BR0207664A - Èmega-aminoalquilamidas de ácidos r-2-aril-propiÈnico como inibidores da quimiotaxia de células polimorfonucleadas e mononucleadas - Google Patents

Èmega-aminoalquilamidas de ácidos r-2-aril-propiÈnico como inibidores da quimiotaxia de células polimorfonucleadas e mononucleadas

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Publication number
BR0207664A
BR0207664A BR0207664-0A BR0207664A BR0207664A BR 0207664 A BR0207664 A BR 0207664A BR 0207664 A BR0207664 A BR 0207664A BR 0207664 A BR0207664 A BR 0207664A
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Prior art keywords
polymorphonucleated
aryl
inhibitors
formula
compounds
Prior art date
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BR0207664-0A
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English (en)
Inventor
Marcello Allegretti
Riccardo Bertini
Valerio Berdini
Cinzia Bizzarri
Maria Candida Cesta
Vito Di Cioccio
Gianfranco Caselli
Francesco Colotta
Carmelo Candolfi
Original Assignee
Dompe Spa
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Publication of BR0207664A publication Critical patent/BR0207664A/pt

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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Hydrogenated Pyridines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

"ÈMEGA-AMINOALQUILAMIDAS DE áCIDOS R-2-ARIL-PROPIÈNICO COMO INIBIDORES DA QUIMIOTAXIA DE CéLULAS POLIMORFONUCLEADAS E MONONUCLEADAS". A patente de invenção refere-se a compostos de (R)-2-arilpropionamida da fórmula (I) que são descritos. O processo para sua preparação e preparações farmacêuticas dos mesmos também são descritos. As 2-arilpropionamidas da invenção são úteis na prevenção e tratamento de dano tecidual devido ao recrutamento exacerbado de leucócitos polimorfonucleados (leucócitos PMN) e de monócitos nos locais de inflamação. Em particular, a invenção refere-se aos enanciómeros R de ómega-aminoalquilamidas de ácidos 2-aril propiónicos, da fórmula (I), para uso na inibição da quimiotaxia de neutrófilos e monócitos induzida pela fração C5a do complemento e por outras proteínas quimiotáticas cuja atividade biológica está associada à ativação de um receptor 7-TD. Compostos selecionados da fórmula (I) são inibidores duplos da quimiotaxia C5a-induzida de neutrófilos e monócitos e da quimiotaxia IL-8-induzida de leucócitos PMN. Os compostos da invenção são usados no tratamento de psoríase, colite ulcerativa, nefrite glomerular, insuficiência respiratória aguda, fibrose idiopática, artrite reumatóide e na prevenção e tratamento de dano causado por isquemia e reperfusão.
BR0207664-0A 2001-02-27 2002-02-25 Èmega-aminoalquilamidas de ácidos r-2-aril-propiÈnico como inibidores da quimiotaxia de células polimorfonucleadas e mononucleadas BR0207664A (pt)

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IT2001MI000395A ITMI20010395A1 (it) 2001-02-27 2001-02-27 Omega-amminoalchilammidi di acidi r-2-aril-propionici come inibitori della chemiotassi di cellule polimorfonucleate e mononucleate
PCT/EP2002/001974 WO2002068377A1 (en) 2001-02-27 2002-02-25 Omega-aminoalkylamides of r-2-aryl-propionic acids as inhibitors of the chemotaxis of polymorphonucleate and mononucleate cells

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BRPI0207664-0A BRPI0207664B1 (pt) 2001-02-27 2002-02-25 Omega-aminoalkylamides of (R) -2-aryl-propionic acids as inhibitors of polymorphonuclear and mononuclear cell chemotaxis, their preparation process, and pharmaceutical composition

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Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ITMI20010395A1 (it) 2001-02-27 2002-08-27 Dompe Spa Omega-amminoalchilammidi di acidi r-2-aril-propionici come inibitori della chemiotassi di cellule polimorfonucleate e mononucleate
ITMI20012025A1 (it) * 2001-09-28 2003-03-28 Dompe Spa Sali di ammonio quaternari di omega-amminoalchilammidi di acidi r 2-aril-propionici e composizioni farmaceutiche che li contengono
JP5208411B2 (ja) * 2003-02-06 2013-06-12 ドムペ・ファ.ル.マ・ソチエタ・ペル・アツィオーニ 2−アリール−酢酸、その誘導体、及びそれらを含有する医薬組成物
EP1457485A1 (en) * 2003-03-14 2004-09-15 Dompé S.P.A. Sulfonic acids, their derivatives and pharmaceutical compositions containing them
US7893094B2 (en) * 2003-06-27 2011-02-22 The Henry M. Jackson Foundation For The Advancement Of Military Medicine, Inc. Amphiphilic pyridinium compounds, method of making and use thereof
CN1934077B (zh) 2004-03-23 2010-09-29 冬姆佩制药股份公司 2-苯基丙酸衍生物及含有它们的药物组合物
US7939521B2 (en) * 2004-12-15 2011-05-10 DompePHA.R.MA S.p.A. 2-arylpropionic acid derivatives and pharmaceutical compositions containing them
US20090131441A1 (en) * 2005-01-25 2009-05-21 Dompe Phar.R.Ma S.P.A. Metabolites Of 2-Arylpropionic Acid Derivatives And Pharmaceutical Compositions Containing Them
EP1739078A1 (de) 2005-05-30 2007-01-03 Jerini AG C5a-Rezeptor-Antagonisten
RU2458051C2 (ru) * 2005-11-24 2012-08-10 ДОМПЕ ФА.Р.МА С.п.А. (r)-арилалкиламинопроизводные и содержащие их фармацевтические композиции
US20090221703A1 (en) 2006-07-09 2009-09-03 Chongxi Yu High penetration composition and uses thereof
US20090238763A1 (en) 2006-07-09 2009-09-24 Chongxi Yu High penetration compositions and uses thereof
CA2657636C (en) * 2006-07-18 2021-11-09 Techfields Biochem Co. Ltd Positively charged water soluble prodrugs of ibuprofen with very fast skin penetration rate
CN103948571A (zh) * 2006-07-18 2014-07-30 天津昕晨泰飞尔医药科技有限公司 具有快速皮肤穿透率的带正电荷的水溶性布洛芬前药
CN101500984A (zh) * 2006-07-27 2009-08-05 于崇曦 具有快速皮肤穿透速度的带正电荷的水溶性酮洛芬及相关化合物的前药
HUE028425T2 (en) * 2006-08-08 2016-12-28 Techfields Biochem Co Ltd Positive charged water-soluble prodrugs of aryl and heteroarylacetic acids with very fast skin penetration rate
CN103772259B (zh) * 2006-08-08 2016-08-31 于崇曦 具有快速皮肤穿透速度的带正电荷的芳基和杂芳基乙酸类前药
CN103772258B (zh) * 2006-08-08 2016-09-28 于崇曦 具有快速皮肤穿透速度的带正电荷的芳基和杂芳基乙酸类前药
EP2054384A4 (en) * 2006-08-15 2010-11-03 Techfields Biochem Co Ltd POSITIVELY LOADED WATER-SOLUBLE PRODRUGS OF ARYL AND HETEROARYLPROPIONIC ACIDS WITH A VERY FAST SKIN PUNCHING RATE
WO2008110351A2 (en) * 2007-03-15 2008-09-18 Dompe' Pha.R.Ma S.P.A. Use of (r) and (s)-2-aryl-propionic acid derivatives as antiseptic agents
CN105669531B (zh) * 2007-06-04 2019-05-07 于崇曦 具有快速皮肤和生物膜穿透速度的非甾体抗炎药的前药及其新的医药用途
JP2010529101A (ja) * 2007-06-04 2010-08-26 テックフィールズ インコーポレイテッド 非常に速い皮膚及び膜浸透速度を有するnsaiaプロドラッグ及びその新規医薬使用
KR101225223B1 (ko) * 2008-04-29 2013-01-22 에프. 호프만-라 로슈 아게 4-다이메틸아미노부티르산 유도체
JP2012511027A (ja) 2008-12-04 2012-05-17 チョンシー ユー 高透過性組成物およびその用途
EP2316820A1 (en) * 2009-10-28 2011-05-04 Dompe S.p.A. 2-aryl-propionamide derivatives useful as bradykinin receptor antagonists and pharmaceutical compositions containing them
KR102332837B1 (ko) 2012-05-16 2021-12-01 테크필즈 파마 코., 엘티디. 폐 병태의 치료를 위한 고침투 전구약물 조성물 및 그의 약제학적 조성물
JP5997658B2 (ja) * 2013-05-08 2016-09-28 テックフィールズ インコーポレイテッド 非常に速い皮膚及び膜浸透速度を有するnsaiaプロドラッグ及びその新規医薬使用
RU2016152499A (ru) * 2014-05-30 2018-07-04 Драг Дискавери Ресеч Сентэ Новые соединения в качестве противотуберкулезных препаратов
JP6153264B2 (ja) * 2015-01-05 2017-06-28 テックフィールズ インコーポレイテッド 非常に速い皮膚及び膜浸透速度を有するnsaiaプロドラッグ及びその新規医薬使用
JP6621775B2 (ja) * 2017-03-22 2019-12-18 テックフィールズ インコーポレイテッド 非常に速い皮膚及び膜浸透速度を有するnsaiaプロドラッグ及びその新規医薬使用
EP4004002A1 (en) 2019-07-22 2022-06-01 Lupin Limited Macrocyclic compounds as sting agonists and methods and uses thereof
JP2020147604A (ja) * 2020-06-17 2020-09-17 テックフィールズ インコーポレイテッド 非常に速い皮膚及び膜浸透速度を有するnsaiaプロドラッグ及びその新規医薬使用

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL33051A (en) * 1968-10-11 1974-05-16 Ciba Geigy Ag Alpha-cycloalkenyl-phenyl-fatty acid derivatives and process for their manufacture
SE385883B (sv) 1972-04-10 1976-07-26 Ciba Geigy Ag Forfarande for framstellning av nya pyridinkarbonsyraestrar
JPS4918875A (pt) * 1972-06-17 1974-02-19
NL7407668A (pt) 1973-06-11 1974-12-13
US4025528A (en) 1973-10-24 1977-05-24 Shionogi & Co., Ltd. Thiazole derivatives of benzoic and phenylalkanoic acids
CA1051906A (en) 1973-10-24 1979-04-03 Shionogi And Co. Thiazole derivatives and production thereof
JPS5277030A (en) 1975-12-23 1977-06-29 Toyo Pharma Kk Production of novel benzyl sulphonic acid derivatives
US4151172A (en) 1977-08-11 1979-04-24 E. R. Squibb & Sons, Inc. Phosphonoacyl prolines and related compounds
IT1193955B (it) 1980-07-22 1988-08-31 Real Di Alberto Reiner S A S Derivati ammidici dell'acido p-isobutilfenilpropionico, procedimento per la loro preparazione e relative composizioni farmaceutici
US4879283A (en) * 1985-10-03 1989-11-07 Wisconsin Alumni Research Foundation Solution for the preservation of organs
US5216026A (en) * 1990-07-17 1993-06-01 Eli Lilly And Company Antitumor compositions and methods of treatment
AU644281B2 (en) 1991-04-24 1993-12-02 Sumitomo Pharmaceuticals Company, Limited Novel thiazole derivatives
JPH05286902A (ja) 1992-04-10 1993-11-02 Sumitomo Pharmaceut Co Ltd α−クロロ−β−ケトエステル誘導体の製造方法
AU4682193A (en) 1992-07-29 1994-03-03 Merck & Co., Inc. Dexibuprofen/antacid/simethicone combinations
JPH11503110A (ja) * 1995-02-17 1999-03-23 スミスクライン・ビーチャム・コーポレイション Il−8受容体拮抗剤
JP3136953B2 (ja) 1995-06-29 2001-02-19 日本電気株式会社 データ処理装置
US6262113B1 (en) * 1996-03-20 2001-07-17 Smithkline Beecham Corporation IL-8 receptor antagonists
US6410584B1 (en) * 1998-01-14 2002-06-25 Cell Pathways, Inc. Method for inhibiting neoplastic cells with indole derivatives
IT1298214B1 (it) 1998-01-28 1999-12-20 Dompe Spa Sali dell'acido (r) 2-(3-benzoilfenil) propionico e loro composizioni farmaceutiche.
IT1303249B1 (it) 1998-10-23 2000-11-06 Dompe Spa Alcune n-(2-aril-propionil)-solfonammidi e preparazionifarmaceutiche che le contengono.
US6348032B1 (en) * 1998-11-23 2002-02-19 Cell Pathways, Inc. Method of inhibiting neoplastic cells with benzimidazole derivatives
US6147155A (en) * 1999-06-08 2000-11-14 Bayer Corporation Aqueous polyurethane dispersions containing non-cyclic diisocyanates and a process for their preparation
CA2390349A1 (en) * 1999-12-03 2001-06-07 Bristol-Myers Squibb Pharma Company Alpha-ketoamide inhibitors of hepatitis c virus ns3 protease
IT1317826B1 (it) 2000-02-11 2003-07-15 Dompe Spa Ammidi, utili nell'inibizione della chemiotassi dei neutrofiliindotta da il-8.
IT1318466B1 (it) * 2000-04-14 2003-08-25 Dompe Spa Ammidi di acidi r-2-(amminoaril)-propionici, utili nella prevenzionedell'attivazione leucocitaria.
ITMI20010395A1 (it) 2001-02-27 2002-08-27 Dompe Spa Omega-amminoalchilammidi di acidi r-2-aril-propionici come inibitori della chemiotassi di cellule polimorfonucleate e mononucleate
US6355682B1 (en) * 2001-05-11 2002-03-12 Assa Weinberg Treatment of acute renal failure by administration of N-acetylcysteine
US20050143372A1 (en) * 2001-10-30 2005-06-30 Shomir Ghosh Compounds, pharmaceutical compositions and methods of use therefor
ITMI20012434A1 (it) 2001-11-20 2003-05-20 Dompe Spa Acidi 2-aril-propionici e composizioni farmaceutiche che li contengono
JP5286902B2 (ja) 2008-04-09 2013-09-11 富士ゼロックス株式会社 濃度制御システム、印刷装置、および濃度制御プログラム

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