Composition and method for inhibiting platelet aggregation

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Carbohydrate doai

Reexamination Certificate

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C514S043000, C514S046000, C514S047000, C514S048000

Reexamination Certificate

active

07132408

ABSTRACT:
This invention is directed to a method of preventing or treating diseases or conditions associated with platelet aggregation. The method is also directed to a method of treating thrombosis. The method comprises administering to a subject a pharmaceutical composition comprising a therapeutic effective amount of P2Y12receptor antagonist compound, wherein said amount is effective to bind the P2Y12receptors on platelets and inhibit ADP-induced platelet aggregation. The P2Y12receptor antagonist compounds useful for this invention include mononucleoside 5′-monophosphates, mononucleoside polyphosphates, and dinucleoside polyphosphates of general Formula I, or salts thereof. The present invention also provides novel compounds of mononucleoside 5′-monophosphates, mononucleoside polyphosphates, and dinucleoside polyphosphates. The present invention further provides pharmaceutical formulations comprising mononucleoside 5′-monophosphates, mononucleoside polyphosphates, or dinucleoside polyphosphates.

REFERENCES:
patent: 3321463 (1967-05-01), Moffatt et al.
patent: 4330550 (1982-05-01), Lautenschlager et al.
patent: 4621076 (1986-11-01), Kuzuya et al.
patent: 5049550 (1991-09-01), Zamecnik
patent: 5654285 (1997-08-01), Ingall et al.
patent: 5681823 (1997-10-01), Kim et al.
patent: 5721219 (1998-02-01), Ingall et al.
patent: 5747496 (1998-05-01), Cox et al.
patent: 5814609 (1998-09-01), Markland, Jr. et al.
patent: 5837861 (1998-11-01), Pendergast et al.
patent: 5900407 (1999-05-01), Yerxa et al.
patent: 5955447 (1999-09-01), Ingall et al.
patent: 6166022 (2000-12-01), Brown et al.
patent: 6323187 (2001-11-01), Yerxa et al.
patent: 6348589 (2002-02-01), Pendergast et al.
patent: 6596725 (2003-07-01), Peterson et al.
patent: 1407903 (1975-10-01), None
patent: WO 89/04321 (1989-05-01), None
patent: WO 92/01673 (1992-02-01), None
patent: WO 92/17488 (1992-10-01), None
patent: WO 94/08593 (1994-04-01), None
patent: WO 94/18216 (1994-08-01), None
patent: WO 97/03084 (1997-01-01), None
patent: WO 97/29456 (1997-08-01), None
patent: WO 98/03182 (1998-01-01), None
patent: WO 98/28300 (1998-07-01), None
patent: WO 98/34593 (1998-08-01), None
patent: WO 99/01138 (1999-01-01), None
patent: WO 99/32085 (1999-07-01), None
patent: WO 99/61012 (1999-12-01), None
patent: WO 00/33080 (2000-06-01), None
patent: WO 00/34283 (2000-06-01), None
patent: WO 00/39145 (2000-07-01), None
patent: WO 00/50024 (2000-08-01), None
patent: WO 01/19826 (2001-03-01), None
patent: WO 01/36421 (2001-05-01), None
patent: WO 01/39781 (2001-06-01), None
patent: WO 02/16381 (2002-02-01), None
Moffatt, et al., “Nucleoside polyphosphates . . . ”, Journal of the American Chemical Society (1958), 80, 3756-61.
International Search Report PCT/US01/41818, Mar. 11, 2002, PCT.
Hamilton, A. et al., “Design of Substrate-Site-Directed Inhibitors of Adenylate Kinase and Hexokinase. Effect of Substrate Substituents on Affinity for the Adenine Nucleotide Sites”,J. Med. Chem.,19:1371-1377 (1976).
Hiratsuka T., “Affinity Labeling of the Myosin ATPase with Riobse-Modified Fluroescent Nucleotides and Vanadate”,J. Biochem.,96:147-154 (1984).
Martin, P. et al., “Structure-Activity Studies of Analogs of β,γ-Methylene-ATP at P2x-Purinoceptors in the Rabbit Ear Central Artery”,Drug Development Research,36: 153-165 (1995).
Metzker, M. et al., “Termination of DNA synthesis by novel3′-modified-deoxyribonucleoside 5′-triphophate”,Nucleic Acids Research,22:4259-4267 (1994).
Pelicano, H. et al., “Study of the substrate-binding properties of bovine liver adenosine kinase and inhibition by fluorescent nucleoside analogues”,Eur. J. Biochem.,248:930-937 (1997).
Richard, J. and Frey, P.A., “Stereochemical Course of Thiophosphoryl Group Transfer Catalyzed by Adenylate Kinase”,J. Am. Chem. Soc.,100:7757-7758 (1978).
Sekine, M. et al., “New Type of Chemical Oxidative Phosphorylation: Activation of Phosphonate Function by Use of Triisoprobylbenzenesulfonyl Chloride”,Tetrahedron Letters,1145-1148 (1997).
Zatorski, A. et al., “Chemical Synthesis of Benzamide Adenine Dinucleotide: Inhibition of Inosine Monophosphate Dehydrogenase (Types I and II)”,Journal of Medicinal Chemistry, American Chemical Society,39:2422-2426 (1996).
Alessi, D. et al., “Synthesis and Properties of a Conformationally Restricted Spin-Labeled Analog of ATP and Its Interaction with Myosin and Skeletal Muscle”Biochemistry(1992), 31(34), 8043-54.
Antiplatelet Trialists'Collaberation., “Collaborative overview of randomised trials of antiplatelet therapy-I : Prevention of Death, myocardial infarction, and stroke by prolonged antiplatelet therapy in various categories of patients,”Br. Med. J.308: 81-106 (1994).
Antiplatelet Trialists'Collaberation., “Collaborative overview of randimised trials of antiplatelet therapy-II : maintenance of Vascular graft or arterial patency by antiplatelet therapy,”Br. Med. J.308: 159-168 (1994).
Antman, E, for The TIMI 9a investigators, “Hirudin in Acute Myocardial Infarction,” ,Circulation,90(4):1624-1630 (1994).
Bernat, A., et al., “Effect of Various Antiplatelet Agents on Acute Arterial Thrombosis in the Rat,”Thromb. Haemostas.(1993) 70(5):812-816.
Bujalowski, W. et al., “Structural Characteristics of the Nucleotide-Binding Site ofEscherichia coliPrimary Replicative Helicase DnaB Protein. Studies with Ribose and Base-Modified Fluorescent Nucleotide Analogs”Biochemistry(1994), 33(15), 4682-94.
Bush, L., et al., “Effects of the selective thromboxane synthetase inhibitor dazoxiben on variations in cyclic blood flow in stenosed canie coronary arteries,” Circulation 69(6):1161-1170, (1984).
Cardullo, R. A. et al., “Synthesis, Purification, and Characterization of 2,4,6-Trinitrophenyl-UDP-galactose: A Fluorescent Substrate for Galactosyltransferase”Analytical Biochemistry(1990), 188(2), 305-9.
Carvalho-Alves, P. et al., “Stoichiometric Photlabeling of Two Distinct Low and High Affinity Nucleotide Sites in Sarcoplasmic Reticulum ATPase”Journal of Biological Chemistry(1985), 260(7), 4282-7.
Chapal, J. et al., “Comparitive effects of adenosine-5′-triphosphate and related analogs on insulin secretion from the rat pancreas”Fundamental&Clinical Pharmacology(1997), 11(6), 537-545.
Folts, J. et al., “Platelet Aggregation in Partially Obstructed Vessels and its Elimination with Asprian,” Circulation 54(3):365-370 (1976).
Frederick, L.G., et al., “The Protective Dose of the Potent GPIIb/IIIa Antagonist SC-54701A is Reduced When Used in Combination with Asprian and Heparin in a Canie Model of Coronary Artery Thrombosis,” Circulation 93(1):129-134 (1996).
Geiger, J., et al., “Specific Impairment of Human Platelet P2Y ac ADP Receptor-Mediated Signaling by the Antiplatelet Drug Clopidogrel,”Aterioscler. Thromb. Vasc. Biol.19:2007-2011 (1999).
Hass, W., et al., “A Randomized Trial Comparing Ticlopidine Hydrochloride with Asprian for the Prevention of Stroke for High-Risk Patients,”N. Engl. J. Med.,321(8):501-507 (1989).
Herbert, J.M. et al., Inhibitory Effect of Clopidogrel on Platelet Adhesion and Intimal Proliferation After Arterial Injury in Rabbits,Arterioscl. Thromb.(1993) 13(8):1171-1179.
Hiratsuka, Toshiaki, “Biological Activities and Spectroscopic Properties of Chromophoric and Fluorescent Analogs of Adenine Nucleoside and Nucleotides, 2′,3′-O-(2,4,6-Trinitrocyclohexadienylidene) Adenosine Derivatives”Biochemicha et Biophysica Acta(1982), 719(3), 509-17.
Hiratsuka, Toshiaki “Monitoring the Myosin ATPase Reaction Using a Sensitive Fluorescent Probe: Pyrene-Labeled ATP”Biophysical Journal(1997), 72(2, Pt. 1), 843-849.
Hourani, et al., The Platelet ADP Receptors Meeting, La Thuile, Italy, Mar. 29-31, 2000.
Humphries, R.G., et al., “Pharmacological profile of the n

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