JP2007535478A5 - - Google Patents

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Publication number
JP2007535478A5
JP2007535478A5 JP2006520420A JP2006520420A JP2007535478A5 JP 2007535478 A5 JP2007535478 A5 JP 2007535478A5 JP 2006520420 A JP2006520420 A JP 2006520420A JP 2006520420 A JP2006520420 A JP 2006520420A JP 2007535478 A5 JP2007535478 A5 JP 2007535478A5
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JP
Japan
Prior art keywords
substituted
formula
group
independently selected
alkyl
Prior art date
Legal status (The legal status 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 status listed.)
Abandoned
Application number
JP2006520420A
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English (en)
Japanese (ja)
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JP2007535478A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2004/023776 external-priority patent/WO2005007652A2/en
Publication of JP2007535478A publication Critical patent/JP2007535478A/ja
Publication of JP2007535478A5 publication Critical patent/JP2007535478A5/ja
Abandoned legal-status Critical Current

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JP2006520420A 2003-07-14 2004-07-14 置換キノリン−4−イルアミン類縁体 Abandoned JP2007535478A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US48694803P 2003-07-14 2003-07-14
PCT/US2004/023776 WO2005007652A2 (en) 2003-07-14 2004-07-14 Substituted quinolin-4-ylamine analogues

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2011032423A Division JP2011137018A (ja) 2003-07-14 2011-02-17 置換キノリン−4−イルアミン類縁体

Publications (2)

Publication Number Publication Date
JP2007535478A JP2007535478A (ja) 2007-12-06
JP2007535478A5 true JP2007535478A5 (enExample) 2011-04-07

Family

ID=34079320

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2006520420A Abandoned JP2007535478A (ja) 2003-07-14 2004-07-14 置換キノリン−4−イルアミン類縁体
JP2011032423A Pending JP2011137018A (ja) 2003-07-14 2011-02-17 置換キノリン−4−イルアミン類縁体

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2011032423A Pending JP2011137018A (ja) 2003-07-14 2011-02-17 置換キノリン−4−イルアミン類縁体

Country Status (8)

Country Link
US (2) US7488740B2 (enExample)
EP (1) EP1644372A2 (enExample)
JP (2) JP2007535478A (enExample)
CN (1) CN1820008A (enExample)
AU (1) AU2004257296A1 (enExample)
CA (1) CA2531535A1 (enExample)
TW (1) TW200510373A (enExample)
WO (1) WO2005007652A2 (enExample)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR042461A1 (es) * 2002-12-13 2005-06-22 Neurogen Corp Analogos 2-sustituidos de quinazolin-4-il - amina. composiciones farmaceuticas
US20040142958A1 (en) * 2002-12-13 2004-07-22 Neurogen Corporation Combination therapy for the treatment of pain
TW200510373A (en) * 2003-07-14 2005-03-16 Neurogen Corp Substituted quinolin-4-ylamine analogues
AU2004270740A1 (en) * 2003-09-09 2005-03-17 Neurogen Corporation 4 - heterobicyclyamino - substituted quinazolines and analogues therof as capsaicin - antagonists
JP2007526323A (ja) * 2004-03-04 2007-09-13 ニューロジェン・コーポレーション アリールアルキルアミノ置換キナゾリン類縁体
EP1732560A4 (en) * 2004-04-08 2010-08-18 Neurogen Corp SUBSTITUTED CINNOLINE-4-YLAMINE
TW200621251A (en) * 2004-10-12 2006-07-01 Neurogen Corp Substituted biaryl quinolin-4-ylamine analogues
AP2008004432A0 (en) 2005-10-07 2008-04-30 Glenmark Pharmaceuticals Sa Substituted benzofused derivatives and their use as vanilloid receptor ligands
RU2441869C2 (ru) 2005-12-21 2012-02-10 Эбботт Лэборетриз Противовирусные соединения
RU2467007C2 (ru) 2005-12-21 2012-11-20 Эбботт Лэборетриз Производные [1,8]нафтиридина, полезные в качестве ингибиторов репликации вируса hcv
ES2395386T3 (es) 2005-12-21 2013-02-12 Abbott Laboratories Compuestos antivirales
EP2096923B1 (en) 2006-11-27 2014-01-22 H. Lundbeck A/S Heteroaryl amide derivatives
CA2672737A1 (en) 2006-12-20 2008-11-06 Abbott Laboratories Anti-viral compounds
JP2010043063A (ja) 2008-05-09 2010-02-25 Agency For Science Technology & Research 川崎病の診断及び治療
US8759362B2 (en) * 2008-10-24 2014-06-24 Purdue Pharma L.P. Bicycloheteroaryl compounds and their use as TRPV1 ligands
US8703962B2 (en) * 2008-10-24 2014-04-22 Purdue Pharma L.P. Monocyclic compounds and their use as TRPV1 ligands
US8546388B2 (en) * 2008-10-24 2013-10-01 Purdue Pharma L.P. Heterocyclic TRPV1 receptor ligands
AU2010303822A1 (en) * 2009-10-07 2012-03-15 Merck Sharp & Dohme Corp. Novel TRPA1 antagonists
JP6104824B2 (ja) 2011-03-09 2017-03-29 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung ピリド[2,3−b]ピラジン誘導体およびそれらの治療的使用
JP2015521603A (ja) * 2012-06-15 2015-07-30 ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニアThe Regents Of The University Of California 脳癌の新規治療薬
HUE050761T2 (hu) 2014-01-01 2021-01-28 Medivation Tech Llc Vegyületek és alkalmazási eljárások
US10227333B2 (en) 2015-02-11 2019-03-12 Curtana Pharmaceuticals, Inc. Inhibition of OLIG2 activity
WO2016138479A1 (en) 2015-02-27 2016-09-01 Curtana Pharmaceuticals, Inc. Inhibition of olig2 activity
WO2017031427A1 (en) * 2015-08-19 2017-02-23 3-V Biosciences, Inc. COMPOUNDS AND METHODS FOR INHIBITING mTOR
WO2020168927A1 (zh) * 2019-02-19 2020-08-27 四川科伦博泰生物医药股份有限公司 含氮并环化合物、其制备方法及用途
DE102022104759A1 (de) 2022-02-28 2023-08-31 SCi Kontor GmbH Co-Kristall-Screening Verfahren, insbesondere zur Herstellung von Co-Kristallen

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Publication number Priority date Publication date Assignee Title
GB8928281D0 (en) 1989-12-14 1990-02-21 Smith Kline French Lab Compounds
GB9510757D0 (en) 1994-09-19 1995-07-19 Wellcome Found Therapeuticaly active compounds
AR004010A1 (es) 1995-10-11 1998-09-30 Glaxo Group Ltd Compuestos heterociclicos
GB9603097D0 (en) 1996-02-14 1996-04-10 Zeneca Ltd Quinazoline compounds
JP4386967B2 (ja) 1996-07-13 2009-12-16 グラクソ、グループ、リミテッド プロテインチロシンキナーゼ阻害剤としての縮合複素環式化合物
HRP970371A2 (en) 1996-07-13 1998-08-31 Kathryn Jane Smith Heterocyclic compounds
ES2191187T3 (es) 1996-07-13 2003-09-01 Glaxo Group Ltd Compuestos heteroaromaticos biciclicos como inhibidores de la proteina tirosin-quinasa.
US5863016A (en) 1997-02-28 1999-01-26 The Wiremold Company Modular faceplate assembly having concealed latching means
MA26473A1 (fr) * 1997-03-01 2004-12-20 Glaxo Group Ltd Composes pharmacologiquement actifs.
GB9800569D0 (en) 1998-01-12 1998-03-11 Glaxo Group Ltd Heterocyclic compounds
BRPI9914164B8 (pt) * 1998-09-29 2021-05-25 American Cyanamid Co compostos de 3-ciano quinolina
GB2345486A (en) * 1999-01-11 2000-07-12 Glaxo Group Ltd Heteroaromatic protein tyrosine kinase inhibitors
US6521618B2 (en) 2000-03-28 2003-02-18 Wyeth 3-cyanoquinolines, 3-cyano-1,6-naphthyridines, and 3-cyano-1,7-naphthyridines as protein kinase inhibitors
AU8066701A (en) 2000-07-20 2002-02-05 Neurogen Corp Capsaicin receptor ligands
DK1318997T3 (da) 2000-09-15 2006-09-25 Vertex Pharma Pyrazolforbindelser der er nyttige som proteinkinase-inhibitorer
WO2003014064A1 (en) * 2001-07-31 2003-02-20 Bayer Healthcare Ag Naphthylurea and naphthylacetamide derivatives as vanilloid receptor 1 (vr1) antagonists
RS63204A (sr) 2002-01-17 2006-10-27 Neurogen Corporation Supstituisani analozi hinazolin-4-ilamina kao modulatori kapsaicina
WO2004005472A2 (en) * 2002-07-02 2004-01-15 Southern Research Institute Inhibitors of ftsz and uses thereof
US20040142958A1 (en) * 2002-12-13 2004-07-22 Neurogen Corporation Combination therapy for the treatment of pain
AR042461A1 (es) * 2002-12-13 2005-06-22 Neurogen Corp Analogos 2-sustituidos de quinazolin-4-il - amina. composiciones farmaceuticas
TW200510373A (en) * 2003-07-14 2005-03-16 Neurogen Corp Substituted quinolin-4-ylamine analogues
TW200621251A (en) 2004-10-12 2006-07-01 Neurogen Corp Substituted biaryl quinolin-4-ylamine analogues
CA2594998A1 (en) * 2005-01-25 2006-08-03 Neurogen Corporation Substituted pyridazinyl-and pyrimidinyl-quinolin-4-ylamine analogues

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