MA33085B1 - Pyrimidine-4 carboxamides cycliques en tant qu'antagonistes du recepteur ccr2 pour le traitement d'inflammations, de l'asthme et des broncho-pneumopathies chroniques obstructives - Google Patents

Pyrimidine-4 carboxamides cycliques en tant qu'antagonistes du recepteur ccr2 pour le traitement d'inflammations, de l'asthme et des broncho-pneumopathies chroniques obstructives

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Publication number
MA33085B1
MA33085B1 MA33952A MA33952A MA33085B1 MA 33085 B1 MA33085 B1 MA 33085B1 MA 33952 A MA33952 A MA 33952A MA 33952 A MA33952 A MA 33952A MA 33085 B1 MA33085 B1 MA 33085B1
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MA
Morocco
Prior art keywords
treatment
asthma
antagonists
premedine
copd
Prior art date
Application number
MA33952A
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Arabic (ar)
English (en)
Inventor
Heiner Ebel
Sara Frattini
Riccardo Giovannini
Christoph Hoenke
Thomas Trieselmann
Patrick Tielmann
Stefan Scheuerer
Silke Marie Katrin Hobbie
Frank Buettner
Original Assignee
Boehringer Ingelheim Int
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=42049604&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA33085(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of MA33085B1 publication Critical patent/MA33085B1/fr

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Abstract

CETTE INVENTION CONCERNE DE NOUVEAUX ANTAGONISTES DE CCR2 (RÉCEPTEUR 2 DE CHIMIOKINE CC) ET LEUR UTILISATION DANS DES MÉDICAMENTS DESTINÉS AU TRAITEMENT D'ÉTATS PATHOLOGIQUES ET DE MALADIES, EN PARTICULIER DE L'ASTHME ET LES BRONCHO-PNEUMOPATHIES CHRONIQUES OBSTRUCTIVES, COMME REPRÉSENTÉ DANS LA FORMULE (I), OÙ A EST PRIS DANS UNE LIAISON UNIQUE, =CH-, -CH2-, -O-, -S-, AND -NH-; N VAUT 1, 2 OU 3; Z EST C OU N, LES AUTRES VARIABLES ÉTANT COMME DÉFINIES DANS LES REVENDICATIONS, AINSI QUE LEURS FORMES DE SELS D'ADJONCTION ACIDES AVEC DES ACIDES DE QUALITÉ PHARMACOLOGIQUE.
MA33952A 2008-12-19 2009-12-17 Pyrimidine-4 carboxamides cycliques en tant qu'antagonistes du recepteur ccr2 pour le traitement d'inflammations, de l'asthme et des broncho-pneumopathies chroniques obstructives MA33085B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP08172336 2008-12-19
EP09160416 2009-05-15
PCT/EP2009/067378 WO2010070032A1 (fr) 2008-12-19 2009-12-17 Pyrimidine-4 carboxamides cycliques en tant qu'antagonistes du récepteur ccr2 pour le traitement d'inflammations, de l'asthme et des broncho-pneumopathies chroniques obstructives

Publications (1)

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MA33085B1 true MA33085B1 (fr) 2012-03-01

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US (3) US20120053164A1 (fr)
EP (2) EP2816040B1 (fr)
JP (2) JP2012512834A (fr)
KR (1) KR101754698B1 (fr)
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AU (1) AU2009327127C1 (fr)
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Families Citing this family (53)

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Publication number Priority date Publication date Assignee Title
WO2008145681A2 (fr) 2007-05-31 2008-12-04 Boehringer Ingelheim International Gmbh Antagonistes des récepteurs ccr2 et utilisations de ceux-ci
US8193182B2 (en) 2008-01-04 2012-06-05 Intellikine, Inc. Substituted isoquinolin-1(2H)-ones, and methods of use thereof
EP2240452B1 (fr) 2008-01-04 2019-05-29 Intellikine, LLC Dérivés de 1h-pyrazolo[3,4-d]pyrimidin-4-amine en tant que modulateurs de kinase pi3, leurs compositions et utilisations
JP5731978B2 (ja) 2008-09-26 2015-06-10 インテリカイン, エルエルシー 複素環キナーゼ阻害剤
JP2012512834A (ja) 2008-12-19 2012-06-07 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 炎症、喘息及びcopdの処置のためのccr2受容体アンタゴニストとしての環状ピリミジン−4−カルボキサミド
EP2415765A4 (fr) * 2009-03-30 2012-08-15 Astellas Pharma Inc Composé pyrimidine
JP5789252B2 (ja) 2009-05-07 2015-10-07 インテリカイン, エルエルシー 複素環式化合物およびその使用
US8338441B2 (en) 2009-05-15 2012-12-25 Gilead Sciences, Inc. Inhibitors of human immunodeficiency virus replication
WO2011073155A1 (fr) * 2009-12-17 2011-06-23 Boehringer Ingelheim International Gmbh Nouveaux antagonistes du récepteur ccr2 et leurs utilisations
PL3091012T3 (pl) * 2009-12-17 2018-08-31 Centrexion Therapeutics Corporation Antagoniści receptora CCR2 i ich zastosowanie
US8946218B2 (en) 2010-05-12 2015-02-03 Boehringer Ingelheim International Gmbh CCR2 receptor antagonists, method for producing the same, and use thereof as medicaments
JP2013526507A (ja) * 2010-05-12 2013-06-24 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 新規ccr2受容体アンタゴニスト、その製造方法及び薬物としてのその使用
WO2011144501A1 (fr) 2010-05-17 2011-11-24 Boehringer Ingelheim International Gmbh Antagonistes du récepteur ccr2 et leurs utilisations
AU2011255218B2 (en) 2010-05-21 2015-03-12 Infinity Pharmaceuticals, Inc. Chemical compounds, compositions and methods for kinase modulation
US9018212B2 (en) 2010-05-25 2015-04-28 Boehringer Ingelheim International Gmbh Pyridazine carboxamides as CCR2 receptor antagonists
JP5721242B2 (ja) 2010-06-01 2015-05-20 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 新規ccr2アンタゴニスト
WO2012064973A2 (fr) 2010-11-10 2012-05-18 Infinity Pharmaceuticals, Inc. Composés hétérocycliques et utilisations de ceux-ci
NZ612909A (en) 2011-01-10 2015-09-25 Infinity Pharmaceuticals Inc Processes for preparing isoquinolinones and solid forms of isoquinolinones
EP2721025B1 (fr) * 2011-06-16 2015-11-25 Boehringer Ingelheim International Gmbh Nouveaux antagonistes sélectifs de ccr2
EP2731941B1 (fr) 2011-07-15 2019-05-08 Boehringer Ingelheim International GmbH Antagonistes ccr2, nouveaux et sélectifs
MX2014000648A (es) 2011-07-19 2014-09-25 Infinity Pharmaceuticals Inc Compuestos heterociclicos y sus usos.
CN103930422A (zh) 2011-07-19 2014-07-16 无限药品股份有限公司 杂环化合物及其用途
AR091790A1 (es) 2011-08-29 2015-03-04 Infinity Pharmaceuticals Inc Derivados de isoquinolin-1-ona y sus usos
EP2771484A1 (fr) 2011-10-28 2014-09-03 Galderma Research & Development Nouveaux marqueurs d'infiltrat leucocytaire de rosacée et utilisations de ceux-ci
GB2511685A (en) 2011-11-18 2014-09-10 Heptares Therapeutics Ltd Muscarinic m1 receptor agonists
US8940742B2 (en) 2012-04-10 2015-01-27 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
US8828998B2 (en) 2012-06-25 2014-09-09 Infinity Pharmaceuticals, Inc. Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors
WO2014019023A1 (fr) * 2012-08-01 2014-02-06 Bionomics Limited Modulateurs du récepteur α7 nicotinique d'acétylcholine et leurs utilisations
UA110688C2 (uk) 2012-09-21 2016-01-25 Пфайзер Інк. Біциклічні піридинони
CN105102612B (zh) 2012-12-06 2020-11-17 恩立夫克治疗有限责任公司 治疗性凋亡细胞制剂、其制备方法以及其用途
CN103102261A (zh) * 2013-02-06 2013-05-15 上海药明康德新药开发有限公司 一种螺[2.5]辛烷-5-羧酸的合成方法
US9481667B2 (en) 2013-03-15 2016-11-01 Infinity Pharmaceuticals, Inc. Salts and solid forms of isoquinolinones and composition comprising and methods of using the same
SG10201902074UA (en) 2013-10-04 2019-04-29 Infinity Pharmaceuticals Inc Heterocyclic compounds and uses thereof
WO2015051241A1 (fr) 2013-10-04 2015-04-09 Infinity Pharmaceuticals, Inc. Composés hétérocycliques et leurs utilisations
JOP20200052A1 (ar) * 2013-12-19 2017-06-16 Bayer Pharma AG بيبريدينيل تتراهيدرو كوينولينات مستبدلة واستخدامها كمعضدات مستقبل أدريني ألفا- 2c
CA2943075C (fr) 2014-03-19 2023-02-28 Infinity Pharmaceuticals, Inc. Composes heterocycliques destines a etre utilises dans le traitement de troubles medies par pi3k-gamma
US20150320755A1 (en) 2014-04-16 2015-11-12 Infinity Pharmaceuticals, Inc. Combination therapies
WO2016054491A1 (fr) 2014-10-03 2016-04-07 Infinity Pharmaceuticals, Inc. Composés hétérocycliques et leurs utilisations
EP3050574B1 (fr) 2015-01-28 2019-10-09 Universite De Bordeaux Utilisation de plerixafor pour le traitement et/ou la prévention des exacerbations aiguës de la bronchopneumopathie chronique obstructive
JP6917910B2 (ja) * 2015-07-02 2021-08-11 セントレクシオン セラピューティクス コーポレイション (4−((3r,4r)−3−メトキシテトラヒドロ−ピラン−4−イルアミノ)ピペリジン−1−イル)(5−メチル−6−(((2r,6s)−6−(p−トリル)テトラヒドロ−2h−ピラン−2−イル)メチルアミノ)ピリミジン−4イル)メタノンクエン酸塩
GB201513743D0 (en) 2015-08-03 2015-09-16 Heptares Therapeutics Ltd Muscarinic agonists
US10160761B2 (en) 2015-09-14 2018-12-25 Infinity Pharmaceuticals, Inc. Solid forms of isoquinolinones, and process of making, composition comprising, and methods of using the same
GB201519194D0 (en) * 2015-10-30 2015-12-16 Heptares Therapeutics Ltd CGRP receptor antagonists
US10759806B2 (en) 2016-03-17 2020-09-01 Infinity Pharmaceuticals, Inc. Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as PI3K kinase inhibitors
MY195948A (en) 2016-03-22 2023-02-27 Merck Sharp & Dohme Allosteric Modulators of Nicotinic Acetylcholine Receptors
WO2017214269A1 (fr) 2016-06-08 2017-12-14 Infinity Pharmaceuticals, Inc. Composés hétérocycliques et leurs utilisations
SG11201811237WA (en) 2016-06-24 2019-01-30 Infinity Pharmaceuticals Inc Combination therapies
GB201617454D0 (en) 2016-10-14 2016-11-30 Heptares Therapeutics Limited Pharmaceutical compounds
CN108017599B (zh) * 2016-11-04 2020-03-03 上海爱科百发生物医药技术有限公司 [3-(胺甲基)-氧杂环丁烷-3-基]氨基甲酸对甲氧基苄酯对氯苯甲酸盐合成方法
GB201810239D0 (en) 2018-06-22 2018-08-08 Heptares Therapeutics Ltd Pharmaceutical compounds
GB201819960D0 (en) 2018-12-07 2019-01-23 Heptares Therapeutics Ltd Pharmaceutical compounds
GB202020191D0 (en) 2020-12-18 2021-02-03 Heptares Therapeutics Ltd Pharmaceutical compounds
WO2022271982A1 (fr) * 2021-06-23 2022-12-29 Synaptive Therapeutics, Llc Phénéthylamine substituée pour le traitement d'une inflammation et de troubles psychologiques

Family Cites Families (122)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4032526A (en) 1975-10-02 1977-06-28 American Cyanamid Company 1,2-dimethyl-3 or 5-piperazinyl-pyrazolium salts
GB2068961B (en) 1980-02-13 1983-11-30 Sankyo Co Quinazoline derivatives
US4621305A (en) 1984-08-22 1986-11-04 General Motors Corporation Header connector and attachment
DE3517617A1 (de) 1985-05-15 1986-11-20 Lentia GmbH Chem. u. pharm. Erzeugnisse - Industriebedarf, 8000 München Neue pyridaziniumverbindungen, verfahren zu deren herstellung und diese enthaltende fungizide und algizide mittel
DE3931432A1 (de) * 1989-09-21 1991-04-04 Hoechst Ag Pyrimidin-4,6-dicarbonsaeurediamide, verfahren zu deren herstellung sowie verwendung derselben sowie arzneimittel auf basis dieser verbindungen
US5096916A (en) * 1990-05-07 1992-03-17 Aegis Technology, Inc. Treatment of chronic obstructive pulmonary disease (copd) by inhalation of an imidazoline
EP0665833B1 (fr) 1992-10-23 1999-07-14 MERCK SHARP &amp; DOHME LTD. Ligands pour les sous-types de recepteurs de dopamine
JP3166376B2 (ja) 1993-02-03 2001-05-14 松下電器産業株式会社 熱利用装置
TW531537B (en) * 1995-12-27 2003-05-11 Janssen Pharmaceutica Nv 1-(1,2-disubstituted piperidinyl)-4-substituted piperidine derivatives
US5629325A (en) 1996-06-06 1997-05-13 Abbott Laboratories 3-pyridyloxymethyl heterocyclic ether compounds useful in controlling chemical synaptic transmission
US6437138B1 (en) 1996-06-06 2002-08-20 Abbott Laboratories 3-pyridyloxymethyl heterocyclic ether compounds useful in controlling chemical synaptic transmission
US6514977B1 (en) 1997-05-22 2003-02-04 G.D. Searle & Company Substituted pyrazoles as p38 kinase inhibitors
US6979686B1 (en) 2001-12-07 2005-12-27 Pharmacia Corporation Substituted pyrazoles as p38 kinase inhibitors
EE04588B1 (et) 1997-10-27 2006-02-15 Neurosearch A/S Heteroarüüldiasatsükloalkaanid kui atsetüülkoliini nikotiinretseptorite kolinergilised ligandid, nende kasutamine ravimitena ning neid sisaldav farmatseutiline kompositsioon
ATE262523T1 (de) 1998-11-20 2004-04-15 Searle Llc Verfahren zur herstellung 5-substituierter pyrazole unter verwendung von dithietane
US6248755B1 (en) 1999-04-06 2001-06-19 Merck & Co., Inc. Pyrrolidine modulators of chemokine receptor activity
EP1632479B1 (fr) 1999-05-04 2011-01-12 Schering Corporation Compositions pharmaceutiques contenant des derives de piperazine antagonistes du ccr5
WO2001052902A1 (fr) 2000-01-24 2001-07-26 Isis Pharmaceuticals, Inc. Modulation antisens de l'expression de l'oxyde nitrique synthase inductible
GB0004153D0 (en) 2000-02-23 2000-04-12 Astrazeneca Uk Ltd Novel use
US20020045613A1 (en) 2000-04-27 2002-04-18 Heinz Pauls 1-aroyl-piperidinyl benzamidines
AU5741301A (en) 2000-05-22 2001-12-03 Aventis Pharm Prod Inc Arylmethylamine derivatives for use as tryptase inhibitors
TR200402579T4 (tr) 2000-10-12 2004-12-21 Boehringer Ingelheim Pharma Gmbh & Co. Kg Kristalin monohidrat, bunun imalat yöntemi ve bir ilaç maddesinin imalatında kullanımı
AR035700A1 (es) 2001-05-08 2004-06-23 Astrazeneca Ab Derivados de arilheteroalquilamina, composicion farmaceutica, usos de estos derivados para la fabricacion de medicamentos, metodos de tratamiento, y proceso para la preparacion de estos derivados
SK287262B6 (sk) 2001-06-22 2010-04-07 Boehringer Ingelheim Pharma Gmbh & Co. Kg Kryštalický bezvodný tiotropiumbromid, spôsob jeho výroby, farmaceutický prostriedok s jeho obsahom a jeho použitie
US20050143372A1 (en) 2001-10-30 2005-06-30 Shomir Ghosh Compounds, pharmaceutical compositions and methods of use therefor
US6806279B2 (en) 2001-12-17 2004-10-19 Sunesis Pharmaceuticals, Inc. Small-molecule inhibitors of interleukin-2
WO2003066604A2 (fr) 2002-02-05 2003-08-14 Novo Nordisk A/S Nouvelles aryl- et heteroarylpiperazines
HUP0200849A2 (hu) 2002-03-06 2004-08-30 Sanofi-Synthelabo N-aminoacetil-2-ciano-pirrolidin-származékok, e vegyületeket tartalmazó gyógyszerkészítmények és eljárás előállításukra
US20030195192A1 (en) 2002-04-05 2003-10-16 Fortuna Haviv Nicotinamides having antiangiogenic activity
IL164002A0 (en) 2002-03-13 2005-12-18 Janssen Pharmaceutica Nv Sulfonyl-derivatives as novel inhibitors of histone deacetylase
US20040014744A1 (en) 2002-04-05 2004-01-22 Fortuna Haviv Substituted pyridines having antiangiogenic activity
AU2003235097A1 (en) 2002-04-24 2003-11-10 Takeda Pharmaceutical Company Limited Use of compounds having ccr antagonism
CA2483752C (fr) 2002-04-29 2011-03-29 Merck & Co., Inc. Modulateurs tetrahydropyranyl cyclopentyl tetrahydropyridopyridine de l'activite des recepteurs de chimiokine
AR040442A1 (es) 2002-06-05 2005-04-06 Pharmacia Corp Derivados de pirazol como inhibidores de la quinasa p38
WO2004024710A1 (fr) 2002-09-13 2004-03-25 Glaxo Group Limited Composes a base d'uree, actifs en tant qu'antagonistes du recepteur de la vanilloide et utilises pour traiter les douleurs
SE0203304D0 (sv) 2002-11-07 2002-11-07 Astrazeneca Ab Novel Coumpounds
GB0229618D0 (en) 2002-12-19 2003-01-22 Cancer Rec Tech Ltd Pyrazole compounds
US20040147561A1 (en) 2002-12-27 2004-07-29 Wenge Zhong Pyrid-2-one derivatives and methods of use
WO2004074438A2 (fr) 2003-02-14 2004-09-02 Smithkline Beecham Corporation Antagonistes de ccr8
NZ542680A (en) 2003-03-12 2008-08-29 Kudos Pharm Ltd Phthalazinone derivatives
DK1615909T3 (da) 2003-04-23 2008-11-17 Glaxo Group Ltd Piperazin-derivater og deres anvendelse til behandling af neurologiske og psykiatriske sygdomme
FR2854158B1 (fr) 2003-04-25 2006-11-17 Sanofi Synthelabo Derives de 2-acylamino-4-phenylethiazole, leur preparation et leur application en therapeutique
TW200514781A (en) 2003-07-18 2005-05-01 Glaxo Group Ltd Novel compounds
KR20060054392A (ko) 2003-07-29 2006-05-22 노보 노르디스크 에이/에스 피리다지닐-피페라진 및 히스타민 h3 수용체 리간드로서그들의 사용
AP2439A (en) 2003-12-18 2012-08-31 Incyte Corp 3-Cycloalkylaminopyrrolidine derivatives as modulators of chemokine receptors
GB0403155D0 (en) * 2004-02-12 2004-03-17 Vernalis Res Ltd Chemical compounds
EP1720545B1 (fr) 2004-03-03 2014-10-29 ChemoCentryx, Inc. Heterocycles d'azote bicycliques et ponts
PE20060285A1 (es) 2004-03-30 2006-05-08 Aventis Pharma Inc Piridonas sustituidas como inhibidores de pol(adp-ribosa)-polimerasa (parp)
US7423147B2 (en) 2004-03-31 2008-09-09 Janssen Pharmaceutical, N.V. Pyridine compounds as histamine H3 modulators
JP5213229B2 (ja) 2004-04-23 2013-06-19 エグゼリクシス, インコーポレイテッド キナーゼ調節因子および使用方法
CA2567851A1 (fr) 2004-05-21 2006-01-05 Merck & Co., Inc. Modulateurs heterocycliques et carbocycliques d'amino cyclopentyle de l'activite du recepteur de la chimiokine
GEP20105024B (en) 2004-06-02 2010-06-25 Takeda Pharmaceuticals Co Fused heterocyclic compound
FR2871157A1 (fr) 2004-06-04 2005-12-09 Aventis Pharma Sa Produits biaryl aromatiques, compositions les contenant et utilisation
EA200700117A1 (ru) 2004-06-24 2007-06-29 Инсайт Корпорейшн N-замещенные пиперидины и их применение в качестве фармацевтических препаратов
UA85597C2 (ru) 2004-06-25 2009-02-10 Янссен Фармацевтика Н.В. Четвертичные соли как антагонисты ccr2
GEP20094844B (en) 2004-06-28 2009-11-25 Incyte Corp 3-aminocyclopentane carboxamides as modulators of chemokine receptors
GB0419072D0 (en) * 2004-08-26 2004-09-29 Kudos Pharm Ltd Phthalazinone derivatives
BRPI0514632A (pt) * 2004-08-26 2008-06-17 Kudos Pharm Ltd derivados de ftalazinona 4-heteroarilmetila substituìdos
GB0420831D0 (en) 2004-09-17 2004-10-20 Glaxo Group Ltd Novel compounds
EP2266569A3 (fr) 2004-09-20 2011-03-09 Xenon Pharmaceuticals Inc. Dérivés hétérocycliques et leur utilisation en tant qu'inhibiteurs de la stearoyl-coa desaturase
GB0421525D0 (en) * 2004-09-28 2004-10-27 Novartis Ag Inhibitors of protein kineses
WO2006038734A1 (fr) 2004-10-08 2006-04-13 Astellas Pharma Inc. Dérivés de la pyridazinone inhibiteurs de cytokines
ES2441718T3 (es) 2004-11-02 2014-02-06 Northwestern University Compuestos de piridazina, composiciones y métodos
UY29219A1 (es) 2004-11-22 2006-04-28 Incyte Corp Sales de la n-(2- (((3r)-1-(trans-4-hidroxi-4-(6-metoxipiridin-3-il)-cilohexil) pirrolidin-3-il)amino)-2-oxoetil)-3- (trifluorometil) benzamida
DE102004061751A1 (de) 2004-12-22 2006-07-06 Bayer Healthcare Ag Cyanoguanidin-substituierte Pyrazoline
BRPI0608205B8 (pt) 2005-02-17 2021-05-25 Astellas Pharma Inc derivado heterocíclico-1-carboxilato de piridila não-aromático nitrogenado, composição farmacêutica e uso do dito composto para o tratamento de frequência urinária, incontinência urinária, bexiga hiperativa e dor
EP1879881A2 (fr) 2005-04-14 2008-01-23 Bristol-Myers Squibb Company Inhibiteurs de la 11-beta hydroxysteroide deshydrogenase de type i
WO2006113140A2 (fr) 2005-04-15 2006-10-26 Elan Pharmaceuticals, Inc. Nouveaux composes s'utilisant dans l'antagonisme du recepteur de bradykinine b1
AU2006236387A1 (en) 2005-04-18 2006-10-26 Neurogen Corporation Subtituted heteroaryl CB1 antagonists
US20080221111A1 (en) 2005-05-11 2008-09-11 Nycomed Gmbh Combination of a Pd4 Inhibitor and a Tetrahydrobiopterin Derivative
CN101228161B (zh) 2005-05-20 2012-10-10 沃泰克斯药物股份有限公司 适用作蛋白激酶抑制剂的吡咯并吡啶类
CN103110635A (zh) 2005-07-04 2013-05-22 海波因特制药有限责任公司 组胺h3受体拮抗剂
AU2006275568A1 (en) 2005-08-02 2007-02-08 Neurogen Corporation Dipiperazinyl ketones and related analogues
GB0517184D0 (en) 2005-08-22 2005-09-28 Glaxo Group Ltd Compounds
AR055203A1 (es) * 2005-08-31 2007-08-08 Otsuka Pharma Co Ltd Derivados de benzotiofeno con propiedades antipsicoticas
TW200800999A (en) 2005-09-06 2008-01-01 Astrazeneca Ab Novel compounds
WO2007038669A2 (fr) 2005-09-27 2007-04-05 Irm Llc Composes et compositions contenant de la diarylamine, et utilisation en tant que modulateurs de recepteurs de c-kit
JO2769B1 (en) 2005-10-26 2014-03-15 جانسين فارماسوتيكا ان. في Rapid decomposition of physiologically antagonistic agents of the 2-dopamine receptor
US20100016289A1 (en) 2005-11-01 2010-01-21 Kevin Sprott Compounds Useful as Antagonists of CCR2
US8067457B2 (en) 2005-11-01 2011-11-29 Millennium Pharmaceuticals, Inc. Compounds useful as antagonists of CCR2
AU2006337682A1 (en) 2005-11-14 2007-08-16 Irm Llc Compounds and compositions as LXR modulators
BRPI0620066A2 (pt) * 2005-12-20 2011-11-01 Novartis Ag derivados de ácido nicotìnico como moduladores do receptor de glutamato metabotrópico, processo para preparação dos mesmos, composição farmacêutica e uso dos referidos derivados
WO2007084868A2 (fr) 2006-01-17 2007-07-26 Kalypsys, Inc. Traitement d'une inflammation et de troubles associes par l'activation de la reponse upr (proteine depliee)
JO2660B1 (en) 2006-01-20 2012-06-17 نوفارتيس ايه جي Pi-3 inhibitors and methods of use
NZ595571A (en) 2006-02-28 2013-04-26 Helicon Therapeutics Inc Pyrazole compounds and uses thereof
CA2643066A1 (fr) 2006-03-16 2007-09-20 Pfizer Products Inc. Pyrazoles
CN101466677A (zh) 2006-04-11 2009-06-24 默克公司 二芳基取代的烷烃
US7807671B2 (en) 2006-04-25 2010-10-05 Bristol-Myers Squibb Company Diketo-piperazine and piperidine derivatives as antiviral agents
CA2650704A1 (fr) 2006-04-28 2007-11-08 Northwestern University Sels de composes de pyridazine
JP2009541268A (ja) 2006-06-22 2009-11-26 ビオヴィトルム・アクチボラゲット(プブリクト) Mnkキナーゼ阻害剤としてのピリジンおよびピラジン誘導体
GB0617575D0 (en) 2006-09-06 2006-10-18 Syngenta Ltd Herbicidal compounds and compositions
JP2010510224A (ja) * 2006-11-17 2010-04-02 アボット・ラボラトリーズ ケモカイン受容体拮抗薬としてのアミノピロリジン類
SG193664A1 (en) 2006-12-28 2013-10-30 Abbott Lab Inhibitors of poly(adp-ribose)polymerase
CA2676715A1 (fr) 2007-02-12 2008-08-21 Merck & Co., Inc. Derives de piperazine pour le traitement de la maladie d'alzheimer et des conditions apparentees
JP4785881B2 (ja) 2007-02-27 2011-10-05 大塚製薬株式会社 医薬
FR2915552B1 (fr) 2007-04-27 2009-11-06 Technip France Conduite tubulaire flexible pour le transport d'hydrocarbures gazeux.
WO2008145681A2 (fr) 2007-05-31 2008-12-04 Boehringer Ingelheim International Gmbh Antagonistes des récepteurs ccr2 et utilisations de ceux-ci
EP2173735B1 (fr) 2007-07-02 2012-01-11 F. Hoffmann-La Roche AG Dérivés imidazolés comme antagonistes du récepteur ccr2
US7977358B2 (en) 2007-07-26 2011-07-12 Hoffmann-La Roche Inc. Pyrazol derivatives
EP2042516A1 (fr) 2007-09-27 2009-04-01 Protaffin Biotechnologie AG Mutants de MCP-1 capable d'antagonisé des glycosaminoglycans et leurs procédés d'utilisation
EP2190836B1 (fr) 2007-08-22 2011-08-17 Irm Llc Derives de 2-heteroarylamino-pyrimidine en tant qu'inhibiteurs de kinase
KR20100050570A (ko) 2007-10-01 2010-05-13 에프. 호프만-라 로슈 아게 Ccr 수용체 길항제로서의 n-헤테로사이클릭 바이아릴 카복스아마이드
EP2200470A4 (fr) 2007-10-12 2013-11-20 Jong O Whang Outil de serrage pour lacet de chaussure
US20090131417A1 (en) 2007-11-20 2009-05-21 Letavic Michael A Substituted pyridyl amide compounds as modulators of the histamine h3 receptor
WO2009066084A1 (fr) * 2007-11-21 2009-05-28 F. Hoffmann-La Roche Ag 2-morpholinopyrimidines et leur utilisation en tant qu'inhibiteurs de kinase pi3
JP5385297B2 (ja) * 2007-11-22 2014-01-08 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 新規化合物
EP2062889A1 (fr) * 2007-11-22 2009-05-27 Boehringer Ingelheim Pharma GmbH & Co. KG Composés
WO2009153182A1 (fr) 2008-06-18 2009-12-23 F. Hoffmann-La Roche Ag Nouveaux dérivés de carboxamide d’hétéroaryle
NZ601483A (en) * 2008-08-04 2013-10-25 Chdi Foundation Inc Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof
GB0815369D0 (en) * 2008-08-22 2008-10-01 Summit Corp Plc Compounds for treatment of duchenne muscular dystrophy
NZ591226A (en) * 2008-09-02 2012-11-30 Boehringer Ingelheim Int Benzoic acid amides, production thereof, and use thereof as medicaments
JP2012512834A (ja) 2008-12-19 2012-06-07 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 炎症、喘息及びcopdの処置のためのccr2受容体アンタゴニストとしての環状ピリミジン−4−カルボキサミド
CA2750635A1 (fr) 2009-02-23 2010-08-26 Merck Canada Inc. Derives heterocycliques comme inhibiteurs de la stearoyl-coenzyme a delta-9 desaturase
PL3091012T3 (pl) * 2009-12-17 2018-08-31 Centrexion Therapeutics Corporation Antagoniści receptora CCR2 i ich zastosowanie
WO2011073155A1 (fr) 2009-12-17 2011-06-23 Boehringer Ingelheim International Gmbh Nouveaux antagonistes du récepteur ccr2 et leurs utilisations
JP2013526507A (ja) 2010-05-12 2013-06-24 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 新規ccr2受容体アンタゴニスト、その製造方法及び薬物としてのその使用
US8946218B2 (en) 2010-05-12 2015-02-03 Boehringer Ingelheim International Gmbh CCR2 receptor antagonists, method for producing the same, and use thereof as medicaments
WO2011144501A1 (fr) 2010-05-17 2011-11-24 Boehringer Ingelheim International Gmbh Antagonistes du récepteur ccr2 et leurs utilisations
US9018212B2 (en) 2010-05-25 2015-04-28 Boehringer Ingelheim International Gmbh Pyridazine carboxamides as CCR2 receptor antagonists
JP5721242B2 (ja) 2010-06-01 2015-05-20 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 新規ccr2アンタゴニスト
EP2721025B1 (fr) 2011-06-16 2015-11-25 Boehringer Ingelheim International Gmbh Nouveaux antagonistes sélectifs de ccr2
EP2731941B1 (fr) 2011-07-15 2019-05-08 Boehringer Ingelheim International GmbH Antagonistes ccr2, nouveaux et sélectifs

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CN103724328A (zh) 2014-04-16
US8835440B2 (en) 2014-09-16
HUE025547T2 (en) 2016-02-29
DK2379525T3 (en) 2015-10-19
CA2747677A1 (fr) 2010-06-24
US20130324517A1 (en) 2013-12-05
ZA201103158B (en) 2011-12-28
JP2012512834A (ja) 2012-06-07
AR074814A1 (es) 2011-02-16
EA201100942A1 (ru) 2012-01-30
WO2010070032A1 (fr) 2010-06-24
BRPI0923051A2 (pt) 2021-06-15
TN2011000310A1 (en) 2012-12-17
US20140336374A1 (en) 2014-11-13
EA020548B1 (ru) 2014-12-30
IL212605A (en) 2015-06-30
TWI478913B (zh) 2015-04-01
CN103724328B (zh) 2015-10-14
TW201026683A (en) 2010-07-16
KR101754698B1 (ko) 2017-07-26
CN102256963B (zh) 2014-06-11
PL2379525T3 (pl) 2016-01-29
EP2379525A1 (fr) 2011-10-26
ECSP11011163A (es) 2011-07-29
AU2009327127A1 (en) 2010-06-24
CO6382124A2 (es) 2012-02-15
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US9067951B2 (en) 2015-06-30
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HK1159099A1 (en) 2012-07-27
EP2816040B1 (fr) 2018-10-17
NZ592723A (en) 2013-06-28
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JP5686916B2 (ja) 2015-03-18
EP2816040A1 (fr) 2014-12-24
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AU2009327127C1 (en) 2017-03-09
PE20120061A1 (es) 2012-02-19
MX2011005150A (es) 2011-05-30
ES2551557T3 (es) 2015-11-19
US20120053164A1 (en) 2012-03-01
BRPI0923051B1 (pt) 2022-07-19
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KR20110111380A (ko) 2011-10-11
CL2011001322A1 (es) 2011-11-11

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