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  • Springer  (3)
  • American Institute of Physics
  • 1990-1994  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Perspectives in drug discovery and design 1 (1994), S. 419-422 
    ISSN: 1573-9023
    Keywords: Hemostasis ; Factor Xa ; Thrombin ; Antithrombin III ; Protein C ; Protein S ; Thrombomodulin ; ADP receptor ; Thrombin receptor ; Fibrinogen receptor ; Glycoprotein IIb/IIIa
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A brief overview of the control of hemostasis is presented that relates physiologically important functions and interactions of the proteins discussed in this volume, i.e.: factor Xa, thrombin, antithrombin III, protein C, protein S, thrombomodulin, ADP receptor, thrombin receptor and fibrinogen receptor.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Perspectives in drug discovery and design 1 (1994), S. 537-548 
    ISSN: 1573-9023
    Keywords: Glycoprotein IIb/IIIa ; Fibrinogen receptor ; Integrin ; Antithrombotic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The objective of this paper is to review briefly the normal physiology of platelet activation which leads to aggregation, to summarize the evidence for the critical role of platelet activation and aggregation in thrombosis, to highlight the key role of the membrane-protein complex glycoprotein IIb/IIIa in this process, and to provide examples of how small molecules can inhibit the aggregatory function of this complex.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-904X
    Keywords: fibrinogen receptor antagonist ; pharmacokinetics ; pharmacodynamics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pharmacokinetics and pharmacodynamics of L-703,014, a fibrinogen receptor antagonist, have been examined in the dog. An analytical method which utilizes methanol precipitation of dog plasma proteins followed by HPLC with an automated column switching technique using the chemical analogue L-704,326 as internal standard was developed for the determination of L-703,014 in dog plasma. The compound was not metabolized in the dog and was eliminated in the kidneys and into bile. Of the administered dose, 68.9 ± 1.3% (i.v.) and 80.5 ± 11.9% (p.o.) were recovered in the feces; 20.3 ± 3% (i.v.) and 2.2 ± 0.2% (p.o.) were recovered in the urine by 72 hr. L-703,014 was 23 ± 3.4% bound in dog plasma protein and the mean ratio of plasma/whole blood was 1.22 ± 0.05. The mean terminal half-life was 118 ± 36 min, the mean steady-state volume of distribution was 0.61 ± 0.22 L/kg, and the mean plasma clearance was 8 ± 2 mL/min/kg. Ex vivo platelet aggregation measurements were made by inducing platelet aggregation with 10 µg/ mL collagen in the presence of 1 µM epinephrine as an agonist. The mean C 50 was 44.4 ± 6.0 ng/mL, and the mean Hill coefficient was 1.5 ± 0.3. The mean bioavailability was 4.9 ± 1.4% in dogs administered 2.0 mg/kg (p.o.).
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