de malt1, e pode exibir um efeito terapêutico ou um efeito profilático em doenças autoimunes in¬cluindo psoríase ou doenças alérgicas incluindo dermatite atópica. a presente inven¬ção fornece um derivado de guanidina tipificado pela fórmula (1) ou um sal farmacologicamente aceitável do mesmo.
BR112018076800-6A 2016-07-29 2017-07-28 derivado de guanidina, medicamento, inibidor da proteína 1 da translocação de linfoma de tecido linfóide associado com mucosa, e, agente terapêutico ou profilático. BR112018076800A2 (pt)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP2016-150467 2016-07-29
JP2016150467 2016-07-29
JP2017-036506 2017-02-28
JP2017036506 2017-02-28
PCT/JP2017/027395 WO2018021520A1 (ja) 2016-07-29 2017-07-28 グアニジン誘導体及びその医薬用途

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BR112018076800A2 true BR112018076800A2 (pt) 2019-04-02

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BR112018076800-6A BR112018076800A2 (pt) 2016-07-29 2017-07-28 derivado de guanidina, medicamento, inibidor da proteína 1 da translocação de linfoma de tecido linfóide associado com mucosa, e, agente terapêutico ou profilático.

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US (1) US10662156B2 (pt)
EP (1) EP3495348A4 (pt)
JP (1) JP6927042B2 (pt)
CN (1) CN109476599A (pt)
BR (1) BR112018076800A2 (pt)
CA (1) CA3030949A1 (pt)
WO (1) WO2018021520A1 (pt)

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WO2018159650A1 (ja) * 2017-02-28 2018-09-07 東レ株式会社 グアニジン誘導体及びその医薬用途
CN110590656B (zh) * 2019-09-27 2020-10-09 中国农业大学 含吡啶酰胺的胍基类衍生物及其制备方法与应用
US20230210849A1 (en) * 2020-06-05 2023-07-06 Georgetown University Cadherin-11 inhibitor formulation and its uses in immunotherapy
WO2021262969A1 (en) 2020-06-24 2021-12-30 The General Hospital Corporation Materials and methods of treating cancer
IL313925A (en) 2021-12-30 2024-08-01 Jiangsu Hansoh Pharmaceutical Group Co Ltd Inhibitor of tricyclic derivatives, method of preparation therefor and application
CN114292225B (zh) * 2022-01-10 2023-07-11 万华化学集团股份有限公司 一种季铵型强碱性阴离子交换树脂及其催化制备甲基丙烯酸缩水甘油酯的方法

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NL299931A (pt) * 1962-10-30
CA2433623A1 (en) 2001-01-02 2002-07-18 Fujisawa Pharmaceutical Co., Ltd. Pyridine derivatives useful as cyclooxygenase inhibitor
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