BR112016002459A2 - Derivados de benzimidazolil-metil ureia como agonistas receptores de alx - Google Patents

Derivados de benzimidazolil-metil ureia como agonistas receptores de alx

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Publication number
BR112016002459A2
BR112016002459A2 BR112016002459A BR112016002459A BR112016002459A2 BR 112016002459 A2 BR112016002459 A2 BR 112016002459A2 BR 112016002459 A BR112016002459 A BR 112016002459A BR 112016002459 A BR112016002459 A BR 112016002459A BR 112016002459 A2 BR112016002459 A2 BR 112016002459A2
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BR
Brazil
Prior art keywords
benzimidazolyl
urea derivatives
methyl urea
receptor agonists
alx receptor
Prior art date
Application number
BR112016002459A
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English (en)
Other versions
BR112016002459A8 (pt
Inventor
Corminboeuf Olivier
Cren Sylvaine
Leroy Xavier
Pozzi Davide
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Actelion Pharmaceuticals Ltd
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Publication date
Application filed by Actelion Pharmaceuticals Ltd filed Critical Actelion Pharmaceuticals Ltd
Publication of BR112016002459A2 publication Critical patent/BR112016002459A2/pt
Publication of BR112016002459A8 publication Critical patent/BR112016002459A8/pt

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    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/14Radicals substituted by nitrogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P11/06Antiasthmatics
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P11/00Drugs for disorders of the respiratory system
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    • A61P25/00Drugs for disorders of the nervous system
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    • A61P25/00Drugs for disorders of the nervous system
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
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    • A61P31/18Antivirals for RNA viruses for HIV
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • AHUMAN NECESSITIES
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/16Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
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    • 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
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Abstract

DERIVADOS DE BENZIMIDAZOLIL-METIL UREIA COMO AGONISTAS RECEPTORES DE ALX. A presente invenção diz respeito a derivados de benzimidazolil-metil ureia da fórmula (I), em que D, E, R1, R2, R3, R4, R6, R7, R8 e R9 são como definidos na descrição, sua preparação e seu uso como compostos farmaceuticamente ativos.
BR112016002459A 2013-08-09 2014-08-08 Derivados de benzimidazolil-metil ureia como agonistas receptores de alx BR112016002459A8 (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IB2013056530 2013-08-09
PCT/IB2014/063795 WO2015019325A1 (en) 2013-08-09 2014-08-08 Benzimidazolyl-methyl urea derivatives as alx receptor agonists

Publications (2)

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BR112016002459A2 true BR112016002459A2 (pt) 2017-08-22
BR112016002459A8 BR112016002459A8 (pt) 2017-12-26

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US (1) US9663473B2 (pt)
EP (1) EP3030560B1 (pt)
JP (1) JP6387411B2 (pt)
KR (1) KR20160042019A (pt)
CN (1) CN105473575B (pt)
AR (1) AR097279A1 (pt)
AU (1) AU2014304046B2 (pt)
BR (1) BR112016002459A8 (pt)
CA (1) CA2917954A1 (pt)
ES (1) ES2641172T3 (pt)
MX (1) MX2016001788A (pt)
RU (1) RU2016107974A (pt)
TW (1) TW201536756A (pt)
WO (1) WO2015019325A1 (pt)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR096686A1 (es) 2013-06-25 2016-01-27 Actelion Pharmaceuticals Ltd Derivados de espiro[2.4]heptano puenteados sustituidos con difluoroetil-oxazol como agonistas del receptor de alx
JP6330038B2 (ja) 2013-07-18 2018-05-23 イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd Alx受容体アゴニストとしてのピペラジン置換架橋スピロ[2.4]ヘプタン誘導体
TN2016000210A1 (en) 2013-11-28 2017-10-06 Kyorin Seiyaku Kk Urea derivative or pharmacologically acceptable salt thereof.
EA201792382A1 (ru) 2015-05-27 2018-04-30 Киорин Фармасютикал Ко., Лтд. Производное мочевины или его фармакологически приемлемая соль
EP3303284B1 (en) 2015-05-27 2020-04-08 Kyorin Pharmaceutical Co., Ltd. Urea derivative or pharmacologically acceptable salt thereof
MX2018004882A (es) 2015-10-23 2018-08-01 Vifor Int Ag Inhibidores de ferroportina novedosos.
JP6919976B2 (ja) * 2015-11-20 2021-08-18 ミングサイト ファーマシューティカルズ,インク. 自己免疫疾患の処置
JP2019530678A (ja) * 2016-09-18 2019-10-24 エイチ リー モフィット キャンサー センター アンド リサーチ インスティテュート インコーポレイテッド Yap1のoct4との相互作用を標的とするyap1阻害剤
JOP20180036A1 (ar) 2017-04-18 2019-01-30 Vifor Int Ag أملاح لمثبطات فروبورتين جديدة
US20210147405A1 (en) * 2017-06-14 2021-05-20 European Molecular Biology Laboratory Bicyclic heteroaromatic urea or carbamate compounds for use in therapy
CN108003048A (zh) * 2017-12-07 2018-05-08 滨海吉尔多肽有限公司 一种o-甲基-苏/酪氨酸的制备方法
EP3762380B1 (en) 2018-03-05 2021-12-15 Bristol-Myers Squibb Company Phenylpyrrolidinone formyl peptide 2 receptor agonists
BR112020018642A2 (pt) 2018-03-14 2020-12-29 H. Lee Moffitt Cancer Center And Research Institute, Inc. Composto da fórmula i, composição farmacêutica, método de tratamento de câncer em um sujeito em necessidade, método de eliminação de uma célula tumoral em um sujeito
US20210401798A1 (en) * 2018-10-23 2021-12-30 The Brigham And Women's Hospital, Inc. Lipoxin a4 analogs and uses thereof
CN112341450B (zh) * 2019-08-09 2022-05-17 成都先导药物开发股份有限公司 一种免疫调节剂
CN112341451B (zh) * 2019-08-09 2022-06-17 成都先导药物开发股份有限公司 一种免疫调节剂
CN114644577B (zh) * 2020-12-18 2023-06-27 新发药业有限公司 一种取代异腈化合物的环保制备方法

Family Cites Families (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4407746A (en) 1981-12-14 1983-10-04 G. D. Searle & Co. Cyclohexyl and phenyl substituted enkephalins
RU2106592C1 (ru) 1996-07-12 1998-03-10 Слипченко Николай Николаевич Подводный спортивный пистолет
WO1998027108A2 (en) * 1996-12-16 1998-06-25 Fujisawa Pharmaceutical Co., Ltd. New amide compounds and their use as nitric oxide synthase inhibitors
AU763636C (en) 1998-01-29 2004-05-27 Daiichi Asubio Pharma Co., Ltd. 1-cycloalkyl-1,8-naphthyridin-4-one derivatives with phosphodiesterase IV inhibitory activity
EP1387680A4 (en) 2001-03-05 2010-01-13 Transtech Pharma Inc AGENTS TH RAPEUTICES D RIV S BENZIMIDAZOLE BASE
FR2822827B1 (fr) 2001-03-28 2003-05-16 Sanofi Synthelabo Nouveaux derives de n-(arylsulfonyl) beta-aminoacides comportant un groupe aminomethyle substitue, leur procede de preparation et les compositions pharmaceutiques en contenant
DE10211770A1 (de) 2002-03-14 2003-10-02 Boehringer Ingelheim Pharma Neue substituierte Piperidine, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung
JP2005536187A (ja) 2002-04-03 2005-12-02 バイエル・ヘルスケア・アクチェンゲゼルシャフト N−ホルミルペプチド受容体様1(fprl1)に関連する疾患の診断および治療
AU2003251828A1 (en) 2002-07-12 2004-02-02 Janssen Pharmaceutica N.V. Naphthol, quinoline and isoquinoline-derivatives as modulators of vanilloid vr1 receptor
PE20040804A1 (es) 2002-12-19 2004-12-31 Boehringer Ingelheim Pharma DERIVADOS DE CARBOXAMIDAS COMO INHIBIDORES DEL FACTOR Xa
DE602004011064T2 (de) 2003-05-30 2008-12-11 Eli Lilly And Co., Indianapolis Antitrombotische aether
US7141596B2 (en) 2003-10-08 2006-11-28 Incyte Corporation Inhibitors of proteins that bind phosphorylated molecules
CN1894580A (zh) * 2003-11-07 2007-01-10 阿卡蒂亚药品公司 脂氧素受体fprl1作为一种用于鉴定能有效治疗疼痛和炎症化合物的工具
KR20060130064A (ko) * 2003-11-07 2006-12-18 아카디아 파마슈티칼스 인코포레이티드 통증 및 염증 치료에 효과적인 화합물을 동정하기 위한도구로서의 리폭신 수용체, fprl1의 용도
US7371743B2 (en) 2004-02-28 2008-05-13 Boehringer Ingelheim International Gmbh Carboxylic acid amides, the preparation thereof and their use as medicaments
TW200538098A (en) 2004-03-22 2005-12-01 Astrazeneca Ab Therapeutic agents
US7453002B2 (en) 2004-06-15 2008-11-18 Bristol-Myers Squibb Company Five-membered heterocycles useful as serine protease inhibitors
DK1778637T3 (da) 2004-06-29 2012-06-18 Aventis Pharma Inc FKBP-bindingssammensætninger og farmaceutisk anvendelse deraf
EP1915345B1 (en) 2005-08-12 2010-12-22 F. Hoffmann-La Roche AG Fluoro substituted 2-oxo azepan derivatives
AR066379A1 (es) 2007-05-02 2009-08-12 Boehringer Ingelheim Int Amidas de acido carboxilico su preparacion y su uso como medicamentos
US7557221B2 (en) 2007-08-16 2009-07-07 Hoffman-La Roche Inc. Substituted hydantoins
AR069650A1 (es) 2007-12-14 2010-02-10 Actelion Pharmaceuticals Ltd Derivados de aminopirazol como agonistas no peptidicos del receptor alx humano
AU2008337097B2 (en) 2007-12-18 2014-03-20 Idorsia Pharmaceuticals Ltd Aminotriazole derivatives as ALX agonists
CN102083794A (zh) * 2008-05-05 2011-06-01 安姆根有限公司 作为γ分泌酶调节剂的脲化合物
JP5476305B2 (ja) 2008-08-07 2014-04-23 杏林製薬株式会社 ビシクロ[2.2.2]オクチルアミン誘導体の製造方法
WO2010083246A1 (en) 2009-01-15 2010-07-22 Amgen Inc. Fluoroisoquinoline substituted thiazole compounds and methods of use
MX2011012264A (es) 2009-05-18 2011-12-12 Actelion Pharmaceuticals Ltd Derivados spiro[2.4]heptano puenteados como agonistas del receptor de lipoxina a(alx) y/o de formil peptido tipo 2 (fprl2).
MX342440B (es) 2009-06-09 2016-09-29 Actelion Pharmaceuticals Ltd * Derivados fluorados de aminotriazol.
US8674111B2 (en) 2009-06-12 2014-03-18 Actelion Pharmaceuticals Ltd. Oxazole and thiazole derivatives as ALX receptor agonists
CN102574843B (zh) * 2009-10-22 2015-06-17 法博太科制药有限公司 抗纤维化剂的稠环类似物
GB201009731D0 (en) 2010-06-10 2010-07-21 Pulmagen Therapeutics Inflamma Kinase inhibitors
CA2814826C (en) 2010-11-17 2019-02-12 Actelion Pharmaceuticals Ltd Bridged spiro[2.4]heptane ester derivatives
TW201305150A (zh) 2010-12-07 2013-02-01 Actelion Pharmaceuticals Ltd 作為脂氧素(alx)受體激動劑之羥基化胺基三唑衍生物
DK2649068T3 (en) 2010-12-07 2014-12-08 Actelion Pharmaceuticals Ltd OXAZOLYL METHYLETHER DERIVATIVES AS ALX RECEPTOR AGONISTS
TR201820873T4 (tr) 2011-08-01 2019-01-21 Hoffmann La Roche Pd-1 ekseni bağlayıcı antagonistler ve mek inhibitörlerinin kullanıldığı kanser tedavisine yönelik yöntemler.
KR102051687B1 (ko) 2011-10-26 2019-12-17 알러간, 인코포레이티드 포르밀 펩티드 수용체 유사-1 (fprl-1) 수용체 조절자로서의 n-유레아 치환된 아미노산의 아미드 유도체
US8541577B2 (en) 2011-11-10 2013-09-24 Allergan, Inc. Aryl urea derivatives as N-formyl peptide receptors like-1 (FPRL-1) receptor modulators
US8492556B2 (en) * 2011-11-10 2013-07-23 Allergan, Inc. 2,5-Dioxoimidazolidin-1-yl-3-phenylurea derivatives as formyl peptide receptor like-1 (FPRL-1) receptor modulators
MA37618B1 (fr) 2012-05-16 2017-08-31 Actelion Pharmaceuticals Ltd Dérivés pontés fluorés de spiro[2.4]heptane en tant qu'agonistes de récepteur alx
JP6101788B2 (ja) 2012-05-16 2017-03-22 アクテリオン ファーマシューティカルズ リミテッドActelion Pharmaceuticals Ltd ALX受容体アゴニストとしての1−(p−トリル)シクロプロピル置換架橋スピロ[2.4]ヘプタン誘導体
BR112015021371B1 (pt) 2013-03-06 2021-04-13 Allergan, Inc Uso de agonistas de receptor de formil peptídeo 2 para tratar doenças inflamatórias oculares
BR122017004256A2 (pt) 2013-03-06 2019-09-10 Allergan Inc uso de agonistas do receptor de peptídeo formil 2 para tratar doenças dermatológicas
AR096686A1 (es) 2013-06-25 2016-01-27 Actelion Pharmaceuticals Ltd Derivados de espiro[2.4]heptano puenteados sustituidos con difluoroetil-oxazol como agonistas del receptor de alx
JP6330038B2 (ja) 2013-07-18 2018-05-23 イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd Alx受容体アゴニストとしてのピペラジン置換架橋スピロ[2.4]ヘプタン誘導体
WO2015042071A1 (en) 2013-09-19 2015-03-26 Allergan, Inc. Diphenyl urea derivatives as formyl peptide receptor modulators

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EP3030560B1 (en) 2017-06-21
WO2015019325A1 (en) 2015-02-12
BR112016002459A8 (pt) 2017-12-26
AU2014304046B2 (en) 2018-07-05
EP3030560A1 (en) 2016-06-15
RU2016107974A (ru) 2017-09-15
US9663473B2 (en) 2017-05-30
JP6387411B2 (ja) 2018-09-05
TW201536756A (zh) 2015-10-01
US20160200686A1 (en) 2016-07-14
KR20160042019A (ko) 2016-04-18
ES2641172T3 (es) 2017-11-08
AU2014304046A1 (en) 2016-03-17
CN105473575B (zh) 2017-11-24
JP2016529251A (ja) 2016-09-23
CN105473575A (zh) 2016-04-06
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