JPH0625181A - 縮合5員複素環式化合物、それらの調製法およびこれらの化合物を含む製薬製剤 - Google Patents

縮合5員複素環式化合物、それらの調製法およびこれらの化合物を含む製薬製剤

Info

Publication number
JPH0625181A
JPH0625181A JP4237334A JP23733492A JPH0625181A JP H0625181 A JPH0625181 A JP H0625181A JP 4237334 A JP4237334 A JP 4237334A JP 23733492 A JP23733492 A JP 23733492A JP H0625181 A JPH0625181 A JP H0625181A
Authority
JP
Japan
Prior art keywords
group
phenyl
ethyl
atom
amidino
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.)
Pending
Application number
JP4237334A
Other languages
English (en)
Japanese (ja)
Inventor
Volkhard Austel
アウシュテル フォルクハルト
Helmut Pieper
ピーペル ヘルムート
Frank Himmelsbach
ヒンメルスバッハ フランク
Guenter Linz
リンツ ギュンター
Thomas Dr Mueller
ミューラー トーマス
Johannes Weisenberger
ヴァイゼンベルガー ヨハネス
Elke Seewaldt-Becker
ゼーワルト ベッカー エルク
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Boehringer Ingelheim Pharma GmbH and Co KG
Original Assignee
Dr Karl Thomae GmbH
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 Dr Karl Thomae GmbH filed Critical Dr Karl Thomae GmbH
Publication of JPH0625181A publication Critical patent/JPH0625181A/ja
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/12Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/06Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • C07D235/14Radicals substituted by nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/18Benzimidazoles; Hydrogenated benzimidazoles with aryl radicals directly attached in position 2
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6503Five-membered rings
    • C07F9/6506Five-membered rings having the nitrogen atoms in positions 1 and 3
    • C07F9/65068Five-membered rings having the nitrogen atoms in positions 1 and 3 condensed with carbocyclic rings or carbocyclic ring systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Molecular Biology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biochemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Plural Heterocyclic Compounds (AREA)
JP4237334A 1991-09-06 1992-09-04 縮合5員複素環式化合物、それらの調製法およびこれらの化合物を含む製薬製剤 Pending JPH0625181A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4129603A DE4129603A1 (de) 1991-09-06 1991-09-06 Kondensierte 5-gliedrige heterocyclen, verfahren zu ihrer herstellung und diese verbindungen enthaltende arzneimittel
DE4129603:6 1991-09-06

Publications (1)

Publication Number Publication Date
JPH0625181A true JPH0625181A (ja) 1994-02-01

Family

ID=6439971

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4237334A Pending JPH0625181A (ja) 1991-09-06 1992-09-04 縮合5員複素環式化合物、それらの調製法およびこれらの化合物を含む製薬製剤

Country Status (17)

Country Link
US (1) US5434150A (cg-RX-API-DMAC7.html)
EP (1) EP0531883A1 (cg-RX-API-DMAC7.html)
JP (1) JPH0625181A (cg-RX-API-DMAC7.html)
KR (1) KR930005983A (cg-RX-API-DMAC7.html)
AU (1) AU657350B2 (cg-RX-API-DMAC7.html)
CA (1) CA2077577A1 (cg-RX-API-DMAC7.html)
DE (1) DE4129603A1 (cg-RX-API-DMAC7.html)
FI (1) FI923960A7 (cg-RX-API-DMAC7.html)
HU (1) HUT61984A (cg-RX-API-DMAC7.html)
IL (1) IL103053A (cg-RX-API-DMAC7.html)
MX (1) MX9205064A (cg-RX-API-DMAC7.html)
NO (1) NO923466L (cg-RX-API-DMAC7.html)
NZ (1) NZ244211A (cg-RX-API-DMAC7.html)
PL (1) PL295818A1 (cg-RX-API-DMAC7.html)
RU (1) RU2041211C1 (cg-RX-API-DMAC7.html)
TW (1) TW221436B (cg-RX-API-DMAC7.html)
ZA (1) ZA926700B (cg-RX-API-DMAC7.html)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002522432A (ja) * 1998-08-01 2002-07-23 ベーリンガー インゲルハイム ファルマ コマンディトゲゼルシャフト 二置換二環式複素環化合物、それらの調製及び医薬組成物としてのそれらの使用
JP2003513959A (ja) * 1999-11-10 2003-04-15 ベーリンガー インゲルハイム ファルマ コマンディトゲゼルシャフト カルボキサミド置換ベンゾイミダゾール誘導体、それらの調製方法及び医薬組成物としてのそれらの使用
JP2003523961A (ja) * 2000-01-14 2003-08-12 シエーリング アクチエンゲゼルシャフト 小グリア細胞活性化に関連する疾病の処理のための1,2−ジアリールベンズイミダゾール
JP2004502761A (ja) * 2000-07-06 2004-01-29 ベーリンガー インゲルハイム (カナダ) リミテッド ウイルスポリメラーゼ阻害剤
JP2007502822A (ja) * 2003-08-21 2007-02-15 オーエスアイ・ファーマスーティカルズ・インコーポレーテッド c−Kit阻害剤としてのN3−置換イミダゾピリジン誘導体
JP2007217427A (ja) * 2000-09-01 2007-08-30 Chiron Corp アザ複素環式誘導体およびその治療的使用
JP2009507779A (ja) * 2005-08-15 2009-02-26 シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト 新規な殺虫剤
WO2011074658A1 (ja) * 2009-12-18 2011-06-23 田辺三菱製薬株式会社 新規抗血小板薬
JP2013018771A (ja) * 2011-06-17 2013-01-31 Mitsubishi Tanabe Pharma Corp 新規抗血小板薬

Families Citing this family (83)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6087380A (en) * 1949-11-24 2000-07-11 Boehringer Ingelheim Pharma Kg Disubstituted bicyclic heterocycles, the preparations and the use thereof as pharmaceutical compositions
DK0567967T3 (da) * 1992-04-28 1996-11-18 Thomae Gmbh Dr K Tritium-mærkede fibrinogen-receptor-antagonister, deres anvendelse og fremgangsmåde til deres fremstilling
DE4304650A1 (de) * 1993-02-16 1994-08-18 Thomae Gmbh Dr K Kondensierte 5-gliedrige Heterocyclen, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel
GB9312853D0 (en) 1993-06-22 1993-08-04 Euro Celtique Sa Chemical compounds
US5731324A (en) * 1993-07-22 1998-03-24 Eli Lilly And Company Glycoprotein IIb/IIIa antagonists
US6137002A (en) * 1993-07-22 2000-10-24 Eli Lilly And Company Glycoprotein IIb/IIIa antagonists
US6448269B1 (en) 1993-07-22 2002-09-10 Eli Lilly And Company Glycoprotein IIb/IIIa antagonists
DE4330959A1 (de) * 1993-09-09 1995-03-16 Schering Ag Neue Benzimidazolderivate, Verfahren zu ihrer Herstellung und ihre pharmazeutische Verwendung
DE4405378A1 (de) * 1994-02-19 1995-08-24 Merck Patent Gmbh Adhäsionsrezeptor-Antagonisten
US5591776A (en) * 1994-06-24 1997-01-07 Euro-Celtique, S.A. Pheynl or benzyl-substituted rolipram-based compounds for and method of inhibiting phosphodiesterase IV
US5922751A (en) * 1994-06-24 1999-07-13 Euro-Celtique, S.A. Aryl pyrazole compound for inhibiting phosphodiesterase IV and methods of using same
US6025361A (en) * 1994-12-13 2000-02-15 Euro-Celtique, S.A. Trisubstituted thioxanthines
DE69531506T2 (de) * 1994-12-13 2004-06-24 Euroceltique S.A. Arylthioxanthine
CA2206804C (en) * 1994-12-13 2002-03-19 Euro-Celtique, S.A. Trisubstituted thioxanthines
US6166041A (en) 1995-10-11 2000-12-26 Euro-Celtique, S.A. 2-heteroaryl and 2-heterocyclic benzoxazoles as PDE IV inhibitors for the treatment of asthma
EP0862457A1 (en) * 1995-10-25 1998-09-09 Janssen Pharmaceutica N.V. Infusions of neuroprotectants and thrombolytic agents
US6075016A (en) 1996-04-10 2000-06-13 Euro-Celtique S.A. 6,5-fused aromatic ring systems having enhanced phosphodiesterase IV inhibitory activity
US5864037A (en) 1996-06-06 1999-01-26 Euro-Celtique, S.A. Methods for the synthesis of chemical compounds having PDE-IV inhibitory activity
EP0927167A1 (en) 1996-08-14 1999-07-07 Warner-Lambert Company 2-phenyl benzimidazole derivatives as mcp-1 antagonists
US6630496B1 (en) 1996-08-26 2003-10-07 Genetics Institute Llc Inhibitors of phospholipase enzymes
US5786360A (en) 1996-11-19 1998-07-28 Link Technology Incorporated A1 adenosine receptor antagonists
DE19653646A1 (de) * 1996-12-20 1998-06-25 Hoechst Ag Substituierte Purinderivate, Verfahren zu deren Herstellung, sie enthaltende Mittel und deren Verwendung
DE19653647A1 (de) 1996-12-20 1998-06-25 Hoechst Ag Vitronectin - Rezeptorantagonisten, deren Herstellung sowie deren Verwendung
US6218387B1 (en) 1996-12-20 2001-04-17 Hoechst Aktiengesellschaft Vitronectin receptor anatagonists, their preparation and their use
US6482821B2 (en) 1996-12-20 2002-11-19 Hoechst Aktiengellschaft Vitronectin receptor antagonists, their preparation and their use
DE19653645A1 (de) * 1996-12-20 1998-06-25 Hoechst Ag Vitronectin - Rezeptorantagonisten, deren Herstellung sowie deren Verwendung
PE121699A1 (es) * 1997-02-18 1999-12-08 Boehringer Ingelheim Pharma Heterociclos biciclicos disustituidos como inhibidores de la trombina
EE04280B1 (et) 1997-07-03 2004-04-15 Dupont Pharmaceuticals Company Imidasopürimidiinid ja imidasopüridiinid neuroloogiliste häirete käitlemiseks
US6114532A (en) * 1998-02-03 2000-09-05 Boehringer Ingelheim Pharma Kg Bicyclic heterocycles, the preparation thereof, and their use as pharmaceuticals
EP1060166A1 (de) * 1998-02-03 2000-12-20 Boehringer Ingelheim Pharma KG 5-gliedrige benzokondensierte heterocyclen als antithrombotika
US6828344B1 (en) 1998-02-25 2004-12-07 Genetics Institute, Llc Inhibitors of phospholipase enzymes
US6916841B2 (en) * 1998-02-25 2005-07-12 Genetics Institute, Llc Inhibitors of phospholipase enzymes
US6500853B1 (en) 1998-02-28 2002-12-31 Genetics Institute, Llc Inhibitors of phospholipase enzymes
US6365589B1 (en) 1998-07-02 2002-04-02 Bristol-Myers Squibb Pharma Company Imidazo-pyridines, -pyridazines, and -triazines as corticotropin releasing factor antagonists
US6124463A (en) * 1998-07-02 2000-09-26 Dupont Pharmaceuticals Benzimidazoles as corticotropin release factor antagonists
RU2236222C2 (ru) * 1998-09-11 2004-09-20 Айлексус Пти Лимитед Модуляторы fc-рецептора и их применение
DE19907813A1 (de) * 1999-02-24 2000-08-31 Boehringer Ingelheim Pharma Substituierte bicyclische Heterocyclen, deren Herstellung und deren Verwendung als Arzneimittel
US6420384B2 (en) * 1999-12-17 2002-07-16 Ariad Pharmaceuticals, Inc. Proton pump inhibitors
US6451832B2 (en) 1999-12-23 2002-09-17 Boehringer Ingelheim Pharma Kg Benzimidazoles with antithrombotic activity
DE19962329A1 (de) * 1999-12-23 2001-06-28 Boehringer Ingelheim Pharma Benzimidazole, deren Herstellung und deren Verwendung als Arzneimittel
US7115645B2 (en) 2000-01-14 2006-10-03 Schering Aktiengesellschaft 1,2 diarylbenzimidazoles and their pharmaceutical use
US7329679B2 (en) 2000-01-27 2008-02-12 Schering Aktiengesellschaft 1,2 Diarylbenzimidazoles and their pharmaceutical use
AU2001281246A1 (en) * 2000-08-23 2002-03-04 The Procter And Gamble Company Benzimidazoles and analogues and their use as neutrophil inhibitors
US6903126B2 (en) 2001-07-09 2005-06-07 Schering Ag 1-Aryl-2-N-, S- or O-substituted benzimidazole derivatives, their use for the production of pharmaceutical agents as well as pharmaceutical preparations that contain these derivatives
DE10135050A1 (de) * 2001-07-09 2003-02-06 Schering Ag 1-Ary1-2-N-, S- oder O-substituierte Benzimidazolderivate, deren Verwendung zur Herstellung von Arzneimitteln sowie diese Derivate enthaltende pharmazeutische Präparate
DE10207844A1 (de) * 2002-02-15 2003-09-04 Schering Ag 1-Phenyl-2-heteroaryl-substituierte Benzimidazolderivate, deren Verwendung zur Herstellung von Arzneimitteln sowie diese Derivate enthaltende pharmazeutische Präparate
US20030181488A1 (en) 2002-03-07 2003-09-25 Boehringer Ingelheim Pharma Gmbh & Co. Kg Administration form for the oral application of 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1H-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionic acid ethyl ester and the salts thereof
US7202252B2 (en) 2003-02-19 2007-04-10 Endacea, Inc. A1 adenosine receptor antagonists
EP1636229A4 (en) * 2003-06-06 2008-07-30 Endacea Inc ADENOSINE A1 RECEPTOR ANTAGONISTS
JP2007506804A (ja) * 2003-06-09 2007-03-22 エンダセア, インコーポレイテッド A1アデノシンレセプターアンタゴニスト
US7202363B2 (en) * 2003-07-24 2007-04-10 Abbott Laboratories Thienopyridine and furopyridine kinase inhibitors
EP1651631A1 (en) * 2003-08-01 2006-05-03 Genelabs Technologies, Inc. Bicyclic imidazol derivatives against flaviviridae
DE10339862A1 (de) * 2003-08-29 2005-03-24 Boehringer Ingelheim Pharma Gmbh & Co. Kg 3-[(2-{[4-(Hexyloxycarbonylamino-imino-methyl)- phenylamino]-methyl}-1-methyl-1H-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionsäure-ethylester-Methansulfonat und dessen Verwendung als Arzneimittel
ES2317244T3 (es) 2004-06-09 2009-04-16 Glaxo Group Limited Derivados de pirrolopiridina.
US7868037B2 (en) 2004-07-14 2011-01-11 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US7772271B2 (en) 2004-07-14 2010-08-10 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US7781478B2 (en) 2004-07-14 2010-08-24 Ptc Therapeutics, Inc. Methods for treating hepatitis C
WO2006019832A1 (en) 2004-07-22 2006-02-23 Ptc Therapeutics, Inc. Thienopyridines for treating hepatitis c
US20060211698A1 (en) * 2005-01-14 2006-09-21 Genelabs, Inc. Bicyclic heteroaryl derivatives for treating viruses
US8618115B2 (en) * 2005-10-26 2013-12-31 Bristol-Myers Squibb Company Substituted thieno[3,2-d]pyrimidinones as MCHR1 antagonists and methods for using them
US7553836B2 (en) * 2006-02-06 2009-06-30 Bristol-Myers Squibb Company Melanin concentrating hormone receptor-1 antagonists
WO2009112445A1 (en) * 2008-03-10 2009-09-17 Novartis Ag Method of increasing cellular phosphatidyl choline by dgat1 inhibition
PE20091928A1 (es) * 2008-05-29 2009-12-31 Bristol Myers Squibb Co Tienopirimidinas hidroxisustituidas como antagonistas de receptor-1 de hormona concentradora de melanina no basicos
TWI453207B (zh) * 2008-09-08 2014-09-21 Signal Pharm Llc 胺基三唑并吡啶,其組合物及使用其之治療方法
JP4913926B2 (ja) * 2008-10-22 2012-04-11 アクテリオン ファーマシューティカルズ リミテッド イソ酪酸(1r*,2r*,4r*)−2−(2−{[3−(4,7−ジメトキシ−1h−ベンゾイミダゾール−2−イル)−プロピル]−メチル−アミノ}−エチル)−5−フェニル−ビシクロ[2.2.2]オクト−5−エン−2−イルエステルの塩
CN102239171B (zh) 2008-12-05 2014-06-11 艾伯维巴哈马有限公司 作为激酶抑制剂用于治疗癌症的噻吩并[3,2-c]吡啶衍生物
DK2519522T3 (en) 2009-12-30 2014-12-08 Arqule Inc SUBSTITUTED IDAZOPYRIDINYL AMINOPYRIDINE COMPOUNDS
JP6046710B2 (ja) 2011-06-24 2016-12-21 アーキュール,インコーポレイティド 置換されたイミダゾピリジニル−アミノピリジン化合物
WO2012177852A1 (en) 2011-06-24 2012-12-27 Arqule, Inc Substituted imidazopyridinyl compounds
WO2013012909A1 (en) 2011-07-20 2013-01-24 Abbott Laboratories Kinase inhibitor with improved aqueous solubility
WO2014151630A2 (en) 2013-03-15 2014-09-25 Irm Llc Compounds and compositions for the treatment of parasitic diseases
US9186361B2 (en) 2013-03-15 2015-11-17 Novartis Ag Compounds and compositions for the treatment of parasitic diseases
US9296754B2 (en) 2013-03-15 2016-03-29 Novartis Ag Compounds and compositions for the treatment of parasitic diseases
TN2016000253A1 (en) 2013-12-19 2017-10-06 Novartis Ag [1,2,4]triazolo[1,5-a]pyrimidine derivatives as protozoan proteasome inhibitors for the treatment of parasitic diseases such as leishmaniasis.
US10300154B2 (en) 2014-09-17 2019-05-28 David R Elmaleh Anticoagulant derivatives for cardiovascular imaging
EP3319945B1 (en) 2015-07-07 2021-04-28 Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts 2-aryl- and 2-arylalkyl-benzimidazoles as midh1 inhibitors
WO2017106134A1 (en) * 2015-12-16 2017-06-22 Merck Sharp & Dohme Corp. Benzimidazoles and indoles as taro inhibitors
EP3416639B1 (en) * 2016-02-16 2022-06-08 Vanderbilt University Positive allosteric modulators of the muscarinic acetylcholine receptor m1
IL279977B2 (en) 2018-07-09 2024-06-01 Boehringer Ingelheim Animal Health Usa Inc Heterocyclic anthelmintic compounds
HUE066335T2 (hu) 2018-10-05 2024-07-28 Annapurna Bio Inc Vegyületek és készítmények APJ receptor aktivitáshoz kapcsolódó állapotok kezelésére
JP7637630B2 (ja) 2019-03-19 2025-02-28 ベーリンガー インゲルハイム フェトメディカ ゲーエムベーハー 駆虫性アザベンゾチオフェンおよびアザベンゾフラン化合物
CA3183100A1 (en) 2020-05-29 2021-12-02 Boehringer Ingelheim Pharma Gmbh & Co. Kg Anthelmintic heterocyclic compounds
KR20240112282A (ko) 2021-11-01 2024-07-18 베링거잉겔하임베트메디카게엠베하 구충제 피롤로피리다진 화합물

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1141936A (en) * 1966-03-26 1969-02-05 Shionogi & Co Improvements in or relating to benzimidazole derivatives
EP0010063B1 (de) * 1978-10-04 1982-12-29 Ciba-Geigy Ag Verfahren zur Herstellung von Furanyl-benzazolen
US4563526A (en) * 1980-09-19 1986-01-07 Forsyth Dental Infirmary For Children Substituted 2-(arylmethoxy) phenol compounds for the treatment of inflammation
US4588722A (en) * 1984-01-09 1986-05-13 Janssen Pharmaceutica N.V. N-(4-piperidinyl) bicyclic condensed 2-imidazolamine derivatives
GB8417194D0 (en) * 1984-07-05 1984-08-08 Boots Co Plc Therapeutic agents
US4581457A (en) * 1984-09-21 1986-04-08 American Home Products Corporation Heterocyclic sulfonamides
DE3445299A1 (de) * 1984-12-12 1986-06-19 Dr. Karl Thomae Gmbh, 7950 Biberach Neue imidazoderivate, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung
GB8510758D0 (en) * 1985-04-27 1985-06-05 Wellcome Found Compounds
HU197746B (en) * 1985-09-05 1989-05-29 Sandoz Ag Process for producing xantin derivatives and pharmaceutical compositions containing them
EP0258191B1 (en) * 1986-08-28 1992-05-27 Sandoz Ag Xanthine derivatives
US4783530A (en) * 1986-11-13 1988-11-08 Marion Laboratories, Inc. 8-arylxanthines
US4942245A (en) * 1987-04-20 1990-07-17 Kyorin Pharmaceutical Co., Ltd. Benzimidazole Derivatives
FR2650592B1 (cg-RX-API-DMAC7.html) * 1989-08-07 1991-11-15 Science Organisation
EP0470543A1 (de) * 1990-08-10 1992-02-12 Dr. Karl Thomae GmbH Heterocyclische Imidazole, diese Verbindungen enthaltende Arzneimittel und Verfahren zur ihrer Herstellung
US5208240A (en) * 1991-03-12 1993-05-04 Merrell Dow Pharmaceuticals Inc. 8-substituted purines as selective adenosine receptor agents
PH31294A (en) * 1992-02-13 1998-07-06 Thomae Gmbh Dr K Benzimidazolyl derivatives, pharmaceutical compositions containing these compounds and process for preparing them.

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002522432A (ja) * 1998-08-01 2002-07-23 ベーリンガー インゲルハイム ファルマ コマンディトゲゼルシャフト 二置換二環式複素環化合物、それらの調製及び医薬組成物としてのそれらの使用
JP2003513959A (ja) * 1999-11-10 2003-04-15 ベーリンガー インゲルハイム ファルマ コマンディトゲゼルシャフト カルボキサミド置換ベンゾイミダゾール誘導体、それらの調製方法及び医薬組成物としてのそれらの使用
JP2003523961A (ja) * 2000-01-14 2003-08-12 シエーリング アクチエンゲゼルシャフト 小グリア細胞活性化に関連する疾病の処理のための1,2−ジアリールベンズイミダゾール
JP2004502761A (ja) * 2000-07-06 2004-01-29 ベーリンガー インゲルハイム (カナダ) リミテッド ウイルスポリメラーゼ阻害剤
JP2007217427A (ja) * 2000-09-01 2007-08-30 Chiron Corp アザ複素環式誘導体およびその治療的使用
JP2007502822A (ja) * 2003-08-21 2007-02-15 オーエスアイ・ファーマスーティカルズ・インコーポレーテッド c−Kit阻害剤としてのN3−置換イミダゾピリジン誘導体
JP2009507779A (ja) * 2005-08-15 2009-02-26 シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト 新規な殺虫剤
WO2011074658A1 (ja) * 2009-12-18 2011-06-23 田辺三菱製薬株式会社 新規抗血小板薬
JPWO2011074658A1 (ja) * 2009-12-18 2013-05-02 田辺三菱製薬株式会社 新規抗血小板薬
US8703760B2 (en) 2009-12-18 2014-04-22 Mitsubishi Tanabe Pharma Corporation Antiplatelet agent
US9533983B2 (en) 2009-12-18 2017-01-03 Mitsubishi Tanabe Pharma Corporation Antiplatelet agent
JP2013018771A (ja) * 2011-06-17 2013-01-31 Mitsubishi Tanabe Pharma Corp 新規抗血小板薬

Also Published As

Publication number Publication date
NO923466L (no) 1993-03-08
RU2041211C1 (ru) 1995-08-09
FI923960L (fi) 1993-03-07
KR930005983A (ko) 1993-04-20
DE4129603A1 (de) 1993-03-11
AU2217892A (en) 1993-03-11
CA2077577A1 (en) 1993-03-07
NZ244211A (en) 1995-12-21
EP0531883A1 (de) 1993-03-17
HUT61984A (en) 1993-03-29
FI923960A7 (fi) 1993-03-07
PL295818A1 (en) 1993-11-02
HU9202857D0 (en) 1992-11-30
IL103053A (en) 1996-08-04
AU657350B2 (en) 1995-03-09
ZA926700B (en) 1994-03-04
US5434150A (en) 1995-07-18
TW221436B (cg-RX-API-DMAC7.html) 1994-03-01
MX9205064A (es) 1993-03-01
IL103053A0 (en) 1993-02-21
NO923466D0 (no) 1992-09-04
FI923960A0 (fi) 1992-09-04

Similar Documents

Publication Publication Date Title
JPH0625181A (ja) 縮合5員複素環式化合物、それらの調製法およびこれらの化合物を含む製薬製剤
US5827849A (en) Cyclic dericatives, pharmaceutical compositions containing these compounds and processes for preparing them
JP2923742B2 (ja) 4−アミノキナゾリン誘導体、その製造方法およびそれを含有する医薬品
EP1812439B1 (en) Kinase inhibitors
RU2053229C1 (ru) Производные бензимидазола и фармацевтическая композиция, обладающая антагонистической активностью в отношении ангиотензина, на их основе
US5159083A (en) Certain aminomethyl phenylimidazole derivatives; a class of dopamine receptor subtype specific ligands
US5463071A (en) 5-membered heterocyclic compounds, processes for preparing them and pharmaceutical compositions containing these compounds
US5478942A (en) Cyclic urea derivatives and pharmaceutical compositions containing these compounds
HU223754B1 (hu) Diszubsztituált biciklusos, heterociklusos vegyületek, ezeket tartalmazó gyógyszerkészítmények és eljárás előállításukra
JPH072851A (ja) 5員複素環化合物、それらの調製方法及びこれらの化合物を含む医薬組成物
US5565469A (en) Benzimidazoles and pharmaceutical compositions containing them
JPH06263740A (ja) 環状尿素誘導体、これらの化合物を含む医薬組成物及びそれらの調製方法
DE69724098T2 (de) Chinolin- und benzimidazolderivate als bradykinin agonisten
RU2126401C1 (ru) Производные бензимидазола, их таутомеры или их соли и лекарственное средство с антагонистическим в отношении ангиотензина ii действием
JPH05247074A (ja) フェニルアルキル誘導体、これらの化合物を含む製薬組成物及びそれらの調製法
JPH072839A (ja) 縮合5員複素環化合物、それらの調製方法及びこれらの化合物を含む医薬組成物
EP1196419B1 (en) Potassium channel blocking agents
JPS6110584A (ja) イミダゾイソキノリン化合物およびその製造方法
JP2003519129A (ja) ベンズイミダゾール、その調製及び医薬組成物としての使用
JPH04346980A (ja) 4−ピリミジノン誘導体、その製造方法および治療への適用
CA2569088C (en) Pyrrolobenzimidazolones and their use as antiproliferative agents
US5459147A (en) Substituted benzimidazolyl derivatives and pharmaceutical compositions containing these compounds
JP2860688B2 (ja) インドール誘導体
JPH07157485A (ja) 縮合ピリミジノン誘導体及びそれらを含有するアンジオテンシンii拮抗剤
JPWO2000076980A1 (ja) 新規な含窒素複素環誘導体又はその塩