DE202010018378U1 - PAR-1-Aktivierung durch Metalloproteinase-1 (MMP-1) - Google Patents
PAR-1-Aktivierung durch Metalloproteinase-1 (MMP-1) Download PDFInfo
- Publication number
- DE202010018378U1 DE202010018378U1 DE202010018378.2U DE202010018378U DE202010018378U1 DE 202010018378 U1 DE202010018378 U1 DE 202010018378U1 DE 202010018378 U DE202010018378 U DE 202010018378U DE 202010018378 U1 DE202010018378 U1 DE 202010018378U1
- Authority
- DE
- Germany
- Prior art keywords
- mmp
- par
- par1
- platelet
- collagen
- 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.)
- Expired - Lifetime
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/10—Peptides having 12 to 20 amino acids
-
- 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
-
- 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
- A61K31/65—Tetracyclines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/08—Peptides having 5 to 11 amino acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L17/00—Materials for surgical sutures or for ligaturing blood vessels ; Materials for prostheses or catheters
- A61L17/005—Materials for surgical sutures or for ligaturing blood vessels ; Materials for prostheses or catheters containing a biologically active substance, e.g. a medicament or a biocide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L27/54—Biologically active materials, e.g. therapeutic substances
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L29/00—Materials for catheters, medical tubing, cannulae, or endoscopes or for coating catheters
- A61L29/14—Materials characterised by their function or physical properties, e.g. lubricating compositions
- A61L29/16—Biologically active materials, e.g. therapeutic substances
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
- A61L31/14—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L31/16—Biologically active materials, e.g. therapeutic substances
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/40—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/40—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
- A61L2300/42—Anti-thrombotic agents, anticoagulants, anti-platelet agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/40—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
- A61L2300/432—Inhibitors, antagonists
- A61L2300/434—Inhibitors, antagonists of enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/40—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
- A61L2300/432—Inhibitors, antagonists
- A61L2300/436—Inhibitors, antagonists of receptors
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Organic Chemistry (AREA)
- Immunology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Vascular Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Surgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Materials Engineering (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Biophysics (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- Endocrinology (AREA)
- Genetics & Genomics (AREA)
- Urology & Nephrology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16835309P | 2009-04-10 | 2009-04-10 | |
| US16836009P | 2009-04-10 | 2009-04-10 | |
| US61/168,353 | 2009-04-10 | ||
| US61/168,360 | 2009-04-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE202010018378U1 true DE202010018378U1 (de) | 2016-04-07 |
Family
ID=42936908
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE202010018378.2U Expired - Lifetime DE202010018378U1 (de) | 2009-04-10 | 2010-04-12 | PAR-1-Aktivierung durch Metalloproteinase-1 (MMP-1) |
Country Status (7)
| Country | Link |
|---|---|
| US (3) | US20120121706A1 (https=) |
| EP (3) | EP2416799B1 (https=) |
| JP (1) | JP2012523438A (https=) |
| AU (1) | AU2010233089B2 (https=) |
| CA (1) | CA2758322C (https=) |
| DE (1) | DE202010018378U1 (https=) |
| WO (1) | WO2010118435A2 (https=) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9745347B2 (en) | 2010-12-30 | 2017-08-29 | Hadasit Medical Research Services And Development Ltd. | PAR1 and PAR2 c-tail peptides and peptide mimetics |
| EP2606828B1 (en) * | 2011-12-20 | 2018-04-11 | Angioclinic AG | Hyaluronic acid and its use for treating venous insufficiency and varicose veins |
| EP2681209B1 (en) * | 2011-03-02 | 2018-05-09 | Aquilus Pharmaceuticals, Inc | Compounds and methods for the treatment of pain and other disorders |
| EP3351641A1 (en) * | 2011-04-08 | 2018-07-25 | Tufts Medical Center, Inc. | Pepducin design and use |
| CN104271150A (zh) | 2012-01-12 | 2015-01-07 | 比奥根艾迪克Ma公司 | 嵌合因子viii多肽及其用途 |
| JP6256882B2 (ja) | 2012-02-15 | 2018-01-10 | アムニクス オペレーティング インコーポレイテッド | 第viii因子組成物、ならびに組成物の作製方法および用途 |
| EP2822577B1 (en) | 2012-02-15 | 2019-02-06 | Bioverativ Therapeutics Inc. | Recombinant factor viii proteins |
| WO2013183725A1 (ja) * | 2012-06-06 | 2013-12-12 | 国立大学法人九州大学 | 非ヒトモデル動物、非ヒトモデル動物の作製方法及び抗血栓薬のスクリーニング方法 |
| CN104661674A (zh) | 2012-07-11 | 2015-05-27 | 阿穆尼克斯运营公司 | 具有xten和血管性血友病因子蛋白的因子viii复合物、及其用途 |
| US9789209B2 (en) * | 2013-03-14 | 2017-10-17 | The Regents Of The University Of California, Berke | Activatable membrane-interacting peptides and methods of use |
| EP3013359A4 (en) * | 2013-06-28 | 2017-01-25 | Biogen MA Inc. | Thrombin cleavable linker |
| TW202003554A (zh) | 2013-08-14 | 2020-01-16 | 美商百歐維拉提夫治療公司 | 因子viii-xten融合物及其用途 |
| HK1223096A1 (zh) | 2013-09-25 | 2017-07-21 | Vertex Pharmaceuticals Incorporated | 用作par-2信號通路抑制劑的咪唑並噠嗪 |
| AU2015204646B2 (en) | 2014-01-10 | 2020-08-27 | Bioverativ Therapeutics Inc. | Factor VIII chimeric proteins and uses thereof |
| WO2015107139A1 (en) * | 2014-01-17 | 2015-07-23 | Proyecto De Biomedicina Cima, S.L. | Compounds for use as antifibrinolytic agents |
| US20160000791A1 (en) | 2014-07-07 | 2016-01-07 | Mayo Foundation For Medical Education And Research | Par1 modulation to alter myelination |
| WO2016205062A1 (en) * | 2015-06-15 | 2016-12-22 | Shifa Biomedical Corporation | Antithrombotic therapies |
| CN106551944A (zh) * | 2015-09-25 | 2017-04-05 | 南开大学 | 四环素类衍生物作为par-1抑制剂的用途 |
| MX2019006444A (es) | 2016-12-02 | 2019-10-30 | Bioverativ Therapeutics Inc | Métodos de tratamiento de artropatía hemofílica utilizando factores de coagulación quiméricos. |
| JP7257333B2 (ja) * | 2017-12-28 | 2023-04-13 | 株式会社カネカ | 細胞凝集抑制剤 |
| PL3793588T3 (pl) | 2018-05-18 | 2025-09-01 | Bioverativ Therapeutics Inc. | Sposoby leczenia hemofilii a |
| WO2020172113A1 (en) * | 2019-02-18 | 2020-08-27 | Lankenau Institute For Medical Research | Scar reducing wound closure materials |
| US11419809B2 (en) | 2019-06-27 | 2022-08-23 | L'oreal | Hair treatment compositions and methods for treating hair |
| KR102612229B1 (ko) * | 2021-05-21 | 2023-12-08 | 가천대학교 산학협력단 | N-[(4'-브로모[1,1'-바이페닐]-4-일)설포닐]-l-발린 또는 이의 약제학적으로 허용 가능한 염을 포함하는 아밀로이드 베타의 올리고머화 및 피브릴화 억제용 조성물 |
| US20230011767A1 (en) * | 2021-07-09 | 2023-01-12 | Boston Scientific Scimed, Inc. | Direct oral anticoagulant-eluting medical device |
Citations (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2980584A (en) | 1957-10-29 | 1961-04-18 | Pfizer & Co C | Parenteral magnesium oxytetracycline acetic or lactic acid carboxamide vehicle preparation |
| US2990331A (en) | 1956-11-23 | 1961-06-27 | Pfizer & Co C | Stable solutions of salts of tetracyclines for parenteral administration |
| US3062717A (en) | 1958-12-11 | 1962-11-06 | Pfizer & Co C | Intramuscular calcium tetracycline acetic or lactic acid carboxamide vehicle preparation |
| US3165531A (en) | 1962-03-08 | 1965-01-12 | Pfizer & Co C | 13-substituted-6-deoxytetracyclines and process utilizing the same |
| US3454697A (en) | 1965-06-08 | 1969-07-08 | American Cyanamid Co | Tetracycline antibiotic compositions for oral use |
| US3557280A (en) | 1966-05-31 | 1971-01-19 | Koninklijke Gist Spiritus | Stable solutions of oxytetracycline suitable for parenteral and peroral administration and process of preparation |
| US3674859A (en) | 1968-06-28 | 1972-07-04 | Pfizer | Aqueous doxycycline compositions |
| US3784701A (en) | 1970-09-21 | 1974-01-08 | American Cyanamid Co | Compositions containing substituted benzoylpropionic acids and method of use to treat inflammation and pain |
| US3957980A (en) | 1972-10-26 | 1976-05-18 | Pfizer Inc. | Doxycycline parenteral compositions |
| US4018889A (en) | 1976-01-02 | 1977-04-19 | Pfizer Inc. | Oxytetracycline compositions |
| US4024272A (en) | 1974-09-06 | 1977-05-17 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Tetracyclic compounds |
| US4126680A (en) | 1977-04-27 | 1978-11-21 | Pfizer Inc. | Tetracycline antibiotic compositions |
| US4529596A (en) | 1982-07-13 | 1985-07-16 | Sanofi, S.A. | Thieno [3,2-c] pyridine derivatives and their therapeutic application |
| WO1986001533A1 (en) | 1984-09-03 | 1986-03-13 | Celltech Limited | Production of chimeric antibodies |
| US4816397A (en) | 1983-03-25 | 1989-03-28 | Celltech, Limited | Multichain polypeptides or proteins and processes for their production |
| US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
| US4847265A (en) | 1987-02-17 | 1989-07-11 | Sanofi | Dextro-rotatory enantiomer of methyl alpha-5 (4,5,6,7-tetrahydro (3,2-c) thieno pyridyl) (2-chlorophenyl)-acetate and the pharmaceutical compositions containing it |
| US4868103A (en) | 1986-02-19 | 1989-09-19 | Enzo Biochem, Inc. | Analyte detection by means of energy transfer |
| US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
| WO1991019813A1 (en) | 1990-06-11 | 1991-12-26 | The University Of Colorado Foundation, Inc. | Nucleic acid ligands |
| EP0519596A1 (en) | 1991-05-17 | 1992-12-23 | Merck & Co. Inc. | A method for reducing the immunogenicity of antibody variable domains |
| US5223409A (en) | 1988-09-02 | 1993-06-29 | Protein Engineering Corp. | Directed evolution of novel binding proteins |
| US5225539A (en) | 1986-03-27 | 1993-07-06 | Medical Research Council | Recombinant altered antibodies and methods of making altered antibodies |
| US5270163A (en) | 1990-06-11 | 1993-12-14 | University Research Corporation | Methods for identifying nucleic acid ligands |
| US5283317A (en) | 1987-08-03 | 1994-02-01 | Ddi Pharmaceuticals, Inc. | Intermediates for conjugation of polypeptides with high molecular weight polyalkylene glycols |
| US5288726A (en) | 1991-09-09 | 1994-02-22 | Ube Industries Limited | Tetrahydrothienopyridine derivatives, furo and pyrrolo analogs thereof and their preparation and uses for inhibiting blood platelet aggregation |
| US5300501A (en) | 1990-12-03 | 1994-04-05 | Celltech Limited | Peptidyl derivatives |
| WO1994010300A1 (en) | 1992-10-30 | 1994-05-11 | The General Hospital Corporation | Interaction trap system for isolating novel proteins |
| EP0239400B1 (en) | 1986-03-27 | 1994-08-03 | Medical Research Council | Recombinant antibodies and methods for their production |
| WO1995013289A1 (en) | 1993-11-10 | 1995-05-18 | Chiroscience Limited | Peptidyl compounds and their therapeutic use as inhibitors of metalloproteinases |
| US5455258A (en) | 1993-01-06 | 1995-10-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
| EP0451216B1 (en) | 1988-12-28 | 1996-01-24 | Protein Design Labs, Inc. | Humanized immunoglobulins and their production and use |
| WO1996011209A1 (en) | 1994-10-05 | 1996-04-18 | Chiroscience Limited | Peptidyl compounds and their therapeutic use as inhibitors of metalloproteases |
| WO1996015096A1 (en) | 1994-11-15 | 1996-05-23 | Bayer Corporation | Substituted 4-biarylbutyric or 5-biarylpentanoic acids and derivatives as matrix metalloprotease inhibitiors |
| US5525348A (en) | 1989-11-02 | 1996-06-11 | Sts Biopolymers, Inc. | Coating compositions comprising pharmaceutical agents |
| US5530128A (en) | 1992-06-03 | 1996-06-25 | Celltech Therapeutics Limited | N-sulphonylamino derivatives of dipetide compounds as metalloproteinase inhibitors |
| US5552419A (en) | 1993-01-06 | 1996-09-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
| US5631169A (en) | 1992-01-17 | 1997-05-20 | Joseph R. Lakowicz | Fluorescent energy transfer immunoassay |
| US5837313A (en) | 1995-04-19 | 1998-11-17 | Schneider (Usa) Inc | Drug release stent coating process |
| US6326155B1 (en) | 1995-03-20 | 2001-12-04 | Dyax Corp. | Engineering affinity ligands for macromolecules |
| US6429210B1 (en) | 1998-06-15 | 2002-08-06 | Sanofi-Synthelabo | Polymorphic clopidogrel hydrogenesulphate form |
| US6693115B2 (en) | 2000-07-06 | 2004-02-17 | Sankyo Company, Limited | Acid addition salts of hydropyridine derivatives |
| US20040127420A1 (en) | 2001-08-16 | 2004-07-01 | Stephen Quirk | Metalloproteinase inhibitors for wound healing |
| US20050020607A1 (en) | 1999-05-03 | 2005-01-27 | Newton Roger Schofield | Statin-MMP inhibitor combinations |
| US20050191333A1 (en) | 2002-08-26 | 2005-09-01 | Biotegra, Inc. | Drug eluting coatings for medical implants and methods of use |
| WO2005097223A1 (en) | 2004-03-26 | 2005-10-20 | Surmodics, Inc. | Composition and method for preparing biocompatible surfaces |
| US20060204533A1 (en) | 2005-03-14 | 2006-09-14 | Biotegra, Inc. | Drug Delivery Compositions and Related Methods |
| US20070179090A1 (en) | 2000-04-21 | 2007-08-02 | Athan Kuliopulos | G protein coupled receptor agonists and antagonists and methods of activating and inhibiting G protein coupled receptors using the same |
| WO2008011107A2 (en) | 2006-07-18 | 2008-01-24 | Irm Llc | Antagonists of protease activated receptor-1 (par1) |
| US20090018646A1 (en) | 2007-07-10 | 2009-01-15 | Zhao Jonathon Z | Coating Employing an Anti-Thrombotic Conjugate |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6858577B1 (en) | 1999-06-29 | 2005-02-22 | Ortho-Mcneil Pharmaceutical, Inc. | Indole peptidomimetics as thrombin receptor antagonists |
| EP2348047A1 (en) * | 2000-04-21 | 2011-07-27 | New England Medical Center | G protein coupled receptor (GPCR) agonists and antagonists and methods of activating and inhibiting GPCR using the same |
| JP4469467B2 (ja) * | 2000-06-29 | 2010-05-26 | 帝人株式会社 | 細胞増殖抑制剤 |
| US20050120392A1 (en) | 2002-02-28 | 2005-06-02 | Rubinstein Amy L. | Transgenic zebrafish models for thrombosis |
| AU2004213050B2 (en) * | 2003-02-20 | 2010-09-09 | Proteon Therapeutics, Inc. | Methods for the treatment and prevention of diseases of biological conduits |
| US20050025705A1 (en) | 2003-07-22 | 2005-02-03 | Xinkang Wang | Thrombosis animal models and their use in drug discovery and development |
| US20080069814A1 (en) * | 2005-01-05 | 2008-03-20 | Novacea, Inc. | Prevention of Thrombotic Disorders with Active Vitamin D Compounds or Mimics Thereof |
| CA2843097C (en) * | 2005-05-24 | 2015-10-27 | Inspire M.D Ltd. | Stent apparatuses for treatment via body lumens and methods of use |
| US20080214599A1 (en) | 2005-08-19 | 2008-09-04 | John Thomas Brandt | Use of Par-1/Par-4 Inhibitors for Treating or Preventing Vascular Diseases |
| US20080125354A1 (en) | 2005-11-21 | 2008-05-29 | Florida Atlantic University | Selective inhibition of matrix metalloproteinases |
| JP4861115B2 (ja) * | 2006-09-28 | 2012-01-25 | サントリーホールディングス株式会社 | ラベル、ラベルの製造方法、ラベルの線剥離強度の経時安定化方法、及び容器 |
| US7838232B2 (en) * | 2006-10-19 | 2010-11-23 | Auburn University | CaIDAG-GEF1 gene mutations associated with thrombopathy in canines |
| US9719191B2 (en) | 2006-11-29 | 2017-08-01 | The Research Foundation For The State University Of New York | Methods for identifying ligands that target nucleic acid molecules and nucleic acid structural motifs |
| US7947447B2 (en) | 2007-01-16 | 2011-05-24 | Somalogic, Inc. | Method for generating aptamers with improved off-rates |
| WO2008118320A1 (en) | 2007-03-23 | 2008-10-02 | Schering Corporation | Reduction of adverse events.after percutaneous intervention by use of a thrombin receptor antagonist |
| WO2008116468A2 (en) * | 2007-03-26 | 2008-10-02 | Dako Denmark A/S | Mhc peptide complexes and uses thereof in infectious diseases |
| US8383156B2 (en) | 2007-04-30 | 2013-02-26 | Cordis Corporation | Coating for a medical device having an anti-thrombotic conjugate |
| JP5483023B2 (ja) * | 2008-03-27 | 2014-05-07 | 国立大学法人東北大学 | がん細胞運動およびがん細胞浸潤抑制剤 |
| WO2010119455A2 (en) * | 2009-04-15 | 2010-10-21 | Sun Pharma Advanced Research Company Ltd. | An injectable sustained release pharmaceutical composition |
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-
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- 2014-08-14 US US14/460,353 patent/US9376499B2/en active Active
-
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- 2016-05-26 US US15/165,988 patent/US20170065668A1/en not_active Abandoned
Patent Citations (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2990331A (en) | 1956-11-23 | 1961-06-27 | Pfizer & Co C | Stable solutions of salts of tetracyclines for parenteral administration |
| US2980584A (en) | 1957-10-29 | 1961-04-18 | Pfizer & Co C | Parenteral magnesium oxytetracycline acetic or lactic acid carboxamide vehicle preparation |
| US3062717A (en) | 1958-12-11 | 1962-11-06 | Pfizer & Co C | Intramuscular calcium tetracycline acetic or lactic acid carboxamide vehicle preparation |
| US3165531A (en) | 1962-03-08 | 1965-01-12 | Pfizer & Co C | 13-substituted-6-deoxytetracyclines and process utilizing the same |
| US3454697A (en) | 1965-06-08 | 1969-07-08 | American Cyanamid Co | Tetracycline antibiotic compositions for oral use |
| US3557280A (en) | 1966-05-31 | 1971-01-19 | Koninklijke Gist Spiritus | Stable solutions of oxytetracycline suitable for parenteral and peroral administration and process of preparation |
| US3674859A (en) | 1968-06-28 | 1972-07-04 | Pfizer | Aqueous doxycycline compositions |
| US3784701A (en) | 1970-09-21 | 1974-01-08 | American Cyanamid Co | Compositions containing substituted benzoylpropionic acids and method of use to treat inflammation and pain |
| US3957980A (en) | 1972-10-26 | 1976-05-18 | Pfizer Inc. | Doxycycline parenteral compositions |
| US4024272A (en) | 1974-09-06 | 1977-05-17 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Tetracyclic compounds |
| US4018889A (en) | 1976-01-02 | 1977-04-19 | Pfizer Inc. | Oxytetracycline compositions |
| US4126680A (en) | 1977-04-27 | 1978-11-21 | Pfizer Inc. | Tetracycline antibiotic compositions |
| US4529596A (en) | 1982-07-13 | 1985-07-16 | Sanofi, S.A. | Thieno [3,2-c] pyridine derivatives and their therapeutic application |
| EP0120694B1 (en) | 1983-03-25 | 1993-07-21 | Celltech Therapeutics Limited | Processes for the production of multichain polypeptides or proteins |
| US4816397A (en) | 1983-03-25 | 1989-03-28 | Celltech, Limited | Multichain polypeptides or proteins and processes for their production |
| EP0125023B1 (en) | 1983-04-08 | 1991-06-05 | Genentech, Inc. | Recombinant immunoglobulin preparations, methods for their preparation, dna sequences, expression vectors and recombinant host cells therefor |
| US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
| WO1986001533A1 (en) | 1984-09-03 | 1986-03-13 | Celltech Limited | Production of chimeric antibodies |
| EP0194276B1 (en) | 1984-09-03 | 1993-08-11 | Celltech Therapeutics Limited | Production of chimeric antibodies |
| US4868103A (en) | 1986-02-19 | 1989-09-19 | Enzo Biochem, Inc. | Analyte detection by means of energy transfer |
| EP0239400B1 (en) | 1986-03-27 | 1994-08-03 | Medical Research Council | Recombinant antibodies and methods for their production |
| US5225539A (en) | 1986-03-27 | 1993-07-06 | Medical Research Council | Recombinant altered antibodies and methods of making altered antibodies |
| US4847265A (en) | 1987-02-17 | 1989-07-11 | Sanofi | Dextro-rotatory enantiomer of methyl alpha-5 (4,5,6,7-tetrahydro (3,2-c) thieno pyridyl) (2-chlorophenyl)-acetate and the pharmaceutical compositions containing it |
| US5283317A (en) | 1987-08-03 | 1994-02-01 | Ddi Pharmaceuticals, Inc. | Intermediates for conjugation of polypeptides with high molecular weight polyalkylene glycols |
| US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
| US5223409A (en) | 1988-09-02 | 1993-06-29 | Protein Engineering Corp. | Directed evolution of novel binding proteins |
| EP0451216B1 (en) | 1988-12-28 | 1996-01-24 | Protein Design Labs, Inc. | Humanized immunoglobulins and their production and use |
| US5525348A (en) | 1989-11-02 | 1996-06-11 | Sts Biopolymers, Inc. | Coating compositions comprising pharmaceutical agents |
| WO1991019813A1 (en) | 1990-06-11 | 1991-12-26 | The University Of Colorado Foundation, Inc. | Nucleic acid ligands |
| US5475096A (en) | 1990-06-11 | 1995-12-12 | University Research Corporation | Nucleic acid ligands |
| US5270163A (en) | 1990-06-11 | 1993-12-14 | University Research Corporation | Methods for identifying nucleic acid ligands |
| US5300501A (en) | 1990-12-03 | 1994-04-05 | Celltech Limited | Peptidyl derivatives |
| EP0519596A1 (en) | 1991-05-17 | 1992-12-23 | Merck & Co. Inc. | A method for reducing the immunogenicity of antibody variable domains |
| US5288726A (en) | 1991-09-09 | 1994-02-22 | Ube Industries Limited | Tetrahydrothienopyridine derivatives, furo and pyrrolo analogs thereof and their preparation and uses for inhibiting blood platelet aggregation |
| US5631169A (en) | 1992-01-17 | 1997-05-20 | Joseph R. Lakowicz | Fluorescent energy transfer immunoassay |
| US5530128A (en) | 1992-06-03 | 1996-06-25 | Celltech Therapeutics Limited | N-sulphonylamino derivatives of dipetide compounds as metalloproteinase inhibitors |
| WO1994010300A1 (en) | 1992-10-30 | 1994-05-11 | The General Hospital Corporation | Interaction trap system for isolating novel proteins |
| US5552419A (en) | 1993-01-06 | 1996-09-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
| US5455258A (en) | 1993-01-06 | 1995-10-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
| WO1995013289A1 (en) | 1993-11-10 | 1995-05-18 | Chiroscience Limited | Peptidyl compounds and their therapeutic use as inhibitors of metalloproteinases |
| WO1996011209A1 (en) | 1994-10-05 | 1996-04-18 | Chiroscience Limited | Peptidyl compounds and their therapeutic use as inhibitors of metalloproteases |
| WO1996015096A1 (en) | 1994-11-15 | 1996-05-23 | Bayer Corporation | Substituted 4-biarylbutyric or 5-biarylpentanoic acids and derivatives as matrix metalloprotease inhibitiors |
| US6326155B1 (en) | 1995-03-20 | 2001-12-04 | Dyax Corp. | Engineering affinity ligands for macromolecules |
| US5837313A (en) | 1995-04-19 | 1998-11-17 | Schneider (Usa) Inc | Drug release stent coating process |
| US6429210B1 (en) | 1998-06-15 | 2002-08-06 | Sanofi-Synthelabo | Polymorphic clopidogrel hydrogenesulphate form |
| US20050020607A1 (en) | 1999-05-03 | 2005-01-27 | Newton Roger Schofield | Statin-MMP inhibitor combinations |
| US20070179090A1 (en) | 2000-04-21 | 2007-08-02 | Athan Kuliopulos | G protein coupled receptor agonists and antagonists and methods of activating and inhibiting G protein coupled receptors using the same |
| US6693115B2 (en) | 2000-07-06 | 2004-02-17 | Sankyo Company, Limited | Acid addition salts of hydropyridine derivatives |
| US20040127420A1 (en) | 2001-08-16 | 2004-07-01 | Stephen Quirk | Metalloproteinase inhibitors for wound healing |
| US20050191333A1 (en) | 2002-08-26 | 2005-09-01 | Biotegra, Inc. | Drug eluting coatings for medical implants and methods of use |
| WO2005097223A1 (en) | 2004-03-26 | 2005-10-20 | Surmodics, Inc. | Composition and method for preparing biocompatible surfaces |
| US20060204533A1 (en) | 2005-03-14 | 2006-09-14 | Biotegra, Inc. | Drug Delivery Compositions and Related Methods |
| WO2006099514A2 (en) | 2005-03-14 | 2006-09-21 | Biotegra, Inc. | Drug delivery compositions and related methods |
| WO2008011107A2 (en) | 2006-07-18 | 2008-01-24 | Irm Llc | Antagonists of protease activated receptor-1 (par1) |
| US20090018646A1 (en) | 2007-07-10 | 2009-01-15 | Zhao Jonathon Z | Coating Employing an Anti-Thrombotic Conjugate |
Non-Patent Citations (99)
| Title |
|---|
| Ausubel et al., Hg., Current Protocols in Molecular Biology, Wiley Interscience, 2006 |
| Ausubel, F. et al., Hg. (1999), Current Protocols in Molecular Biology, J. Wiley: New York |
| Ausubel, F. et al., Hg., Current Protocols in Molecular Biology 1999, J. Wiley: New York |
| Bartel et al. (1993) Biotechniques. 14: 920-924 |
| Bergmeier et al., 2003 |
| Bergmeier et al., 2004 |
| Berman et al., 1992 |
| Bhatt und Topol, 2003 |
| Biomol, Kat.-Nr. SE 361 |
| Bird et al., Science, 242: 423-426 (1988) |
| Boire et al., 2005 |
| Carell et al. (1994) Angew. Chem. Int. Ed. Engl. 33: 2061 |
| Carrell et al. (1994) Angew. Chem. Int. Ed. Engl. 33: 2059 |
| Chang, 1985 |
| Chesney et al., 1974 |
| Cho et al. (1993) Science 261: 1303 |
| Clontech Inc., CA, Gossen und Bujard (1992) Proc. Natl. Acad. Sci. USA 89: 5547 |
| Coughlin, 2000 |
| Covic et al., 2002a |
| Cull et al. (1992) Proc Natl Acad Sci USA 89: 1865-1869 |
| Cwirla et al. (1990) Proc. Natl. Acad. Sci. 87: 6378-6382 |
| De Witt et al. (1993) Proc. Natl. Acad. Sci. U.S.A. 90: 6909 |
| Devlin (1990) Science 249: 404-406 |
| Dollery und Libby, 2006 |
| Egeblad und Werb, 2002 |
| Erb et al. (1994) Proc. Natl. Acad. Sci. USA 91: 11422 |
| Felici (1991) J. Mol. Biol. 222: 301-310 |
| Fodor (1993) Nature 364: 555-556 |
| Fressinaud et al., 1992 |
| Furie und Furie, 2008 |
| Gallop et al. (1994) J. Med. Chem. 37: 1233 |
| Galt et al., 2002 |
| Gast et al., 1994 |
| Giesen et al., 1999 |
| Glass und Witztum, 2001 |
| Glassand Witztum, 2001 |
| Gluzman (1981) Cell 123: 175-182 |
| Goeddel, (1990) Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Kalifornien |
| Gogly et al., 1998 |
| Hage, D. S. und Tweed, S. A. (1997) J Chromatogr B Biomed Sci Appl. 699: 499-525 |
| Heegaard, N. H., (1998) J Mol Recognit 11: 141-8 |
| Houghten (1992) Biotechniques 13: 412-421 |
| Huang et al., 2007 |
| Huebner et al., 1998 |
| Inauen et al., 1990 |
| Jackson et al., 2003 |
| Kaneider et al., 2007 |
| Kazes et al., 2000 |
| Kennebunk, ME |
| Kuliopulos 1999 |
| Kuliopulos et al., 1999 |
| Kuliopulos et al., 2004 |
| Kuliopulos, 1999 |
| Ladner s. o. |
| Lam (1991) Nature 354: 82-84 |
| Lam (1997) Anticancer Drug Des. 12: 145 |
| Leger et al., 2006a |
| Leger et al., 2006b |
| Levy et al., 2001 |
| Loew et al., 200 |
| Loew et al., 2000 |
| Mackman, 2004 |
| Madura et al. (1993) J. Biol. Chem. 268: 12046-12054 |
| Mann et al., 2007 |
| McConnell, H. M. et al. (1992) Science 257: 1906-1912 |
| Moers et al., 2003 |
| Nelson, A. et al., (2000) J. Clin. Oncol. 18, 1135-1149 |
| Netzel-Arnett et al., 1991 |
| New England Biolabs, Beverly, Mass. |
| Newman et al., BioTechnology, 10: 1455-1460 (1992) |
| Offermanns et al., 1994 |
| Okorie et al., 2008 |
| Paillard (1989) Human Gene Therapy 9: 983 |
| Parry et al., 1996 |
| Pearce et al., 2005 |
| Pharmacia Biotech Inc.; Smith, D. B. und Johnson, K. S. (1988) Gene 67: 31-40 |
| Pharmacia, Piscataway, N. J. |
| Rand et al., 1996 |
| Rivas, G. und Minton, A. P. (1993) Trends Biochem Sci 18: 284-7 |
| Ruggeri, 2002 |
| Sambrook und Russell, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Press, NY, 2001 |
| Sawicki et al., 1997 |
| Schwertz et al., 2006 |
| Scott und Smith (1990) Science 249: 386-390 |
| Seeley et al., 2003 |
| Sjolander, S., und Urbaniczky, C. (1991) Anal. Chem. 63: 2338-2345 |
| Stephens et al., 2004 |
| Sukhova et al., 1999 |
| Sundaresan und Famdale, 2002 |
| Sundaresan und Farndale, 2002 |
| Szabo et al. (1995) Curr. Opin. Struct. Biol. 5: 699-705 |
| Turk et al., 2001 |
| Veen et al., 1993 |
| Vu et al., 1991 |
| Woessner, J. F. und Nagase, H. (2000) Matrix Metalloproteinases and TIMPs, Oxford University Press, Oxford |
| Woessner, J. F. und Nagase, H., s. o. |
| Zervos et al. (1993) Cell 72: 223-232 |
| Zuckermann et al. (1994). J. Med. Chem. 37: 2678 |
| Zuckermann, R. N. et al. (1994) J. Med. Chem. 37: 2678-85 |
Also Published As
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| US9376499B2 (en) | 2016-06-28 |
| EP2990051B1 (en) | 2016-10-26 |
| EP2416799A2 (en) | 2012-02-15 |
| WO2010118435A2 (en) | 2010-10-14 |
| JP2012523438A (ja) | 2012-10-04 |
| EP3061460A1 (en) | 2016-08-31 |
| AU2010233089B2 (en) | 2016-05-26 |
| EP2990051A1 (en) | 2016-03-02 |
| WO2010118435A3 (en) | 2011-03-17 |
| US20170065668A1 (en) | 2017-03-09 |
| CA2758322C (en) | 2019-04-02 |
| EP2416799B1 (en) | 2017-11-01 |
| CA2758322A1 (en) | 2010-10-14 |
| US20150023975A1 (en) | 2015-01-22 |
| EP2416799A4 (en) | 2013-04-17 |
| US20120121706A1 (en) | 2012-05-17 |
| AU2010233089A1 (en) | 2011-11-03 |
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