WO2007056213A2 - Drug-eluting stents coated with p2y12 receptor antagonist compound - Google Patents
Drug-eluting stents coated with p2y12 receptor antagonist compound Download PDFInfo
- Publication number
- WO2007056213A2 WO2007056213A2 PCT/US2006/043085 US2006043085W WO2007056213A2 WO 2007056213 A2 WO2007056213 A2 WO 2007056213A2 US 2006043085 W US2006043085 W US 2006043085W WO 2007056213 A2 WO2007056213 A2 WO 2007056213A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compound
- acetal
- formula
- receptor antagonist
- substituted
- Prior art date
Links
- 0 CCCCNC(Nc1ncnc2c1nc[n]2[C@@](C1OC(c2ccccc2)OC11)O[C@@]1(COP(*)([O-])=O)N)=O Chemical compound CCCCNC(Nc1ncnc2c1nc[n]2[C@@](C1OC(c2ccccc2)OC11)O[C@@]1(COP(*)([O-])=O)N)=O 0.000 description 1
- RDBQIGAKJJHMIA-BCTLUTKKSA-M CCNC(Nc1c2nc[n]([C@@H]3O[C@H](COP([O-])(O)=O)[C@H]4O[C@H](C5C=CC=CC5)OC34)c2ncn1)=O Chemical compound CCNC(Nc1c2nc[n]([C@@H]3O[C@H](COP([O-])(O)=O)[C@H]4O[C@H](C5C=CC=CC5)OC34)c2ncn1)=O RDBQIGAKJJHMIA-BCTLUTKKSA-M 0.000 description 1
- MPBHAGPNVWBUTJ-PLTGJFJPSA-O OP([OH2+])(OC[C@H](C1OC(C#Cc2ccccc2)OC11)O[C@H]1[n]1c(ncnc2NC(Nc3ccccc3)=O)c2nc1)=O Chemical compound OP([OH2+])(OC[C@H](C1OC(C#Cc2ccccc2)OC11)O[C@H]1[n]1c(ncnc2NC(Nc3ccccc3)=O)c2nc1)=O MPBHAGPNVWBUTJ-PLTGJFJPSA-O 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
- A61K31/7072—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7084—Compounds having two nucleosides or nucleotides, e.g. nicotinamide-adenine dinucleotide, flavine-adenine dinucleotide
-
- 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
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/10—Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
- C07H19/207—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids the phosphoric or polyphosphoric acids being esterified by a further hydroxylic compound, e.g. flavine adenine dinucleotide or nicotinamide-adenine dinucleotide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008539086A JP2009514604A (ja) | 2005-11-04 | 2006-11-02 | P2y12受容体アンタゴニスト化合物でコートされた薬剤溶出ステント |
EP06836933A EP1942910A2 (en) | 2005-11-04 | 2006-11-02 | Drug-eluting stents coated with p2y12 receptor antagonist compound |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/267,834 US7452870B2 (en) | 2000-08-21 | 2005-11-04 | Drug-eluting stents coated with P2Y12 receptor antagonist compound |
US11/267,834 | 2005-11-04 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2007056213A2 true WO2007056213A2 (en) | 2007-05-18 |
WO2007056213A3 WO2007056213A3 (en) | 2009-04-30 |
Family
ID=38023857
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2006/043085 WO2007056213A2 (en) | 2005-11-04 | 2006-11-02 | Drug-eluting stents coated with p2y12 receptor antagonist compound |
Country Status (4)
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7618949B2 (en) | 2000-08-21 | 2009-11-17 | Inspire Pharmaceuticals, Inc. | Drug-eluting stents coated with P2Y12 receptor antagonist compound |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2006204159A1 (en) * | 2005-01-06 | 2006-07-13 | Astrazeneca Ab | Novel pyridine compounds |
JP2008537745A (ja) * | 2005-03-30 | 2008-09-25 | インスパイアー ファーマシューティカルズ,インコーポレイティド | 4,6−二置換−テトラヒドロ−フロ、チエノ、ピロロ及びシクロペンタ−[3,4][1,3]ジオキソールの調製のための方法 |
US20080312208A1 (en) * | 2005-07-13 | 2008-12-18 | Astrazeneca Ab | Pyridine Analogues |
TW200815426A (en) * | 2006-06-28 | 2008-04-01 | Astrazeneca Ab | New pyridine analogues II 333 |
EP2041115A4 (en) * | 2006-07-04 | 2010-07-07 | Astrazeneca Ab | NEW PYRIDINE ANALOG |
CN101511792A (zh) * | 2006-07-04 | 2009-08-19 | 阿斯利康(瑞典)有限公司 | 新的吡啶类似物 |
TW200811133A (en) * | 2006-07-04 | 2008-03-01 | Astrazeneca Ab | New pyridine analogues III 334 |
WO2008004941A1 (en) * | 2006-07-04 | 2008-01-10 | Astrazeneca Ab | New pyridine analogues |
EP2076210A2 (en) * | 2006-10-24 | 2009-07-08 | Paul Zamecnik | Medical device coatings and coated stents |
TW200833333A (en) * | 2007-01-12 | 2008-08-16 | Astrazeneca Ab | New pyridine analogues |
EP2111400A4 (en) * | 2007-01-12 | 2010-07-07 | Astrazeneca Ab | Pyridine compounds and their use as P2Y12 antagonists |
CL2008000093A1 (es) * | 2007-01-12 | 2008-08-22 | Astrazeneca Ab | Compuestos derivados de piridina, inhibidores de p2y12; composicion farmaceutica que comprende a dichos compuestos; y su uso para el tratamiento de un desorden de agregacion plaquetaria. |
PE20081892A1 (es) * | 2007-07-13 | 2009-02-21 | Astrazeneca Ab | Nuevos analogos de amino-piridina como agentes antitromboticos |
EP2153833A1 (en) * | 2008-08-14 | 2010-02-17 | Royal College of Surgeons in Ireland | ADP-receptor antagonist for treatment of inflammatory disease |
US20100286765A1 (en) * | 2009-05-07 | 2010-11-11 | Paul Zamecnik | Medical Device Coatings and Coated Stents |
US8609066B2 (en) * | 2009-08-10 | 2013-12-17 | Jaya Brigitte Rosenmeier | Use of UTP for the diagnosis of stenoses and other conditions of restricted blood flow |
US10307292B2 (en) | 2011-07-18 | 2019-06-04 | Mor Research Applications Ltd | Device for adjusting the intraocular pressure |
WO2013033178A1 (en) | 2011-08-30 | 2013-03-07 | University Of Utah Research Foundation | Methods and compositions for treating nephrogenic diabetes insipidus |
US9388127B2 (en) | 2012-04-17 | 2016-07-12 | University College Dublin, National University Of Ireland, Dublin | Thromboxane receptor antagonists |
US9718781B2 (en) | 2012-04-17 | 2017-08-01 | University College Dublin, National University Of Ireland, Dublin | Methods and compounds for treating proliferative disorders and viral infections |
WO2015153401A1 (en) * | 2014-04-04 | 2015-10-08 | Merck Sharp & Dohme Corp | Phosphate based linkers for intracellular delivery of drug conjugates |
EP3310756B1 (en) | 2015-06-16 | 2020-12-09 | ATXA Therapeutics Limited | Thromboxane receptor antagonists |
US10800826B2 (en) | 2015-10-05 | 2020-10-13 | Merck Sharp & Dohme Corp. | Antibody peptide conjugates that have agonist activity at both the glucagon and glucagon-like peptide 1 receptors |
US11510993B2 (en) | 2015-10-06 | 2022-11-29 | Merck Sharp & Dohme Llc | Antibody drug conjugate for anti-inflammatory applications |
WO2017132103A2 (en) | 2016-01-29 | 2017-08-03 | Merck Sharp & Dohme Corp. | Phosphonate linkers and their use to facilitate cellular retention of compounds |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050233062A1 (en) * | 1999-09-03 | 2005-10-20 | Hossainy Syed F | Thermal treatment of an implantable medical device |
Family Cites Families (54)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US732408A (en) * | 1902-09-17 | 1903-06-30 | William F Hanson | Machine for molding crayons. |
US3321462A (en) * | 1963-07-15 | 1967-05-23 | Syntex Corp | Process for the preparation of nucleoside polyphosphates |
GB1407903A (en) | 1973-03-21 | 1975-10-01 | Ici Ltd | Nucleotide derivatives |
DE2934746A1 (de) | 1979-08-28 | 1981-03-19 | A. Nattermann & Cie GmbH, 5000 Köln | Oxoimidazolinalkansaeuren, deren salze und ester sowie verfahren zu ihrer herstellung und diese enthaltende arzneimittel |
JPS5973524A (ja) * | 1982-10-21 | 1984-04-25 | Meito Sangyo Kk | 血栓性疾患処置剤 |
WO1989004321A1 (en) | 1987-11-05 | 1989-05-18 | The Worcester Foundation For Experimental Biology | Diadenosine 5', 5'''-p1, p4-tetraphosphate and analogs thereof as antithrombotic agents |
US5049550A (en) * | 1987-11-05 | 1991-09-17 | Worcester Foundation For Experimental Biology | Diadenosine 5', 5'"-p1, p4,-tetraphosphate analogs as antithrombotic agents |
US5635180A (en) * | 1988-02-17 | 1997-06-03 | Neorx Corporation | Alteration of pharmacokinetics of proteins by charge modification |
GB9015684D0 (en) | 1990-07-17 | 1990-09-05 | Medical Res Council | Synthesis and uses of spin labelled ribonucleosides and ribonucleotides |
NZ239846A (en) * | 1990-09-27 | 1994-11-25 | Merck & Co Inc | Sulphonamide derivatives and pharmaceutical compositions thereof |
US5654285A (en) * | 1991-04-06 | 1997-08-05 | Astra Pharmaceuticals Limited | ADP and ATP analogues, process for making and administration to inhibit ADP-induced platelet aggregation |
ES2078654T3 (es) | 1991-04-06 | 1995-12-16 | Astra Pharma Prod | Analogos de atp. |
US5292498A (en) | 1991-06-19 | 1994-03-08 | The University Of North Carolina At Chapel Hill | Method of treating lung disease with uridine triphosphates |
ES2108425T3 (es) | 1993-02-10 | 1997-12-16 | Astra Pharma Prod | Analogos de atp sustituidos con n-alquilo-2. |
WO1995010538A1 (en) | 1993-10-15 | 1995-04-20 | The University Of North Carolina At Chapel Hill | Dna encoding the human p2u receptor and null cells expressing p2u receptors |
US5814609A (en) * | 1993-10-22 | 1998-09-29 | University Of Southern California | Compositions containing a disintegrin and methods for its use in preventing metastasis and other conditions |
US5656256A (en) | 1994-12-14 | 1997-08-12 | The University Of North Carolina At Chapel Hill | Methods of treating lung disease by an aerosol containing benzamil or phenamil |
EP0796098A4 (en) * | 1994-12-22 | 1998-04-29 | Smithkline Beecham Corp | FIBRINOGEN RECEPTOR ANTAGONISTS |
US5635160A (en) | 1995-06-07 | 1997-06-03 | The University Of North Carolina At Chapel Hill | Dinucleotides useful for the treatment of cystic fibrosis and for hydrating mucus secretions |
EP0840740B1 (en) | 1995-07-11 | 2002-05-02 | AstraZeneca AB | New inhibitors of platelet aggregation |
US5628984A (en) | 1995-07-31 | 1997-05-13 | University Of North Carolina At Chapel Hill | Method of detecting lung disease |
JP3519199B2 (ja) | 1996-02-06 | 2004-04-12 | 株式会社ソニー・コンピュータエンタテインメント | 画像生成装置 |
CN1229114C (zh) | 1996-03-27 | 2005-11-30 | 印斯拜尔药品股份有限公司 | 用三磷酸尿苷和相关化合物治疗纤毛运动障碍的方法 |
US5837861A (en) * | 1997-02-10 | 1998-11-17 | Inspire Pharmaceuticals, Inc. | Dinucleotides and their use as modulators of mucociliary clearance and ciliary beat frequency |
US5900407A (en) * | 1997-02-06 | 1999-05-04 | Inspire Pharmaceuticals, Inc. | Method of treating dry eye disease with uridine triphosphates and related compounds |
US5681823A (en) * | 1996-05-02 | 1997-10-28 | Prp Inc. | P1, P4 -dithio-P2 -P3 -monochloromethylene 5', 5'"-diadenosine P1, P4 -tetraphosphate as antithrombotic agent |
US5789391A (en) | 1996-07-03 | 1998-08-04 | Inspire Pharmaceuticals, Inc. | Method of treating sinusitis with uridine triphosphates and related compounds |
US5968913A (en) | 1996-07-03 | 1999-10-19 | Inspire Pharmaceuticals, Inc. | Pharmaceutical compositions of uridine triphosphate |
US5962432A (en) | 1996-07-03 | 1999-10-05 | Inspire Pharmaceuticals, Inc. | Sterilized, isotonic and pH-adjusted pharmaceutical formulation of uridine triphosphate |
US5763447C1 (en) | 1996-07-23 | 2002-05-07 | Inspire Pharmaceuticals | Method of preventing or treating pneumonia in immobilized patients with uridine triphosphates and related compounds |
WO1998015835A1 (en) | 1996-10-08 | 1998-04-16 | Inspire Pharmaceuticals, Inc. | Method of early lung cancer detection via sputum induction and analysis of sputum to detect cancer associated substances |
US6159952A (en) | 1996-11-07 | 2000-12-12 | Inspire Pharmaceuticals, Inc. | Method of treating bronchitis with uridine triphosphate and related compounds |
WO1998028300A1 (en) | 1996-12-20 | 1998-07-02 | Astra Pharmaceuticals Ltd. | Triazolo[4,5-d]pyrimidinyl derivatives and their use as medicaments |
DK0981534T3 (da) * | 1997-02-06 | 2006-09-04 | Inspire Pharmaceuticals Inc | Dinukleotider og deres anvendelser |
US6596725B2 (en) * | 1997-02-10 | 2003-07-22 | Inspire Pharmaceuticals, Inc. | Use of certain dinucleotides to stimulate removal of fluid in retinal detachment and retinal edema |
SE9702774D0 (sv) * | 1997-07-22 | 1997-07-22 | Astra Pharma Prod | Novel compounds |
JP3723227B2 (ja) | 1997-07-25 | 2005-12-07 | インスパイアー ファーマシューティカルズ,インコーポレイティド | ジ(ウリジン5’)−テトラホスフェート及びその塩の大規模生産のための方法 |
US6462028B2 (en) | 1997-07-25 | 2002-10-08 | Inspire Pharmaceuticals, Inc. | Method of promoting cervical and vaginal secretions |
ZA987847B (en) | 1997-08-29 | 1999-06-28 | Univ North Carolina | Method of treating lung diseases with uridine 5'-diphosphate and analogs thereof |
US6528640B1 (en) * | 1997-11-05 | 2003-03-04 | Ribozyme Pharmaceuticals, Incorporated | Synthetic ribonucleic acids with RNAse activity |
EP1087777B1 (en) * | 1998-05-22 | 2003-02-19 | Inspire Pharmaceuticals, Inc. | Therapeutic dinucleotide and derivatives |
SE9804175D0 (sv) | 1998-12-02 | 1998-12-02 | Astra Pharma Prod | New assay |
TWI229674B (en) | 1998-12-04 | 2005-03-21 | Astra Pharma Prod | Novel triazolo[4,5-d]pyrimidine compounds, pharmaceutical composition containing the same, their process for preparation and uses |
WO2000039145A1 (en) | 1998-12-23 | 2000-07-06 | The University Of North Carolina At Chapel Hill | Targeted gene transfer using g protein coupled receptors |
CA2359891A1 (en) | 1999-02-26 | 2000-08-31 | Inspire Pharmaceuticals, Inc. | Method of promoting mucosal hydration with certain uridine, adenine and cytidine diphosphates and analogs thereof |
SE9903290D0 (sv) | 1999-09-15 | 1999-09-15 | Astra Pharma Prod | Novel compounds |
SE9904129D0 (sv) | 1999-11-15 | 1999-11-15 | Astra Pharma Prod | Novel compounds |
SE9904377D0 (sv) | 1999-12-01 | 1999-12-01 | Astra Pharma Prod | Pharmaceutical combinations |
US6908624B2 (en) * | 1999-12-23 | 2005-06-21 | Advanced Cardiovascular Systems, Inc. | Coating for implantable devices and a method of forming the same |
US7018985B1 (en) | 2000-08-21 | 2006-03-28 | Inspire Pharmaceuticals, Inc. | Composition and method for inhibiting platelet aggregation |
US7132408B2 (en) * | 2000-08-21 | 2006-11-07 | Inspire Pharmaceuticals, Inc. | Composition and method for inhibiting platelet aggregation |
US7452870B2 (en) | 2000-08-21 | 2008-11-18 | Inspire Pharmaceuticals, Inc. | Drug-eluting stents coated with P2Y12 receptor antagonist compound |
US6654285B1 (en) * | 2002-02-27 | 2003-11-25 | Advanced Micro Devices, Inc. | Method of matching core cell and reference cell source resistances |
US7368438B2 (en) | 2003-10-21 | 2008-05-06 | Inspire Pharmaceuticals, Inc. | Non-nucleotide compositions and method for inhibiting platelet aggregation |
-
2005
- 2005-11-04 US US11/267,834 patent/US7452870B2/en not_active Expired - Fee Related
-
2006
- 2006-11-02 EP EP06836933A patent/EP1942910A2/en not_active Withdrawn
- 2006-11-02 JP JP2008539086A patent/JP2009514604A/ja active Pending
- 2006-11-02 WO PCT/US2006/043085 patent/WO2007056213A2/en active Application Filing
-
2008
- 2008-07-30 US US12/182,935 patent/US7618949B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050233062A1 (en) * | 1999-09-03 | 2005-10-20 | Hossainy Syed F | Thermal treatment of an implantable medical device |
Non-Patent Citations (7)
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7618949B2 (en) | 2000-08-21 | 2009-11-17 | Inspire Pharmaceuticals, Inc. | Drug-eluting stents coated with P2Y12 receptor antagonist compound |
Also Published As
Publication number | Publication date |
---|---|
US20060122143A1 (en) | 2006-06-08 |
US20080287671A1 (en) | 2008-11-20 |
EP1942910A2 (en) | 2008-07-16 |
US7452870B2 (en) | 2008-11-18 |
JP2009514604A (ja) | 2009-04-09 |
US7618949B2 (en) | 2009-11-17 |
WO2007056213A3 (en) | 2009-04-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7618949B2 (en) | Drug-eluting stents coated with P2Y12 receptor antagonist compound | |
US7101860B2 (en) | Composition and method for inhibiting platelet aggregation | |
EP1758915A2 (en) | Composition and method for inhibiting platelet aggregation | |
AU2001285470A1 (en) | Composition and method for inhibiting platelet aggregation | |
US7749981B2 (en) | Drug-eluting stents coated with non-nucleotide P2Y12 receptor antagonist compound | |
US7943760B2 (en) | Non-nucleotide composition for inhibiting platelet aggregation | |
US7504497B2 (en) | Orally bioavailable compounds and methods for inhibiting platelet aggregation | |
EP1685135B1 (en) | TETRAHYDRO-FURO[3,4-d]DIOXOLE COMPOUNDS AND COMPOSITIONS AND METHOD FOR INHIBITING PLATELET AGGREGATION | |
WO2007140333A2 (en) | Mononucleoside phosphonate compounds | |
US7932376B2 (en) | Pyrimidine-based non-nucleotide composition and method for inhibiting platelet aggregation | |
WO2007056217A2 (en) | Drug-eluting stents coated with non-nucleotide p2y12 receptor antagonist compound | |
JP2009520510A (ja) | 非ヌクレオチドp2y12受容体アンタゴニスト化合物でコーティングした薬剤溶出ステント |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2006836933 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 2008539086 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |