JPH11514361A5 - - Google Patents

Info

Publication number
JPH11514361A5
JPH11514361A5 JP1997515680A JP51568097A JPH11514361A5 JP H11514361 A5 JPH11514361 A5 JP H11514361A5 JP 1997515680 A JP1997515680 A JP 1997515680A JP 51568097 A JP51568097 A JP 51568097A JP H11514361 A5 JPH11514361 A5 JP H11514361A5
Authority
JP
Japan
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.)
Withdrawn
Application number
JP1997515680A
Other languages
English (en)
Japanese (ja)
Other versions
JPH11514361A (ja
Filing date
Publication date
Priority claimed from GBGB9521102.5A external-priority patent/GB9521102D0/en
Priority claimed from AUPO1811A external-priority patent/AUPO181196A0/en
Application filed filed Critical
Priority claimed from PCT/JP1996/002981 external-priority patent/WO1997014681A1/en
Publication of JPH11514361A publication Critical patent/JPH11514361A/ja
Publication of JPH11514361A5 publication Critical patent/JPH11514361A5/ja
Withdrawn legal-status Critical Current

Links

JP9515680A 1995-10-16 1996-10-15 H+−ATPaseとしての複素環式化合物 Withdrawn JPH11514361A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
AU1811 1985-08-06
GBGB9521102.5A GB9521102D0 (en) 1995-10-16 1995-10-16 New Heterocyclic compounds
AUPO1811A AUPO181196A0 (en) 1996-08-21 1996-08-21 New heterocyclic compounds
AU9521102.5 1996-08-21
PCT/JP1996/002981 WO1997014681A1 (en) 1995-10-16 1996-10-15 Heterocyclic compounds as h+-atpases

Publications (2)

Publication Number Publication Date
JPH11514361A JPH11514361A (ja) 1999-12-07
JPH11514361A5 true JPH11514361A5 (enExample) 2004-10-14

Family

ID=25645248

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9515680A Withdrawn JPH11514361A (ja) 1995-10-16 1996-10-15 H+−ATPaseとしての複素環式化合物

Country Status (6)

Country Link
US (1) US6008230A (enExample)
EP (1) EP0876345B1 (enExample)
JP (1) JPH11514361A (enExample)
AT (1) ATE273958T1 (enExample)
DE (1) DE69633196D1 (enExample)
WO (1) WO1997014681A1 (enExample)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA73073C2 (uk) * 1997-04-03 2005-06-15 Уайт Холдінгз Корпорейшн Заміщені 3-ціанохіноліни, спосіб їх одержання та фармацевтична композиція
US6002008A (en) * 1997-04-03 1999-12-14 American Cyanamid Company Substituted 3-cyano quinolines
AUPP003197A0 (en) * 1997-09-03 1997-11-20 Fujisawa Pharmaceutical Co., Ltd. New heterocyclic compounds
HUP0101275A3 (en) 1998-03-26 2002-12-28 Japan Tobacco Inc Amide derivatives and pharmaceutical compositions containing them as nociceptin antagonists
US7045519B2 (en) 1998-06-19 2006-05-16 Chiron Corporation Inhibitors of glycogen synthase kinase 3
GB9822440D0 (en) 1998-10-14 1998-12-09 Smithkline Beecham Plc Medicaments
AU5250400A (en) * 1999-06-18 2001-01-09 Mitsubishi Pharma Corporation Osteogenesis promoters
AU6865100A (en) * 1999-09-02 2001-04-10 Mitsubishi Pharma Corporation Osteogenesis promoting agents
SE9903611D0 (sv) * 1999-10-06 1999-10-06 Astra Ab Novel compounds III
DE60143041D1 (de) 2000-08-10 2010-10-21 Pfizer Italia Srl Bizyklische pyrazole wirksam als kinase inhibitoren, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische zubereitungen
DE10060145C1 (de) * 2000-12-04 2002-06-13 Michael Wackernagel Chinolin-Derivate, ihre Verwendung und diese enthaltende pharmazeutische Zusammensetzung
CA2430951A1 (en) * 2000-12-07 2002-06-13 Cv Therapeutics, Inc. Substituted 1, 3, 5-triazines and pyrimidines as abca-1 elevating compounds against coronary artery disease or atherosclerosis
AR038658A1 (es) * 2001-06-15 2005-01-26 Novartis Ag Derivados de 4-aril-2(1h) quinazolinona y 4-aril-quinazolina 2-sustituidas, un proceso para su preparacion, composiciones farmaceuticas y el uso de dichos derivados para la preparacion de un medicamento
GB0130341D0 (en) * 2001-12-19 2002-02-06 Smithkline Beecham Plc Compounds
GB0230015D0 (en) * 2002-12-23 2003-01-29 Novartis Ag Organic compounds
UA80607C2 (en) * 2003-04-09 2007-10-10 White Holdings Corp Process for the preparation of 3-cyano-6-alkoxy-7-nitro-4-quinolines
DE10331675A1 (de) * 2003-07-14 2005-02-10 Bayer Cropscience Ag Hetarylsubstituierte Pyrazolidindion-Derivate
JP4667384B2 (ja) 2003-10-07 2011-04-13 レノビス, インコーポレイテッド イオンチャネルリガンドとしてのアミド誘導体および薬学的組成物、ならびにこれらを使用する方法
SI1746999T1 (sl) * 2004-05-06 2012-01-31 Warner Lambert Co 4-fenilamino-kinazolin-6-il-amidi
WO2005108404A1 (ja) * 2004-05-12 2005-11-17 Ube Industries, Ltd. エチニル基置換縮合ヘテロ環化合物重金属錯体、その製造法、その合成中間体及びその製造法並びに有機エレクトロルミネッセンス素子
FR2874922A1 (fr) * 2004-07-30 2006-03-10 Palumed Sa Molecules hybrides qa ou q est une aminoquinoleine et a est un residu antibiotique, leur synthese et leurs utilisations en tant qu'agent antibacterien
WO2006024741A2 (fr) * 2004-07-30 2006-03-09 Palumed S.A. Molecules hybrides qa ou q est une aminoquinoleine et a est un residu antibiotique, leur synthese et leurs utilisations en tant qu'agent antibacterien
FR2873695A1 (fr) * 2004-07-30 2006-02-03 Palumed Sa Molecules hybrides qa ou q est une aminoquinoleine et a est un antibiotique ou un inhibiteur de resistance), leur synthese et leurs utilisations en tant qu'agent antibacterien
WO2006040645A1 (en) * 2004-10-11 2006-04-20 Ranbaxy Laboratories Limited N-(3,5-dichloropyridin-4-yl)-2,4,5-alkoxy and 2,3,4-alkoxy benzamide derivatives as pde-iv (phophodiesterase type-iv) inhibitors for the treatment of inflammatory diseases such as asthma
US7875627B2 (en) * 2004-12-07 2011-01-25 Abbott Laboratories Thienopyridyl compounds that inhibit vanilloid receptor subtype 1 (VR1) and uses thereof
US7576099B2 (en) 2005-02-28 2009-08-18 Renovis, Inc. Amide derivatives as ion-channel ligands and pharmaceutical compositions and methods of using the same
CA2599688A1 (en) 2005-03-01 2006-09-08 Wyeth Cinnoline compounds and their use as liver x receptor modulators
DE602006016564D1 (de) * 2005-03-03 2010-10-14 Santen Pharmaceutical Co Ltd Neue cyclische verbindung mit chinolylalkylthiogruppe
EP1991540A1 (en) * 2006-02-21 2008-11-19 Amgen Inc. Cinnoline derivatives as phosphodiesterase 10 inhibitors
US20090099175A1 (en) * 2006-03-01 2009-04-16 Arrington Mark P Phosphodiesterase 10 inhibitors
AU2007223801A1 (en) * 2006-03-08 2007-09-13 Amgen Inc. Quinoline and isoquinoline derivatives as phosphodiesterase 10 inhibitors
CA2685888A1 (en) * 2007-05-09 2008-11-20 Pfizer Inc. Substituted heterocyclic derivatives and their pharmaceutical use and compositions
US20110038852A1 (en) * 2009-06-10 2011-02-17 3-V Biosciences, Inc. Antivirals that target transporters, carriers, and ion channels
CN103539734B (zh) * 2013-09-25 2015-10-14 上海交通大学 3-烯丙基喹啉的制备方法
WO2016032569A1 (en) * 2014-08-29 2016-03-03 Celladon Corporation Quinolines and their use for treating endoplasmic reticulum stress-caused diseases
US20200347038A1 (en) 2014-08-29 2020-11-05 Russell Dahl Quinolines that modulate serca and their use for treating disease
US9932310B2 (en) * 2016-02-08 2018-04-03 City Of Hope DNA2 inhibitors for cancer treatment
US11730729B2 (en) 2020-07-20 2023-08-22 Neurodon Corporation Quinolines that modulate SERCA and their use for treating disease
US12486269B2 (en) 2024-02-08 2025-12-02 Aconcagua Bio, Inc. Compounds and compositions for treating conditions associated with calcitonin receptor and/or amylin receptor activity
WO2025171341A2 (en) * 2024-02-08 2025-08-14 Aconcagua Bio, Inc. Compounds and compositions for treating conditions associated with calcitonin receptor and/or amylin receptor activity

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1458332A (fr) * 1965-08-18 1966-03-04 Kuhlmann Ets Procédé de modification des fibres de polyamides
CH508226A (de) * 1969-03-13 1971-05-31 Ciba Geigy Ag Verwendung von Chinoxalinen als Farbbleichkatalysatoren
US4147694A (en) * 1977-02-07 1979-04-03 Riker Laboratories, Inc. 8-(1H-Tetrazol-5-yl-carbamoyl)quinoline compounds
DE3108873A1 (de) * 1981-03-09 1982-09-16 Basf Ag, 6700 Ludwigshafen Dichlorchinolinderivate, ihre herstellung, ihre verwendung als herbizide und mittel dafuer
DE3233089A1 (de) * 1982-09-07 1984-03-08 Basf Ag, 6700 Ludwigshafen Chinolinderivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
EP0224823A3 (de) * 1985-11-26 1988-02-10 BASF Aktiengesellschaft Chinolinderivate und ihre Verwendung zur Bekämpfung von unerwümschtem Pflanzenwachstum
GB8928281D0 (en) * 1989-12-14 1990-02-21 Smith Kline French Lab Compounds
US5574042A (en) * 1992-11-02 1996-11-12 Fujisawa Pharmaceutical Co., Ltd Imidazo [1,2-a] pyridines and their pharmaceutical use
FR2703995B1 (fr) * 1993-04-16 1995-07-21 Sanofi Elf 5-acylamino 1,2,4-thiadiazoles, leur preparation et compositions pharmaceutiques en contenant.
AU680870B2 (en) * 1993-04-28 1997-08-14 Astellas Pharma Inc. New heterocyclic compounds
US5500423A (en) * 1994-09-09 1996-03-19 Hoechst-Roussel Pharmaceuticals Inc. 5,6-dihydro-4H-imidazo[4,5,1-ij]quinolines
JPH08143525A (ja) * 1994-11-21 1996-06-04 Banyu Pharmaceut Co Ltd ヒドロキシ安息香酸アミド誘導体を有効成分とする骨疾患の予防・治療剤
EP0952832B1 (en) * 1996-05-20 2008-08-27 Darwin Discovery Limited Quinoline carboxamides as tnf inhibitors and as pde-iv inhibitors

Similar Documents

Publication Publication Date Title
JP2000500228A5 (enExample)
JP2000500445A5 (enExample)
JPH11511357A5 (enExample)
JP2000500440A5 (enExample)
JP2000500327A5 (enExample)
JP2000500145A5 (enExample)
JP2000500155A5 (enExample)
JP2000500406A5 (enExample)
JP2000500115A5 (enExample)
JPH11506695A5 (enExample)
JP2000500322A5 (enExample)
JP2000500258A5 (enExample)
JP2000500342A5 (enExample)
JP2000500192A5 (enExample)
JP2000500112A5 (enExample)
JPH11514361A5 (enExample)
JP2000500226A5 (enExample)
JP2001500167A5 (enExample)
JP2000500051A5 (enExample)
JP2000500407A5 (enExample)
JP2000500166A5 (enExample)
JP2000501233A5 (enExample)
JP2000500125A5 (enExample)
JP2000500346A5 (enExample)
JP2000500090A5 (enExample)