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
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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 (https=) 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 (https=)
EP (1) EP1644372A2 (https=)
JP (2) JP2007535478A (https=)
CN (1) CN1820008A (https=)
AU (1) AU2004257296A1 (https=)
CA (1) CA2531535A1 (https=)
TW (1) TW200510373A (https=)
WO (1) WO2005007652A2 (https=)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1569925A1 (en) * 2002-12-13 2005-09-07 Neurogen Corporation 2-substituted quinazolin-4-ylamine analogues as capsaicin receptor modulators
CA2509616A1 (en) * 2002-12-13 2004-07-01 Neurogen Corporation Combination therapy for the treatment of pain
TW200510373A (en) * 2003-07-14 2005-03-16 Neurogen Corp Substituted quinolin-4-ylamine analogues
US20070105865A1 (en) * 2003-09-09 2007-05-10 Neurogen Corporation Substituted bicyclic quinazolin-4-ylamine derivatives
CN1950081A (zh) * 2004-03-04 2007-04-18 神经能质公司 芳烷氨基取代的喹唑啉类似物
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
JP2009511465A (ja) 2005-10-07 2009-03-19 グレンマーク・ファーマシューティカルズ・エスエー 置換ベンゾ縮合誘導体およびバニロイド受容体リガンドとしてのその使用
EP1979349B1 (en) 2005-12-21 2010-07-28 Abbott Laboratories Anti-viral compounds
WO2007081517A2 (en) 2005-12-21 2007-07-19 Abbott Laboratories Anti-viral compounds
US7910595B2 (en) 2005-12-21 2011-03-22 Abbott Laboratories Anti-viral compounds
EP2591675A1 (en) 2006-11-27 2013-05-15 H. Lundbeck A/S Heteroaryl amide derivatives
US8236950B2 (en) 2006-12-20 2012-08-07 Abbott Laboratories Anti-viral compounds
SG157299A1 (en) 2008-05-09 2009-12-29 Agency Science Tech & Res Diagnosis and treatment of kawasaki disease
US8703962B2 (en) * 2008-10-24 2014-04-22 Purdue Pharma L.P. Monocyclic compounds and their use as TRPV1 ligands
US8759362B2 (en) * 2008-10-24 2014-06-24 Purdue Pharma L.P. Bicycloheteroaryl compounds and their use as TRPV1 ligands
US8546388B2 (en) * 2008-10-24 2013-10-01 Purdue Pharma L.P. Heterocyclic TRPV1 receptor ligands
CA2773713A1 (en) * 2009-10-07 2011-04-14 Merck Sharp & Dohme Corp. Novel trpa1 antagonists
ES2542647T3 (es) 2011-03-09 2015-08-07 Merck Patent Gmbh Derivados de pirido[2,3 b]pirazina y sus usos terapéuticos
CN106905297A (zh) * 2012-06-15 2017-06-30 加利福尼亚大学董事会 用于脑癌的新颖治疗剂
PL3089971T3 (pl) 2014-01-01 2021-01-25 Medivation Technologies Llc Związki i sposoby ich zastosowania
US10227333B2 (en) 2015-02-11 2019-03-12 Curtana Pharmaceuticals, Inc. Inhibition of OLIG2 activity
MX394452B (es) 2015-02-27 2025-03-21 Curtana Pharmaceuticals Inc Inhibicion de la actividad de olig2.
WO2017031427A1 (en) * 2015-08-19 2017-02-23 3-V Biosciences, Inc. COMPOUNDS AND METHODS FOR INHIBITING mTOR
EP3929185A4 (en) * 2019-02-19 2023-02-15 Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. NITROGEN CONDENSED CYCLIC COMPOUND, METHOD OF PRODUCTION THEREOF AND USE THEREOF
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
HRP970371A2 (en) 1996-07-13 1998-08-31 Kathryn Jane Smith Heterocyclic compounds
EA199900021A1 (ru) 1996-07-13 1999-08-26 Глаксо, Груп Лимитед Бициклические гетероароматические соединения в качестве ингибиторов протеинтирозинкиназы
AR007857A1 (es) 1996-07-13 1999-11-24 Glaxo Group Ltd Compuestos heterociclicos fusionados como inhibidores de proteina tirosina quinasa, sus metodos de preparacion, intermediarios uso en medicina ycomposiciones farmaceuticas que los contienen.
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.
RS49779B (sr) 1998-01-12 2008-06-05 Glaxo Group Limited, Biciklična heteroaromatična jedinjenja kao inhibitori protein tirozin kinaze
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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
EP1301484A2 (en) 2000-07-20 2003-04-16 Neurogen Corporation Capsaicin receptor ligands
WO2002022605A1 (en) 2000-09-15 2002-03-21 Vertex Pharmaceuticals Incorporated Pyrazole compounds useful as protein kinase inhibitors
WO2003014064A1 (en) * 2001-07-31 2003-02-20 Bayer Healthcare Ag Naphthylurea and naphthylacetamide derivatives as vanilloid receptor 1 (vr1) antagonists
HUP0500200A2 (hu) * 2002-01-17 2005-07-28 Neurogen Corporation Szubsztituált kinazolin-4-ilamin analógok, mint kapszaicin modulátorok és ezeket tartalmazó gyógyszerkészítmények
US7718651B2 (en) * 2002-07-02 2010-05-18 Southern Research Institute Inhibitors of FtsZ and uses thereof
CA2509616A1 (en) * 2002-12-13 2004-07-01 Neurogen Corporation Combination therapy for the treatment of pain
EP1569925A1 (en) 2002-12-13 2005-09-07 Neurogen Corporation 2-substituted quinazolin-4-ylamine analogues as capsaicin receptor modulators
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
CN101232885A (zh) * 2005-01-25 2008-07-30 神经能质公司 经取代的哒嗪基喹啉-4-基胺和嘧啶基喹啉-4-基胺类似物

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