BR0012047A - Inibidores da replicação do vìrus sincicial respiratório - Google Patents

Inibidores da replicação do vìrus sincicial respiratório

Info

Publication number
BR0012047A
BR0012047A BR0012047-2A BR0012047A BR0012047A BR 0012047 A BR0012047 A BR 0012047A BR 0012047 A BR0012047 A BR 0012047A BR 0012047 A BR0012047 A BR 0012047A
Authority
BR
Brazil
Prior art keywords
alkyl
hydrogen
formula
optionally substituted
aryl
Prior art date
Application number
BR0012047-2A
Other languages
English (en)
Inventor
Frans Eduard Janssens
Kathleen Petrus Marie Meersman
Francois Maria Sommen
Koenraad Jozef Lodewij Andries
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of BR0012047A publication Critical patent/BR0012047A/pt

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/14—Heterocyclic 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 three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Virology (AREA)
  • Communicable Diseases (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Oncology (AREA)
  • Molecular Biology (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Patente de Invenção: "INIBIDORES DA REPLICAçãO DO VìRUS SINCICIAL RESPIRATóRIO". A invenção diz respeito aos compostos de fórmula (1), pró-drogas, N-óxidos, sais de adição, aminas quaternárias, complexos metálicos ou formas estereoquimicamente isoméricas dos mesmos em que -a^ 1^=a^ 2^-a^ 3^ =a^ 4^- é um radical de fórmula -CH=CH-CH=CH-, -N=CH-CH=CH-, -CH=NCH=CH-, -CH=CH-N=CH-, -CH=CH-CH=N- em que cada átomo de hidrogênio pode ser substituído opcionalmente; Q é um radical de fórmula (b-1), (b-2), (b-3), (b-4), (b-5), (b-6), (b-7), (b-8), em que Alq é C~ 1-6~ alcanodiil; Y^ 1^ é um radical bivalente de fórmula -NR^ 2^- ou -CH(NR^ 2^R^ 4^)-; X^ 1^ é NR^ 4^, S, S(=O), C(=O)~ 2~, O, CH~ 2~, C(=O), CH(=CH~ 2~), CH(OH), CH(CH~ 3~), CH(OCH~ 3~), CH(SCH~ 3~), CH(NR^ 5a^R^ 5b^), CH~ 2~-NR^ 4^ ou NR^ 4^-CH~ 2~; X^ 1^ é uma ligação direta, CH2, C(=O), NR^ 4^, C~ 1-4~ alquil-NR^ 4^, NR^ 4^-C~ 1-4~ alquil; t é 2 a 5; u é 1 a 5; v é 2 ou 3; e em que cada hidrogênio em Alq e em (b-3), (b-4), (b-5), (b-6), (b-7) e (b-8) pode ser substituído opcionalmente por R3; com a condição de que quando R^ 3^ é hidróxi ou C~ 1-6~ alquilóxi, então R^ 3^ não pode substituir um átomo de hidrogênio na posição <244> em relação a um átomo de nitrogênio; G é C~ 1-10 alcanodiil substituído em que o substituinte é ligado através de um átomo de oxigênio; R^ 1^ é um aril ou heterociclo monocíclico opcionalmente substituído; R^ 2^ é hidrogênio, formil, C~ 1-6~ alquilcarbonil, Hetcarbonil, pirrolidinil, piperidinil, homopiperidinil, C3-7 cicioalquil ou C~ 1-10~ alquil substituído com N(R^ 6^)~ 2~ e opcionalmente com outro substituinte; R^ 3^ é hidrogênio, hidróxi, C~ 1-6~ alquil, C~ 1-6~ alquilóxi, aril C~ 1-6~ alquil ou aril C~ 1-6~ alquilóxi; R^ 4^ é hidrogênio, C~ 1-6~ alquil ou aril C~ 1-6~ alquil; R^ 5a^, R^ 5b^, R^ 5c^ e R^ 5d^ são hidrogênio ou C~ 1-6~ alquil; ou R^ 5a^ e R^ 5b^, ou R^ 5c^ e R^ 5d^ tomados juntos formam um radical bivalente de fórmula -(CH~ 2~)~ S~-em que s é 4 ou 5; R^ 6^ é hidrogênio, C~ 1-6~ alquil, formil, hidróxi C~ 1-6~ alquil, C~ 1-6 alquilcarbonil OU C~ 1-6~ alquiloxicarbonil; aril é fenil opcionalmente substituído; Het é piridil, pirimidinil, pirazinil, piridazinil; como inibidores da replicação do vírus sincicial respiratório; sua preparação, composições contendo os mesmos e sua aplicação como um medicamento.
BR0012047-2A 1999-06-28 2000-06-20 Inibidores da replicação do vìrus sincicial respiratório BR0012047A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP99202088 1999-06-28
PCT/EP2000/005675 WO2001000612A2 (en) 1999-06-28 2000-06-20 Respiratory syncytial virus replication inhibitors

Publications (1)

Publication Number Publication Date
BR0012047A true BR0012047A (pt) 2002-03-12

Family

ID=8240373

Family Applications (1)

Application Number Title Priority Date Filing Date
BR0012047-2A BR0012047A (pt) 1999-06-28 2000-06-20 Inibidores da replicação do vìrus sincicial respiratório

Country Status (33)

Country Link
US (3) US6747028B1 (pt)
EP (1) EP1196409B1 (pt)
JP (1) JP2003503402A (pt)
KR (1) KR100731271B1 (pt)
CN (1) CN1210275C (pt)
AR (1) AR035991A1 (pt)
AT (1) ATE258928T1 (pt)
AU (1) AU778218B2 (pt)
BG (1) BG65328B1 (pt)
BR (1) BR0012047A (pt)
CA (1) CA2376676C (pt)
DE (1) DE60008112T2 (pt)
DK (1) DK1196409T3 (pt)
EA (1) EA005027B1 (pt)
EE (1) EE04591B1 (pt)
ES (1) ES2215683T3 (pt)
HK (1) HK1045997A1 (pt)
HR (1) HRP20010935A2 (pt)
HU (1) HUP0201869A3 (pt)
IL (2) IL147327A0 (pt)
MX (1) MXPA02000120A (pt)
MY (1) MY127687A (pt)
NO (1) NO322458B1 (pt)
NZ (1) NZ515664A (pt)
PL (1) PL200674B1 (pt)
PT (1) PT1196409E (pt)
SI (1) SI1196409T1 (pt)
SK (1) SK19122001A3 (pt)
TR (1) TR200103806T2 (pt)
TW (1) TWI278454B (pt)
UA (1) UA74787C2 (pt)
WO (1) WO2001000612A2 (pt)
ZA (1) ZA200110479B (pt)

Families Citing this family (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6495580B1 (en) 1998-01-29 2002-12-17 Viropharma Incorporated Compounds, compositions and methods for treating or preventing pneumovirus infection and associated diseases
MXPA02000120A (es) 1999-06-28 2002-07-02 Janssen Pharmaceutica Nv Inhibidores de la replicacion del virus sincitial respiratorio.
EP1418175A1 (en) * 1999-06-28 2004-05-12 Janssen Pharmaceutica N.V. Respiratory syncytial virus replication inhibitors
US6506738B1 (en) 2000-09-27 2003-01-14 Bristol-Myers Squibb Company Benzimidazolone antiviral agents
US6774134B2 (en) 2000-12-20 2004-08-10 Bristol-Myers Squibb Company Heterocyclic substituted 2-methyl-benzimidazole antiviral agents
US7030150B2 (en) * 2001-05-11 2006-04-18 Trimeris, Inc. Benzimidazole compounds and antiviral uses thereof
US6919331B2 (en) 2001-12-10 2005-07-19 Bristol-Myers Squibb Company Substituted 2-methyl-benzimidazole respiratory syncytial virus antiviral agents
US8202896B2 (en) 2002-08-09 2012-06-19 Microdose Therapeutx, Inc. Compounds, compositions and methods for treating or preventing pneumovirus infection and associated diseases
EP1539691A2 (en) 2002-08-09 2005-06-15 Viropharma Incorporated Compounds, compositions and methods for treating or preventing pneumovirus infection and associated diseases
JP2006505570A (ja) * 2002-10-17 2006-02-16 アムジエン・インコーポレーテツド ベンズイミダゾール誘導体およびそれのバニロイド受容体リガンドとしての使用
WO2005042530A1 (en) 2003-10-30 2005-05-12 Boehringer Ingelheim (Canada) Ltd. Rsv polymerase inhibitors
AR046959A1 (es) * 2003-12-18 2006-01-04 Tibotec Pharm Ltd Morfolinilo que contiene bencimidazoles como inhibidores de la replicacion del virus sincitial respiratorio
ATE435222T1 (de) * 2003-12-18 2009-07-15 Tibotec Pharm Ltd Aminobenzimidazole und benzimidazole als inhibitoren der replikation von respiratory syncytial virus
AR046770A1 (es) * 2003-12-18 2005-12-21 Tibotec Pharm Ltd Derivados bencimidazol 5- o 6-substituidos como inhibidores de la replicacion del virus sincitial respiratorio
AR046972A1 (es) * 2003-12-18 2006-01-04 Tibotec Pharm Ltd Derivados de los amino-bencimidazoles como inhibidores de la replicacion del virus sincitial respiratorio
TWI349007B (en) 2003-12-18 2011-09-21 Tibotec Pharm Ltd Piperidine-amino-benzimidazole derivatives as inhibitors of respiratory syncytial virus replication
MXPA06007110A (es) 2003-12-18 2006-08-23 Tibotec Pharm Ltd Derivados de los amino-bencimidazoles como inhibidores de la replicacion del virus sincitial respiratorio.
DE102004010207A1 (de) * 2004-03-02 2005-09-15 Aventis Pharma S.A. Neue 4-Benzimidazol-2-yl-pyridazin-3-on-Derivate
RU2410382C2 (ru) 2005-03-17 2011-01-27 Тиботек Фармасьютикалз Лтд 1, 3-дигидробензимидазол-2-илиденовые амины в качестве ингибиторов репликации респираторного синцитиального вируса
AU2006260969B2 (en) 2005-06-20 2011-11-17 Janssen Sciences Ireland Uc 1- ( 2-amino-3- (substituted alkyl)-3H-benzimidazolylmethyl) -3-substituted-1,3-dihydro-benzoimidazol-2-ones with activity on respiratory syncytial virus
MX2007016311A (es) * 2005-06-20 2008-03-07 Tibotec Pharm Ltd Bencimidazoles sustituidos con heterociclilaminoalquilo.
PL1896450T3 (pl) * 2005-06-20 2013-01-31 Janssen Sciences Ireland Uc 2-podstawione benzimidazole
WO2011097607A1 (en) * 2010-02-08 2011-08-11 Southern Research Institute Anti-viral treatment and assay to screen for anti-viral agent
TWI515187B (zh) 2010-12-16 2016-01-01 健生科學愛爾蘭無限公司 作為呼吸道融合病毒抗病毒劑之吲哚類
TWI527814B (zh) * 2010-12-16 2016-04-01 健生科學愛爾蘭無限公司 作為呼吸道融合病毒抗病毒劑之氮雜苯并咪唑類
TWI530495B (zh) 2010-12-16 2016-04-21 健生科學愛爾蘭無限公司 苯并咪唑呼吸道融合病毒抑制劑
TWI541241B (zh) 2010-12-16 2016-07-11 健生科學愛爾蘭無限公司 作為呼吸道融合病毒抗病毒劑之咪唑并吡啶類
TWI501967B (zh) * 2010-12-16 2015-10-01 Janssen R&D Ireland 作為呼吸道融合病毒抗病毒劑之氮雜吲哚類
PL2797416T3 (pl) 2011-12-28 2017-12-29 Global Blood Therapeutics, Inc. Podstawione związki benzaldehydowe i sposoby ich zastosowania do zwiększania natlenienia tkanek
US9012450B2 (en) 2011-12-28 2015-04-21 Global Blood Therapeutics, Inc. Substituted heteroaryl aldehyde compounds and methods for their use in increasing tissue oxygenation
CA2873920C (en) 2012-06-15 2021-07-20 Janssen R&D Ireland 1,3-dihydro-2h-benzimidazol-2-one derivatives substituted with heterocycles as respiratory syncytial virus antiviral agents
US8952171B2 (en) 2013-03-15 2015-02-10 Global Blood Therapeutics, Inc. Compounds and uses thereof for the modulation of hemoglobin
WO2014145040A1 (en) 2013-03-15 2014-09-18 Global Blood Therapeutics, Inc. Substituted aldehyde compounds and methods for their use in increasing tissue oxygenation
US9422279B2 (en) 2013-03-15 2016-08-23 Global Blood Therapeutics, Inc. Compounds and uses thereof for the modulation of hemoglobin
EP2968299B1 (en) 2013-03-15 2021-01-20 Global Blood Therapeutics, Inc. Compounds and uses thereof for the modulation of hemoglobin
BR112015021982B1 (pt) 2013-03-15 2022-12-13 Global Blood Therapeutics, Inc Compostos e seus usos para a modulação de hemoglobina
US9604999B2 (en) 2013-03-15 2017-03-28 Global Blood Therapeutics, Inc. Compounds and uses thereof for the modulation of hemoglobin
US10266551B2 (en) 2013-03-15 2019-04-23 Global Blood Therapeutics, Inc. Compounds and uses thereof for the modulation of hemoglobin
US20140274961A1 (en) 2013-03-15 2014-09-18 Global Blood Therapeutics, Inc. Compounds and uses thereof for the modulation of hemoglobin
US9802900B2 (en) 2013-03-15 2017-10-31 Global Blood Therapeutics, Inc. Bicyclic heteroaryl compounds and uses thereof for the modulation of hemoglobin
US9458139B2 (en) 2013-03-15 2016-10-04 Global Blood Therapeutics, Inc. Compounds and uses thereof for the modulation of hemoglobin
JP6426694B2 (ja) 2013-03-15 2018-11-21 グローバル ブラッド セラピューティクス インコーポレイテッド ヘモグロビンの修飾のための化合物及びその使用
EA201992707A1 (ru) 2013-11-18 2020-06-30 Глобал Блад Терапьютикс, Инк. Соединения и их применения для модуляции гемоглобина
AP2016009261A0 (en) 2014-02-07 2016-06-30 Global Blood Therapeutics Inc Crystalline polymorphs of the free base of 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde
JP2016079168A (ja) * 2014-10-17 2016-05-16 塩野義製薬株式会社 9員縮合環誘導体
MA41841A (fr) 2015-03-30 2018-02-06 Global Blood Therapeutics Inc Composés aldéhyde pour le traitement de la fibrose pulmonaire, de l'hypoxie, et de maladies auto-immunes et des tissus conjonctifs
PL3383392T3 (pl) 2015-12-04 2025-11-17 Global Blood Therapeutics, Inc. Schematy dawkowania dla 2-hydroksy-6-((2-(1-izopropylo-1H-pirazol-5-ilo)pirydyn3-ylo)metoksy)benzaldehydu
TWI663160B (zh) 2016-05-12 2019-06-21 全球血液治療公司 用於合成2-羥基-6-((2-(1-異丙基-1h-吡唑-5-基)-吡啶-3-基)甲氧基)苯甲醛之方法
TW202332423A (zh) 2016-10-12 2023-08-16 美商全球血液治療公司 包含2-羥基-6-((2-(1-異丙基-1h-吡唑-5-基)吡啶-3-基)甲氧基)-苯甲醛之片劑
EP3860975B1 (en) 2018-10-01 2023-10-18 Global Blood Therapeutics, Inc. Modulators of hemoglobin for the treatment of sickle cell disease
JP2023528969A (ja) 2020-06-11 2023-07-06 ヤンセン・サイエンシズ・アイルランド・アンリミテッド・カンパニー 3-({5-クロロ-1-[3-(メチルスルホニル)プロピル]-1H-インドール-2 イル}メチル)-1-(2,2,2-トリフルオロエチル)-1,3-ジヒドロ-2H-イミダゾ[4,5-c]ピリジン-2-オンのヘミ(L)-酒石酸塩形態及びそれを含む医薬組成物

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1140119A (en) 1978-04-03 1983-01-25 Joseph Torremans N-heterocyclyl-4-piperidinamines
US4556660A (en) 1982-07-12 1985-12-03 Janssen Pharmaceutica N.V. N-(Bicyclic heterocyclyl)-4-piperidinamines
US4634704A (en) 1983-10-06 1987-01-06 Janssen Pharmaceutica, N.V. Anti-allergic five membered heterocyclic ring containing N-(bicyclic heterocycyl)-4-piperidinamines
EP0144101B1 (en) 1983-11-30 1991-02-06 Janssen Pharmaceutica N.V. Bicyclic heterocyclyl containing n-(bicyclic heterocyclyl)-4-piperidinamines
US4695569A (en) 1983-11-30 1987-09-22 Janssen Pharmaceutica N.V. Bicyclic heterocyclyl containing N-(bicyclic heterocyclyl)-4-piperidinamines
PH23995A (en) 1984-01-09 1990-02-09 Janssen Pharmaceutica Nv 4((bicycle heterocyclyl)-methyl and hetero)piperidines
US4588722A (en) 1984-01-09 1986-05-13 Janssen Pharmaceutica N.V. N-(4-piperidinyl) bicyclic condensed 2-imidazolamine derivatives
ES2052544T3 (es) 1986-02-03 1994-07-16 Janssen Pharmaceutica Nv Composiciones anti-histaminicas que contienen n-heterociclil-4-piperidinaminas.
NZ223654A (en) 1987-03-09 1990-03-27 Janssen Pharmaceutica Nv 1-alkyl-substituted-benzimidazole-4-piperidinamines and pharmaceutical compositions
US4897401A (en) 1987-06-19 1990-01-30 Janssen Pharmaceutical N.V. N-(4-piperidinyl) bicyclic condensed 2-imidazolamine derivatives useful in treating allergic diseases
CA1317939C (en) * 1987-07-01 1993-05-18 Janssen Pharmaceutica Naamloze Vennootschap ¬(bicyclic heterocyclyl)methyl and -hetero| substituted hexahydro-1h-azepines and pyrrolidines
GB8716313D0 (en) 1987-07-10 1987-08-19 Janssen Pharmaceutica Nv 2-(heterocyclylalkyl)imidazopyridines
US5360807A (en) * 1990-07-19 1994-11-01 Janssen Pharmaceutica N.V. Substituted thiazolyl and substituted pyridinyl derivatives
KR100190299B1 (ko) 1990-07-19 1999-06-01 디르크 반테 신규한 옥사졸릴 유도체
NZ238863A (en) 1990-07-19 1993-03-26 Janssen Pharmaceutica Nv Substituted thiazolyl and pyridinyl derivatives
US5693661A (en) 1995-06-07 1997-12-02 Eli Lilly And Company Anti-viral compounds
PE107598A1 (es) 1996-09-11 1999-01-29 Ucb Sa Cetirizina util para el tratamiento de enfermedades de tipo virico
WO1998031363A1 (en) 1997-01-22 1998-07-23 Eli Lilly And Company Anti-viral compounds
EP1001767A4 (en) 1997-06-04 2001-07-04 Lilly Co Eli ANTIVIRAL CONNECTIONS
MXPA02000120A (es) 1999-06-28 2002-07-02 Janssen Pharmaceutica Nv Inhibidores de la replicacion del virus sincitial respiratorio.

Also Published As

Publication number Publication date
MXPA02000120A (es) 2002-07-02
US20070015747A1 (en) 2007-01-18
HUP0201869A3 (en) 2003-12-29
EA005027B1 (ru) 2004-10-28
DE60008112D1 (en) 2004-03-11
MY127687A (en) 2006-12-29
PT1196409E (pt) 2004-06-30
US7528149B2 (en) 2009-05-05
UA74787C2 (en) 2006-02-15
HRP20010935A2 (en) 2003-06-30
CA2376676A1 (en) 2001-01-04
AU778218B2 (en) 2004-11-25
JP2003503402A (ja) 2003-01-28
US7179811B2 (en) 2007-02-20
DK1196409T3 (da) 2004-06-07
EP1196409B1 (en) 2004-02-04
AU5816600A (en) 2001-01-31
ZA200110479B (en) 2003-03-20
IL147327A (en) 2007-06-03
US6747028B1 (en) 2004-06-08
US20070135404A1 (en) 2007-06-14
HUP0201869A2 (hu) 2002-11-28
PL200674B1 (pl) 2009-01-30
KR20020003884A (ko) 2002-01-15
WO2001000612A2 (en) 2001-01-04
WO2001000612A3 (en) 2001-03-29
CN1358181A (zh) 2002-07-10
ES2215683T3 (es) 2004-10-16
NO322458B1 (no) 2006-10-09
BG65328B1 (bg) 2008-02-29
ATE258928T1 (de) 2004-02-15
SI1196409T1 (en) 2004-06-30
BG106286A (en) 2002-10-31
SK19122001A3 (sk) 2003-01-09
PL352378A1 (en) 2003-08-25
EE04591B1 (et) 2006-02-15
CN1210275C (zh) 2005-07-13
DE60008112T2 (de) 2004-09-16
EA200200088A1 (ru) 2002-06-27
TWI278454B (en) 2007-04-11
NZ515664A (en) 2004-01-30
EE200100688A (et) 2003-04-15
NO20016369L (no) 2002-02-20
CA2376676C (en) 2009-01-20
AR035991A1 (es) 2004-08-04
KR100731271B1 (ko) 2007-06-21
NO20016369D0 (no) 2001-12-27
HK1045997A1 (zh) 2002-12-20
TR200103806T2 (tr) 2002-06-21
IL147327A0 (en) 2002-08-14
EP1196409A2 (en) 2002-04-17

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