NO177702C - Analogifremgangsmåte for fremstilling av terapeutisk aktive forbindelser - Google Patents
Analogifremgangsmåte for fremstilling av terapeutisk aktive forbindelserInfo
- Publication number
- NO177702C NO177702C NO913784A NO913784A NO177702C NO 177702 C NO177702 C NO 177702C NO 913784 A NO913784 A NO 913784A NO 913784 A NO913784 A NO 913784A NO 177702 C NO177702 C NO 177702C
- Authority
- NO
- Norway
- Prior art keywords
- opt
- substd
- alkyl
- aryl
- het1
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/03—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C311/06—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by carboxyl groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/12—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/12—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings
- C07C311/13—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings the carbon skeleton containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/20—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
- C07D211/22—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Peptides Or Proteins (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pyrrole Compounds (AREA)
- Pyridine Compounds (AREA)
- Materials For Medical Uses (AREA)
- External Artificial Organs (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US58913090A | 1990-09-27 | 1990-09-27 | |
| US75064791A | 1991-08-30 | 1991-08-30 |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| NO913784D0 NO913784D0 (no) | 1991-09-26 |
| NO913784L NO913784L (no) | 1992-03-30 |
| NO177702B NO177702B (no) | 1995-07-31 |
| NO177702C true NO177702C (no) | 1995-11-08 |
Family
ID=27080454
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO913784A NO177702C (no) | 1990-09-27 | 1991-09-26 | Analogifremgangsmåte for fremstilling av terapeutisk aktive forbindelser |
| NO2000001C NO2000001I2 (no) | 1990-09-27 | 2000-04-13 | Analogifremgangsmaate for fremstilling av terapeutisk aktive forbindelser |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO2000001C NO2000001I2 (no) | 1990-09-27 | 2000-04-13 | Analogifremgangsmaate for fremstilling av terapeutisk aktive forbindelser |
Country Status (32)
| Country | Link |
|---|---|
| US (5) | US5292756A (fr) |
| EP (2) | EP0478363B1 (fr) |
| JP (2) | JPH0794425B2 (fr) |
| KR (1) | KR100216939B1 (fr) |
| CN (1) | CN1038748C (fr) |
| AT (1) | ATE150454T1 (fr) |
| AU (1) | AU655436B2 (fr) |
| BG (1) | BG61810B1 (fr) |
| CA (1) | CA2052073C (fr) |
| CY (1) | CY2048B1 (fr) |
| DE (2) | DE19875054I2 (fr) |
| DK (1) | DK0478363T3 (fr) |
| ES (2) | ES2133892T3 (fr) |
| FI (2) | FI108295B (fr) |
| GR (2) | GR3023226T3 (fr) |
| HR (1) | HRP930779B1 (fr) |
| IE (1) | IE913383A1 (fr) |
| IL (1) | IL99540A (fr) |
| LU (1) | LU90505I2 (fr) |
| LV (1) | LV12089B (fr) |
| NL (1) | NL990040I2 (fr) |
| NO (2) | NO177702C (fr) |
| NZ (1) | NZ239846A (fr) |
| PL (1) | PL172687B1 (fr) |
| PT (1) | PT99098B (fr) |
| RO (1) | RO116621B1 (fr) |
| RU (1) | RU2116296C1 (fr) |
| SI (1) | SI9210306B (fr) |
| SK (1) | SK281233B6 (fr) |
| UA (1) | UA44222C2 (fr) |
| WO (1) | WO1993019046A1 (fr) |
| YU (1) | YU48912B (fr) |
Families Citing this family (140)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ239846A (en) * | 1990-09-27 | 1994-11-25 | Merck & Co Inc | Sulphonamide derivatives and pharmaceutical compositions thereof |
| US5645815A (en) * | 1991-02-08 | 1997-07-08 | Diatide, Inc. | Radiolabled compounds for thrombus imaging |
| US5321034A (en) * | 1991-05-07 | 1994-06-14 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| US5939412A (en) * | 1992-06-26 | 1999-08-17 | Smithkline Beecham Corporation | Bicyclic fibrinogen antagonists |
| WO1993000095A2 (fr) * | 1991-06-28 | 1993-01-07 | Smithkline Beecham Corporation | Antagonistes bicycliques de fibrinogene |
| SG47459A1 (en) * | 1991-09-24 | 1998-04-17 | Janssen Pharmaceutica Nv | Process for preparing enantiomerically pure imidazo(4,5,1)(1,4)benzodiazepin-2(1H)-thiones |
| US5264457A (en) * | 1992-02-14 | 1993-11-23 | G. D. Searle & Co. | Phenyl amidines sulfonamides useful as platelet aggregation inhibitors |
| TW224462B (fr) * | 1992-02-24 | 1994-06-01 | Squibb & Sons Inc | |
| US5312923A (en) * | 1992-02-28 | 1994-05-17 | Merck & Co., Inc. | Process for preparing fibrinogen receptor antagonists |
| US5206373A (en) * | 1992-02-28 | 1993-04-27 | Merck & Co., Inc. | Process for preparing fibrinogen receptor antagonists |
| AU4540693A (en) * | 1992-06-25 | 1994-01-24 | G.D. Searle & Co. | Phenyl amidine alkanoic acids and lactones useful as platelet aggregation inhibitors |
| US5358956A (en) * | 1992-10-14 | 1994-10-25 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| US5340798A (en) * | 1992-10-14 | 1994-08-23 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| JP3322878B2 (ja) * | 1992-10-14 | 2002-09-09 | 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 |
| WO1994008962A1 (fr) * | 1992-10-14 | 1994-04-28 | Merck & Co., Inc. | Antagonistes des recepteurs du fibrinogene |
| CA2150550A1 (fr) * | 1992-12-01 | 1994-06-09 | Melissa S. Egbertson | Antagonistes du recepteur du fibrinogene |
| US5750754A (en) * | 1993-03-29 | 1998-05-12 | Zeneca Limited | Heterocyclic compounds |
| US5753659A (en) * | 1993-03-29 | 1998-05-19 | Zeneca Limited | Heterocyclic compouds |
| GB9406144D0 (en) * | 1993-03-29 | 1994-05-18 | Zeneca Ltd | Heterocyclic compounds |
| JPH08508291A (ja) * | 1993-03-29 | 1996-09-03 | ゼネカ・リミテッド | 複素環誘導体 |
| US5652242A (en) * | 1993-03-29 | 1997-07-29 | Zeneca Limited | Heterocyclic derivatives |
| US5441952A (en) * | 1993-04-05 | 1995-08-15 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| US5334596A (en) * | 1993-05-11 | 1994-08-02 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| SE9301916D0 (sv) * | 1993-06-03 | 1993-06-03 | Ab Astra | New peptides derivatives |
| US6984627B1 (en) * | 1993-06-03 | 2006-01-10 | Astrazeneca Ab | Peptide derivatives |
| US5612355A (en) * | 1993-06-23 | 1997-03-18 | G. D. Searle & Co. | Phenyl amidine lactones useful as platelet aggregation inhibitors |
| 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 |
| WO1995001336A1 (fr) * | 1993-06-30 | 1995-01-12 | Sumitomo Pharmaceuticals Co., Ltd. | Nouveau derive de piperidine |
| US5397791A (en) * | 1993-08-09 | 1995-03-14 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| CA2174516A1 (fr) * | 1993-10-19 | 1995-04-27 | Yoshiharu Ikeda | Derive d'acide 2,3-diaminopropionique |
| US5849736A (en) * | 1993-11-24 | 1998-12-15 | The Dupont Merck Pharmaceutical Company | Isoxazoline and isoxazole fibrinogen receptor antagonists |
| 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 |
| 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 |
| MA23420A1 (fr) * | 1994-01-07 | 1995-10-01 | Smithkline Beecham Corp | Antagonistes bicycliques de fibrinogene. |
| US5821241A (en) * | 1994-02-22 | 1998-10-13 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| ES2186720T3 (es) * | 1994-05-27 | 2003-05-16 | Merck & Co Inc | Composiciones para inhibir la reabsorcion osea mediada por osteoclastos. |
| US6458784B1 (en) | 1994-06-29 | 2002-10-01 | Smithkline Beecham Corporation | Vitronectin receptor antagonists |
| 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 |
| US6117910A (en) * | 1994-12-13 | 2000-09-12 | Smithkline Beecham Corporation | Bicyclic fibrinogen antagonists |
| EP0796098A4 (fr) * | 1994-12-22 | 1998-04-29 | Smithkline Beecham Corp | Antagonistes des recepteurs du fibrinogene |
| US5719144A (en) * | 1995-02-22 | 1998-02-17 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| IL118007A0 (en) * | 1995-05-24 | 1996-08-04 | Du Pont Merck Pharma | Isoxazoline compounds pharmaceutical compositions containing them and their use |
| ZA963391B (en) * | 1995-05-24 | 1997-10-29 | Du Pont Merck Pharma | Isoxazoline fibrinogen receptor antagonists. |
| US5977101A (en) * | 1995-06-29 | 1999-11-02 | Smithkline Beecham Corporation | Benzimidazoles/Imidazoles Linked to a Fibrinogen Receptor Antagonist Template Having Vitronectin Receptor Antagonist Activity |
| AU702487B2 (en) * | 1995-08-30 | 1999-02-25 | G.D. Searle & Co. | Meta-guanidine, urea, thiourea or azacyclic amino benzoic acid derivatives as integrin antagonists |
| US6100423A (en) * | 1995-08-30 | 2000-08-08 | G. D. Searle & Co. | Amino benzenepropanoic acid compounds and derivatives thereof |
| US5789421A (en) * | 1995-10-26 | 1998-08-04 | Merck & Co., Inc. | Fibrinogen receptor antagonist |
| US5733919A (en) * | 1995-10-27 | 1998-03-31 | Merck & Co., Inc. | Compositions for inhibiting platelet aggregation |
| TW385248B (en) * | 1995-10-27 | 2000-03-21 | Merck & Co Inc | Pharmaceutical compositions for intravenous administration for inhibiting platelet aggregation |
| US5972967A (en) * | 1996-10-23 | 1999-10-26 | Merck & Co., Inc. | Compositions for inhibiting platelet aggregation |
| DE19548709A1 (de) * | 1995-12-23 | 1997-07-03 | Merck Patent Gmbh | Tyrosinderivate |
| US5952306A (en) * | 1996-01-16 | 1999-09-14 | Merck & Co., Inc. | Integrin receptor antagonists |
| CA2246756A1 (fr) * | 1996-02-28 | 1997-09-04 | Merck & Co., Inc. | Antagonistes des recepteurs de fibrinogenes |
| US5780480A (en) * | 1996-02-28 | 1998-07-14 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| AU2340997A (en) * | 1996-03-27 | 1997-10-17 | Merck & Co., Inc. | A method for inhibiting clot formation |
| ATE203515T1 (de) * | 1996-03-29 | 2001-08-15 | Searle & Co | Meta-substituierte phenylsulphonamidderivate |
| ES2179318T3 (es) * | 1996-03-29 | 2003-01-16 | Searle & Co | Derivados de acido cinamico y su uso como antagonistas de integrina. |
| WO1997036858A1 (fr) * | 1996-03-29 | 1997-10-09 | G.D. Searle & Co. | Derives de l'acide alcanoique de cyclopropyle |
| PT891325E (pt) * | 1996-03-29 | 2002-07-31 | Searle & Co | Derivados do acido fenilpropanoico para-substituido como antagonistas de integrina |
| CA2250464A1 (fr) * | 1996-03-29 | 1997-10-09 | G.D. Searle & Co. | Derives de phenylene meta-substitues, utilises comme antagonistes ou inhibiteurs de l'integrine alphavbeta3 |
| JP2000515133A (ja) | 1996-07-01 | 2000-11-14 | イーライ・リリー・アンド・カンパニー | 血糖降下性および脂質低下性の化合物 |
| US6653331B2 (en) * | 1996-07-03 | 2003-11-25 | Pharmacia & Upjohn Company | Targeted drug delivery using sulfonamide derivatives |
| WO1998006707A1 (fr) * | 1996-08-15 | 1998-02-19 | Dupont Pharmaceuticals Company | Carbamates et isoxazolidines cycliques antagonistes de l'iib/iiia |
| US5977138A (en) * | 1996-08-15 | 1999-11-02 | Schering Corporation | Ether muscarinic antagonists |
| US6004955A (en) * | 1996-08-15 | 1999-12-21 | Dupont Pharmaceuticals Company | Cyclic carbamates and isoxazolidines as IIb/IIIa antagonists |
| US5900414A (en) * | 1996-08-29 | 1999-05-04 | Merck & Co., Inc. | Methods for administering integrin receptor antagonists |
| US5978698A (en) * | 1996-10-08 | 1999-11-02 | Merck & Co., Inc. | Angioplasty procedure using nonionic contrast media |
| JP4498471B2 (ja) * | 1996-11-27 | 2010-07-07 | アヴェンティス ファーマシューティカルズ インコーポレイテッド | 抗―Xa活性を有する化合物及び血小板凝集拮抗剤化合物を含有する製薬組成物 |
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| US6294549B1 (en) | 1997-07-23 | 2001-09-25 | Merck & Co., Inc. | Method for eliciting an αvβ5 or dual αvβ3/αvβ5 antagonizing effect |
| CA2309204A1 (fr) * | 1997-11-26 | 1999-06-03 | Dupont Pharmaceuticals Company | 1,3,4-thiadiazoles et 1,3,4-oxadiazoles utilises comme antagonistes de .alpha.v.beta.3 |
| 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 |
| CA2318731C (fr) | 1998-01-29 | 2012-05-29 | Tularik Inc. | Modulateurs du recepteur active de la proliferation des peroxysomes (ppar.gamma.) |
| US6583157B2 (en) | 1998-01-29 | 2003-06-24 | Tularik Inc. | Quinolinyl and benzothiazolyl modulators |
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| WO1999038827A1 (fr) * | 1998-02-02 | 1999-08-05 | Merck & Co., Inc. | INHIBITION DE L'AGREGATION PLAQUETTAIRE AU MOYEN D'UNE COMBINAISON D'HEPARINE A FAIBLE POIDS MOLECULAIRE ET D'ANTAGONISTE DE RECEPTEUR DE GP IIb/IIIa |
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| US6136804A (en) | 1998-03-13 | 2000-10-24 | Merck & Co., Inc. | Combination therapy for treating, preventing, or reducing the risks associated with acute coronary ischemic syndrome and related conditions |
| WO1999050249A2 (fr) * | 1998-04-01 | 1999-10-07 | Du Pont Pharmaceuticals Company | Antagonistes de l'integrine |
| AU4584199A (en) | 1998-06-29 | 2000-01-17 | Du Pont Pharmaceuticals Company | Cyclic carbamates and isoxazolidines as iib/iiia antagonists |
| DE69929453T2 (de) * | 1998-11-04 | 2006-07-20 | Rhodia Chimie | Zur sulfonierung von perhalogenierten sulfanilid verwendbare verfahren und reagenz zur sulfonierung |
| JP2002535316A (ja) * | 1999-01-22 | 2002-10-22 | エラン ファーマシューティカルズ,インコーポレイテッド | Vla−4により媒介される白血球接着を阻害する縮合環へテロアリールおよび複素環式化合物 |
| WO2000043354A2 (fr) | 1999-01-22 | 2000-07-27 | Elan Pharmaceuticals, Inc. | Composes inhibant l'adhesion leucocytaire provoquee par vla-4 |
| KR100711840B1 (ko) * | 1999-01-22 | 2007-05-02 | 엘란 파마슈티칼스, 인크. | Vla-4 관련 질환 치료용 아실 유도체 |
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1991
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- 1991-09-20 IL IL9954091A patent/IL99540A/en active Protection Beyond IP Right Term
- 1991-09-23 CA CA002052073A patent/CA2052073C/fr not_active Expired - Lifetime
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- 1991-09-27 DE DE1991625235 patent/DE19875054I2/de active Active
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- 1991-09-27 EP EP91308850A patent/EP0478363B1/fr not_active Expired - Lifetime
- 1991-09-27 DE DE69125235T patent/DE69125235T2/de not_active Expired - Lifetime
- 1991-09-27 EP EP96202038A patent/EP0743302B1/fr not_active Expired - Lifetime
- 1991-09-27 DK DK91308850.6T patent/DK0478363T3/da active
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- 1992-03-18 PL PL92305248A patent/PL172687B1/pl unknown
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- 1992-03-18 SK SK1023-94A patent/SK281233B6/sk not_active IP Right Cessation
- 1992-03-18 RU RU94041739A patent/RU2116296C1/ru active
- 1992-03-18 WO PCT/US1992/002249 patent/WO1993019046A1/fr not_active Ceased
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