MA27144A1 - Benzamide et heteroarylamide servant d'antagonistes du recepteur p2x7 - Google Patents

Benzamide et heteroarylamide servant d'antagonistes du recepteur p2x7

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Publication number
MA27144A1
MA27144A1 MA27660A MA27660A MA27144A1 MA 27144 A1 MA27144 A1 MA 27144A1 MA 27660 A MA27660 A MA 27660A MA 27660 A MA27660 A MA 27660A MA 27144 A1 MA27144 A1 MA 27144A1
Authority
MA
Morocco
Prior art keywords
heteroarylamide
benzamide
preparation
present
inhibitors
Prior art date
Application number
MA27660A
Other languages
English (en)
Inventor
Allen Jacob Duplantier
Chakrapani Subramanyam
Original Assignee
Pfizer Prod 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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of MA27144A1 publication Critical patent/MA27144A1/fr

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    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D253/00Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
    • C07D253/02Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 not condensed with other rings
    • C07D253/061,2,4-Triazines
    • C07D253/0651,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members
    • C07D253/071,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members with hetero atoms, or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D253/075Two hetero atoms, in positions 3 and 5
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Abstract

DEPOSANT Société dite: PFIZER PRODUCTS INC. REVENDICATION DE PRIORITES US 12 Novembre 2001 60/336,781 Voir en annexe le titre de l'invention et le texte de l'abrégé Benzamide et heteroarylamide servant d'antagonistes du récepteur P2X7 La présente invention concerne des inhibiteurs de P2X7 nouveaux répondant à la formule (I) et des procédés pour leur préparation, des intermédiaires utiles dans leur préparation, des compositions pharmaceutiques les contenant, et leur utilisation en thérapeutique. Les composés actifs de la présente invention sont de puissants inhibiteurs de P2X7 et, en tant que tels, sont utiles dans le traitement de l'inflammation, de l'ostéoarthrite, de la polyarthrite rhumatoïde, du cancer, d'une lésion de reperfusion ou ischémie dans le cas d'un ictus ou d'une attaque cardiaque, de maladies auto-immunes et d'autres affections.
MA27660A 2001-11-12 2004-04-28 Benzamide et heteroarylamide servant d'antagonistes du recepteur p2x7 MA27144A1 (fr)

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US33678101P 2001-11-12 2001-11-12

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MA27144A1 true MA27144A1 (fr) 2005-01-03

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MA27660A MA27144A1 (fr) 2001-11-12 2004-04-28 Benzamide et heteroarylamide servant d'antagonistes du recepteur p2x7

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US (2) US7214677B2 (fr)
EP (1) EP1448535B1 (fr)
JP (1) JP4365218B2 (fr)
KR (1) KR20050043785A (fr)
CN (1) CN1585755A (fr)
AP (1) AP2004003028A0 (fr)
AR (1) AR038365A1 (fr)
AT (1) ATE502020T1 (fr)
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CA (1) CA2466724C (fr)
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DK (1) DK1448535T3 (fr)
EA (1) EA200400488A1 (fr)
EC (1) ECSP045097A (fr)
ES (1) ES2358988T3 (fr)
GT (1) GT200200224A (fr)
HN (1) HN2002000319A (fr)
HU (1) HUP0401936A3 (fr)
IL (1) IL161329A0 (fr)
IS (1) IS7216A (fr)
MA (1) MA27144A1 (fr)
MX (1) MXPA04004465A (fr)
NO (1) NO20041922L (fr)
OA (1) OA12718A (fr)
PA (1) PA8557501A1 (fr)
PE (1) PE20030537A1 (fr)
PL (1) PL370762A1 (fr)
PT (1) PT1448535E (fr)
PY (1) PY0227300A (fr)
SV (1) SV2004001393A (fr)
TN (1) TNSN04083A1 (fr)
UY (1) UY27535A1 (fr)
WO (1) WO2003042191A1 (fr)
ZA (1) ZA200402754B (fr)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PA8557501A1 (es) * 2001-11-12 2003-06-30 Pfizer Prod Inc Benzamida, heteroarilamida y amidas inversas
PA8591801A1 (es) * 2002-12-31 2004-07-26 Pfizer Prod Inc Inhibidores benzamidicos del receptor p2x7.
JP2006513205A (ja) * 2002-12-31 2006-04-20 ファイザー・プロダクツ・インク P2x7受容体のベンズアミド阻害剤
US7071223B1 (en) 2002-12-31 2006-07-04 Pfizer, Inc. Benzamide inhibitors of the P2X7 receptor
SE0300480D0 (sv) 2003-02-21 2003-02-21 Astrazeneca Ab Novel compounds
EP1469072B1 (fr) * 2003-04-17 2007-08-29 Affectis Pharmaceuticals AG Dispositifs et méthodes pour le diagnostic et traitement de la maladie affective
ATE355273T1 (de) 2003-05-12 2006-03-15 Pfizer Prod Inc Benzamidinhibitoren des p2x7-rezeptors
EP1837330B1 (fr) * 2003-05-12 2012-10-24 Pfizer Products Inc. Inhibiteurs benzamidiques du recepteur P2X7
GB0312321D0 (en) * 2003-05-29 2003-07-02 Astrazeneca Ab New combination
MXPA05012705A (es) * 2003-05-29 2006-02-08 Astrazeneca Ab Una composicion farmaceutica que comprende un antagonista del receptor p2x7 y un factor alfa de necrosis tumoral.
WO2004105797A1 (fr) * 2003-05-29 2004-12-09 Astrazeneca Ab Nouvelle combinaison
US20070281931A1 (en) * 2003-05-29 2007-12-06 Nigel Boughton-Smith Pharmaceutical Composition Containing a P2x7 Receptor Antagonist and Methotrexate
BR0318394A (pt) * 2003-07-11 2006-08-01 Thomson Licensing estrutura de micro célula sobreposta para rede de sistema de telefonia móvel universal
WO2005019182A1 (fr) * 2003-08-20 2005-03-03 Bayer Healthcare Ag Derives de pyrazolylmethylbenzamide utilises comme antagonistes du recepteur p2xt
SE0302488D0 (sv) * 2003-09-18 2003-09-18 Astrazeneca Ab New combination
MXPA06004005A (es) * 2003-10-08 2006-06-28 Vertex Pharma Moduladores de transportadores con casete de union con atp.
ITMI20040255A1 (it) * 2004-02-17 2004-05-17 Univ Degli Studi Milano Sostanze ad attivita' antiangiogenica
EP1763353A1 (fr) * 2004-06-29 2007-03-21 Warner-Lambert Company LLC THERAPIES COMBINATOIRES DANS LESQUELLES SONT UTILISES DES INHIBITEURS DE BENZAMIDE DU RECEPTEUR P2X<SB>7</SB>
MXPA06015273A (es) * 2004-06-29 2007-03-15 Pfizer Prod Inc Procedimiento para preparar derivados de 5-[4-(2-hidroxi -etil)-3, 5-dioxo-4, 5-dihidro-3h-[1, 2, 4]-triazin -2-il]-benzamida con actividad inhibidora de p2x7 mediante reaccion del derivado no sustituido en posicion 4 de la triazina con un oxirano en
WO2006003500A1 (fr) * 2004-06-29 2006-01-12 Pfizer Products Inc. Procedes permettant de preparer des derives de 5-[4-(2-hydroxy-propyl)-3,5-dioxo-4,5-dihydro-3h-[1,2,4]triazin-2-yl]-benzamides par deprotection des precurseurs proteges par hydroxyle
WO2006083214A1 (fr) * 2005-02-02 2006-08-10 Astrazeneca Ab Composition pharmaceutique comprenant un antagoniste du recepteur p2x7 et un inhibiteur de hmg-coa reductase
JPWO2006104172A1 (ja) * 2005-03-29 2008-09-11 興和株式会社 関節リウマチの予防及び/又は治療薬
WO2007008157A1 (fr) * 2005-07-11 2007-01-18 Astrazeneca Ab Nouvelle combinaison 2
EP1906960A4 (fr) * 2005-07-11 2010-03-10 Astrazeneca Ab Nouvelle combinaison 1
EP1945632B1 (fr) 2005-11-08 2013-09-18 Vertex Pharmaceuticals Incorporated Modulateurs hétérocycliques de transporteurs à cassette liant l' atp
US20070117497A1 (en) * 2005-11-22 2007-05-24 Cabot Microelectronics Corporation Friction reducing aid for CMP
US7671221B2 (en) 2005-12-28 2010-03-02 Vertex Pharmaceuticals Incorporated Modulators of ATP-Binding Cassette transporters
EP2038264B1 (fr) * 2006-06-29 2016-10-26 F.Hoffmann-La Roche Ag Arylamides substitués par tétrazole
DE102006049618A1 (de) * 2006-10-20 2008-05-08 Tschesche, Harald, Prof. Dr. Triazine und Ihre Verwendung als Metalloproteinase-Inhibitoren
US7754739B2 (en) 2007-05-09 2010-07-13 Vertex Pharmaceuticals Incorporated Modulators of CFTR
US8969386B2 (en) 2007-05-09 2015-03-03 Vertex Pharmaceuticals Incorporated Modulators of CFTR
RU2470910C9 (ru) * 2007-06-29 2013-05-20 Акьюсела, Инк. Соединения, представляющие собой алкинилфенильные производные, для лечения офтальмических заболеваний и расстройств
HRP20151052T1 (xx) * 2007-07-19 2015-11-06 H. Lundbeck A/S Peteroäślani heterocikliäśki amidi i srodne tvari
CN103553945B (zh) 2007-10-05 2015-01-07 奥克塞拉有限公司 用于治疗疾病的烷氧基化合物
WO2009053459A1 (fr) 2007-10-26 2009-04-30 Glaxo Group Limited Dérivés de 4-benzoyl-1-substitué-pipérazin-2-one comme modulateurs de p2x7
MY156662A (en) * 2007-11-01 2016-03-15 Acucela Inc Amine derivative compounds for treating ophthalmic diseases and disorders
SI2225230T1 (sl) 2007-12-07 2017-03-31 Vertex Pharmaceuticals Incorporated Trdne oblike 3-(6-(1-2,2-difluorobenzo(d)(1,3)dioxol-5-il)ciklopropan- karboksamido)-3-metilpiridin-2-il) benzojske kisline
EP2639224B1 (fr) 2007-12-07 2016-08-24 Vertex Pharmaceuticals Incorporated Procédés de fabrication d'acides cycloalkylcarboxamido-pyridine benzoïques
GB0724625D0 (en) * 2007-12-18 2008-01-30 Glaxo Group Ltd Novel compounds
NZ720282A (en) 2008-02-28 2017-12-22 Vertex Pharma Heteroaryl derivatives as cftr modulators
BRPI0910034B1 (pt) 2008-03-25 2022-02-08 Affectis Pharmaceuticals Ag Antagonistas do p2x7r e composições farmacêuticas que os compreendem
CA2736229C (fr) * 2008-09-05 2015-06-09 Acucela Inc. Composants a liaison soufre pour le traitement de maladies et de troubles ophtalmiques
JP5773877B2 (ja) * 2008-10-22 2015-09-02 アキュセラ インコーポレイテッド 眼の疾患及び障害を治療する化合物
AU2010237302A1 (en) 2009-04-14 2011-12-01 Affectis Pharmaceuticals Ag Novel P2X7R antagonists and their use
JP5860398B2 (ja) 2009-07-02 2016-02-16 アキュセラ インコーポレイテッド 視覚サイクルモジュレーターの薬理
EP2322149A1 (fr) 2009-11-03 2011-05-18 Universidad del Pais Vasco Procédés et compositions de traitement de l'ischémie
CA2785204C (fr) 2010-01-07 2016-01-05 Selexagen Therapeutics, Inc. Inhibiteurs de la voie hedgehog
WO2011085261A1 (fr) * 2010-01-08 2011-07-14 Selexagen Therapeutics, Inc. Inhibiteurs de hedgehog
EP2542670A2 (fr) 2010-03-05 2013-01-09 President and Fellows of Harvard College Compositions de cellules dendritiques induites et utilisations associées
HRP20211752T1 (hr) 2010-04-07 2022-02-18 Vertex Pharmaceuticals Incorporated Farmaceutski pripravci 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioksol-5-il)ciklopropankarboksamido)-3-metilpiridin-2-il)benzojeve kiseline i njihova primjena
SG185400A1 (en) 2010-05-14 2012-12-28 Affectis Pharmaceuticals Ag Novel methods for the preparation of p2x7r antagonists
WO2012110190A1 (fr) 2011-02-17 2012-08-23 Affectis Pharmaceuticals Ag Nouveaux antagonistes p2x7r et leur utilisation
US20140073651A1 (en) 2011-02-22 2014-03-13 Actelion Pharmaceuticals Ltd. Benzamide derivatives as p2x7 receptor antagonists
WO2012149285A1 (fr) * 2011-04-28 2012-11-01 Claire Mitchell Méthode de traitement d'une dégénérescence maculaire par la modulation des récepteurs p2y12 ou p2x7
WO2012163792A1 (fr) 2011-05-27 2012-12-06 Affectis Pharmaceuticals Ag Nouveaux antagonistes de p2x7r et leur utilisation
WO2012163456A1 (fr) 2011-05-27 2012-12-06 Affectis Pharmaceuticals Ag Nouveaux antagonistes de p2x7r et leur utilisation
CN103687860B (zh) 2011-07-22 2016-06-08 埃科特莱茵药品有限公司 作为p2x7受体拮抗剂的杂环酰胺衍生物
US9707235B1 (en) 2012-01-13 2017-07-18 University Of Kentucky Research Foundation Protection of cells from degeneration and treatment of geographic atrophy
US9409917B2 (en) 2012-01-20 2016-08-09 Actelion Pharmaceuticals Ltd. Heterocyclic amide derivatives as P2X7 receptor antagonists
WO2013112804A1 (fr) 2012-01-25 2013-08-01 Vertex Pharmaceuticals Incorporated Formulations d'acide 3-(6-(1-(2,2-difluorobenzo [d] [1,3]dioxol-5-yl) cyclopropanecarboxamido)-3-méthylpyridin-2-yl) benzoïque
TW201427947A (zh) 2012-10-12 2014-07-16 Lundbeck & Co As H 環狀胺
TWI598325B (zh) * 2012-10-12 2017-09-11 H 朗德貝克公司 苯甲醯胺類
WO2014091415A1 (fr) 2012-12-12 2014-06-19 Actelion Pharmaceuticals Ltd Dérivés d'indole carboxamide utilisés en tant qu'antagonistes du récepteur p2x7
KR102232744B1 (ko) 2012-12-18 2021-03-26 이도르시아 파마슈티컬스 리미티드 P2x7 수용체 길항제로서의 인돌 카르복사미드 유도체
CA2896790C (fr) 2013-01-22 2022-05-10 Actelion Pharmaceuticals Ltd Derives d'amides heterocycliques utilises comme antagonistes du recepteur p2x7
ES2616883T3 (es) 2013-01-22 2017-06-14 Actelion Pharmaceuticals Ltd. Derivados amida heterocíclicos como antagonistas del receptor P2X7
BR112016000241B1 (pt) 2013-07-08 2021-06-22 Bayer Cropscience Aktiengesellschaft Compostos pesticidas derivados de sulfeto de arila e sulfóxido de arila, formulação, seus usos, método para controle de pragas e método de proteção de semente ou planta
JP6963896B2 (ja) 2013-11-12 2021-11-10 バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated Cftr媒介性疾患の処置のための医薬組成物を調製する方法
WO2015099107A1 (fr) * 2013-12-26 2015-07-02 塩野義製薬株式会社 Dérivé cyclique à six chaînons contenant de l'azote et composition pharmaceutique le contenant
PT3221692T (pt) 2014-11-18 2021-09-10 Vertex Pharma Processo de realização de testagem de alta produtividade por cromatografia líquida de alta eficiência
US10774051B2 (en) 2015-04-24 2020-09-15 Shionogi & Co., Ltd. 6-membered heterocyclic derivatives and pharmaceutical composition comprising the same
WO2018074390A1 (fr) 2016-10-17 2018-04-26 塩野義製薬株式会社 Dérivé hétérocyclique azoté bicyclique et composition pharmaceutique le comprenant
CN106674098B (zh) * 2016-12-23 2019-07-02 中国医科大学 N-(3-氰基-4-烷氧基苯基)吡啶甲酰胺类化合物及其用途
WO2020227159A2 (fr) 2019-05-03 2020-11-12 Flagship Pioneering Innovations V, Inc. Métodes de modulation de l'activité immunitaire
CN114315811B (zh) * 2021-11-19 2024-04-30 江苏恒盛药业有限公司 一种三氮唑类似物化合物及其制备方法和应用
WO2026041663A1 (fr) 2024-08-22 2026-02-26 Breye Therapeutics Aps Antagonistes du récepteur p2x7

Family Cites Families (64)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US71529A (en) * 1867-11-26 John e
US123378A (en) * 1872-02-06 Improvement in time-locks
US71509A (en) * 1867-11-26 mcclellan
US146200A (en) * 1874-01-06 Improvement in wind-wheels
US142194A (en) * 1873-08-26 William w
US128498A (en) * 1872-07-02 Improvement in tile-molds
US158883A (en) * 1875-01-19 Improvement in wax-thread sewing-machines
US77018A (en) * 1868-04-21 Improvement in dove-tail mabkers
US144170A (en) * 1873-10-28 Improvement in scarf-clasps
US74576A (en) * 1868-02-18 Adam myers
US144213A (en) * 1873-11-04 Improvement in faucets
AU542544B2 (en) * 1980-03-12 1985-02-28 Nippon Kayaku Kabushiki Kaisha Tetrahydrophthalimide derivatives
EP0077938A3 (fr) * 1981-10-23 1983-08-24 Mitsubishi Kasei Corporation Tétrahydrophtalimides N-(3-substituées aminophényl) et compositions herbicides les contenant
WO1986000072A1 (fr) 1984-06-12 1986-01-03 Fmc Corporation 2-aryl-1,2,4-triazine-3,5(2h,4h)-diones herbicides et leurs analogues sulfures
US4766233A (en) 1984-06-12 1988-08-23 Fmc Corporation Herbicidal 2-aryl-1,2,4-triazine-3,5(2H,4H)-diones and sulfur analogs thereof
AU2328188A (en) * 1987-09-23 1989-04-18 Ciba-Geigy Ag Heterocyclic compounds
US5077409A (en) 1990-05-04 1991-12-31 American Cyanamid Company Method of preparing bis-aryl amide and urea antagonists of platelet activating factor
US5128351A (en) 1990-05-04 1992-07-07 American Cyanamid Company Bis-aryl amide and urea antagonists of platelet activating factor
EP0491441A1 (fr) 1990-12-17 1992-06-24 Shell Internationale Researchmaatschappij B.V. Dérivés d'isoquinolinefongicides
JP3089621B2 (ja) * 1990-12-17 2000-09-18 日産化学工業株式会社 ウラシル誘導体
GB9110679D0 (en) * 1991-05-17 1991-07-10 Sandoz Ltd Improvements in or relating to organic compounds
GB9119467D0 (en) 1991-09-12 1991-10-23 Smithkline Beecham Corp Chemical compounds
US5691376A (en) 1994-02-17 1997-11-25 American Home Products Corporation Substituted biphenyl derivatives
DE4405614A1 (de) * 1994-02-22 1995-08-24 Bayer Ag Substituierte Triazolinone
US5686061A (en) 1994-04-11 1997-11-11 The Board Of Regents Of The University Of Texas System Particulate contrast media derived from non-ionic water soluble contrast agents for CT enhancement of hepatic tumors
GB9412603D0 (en) * 1994-06-23 1994-08-10 Sandoz Ltd Organic compounds
JP3144624B2 (ja) 1995-06-02 2001-03-12 杏林製薬株式会社 N−ベンジルジオキソチアゾリジルベンズアミド誘導体及びその製造法
JP3906935B2 (ja) 1995-12-18 2007-04-18 杏林製薬株式会社 N−置換ジオキソチアゾリジルベンズアミド誘導体及びその製造法
WO1997023212A1 (fr) 1995-12-21 1997-07-03 The Du Pont Merck Pharmaceutical Company ISOXAZOLINE, ISOTHIAZOLINE ET PYRAZOLINE INHIBITEURS DU FACTEUR Xa
DE69706407T2 (de) 1996-03-29 2002-05-29 G.D. Searle & Co., Chicago META-SUBSTITUIERTE PHENYLENDERIVATE UND IHRE VERWENDUNG ALS ALPHAvBETA3 INTERGRIN-ANTAGONISTEN ODER INHIBITOREN
AU730224B2 (en) 1996-12-23 2001-03-01 Du Pont Pharmaceuticals Company Nitrogen containing heteroaromatics as factor Xa inhibitors
US6020357A (en) 1996-12-23 2000-02-01 Dupont Pharmaceuticals Company Nitrogen containing heteroaromatics as factor Xa inhibitors
US6187797B1 (en) 1996-12-23 2001-02-13 Dupont Pharmaceuticals Company Phenyl-isoxazoles as factor XA Inhibitors
DE19701287A1 (de) * 1997-01-16 1998-07-23 Wernicke & Co Gmbh Verfahren zum Erhöhen der Gebrauchsdauer von Schleifscheiben
WO1998042669A1 (fr) 1997-03-25 1998-10-01 Astra Pharmaceuticals Ltd. Nouveaux derives de pyridine et compositions pharmaceutiques les renfermant
WO1998043973A1 (fr) 1997-03-27 1998-10-08 Novartis Ag Produits intermediaires et procede pour preparer des derives de pyrimidine
DE19719621A1 (de) 1997-05-09 1998-11-12 Hoechst Ag Sulfonylaminocarbonsäuren
US6297239B1 (en) 1997-10-08 2001-10-02 Merck & Co., Inc. Inhibitors of prenyl-protein transferase
SE9704272D0 (sv) 1997-11-21 1997-11-21 Astra Pharma Prod Novel Compounds
SE9704545D0 (sv) 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
SE9704546D0 (sv) 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
SE9704544D0 (sv) 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
JPH11318492A (ja) 1998-03-09 1999-11-24 Aisin Seiki Co Ltd 蛍光発生性基質を含有する組成物
US6320078B1 (en) 1998-07-24 2001-11-20 Mitsui Chemicals, Inc. Method of producing benzamide derivatives
FR2783519B1 (fr) 1998-09-23 2003-01-24 Sod Conseils Rech Applic Nouveaux derives d'amidines, leur preparation, leur application a titre de medicaments et les compositions pharmaceutiques les contenant
DE19851184A1 (de) 1998-11-06 2000-05-11 Aventis Pharma Gmbh N-Arylsulfonyl-aminosäure-omega-amide
WO2001028498A2 (fr) 1999-10-18 2001-04-26 University Of Connecticut Retro-anandamides, ligands des recepteurs des cannabinoides presentant une affinite et une stabilite elevees
DE69927050T2 (de) 1998-12-16 2006-06-29 Bayer Healthcare Ag Biphenylverbindungen und biphenyl-analoge als intergrin-antagonisten
CZ20013608A3 (cs) 1999-04-09 2002-05-15 Astrazeneca Ab Adamantanové deriváty
AU5283700A (en) 1999-05-24 2000-12-12 Cor Therapeutics, Inc. Inhibitors of factor xa
SE9901875D0 (sv) * 1999-05-25 1999-05-25 Astra Pharma Prod Novel compounds
EP1088821A1 (fr) 1999-09-28 2001-04-04 Applied Research Systems ARS Holding N.V. Derives des sulfamides pharmaceutiquement actifs
SE9904505D0 (sv) * 1999-12-09 1999-12-09 Astra Pharma Prod Novel compounds
SE9904652D0 (sv) 1999-12-17 1999-12-17 Astra Pharma Prod Novel Compounds
TWI258462B (en) 1999-12-17 2006-07-21 Astrazeneca Ab Adamantane derivative compounds, process for preparing the same and pharmaceutical composition comprising the same
SE9904738D0 (sv) 1999-12-22 1999-12-22 Astra Pharma Prod Novel compounds
DE10005284A1 (de) 2000-02-07 2001-08-09 Bayer Ag Verfahren zur Herstellung von 1-Amino-3-aryl-uracilen
PA8557501A1 (es) * 2001-11-12 2003-06-30 Pfizer Prod Inc Benzamida, heteroarilamida y amidas inversas
WO2003042190A1 (fr) 2001-11-12 2003-05-22 Pfizer Products Inc. Derives de n-adamantylalkyle benzamide en tant qu'antagonistes du recepteur p2x7
PA8591801A1 (es) 2002-12-31 2004-07-26 Pfizer Prod Inc Inhibidores benzamidicos del receptor p2x7.
ATE355273T1 (de) 2003-05-12 2006-03-15 Pfizer Prod Inc Benzamidinhibitoren des p2x7-rezeptors
MXPA06015273A (es) 2004-06-29 2007-03-15 Pfizer Prod Inc Procedimiento para preparar derivados de 5-[4-(2-hidroxi -etil)-3, 5-dioxo-4, 5-dihidro-3h-[1, 2, 4]-triazin -2-il]-benzamida con actividad inhibidora de p2x7 mediante reaccion del derivado no sustituido en posicion 4 de la triazina con un oxirano en
WO2006003500A1 (fr) 2004-06-29 2006-01-12 Pfizer Products Inc. Procedes permettant de preparer des derives de 5-[4-(2-hydroxy-propyl)-3,5-dioxo-4,5-dihydro-3h-[1,2,4]triazin-2-yl]-benzamides par deprotection des precurseurs proteges par hydroxyle
EP1763353A1 (fr) 2004-06-29 2007-03-21 Warner-Lambert Company LLC THERAPIES COMBINATOIRES DANS LESQUELLES SONT UTILISES DES INHIBITEURS DE BENZAMIDE DU RECEPTEUR P2X<SB>7</SB>

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