[go: up one dir, main page]

NO933999L - Fibrinogenreseptorantagonister - Google Patents

Fibrinogenreseptorantagonister

Info

Publication number
NO933999L
NO933999L NO933999A NO933999A NO933999L NO 933999 L NO933999 L NO 933999L NO 933999 A NO933999 A NO 933999A NO 933999 A NO933999 A NO 933999A NO 933999 L NO933999 L NO 933999L
Authority
NO
Norway
Prior art keywords
fibrinogen
inhibiting
platelets
binding
formula
Prior art date
Application number
NO933999A
Other languages
English (en)
Norwegian (no)
Other versions
NO933999D0 (no
Inventor
Mark E Duggan
George Hartman
Melissa E Egbertson
Nathan Ihle
Laura M Turchi
William F Hoffman
Original Assignee
Merck & Co Inc
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 Merck & Co Inc filed Critical Merck & Co Inc
Publication of NO933999L publication Critical patent/NO933999L/no
Publication of NO933999D0 publication Critical patent/NO933999D0/no

Links

Classifications

    • 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
    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • 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
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/72Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D211/74Oxygen atoms
    • C07D211/76Oxygen atoms attached in position 2 or 6
    • 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
    • C07D401/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D453/00Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C07D453/06Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing isoquinuclidine ring systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Peptides Or Proteins (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyrrole Compounds (AREA)
  • Materials For Medical Uses (AREA)
NO1993933999A 1991-05-07 1993-11-05 Fibrinogenreseptorantagonister NO933999D0 (no)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US69689391A 1991-05-07 1991-05-07
US72035791A 1991-06-25 1991-06-25
US87126292A 1992-04-23 1992-04-23
PCT/US1992/003463 WO1992019595A1 (fr) 1991-05-07 1992-04-27 Antagonistes de recepteur de fibrinogene

Publications (2)

Publication Number Publication Date
NO933999L true NO933999L (no) 1993-11-05
NO933999D0 NO933999D0 (no) 1993-11-05

Family

ID=27418643

Family Applications (1)

Application Number Title Priority Date Filing Date
NO1993933999A NO933999D0 (no) 1991-05-07 1993-11-05 Fibrinogenreseptorantagonister

Country Status (20)

Country Link
US (2) US5281585A (fr)
EP (1) EP0512831B1 (fr)
JP (1) JP2531562B2 (fr)
KR (1) KR920021531A (fr)
CN (1) CN1067883A (fr)
AT (1) ATE184874T1 (fr)
AU (1) AU647618B2 (fr)
BG (1) BG98194A (fr)
CA (1) CA2068064C (fr)
DE (1) DE69230013T2 (fr)
ES (1) ES2137175T3 (fr)
FI (1) FI934894A7 (fr)
HU (1) HUT68769A (fr)
IE (1) IE921463A1 (fr)
IL (1) IL101779A0 (fr)
MX (1) MXPA92002103A (fr)
NO (1) NO933999D0 (fr)
NZ (1) NZ242609A (fr)
WO (1) WO1992019595A1 (fr)
YU (1) YU47992A (fr)

Families Citing this family (113)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6521594B1 (en) 1990-04-06 2003-02-18 La Jolla Cancer Research Foundation Method and composition for treating thrombosis
US6017877A (en) * 1990-04-06 2000-01-25 La Jolla Cancer Research Foundation Method and composition for treating thrombosis
US5780303A (en) * 1990-04-06 1998-07-14 La Jolla Cancer Research Foundation Method and composition for treating thrombosis
US5672585A (en) * 1990-04-06 1997-09-30 La Jolla Cancer Research Foundation Method and composition for treating thrombosis
WO1993018058A1 (fr) * 1992-03-06 1993-09-16 G.D. Searle & Co. Imitateurs peptidiques utiles comme inhibiteurs de l'agregation plaquettaire
JPH08504194A (ja) * 1992-12-01 1996-05-07 メルク エンド カンパニー インコーポレーテッド フィブリノーゲンレセプターアンタゴニスト
DE4308034A1 (de) * 1993-03-13 1994-09-15 Cassella Ag Neue Heterocyclen, ihre Herstellung und ihre Verwendung
NZ262941A (en) * 1993-03-29 1997-07-27 Zeneca Ltd Pyridine derivatives and medicaments
US5652242A (en) * 1993-03-29 1997-07-29 Zeneca Limited Heterocyclic derivatives
US5753659A (en) * 1993-03-29 1998-05-19 Zeneca Limited Heterocyclic compouds
GB9406144D0 (en) * 1993-03-29 1994-05-18 Zeneca Ltd Heterocyclic compounds
US5750754A (en) * 1993-03-29 1998-05-12 Zeneca Limited Heterocyclic compounds
US5463011A (en) * 1993-06-28 1995-10-31 Zeneca Limited Acid derivatives
GB9313285D0 (en) * 1993-06-28 1993-08-11 Zeneca Ltd Acid derivatives
GB9313268D0 (en) * 1993-06-28 1993-08-11 Zeneca Ltd Chemical compounds
ES2164109T3 (es) * 1993-09-22 2002-02-16 Fujisawa Pharmaceutical Co Derivados de n-(3-piperidinilcarbonil)-beta-alanina como antagonistas de paf.
US5707994A (en) * 1993-10-19 1998-01-13 Sumitomo Pharmaceuticals Company, Limited 2,3-diaminopropionic acid derivative
DE4427979A1 (de) 1993-11-15 1996-02-15 Cassella Ag Substituierte 5-Ring-Heterocyclen, ihre Herstellung und ihre Verwendung
US5446056A (en) * 1993-11-24 1995-08-29 The Du Pont Merck Pharmaceutical Company Isoxazoline compounds useful as fibrinogen receptor antagonists
US5523302A (en) * 1993-11-24 1996-06-04 The Du Pont Merck Pharmaceutical Company Aromatic compounds containing basic and acidic termini useful as fibrinogen receptor antagonists
US5849736A (en) * 1993-11-24 1998-12-15 The Dupont Merck Pharmaceutical Company Isoxazoline and isoxazole fibrinogen receptor antagonists
CA2174838A1 (fr) * 1993-11-24 1995-06-01 John Wityak Nouveaux antagonistes de recepteur de fibrinogene, a base d'isoxazoline et d'isoxazole
US5563158A (en) * 1993-12-28 1996-10-08 The Dupont Merck Pharmaceutical Company Aromatic compounds containing basic and acidic termini useful as fibrinogen receptor antagonists
DE4405378A1 (de) * 1994-02-19 1995-08-24 Merck Patent Gmbh Adhäsionsrezeptor-Antagonisten
US5821241A (en) * 1994-02-22 1998-10-13 Merck & Co., Inc. Fibrinogen receptor antagonists
JPH09510442A (ja) * 1994-03-11 1997-10-21 ファーマコペイア,インコーポレイテッド スルホンアミド誘導体及びそれらの使用
WO1995025101A1 (fr) * 1994-03-14 1995-09-21 Merck & Co., Inc. Ethylation pyridylique des lactames
WO1995025088A1 (fr) * 1994-03-14 1995-09-21 Merck & Co., Inc. Ethylation pyridylique de derives de lactames
KR100254666B1 (ko) * 1994-07-15 2000-05-01 이치로 키타사토 혈소판 응집 저해 작용을 갖는 신규 화합물
US5451578A (en) * 1994-08-12 1995-09-19 Merck & Co., Inc. Fibrinogen receptor antagonists
US5525617A (en) * 1994-08-24 1996-06-11 Merck & Co., Inc. Fibrinogen receptor antagonists
US5494921A (en) * 1994-09-16 1996-02-27 Merck & Co., Inc. Fibrinogen receptor antagonists
US5686607A (en) * 1994-09-16 1997-11-11 Merck & Co., Inc. Pyridyl ethylation of lactam derivatives
EP0790247A4 (fr) * 1994-11-01 2000-07-19 Terumo Corp Derive de tetrahydroisoquinoleine et preparation medicinale contenant ce derive
US5719144A (en) * 1995-02-22 1998-02-17 Merck & Co., Inc. Fibrinogen receptor antagonists
US5674894A (en) * 1995-05-15 1997-10-07 G.D. Searle & Co. Amidine derivatives useful as platelet aggregation inhibitors and vasodilators
ZA963391B (en) * 1995-05-24 1997-10-29 Du Pont Merck Pharma Isoxazoline fibrinogen receptor antagonists.
US6187757B1 (en) 1995-06-07 2001-02-13 Ariad Pharmaceuticals, Inc. Regulation of biological events using novel compounds
US5852045A (en) * 1995-10-19 1998-12-22 Merck & Co., Inc. Fibrinogen receptor antagonists
JPH11513686A (ja) * 1995-10-19 1999-11-24 メルク エンド カンパニー インコーポレーテッド 線維素原受容体拮抗薬
US5952306A (en) * 1996-01-16 1999-09-14 Merck & Co., Inc. Integrin receptor antagonists
WO1997026250A1 (fr) * 1996-01-16 1997-07-24 Merck & Co., Inc. Antagonistes du recepteur integrine
EP0888302A1 (fr) * 1996-03-13 1999-01-07 Fujisawa Pharmaceutical Co., Ltd. N- (r)-1- 3-(4-piperidyl)propionyl-3-piperidylcarbonyl]-2(s)-acetylamino-beta-alanine utilisee comme antagoniste du recepteur du fibrinogene
GB2312895A (en) * 1996-05-10 1997-11-12 Merck & Co Inc Fibrinogen receptor antagonists
US5889023A (en) * 1996-05-10 1999-03-30 Merck & Co., Inc. Fibrinogen receptor antagonist
AU3404197A (en) * 1996-06-19 1998-01-07 Becton Dickinson & Company Iontophoretic delivery of cell adhesion inhibitors
US6004955A (en) * 1996-08-15 1999-12-21 Dupont Pharmaceuticals Company Cyclic carbamates and isoxazolidines as IIb/IIIa antagonists
US5981546A (en) * 1996-08-29 1999-11-09 Merck & Co., Inc. Integrin antagonists
US6211184B1 (en) * 1996-08-29 2001-04-03 Merck & Co., Inc. Integrin antagonists
US5900414A (en) * 1996-08-29 1999-05-04 Merck & Co., Inc. Methods for administering integrin receptor antagonists
WO1998011896A1 (fr) * 1996-09-18 1998-03-26 Merck & Co., Inc. Traitement combine destine a reduire les risques de maladies cardio-vasculaires
US5978698A (en) * 1996-10-08 1999-11-02 Merck & Co., Inc. Angioplasty procedure using nonionic contrast media
US6063794A (en) * 1996-10-11 2000-05-16 Cor Therapeutics Inc. Selective factor Xa inhibitors
US6194435B1 (en) 1996-10-11 2001-02-27 Cor Therapeutics, Inc. Lactams as selective factor Xa inhibitors
US6262047B1 (en) 1996-10-11 2001-07-17 Cor Therapeutics, Inc. Selective factor Xa inhibitors
US6369080B2 (en) 1996-10-11 2002-04-09 Cor Therapeutics, Inc. Selective factor Xa inhibitors
US5919792A (en) * 1996-10-30 1999-07-06 Merck & Co., Inc. Integrin antagonists
US5952341A (en) * 1996-10-30 1999-09-14 Merck & Co., Inc. Integrin antagonists
US6017925A (en) * 1997-01-17 2000-01-25 Merck & Co., Inc. Integrin antagonists
US5981584A (en) * 1997-02-06 1999-11-09 Merck & Co., Inc. Fibrinogen receptor antagonist prodrugs
NZ500353A (en) 1997-04-14 2002-02-01 Cor Therapeutics Inc Cyclic diaza compounds that are selective inhibitors of factor Xa
EP0975659A1 (fr) * 1997-04-14 2000-02-02 Cor Therapeutics, Inc. INHIBITEURS SELECTIFS DU FACTEUR Xa
WO1998046627A1 (fr) 1997-04-14 1998-10-22 Cor Therapeutics, Inc. INHIBITEURS SELECTIFS DU FACTEUR Xa
CA2285335A1 (fr) 1997-04-14 1998-10-22 Cor Therapeutics, Inc. Inhibiteurs selectifs du facteur xa
US6294549B1 (en) 1997-07-23 2001-09-25 Merck & Co., Inc. Method for eliciting an αvβ5 or dual αvβ3/αvβ5 antagonizing effect
WO1999006402A1 (fr) * 1997-07-31 1999-02-11 Ube Industries, Ltd. Composes amides n-acylamino acides et intermediaires utiles dans la preparation de ceux-ci
US6333321B1 (en) 1997-08-11 2001-12-25 Cor Therapeutics, Inc. Selective factor Xa inhibitors
US6228854B1 (en) 1997-08-11 2001-05-08 Cor Therapeutics, Inc. Selective factor Xa inhibitors
US6218382B1 (en) 1997-08-11 2001-04-17 Cor Therapeutics, Inc Selective factor Xa inhibitors
GB2328871A (en) * 1997-09-05 1999-03-10 Merck & Co Inc Compositions for inhibiting platelet aggregation
US6129932A (en) * 1997-09-05 2000-10-10 Merck & Co., Inc. Compositions for inhibiting platelet aggregation
GB2328873A (en) * 1997-09-08 1999-03-10 Merck & Co Inc The use of [3(R)-[2-(piperidin-4-yl)ethyl]-2-piperidone-1]acetyl-3(R)-methyl-ß-alanine for inhibiting blood platelet aggregation
WO1999026945A1 (fr) * 1997-11-26 1999-06-03 Du Pont Pharmaceuticals Company 1,3,4-THIADIAZOLES ET 1,3,4-OXADIAZOLES UTILISES COMME ANTAGONISTES DE αvβ¿3?
US6017926A (en) * 1997-12-17 2000-01-25 Merck & Co., Inc. Integrin receptor antagonists
US6048861A (en) 1997-12-17 2000-04-11 Merck & Co., Inc. Integrin receptor antagonists
US6066648A (en) * 1997-12-17 2000-05-23 Merck & Co., Inc. Integrin receptor antagonists
US6211191B1 (en) 1997-12-17 2001-04-03 Merck & Co., Inc. Integrin receptor antagonists
US6623981B2 (en) * 1998-01-27 2003-09-23 Bristol-Myers Squibb Company Detection of patients at risk for developing integrin antagonist/agonist mediated disease states
US6984635B1 (en) 1998-02-13 2006-01-10 Board Of Trustees Of The Leland Stanford Jr. University Dimerizing agents, their production and use
EP1091945A1 (fr) 1998-06-29 2001-04-18 Du Pont Pharmaceuticals Company Isoxazolidines et carbamates cycliques utilises comme antagonistes de iib/iiia
CA2338878A1 (fr) * 1998-08-13 2000-02-24 Merck & Co., Inc. Antagonistes de recepteurs d'integrine
US6319937B1 (en) 1998-11-18 2001-11-20 Dupont Pharmaceuticals Company Isoxazoline fibrinogen receptor antagonists
WO2000029406A2 (fr) 1998-11-18 2000-05-25 Du Pont Pharmaceuticals Company Nouveaux antagonistes du recepteur de fibrinogene a base d'isoxazoline
US6723711B2 (en) 1999-05-07 2004-04-20 Texas Biotechnology Corporation Propanoic acid derivatives that inhibit the binding of integrins to their receptors
US6972296B2 (en) 1999-05-07 2005-12-06 Encysive Pharmaceuticals Inc. Carboxylic acid derivatives that inhibit the binding of integrins to their receptors
MXPA01011341A (es) * 1999-05-07 2002-06-21 Texas Biotechnology Corp Derivados de acido propanoico que inhiben la union de las integrinas a sus receptores.
DE60035779T2 (de) 1999-06-02 2008-04-30 Merck & Co., Inc. Alpha v integrin-rezeptor antagonisten
EP1212331B1 (fr) 1999-08-24 2004-04-21 Ariad Gene Therapeutics, Inc. Analogues d'epirapamycine-28
US7067526B1 (en) 1999-08-24 2006-06-27 Ariad Gene Therapeutics, Inc. 28-epirapalogs
AU7743400A (en) 1999-10-04 2001-05-10 Merck & Co., Inc. Integrin receptor antagonists
US6518244B2 (en) 2000-03-09 2003-02-11 Intimax Corporation Combinations of heparin cofactor II agonist and platelet IIb/IIIa antagonist, and uses thereof
AR030817A1 (es) 2000-10-02 2003-09-03 Novartis Ag Derivados de diazacicloalcanodiona
US8048917B2 (en) 2005-04-06 2011-11-01 Xenoport, Inc. Prodrugs of GABA analogs, compositions and uses thereof
US7232924B2 (en) * 2001-06-11 2007-06-19 Xenoport, Inc. Methods for synthesis of acyloxyalkyl derivatives of GABA analogs
US7186855B2 (en) * 2001-06-11 2007-03-06 Xenoport, Inc. Prodrugs of GABA analogs, compositions and uses thereof
US6818787B2 (en) * 2001-06-11 2004-11-16 Xenoport, Inc. Prodrugs of GABA analogs, compositions and uses thereof
JP4336196B2 (ja) 2001-07-18 2009-09-30 メルク エンド カムパニー インコーポレーテッド メラノコルチン受容体作動薬としての架橋ピペリジン誘導体
SI21096B (sl) * 2001-10-09 2012-05-31 Encysive Pharmaceuticals Inc Derivati karboksilne kisline ki inhibirajo vezavo integrinov na njihove receptorje
US10675280B2 (en) 2001-10-20 2020-06-09 Sprout Pharmaceuticals, Inc. Treating sexual desire disorders with flibanserin
UA78974C2 (en) 2001-10-20 2007-05-10 Boehringer Ingelheim Pharma Use of flibanserin for treating disorders of sexual desire
EP1626961B1 (fr) * 2003-05-17 2011-11-02 Korea Research Institute of Bioscience and Biotechnology Nouveaux composes 2-oxo-heterocycliques et compositions pharmaceutiques contenant ces composes
WO2007014929A1 (fr) 2005-08-03 2007-02-08 Boehringer Ingelheim International Gmbh Utilisation de la flibansérine dans le traitement de l'obésité
US20070087061A1 (en) * 2005-10-14 2007-04-19 Medafor, Incorporated Method and composition for creating and/or activating a platelet-rich gel by contact with a porous particulate material, for use in wound care, tissue adhesion, or as a matrix for delivery of therapeutic components
US20070086958A1 (en) * 2005-10-14 2007-04-19 Medafor, Incorporated Formation of medically useful gels comprising microporous particles and methods of use
WO2008000760A1 (fr) 2006-06-30 2008-01-03 Boehringer Ingelheim International Gmbh Flibansérine dans le traitement de l'incontinence urinaire et des maladies associées
PE20091188A1 (es) 2007-09-12 2009-08-31 Boehringer Ingelheim Int Compuesto 1-[2-(4-(3-trifluorometil-fenil)piperazin-1-il)etil]-2,3-dihidro-1h-benzimidazol-2-ona (flibanserina), sus sales de adicion y composiciones farmaceuticas que los contienen
CA2686480A1 (fr) 2008-12-15 2010-06-15 Boehringer Ingelheim International Gmbh Nouveaux sels
NZ598125A (en) * 2009-07-30 2014-05-30 Salvat Lab Sa Apaf-1 inhibitor compounds
JP6228010B2 (ja) 2010-12-27 2017-11-08 ブラウン ユニバーシティ ビグリカンおよびユートロフィンに関する治療法および診断法
US11043823B2 (en) * 2017-04-06 2021-06-22 Tesla, Inc. System and method for facilitating conditioning and testing of rechargeable battery cells
US10792771B2 (en) 2017-09-12 2020-10-06 Raytheon Technologies Corporation Method of making integrally bladed rotor
US10605101B2 (en) 2017-09-12 2020-03-31 United Technologies Corporation Process of making integrally bladed rotor
US10561736B1 (en) 2019-01-09 2020-02-18 Spiral Therapeutics, Inc. Apoptosis inhibitor formulations for prevention of hearing loss

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2549999A1 (de) * 1975-11-07 1977-05-12 Boehringer Mannheim Gmbh Piperidin-derivate und verfahren zu ihrer herstellung
FR2334358A1 (fr) * 1975-12-12 1977-07-08 Sogeras Nouveaux medicaments derives de l'indole
US4064125A (en) * 1976-10-29 1977-12-20 E. R. Squibb And Sons, Inc. Substituted amides having antiinflammatory activity
IL60129A0 (en) * 1979-05-23 1980-07-31 Wuelfing J Kg Phenylsulphonamide derivatives,their preparation and pharmaceutical compositions containing them
KR880007441A (ko) * 1986-12-11 1988-08-27 알렌 제이.스피겔 스피로-치환된 글루타르아미드 이뇨제
US4879313A (en) * 1988-07-20 1989-11-07 Mosanto Company Novel platelet-aggregation inhibitors
US5039805A (en) * 1988-12-08 1991-08-13 Hoffmann-La Roche Inc. Novel benzoic and phenylacetic acid derivatives
US5084466A (en) * 1989-01-31 1992-01-28 Hoffmann-La Roche Inc. Novel carboxamide pyridine compounds which have useful pharmaceutical utility
CA2008116C (fr) * 1989-02-23 2001-11-20 Thomas Weller Derives de glycine
NZ234264A (en) * 1989-06-29 1993-05-26 Warner Lambert Co N-substituted cycloalkyl and polycycloalkyl alpha-substituted trp-phe- and phenethylamine derivatives, and pharmaceutical compositions
US5064814A (en) * 1990-04-05 1991-11-12 Rhone-Poulenc Rorer Pharmaceuticals Inc. Anti-thrombotic peptide and pseudopeptide derivatives
IL99537A (en) * 1990-09-27 1995-11-27 Merck & Co Inc Fibrinogen receptor antagonists and pharmaceutical compositions containing them
NZ239876A (en) * 1990-09-27 1993-12-23 Merck & Co Inc Glycyl-b-alanine derivatives and pharmaceutical compositions thereof.

Also Published As

Publication number Publication date
AU1611192A (en) 1992-11-12
YU47992A (sh) 1995-03-27
IE921463A1 (en) 1992-11-18
ES2137175T3 (es) 1999-12-16
US5455243A (en) 1995-10-03
CN1067883A (zh) 1993-01-13
ATE184874T1 (de) 1999-10-15
JP2531562B2 (ja) 1996-09-04
JPH069525A (ja) 1994-01-18
NZ242609A (en) 1995-04-27
HUT68769A (en) 1995-07-28
NO933999D0 (no) 1993-11-05
US5281585A (en) 1994-01-25
EP0512831B1 (fr) 1999-09-22
CA2068064C (fr) 2001-01-02
DE69230013T2 (de) 2000-04-27
BG98194A (bg) 1994-09-30
CA2068064A1 (fr) 1992-11-08
FI934894A0 (fi) 1993-11-05
KR920021531A (ko) 1992-12-18
WO1992019595A1 (fr) 1992-11-12
AU647618B2 (en) 1994-03-24
HU9303145D0 (en) 1994-01-28
DE69230013D1 (de) 1999-10-28
FI934894L (fi) 1993-11-05
EP0512831A1 (fr) 1992-11-11
FI934894A7 (fi) 1993-11-05
MXPA92002103A (es) 2005-08-25
IL101779A0 (en) 1992-12-30

Similar Documents

Publication Publication Date Title
NO933999L (no) Fibrinogenreseptorantagonister
ATE163646T1 (de) Fibrinogen-rezeptor-antagonisten
ATE181064T1 (de) Fibrinogen-rezeptor-antagonisten
CA2109613A1 (fr) Derives fluoroalcoxybenzylamines d'heterocycles azotes
ATE188379T1 (de) Fibrinogenrezeptor-antagonisten
MY104685A (en) Substituted thiazoles and their use as fungicides.
IT1199243B (it) Composti eterociclici,loro preparazione e loro impiego come medicamenti
BR8406642A (pt) Bismaleimida,composicao de resina"prepregavel",prepreg e composto
CA2118704A1 (fr) Heterocycles azotes tricycliques fusionnes utilises comme antagonistes des recepteurs a substance p
NZ502181A (en) Triazole compounds and the use thereof as dopamine-D 3-ligands
DE3574871D1 (de) Heterozyklische verbindungen enthaltende zusammensetzungen und ihre verwendung als herbizide.
KR950700321A (ko) 혈소판 응집 억제제로서의 4-옥소-2-티옥소이미다졸리딘 유도체(4-Oxo-2-thioxoimidazolidine derivatives as inhibitors of blood platelet aggregation)
JO1406B1 (en) Chemical compounds
ATE188692T1 (de) Fibrinogenrezeptorantagonisten
ES2044100T3 (es) Ciertas combinaciones de antagonistas del "paf" y antihistaminicos y metodos.
DK133587D0 (da) 2-heterocyclylthio-penemer, deres anvendelse og farmaceutisk komposition indeholdende forbindelserne
ATE256661T1 (de) Bispiperidine mit antithrombotischer wirkung
ES8505363A1 (es) Un procedimiento para preparar una 3-(2-furoil)-5-2,6-dimetil-4-(2-nitrofenil)-1,4-dihidropiridina
FI875538A7 (fi) Uudet maleimideihin perustuvat yhdisteet ja uudet, niitä sisältävät valolla kovettuvat koostumukset.
NO305556B1 (no) Tiokarbamoylforbindelser og anvendelse derav samt middel for beskyttelse av tekniske materialer
IT1213208B (it) Composizioni iniettabili,contenenti metronidazolo
ATE81589T1 (de) Verwendung von folinsaeurederivaten als plaettchenaggregationshemmstoffe.
DE3574926D1 (de) Heterocyclische verbindungen enthaltende zusammensetzungen und ihre verwendung als herbizide.
IT8821386A0 (it) 5 pirimidincarbossamidi sostituite e composizioni farmaceutiche contenenti le stesse per il trattamento di leucemia.
IT8821384A0 (it) 5 pirimidincarbossamidi sostituite e composizioni farmaceutiche contenenti le stesse per il trattamento di leucemia.