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A novel inhibitor of plasminogen activator inhibitor-1 provides antithrombotic benefits devoid of bleeding effect in nonhuman primates.

Abstract
Inhibition of plasminogen activator inhibitor (PAI)-1 is useful to treat several disorders including thrombosis. An inhibitor of PAI-1 (TM5275) was newly identified by an extensive study of structure-activity relationship based on a lead compound (TM5007) which was obtained through virtual screening by docking simulations. Its antithrombotic efficacy and adverse effects were tested in vivo in rats and nonhuman primates (cynomolgus monkey). TM5275, administered orally in rats (1 to 10 mg/kg), has an antithrombotic effect equivalent to that of ticlopidine (500 mg/kg) in an arterial venous shunt thrombosis model and to that of clopidogrel (3 mg/kg) in a ferric chloride-treated carotid artery thrombosis model. TM5275 does not modify activated partial thromboplastin time and prothrombin time or platelet activity and does not prolong bleeding time. Combined with tissue plasminogen activator, TM5275 improves the latter's therapeutic efficacy and reduces its adverse effect. Administered to a monkey model of photochemical induced arterial thrombosis, TM5275 (10 mg/kg) has the same antithrombotic effect as clopidogrel (10 mg/kg), without enhanced bleeding. This study documents the antithrombotic benefits of a novel, more powerful, PAI-1 inhibitor in rats and, for the first time, in nonhuman primates. These effects are obtained without adverse effect on bleeding time.
AuthorsYuko Izuhara, Nagahisa Yamaoka, Hidehiko Kodama, Takashi Dan, Shunya Takizawa, Noriaki Hirayama, Kanji Meguro, Charles van Ypersele de Strihou, Toshio Miyata
JournalJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism (J Cereb Blood Flow Metab) Vol. 30 Issue 5 Pg. 904-12 (May 2010) ISSN: 1559-7016 [Electronic] United States
PMID20087372 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • 5-chloro-2-(((2-(4-(diphenylmethyl)piperazin-1-yl)-2-oxoethoxy)acetyl)amino)benzoate
  • Fibrinolytic Agents
  • Piperazines
  • Plasminogen Activator Inhibitor 1
  • Serine Proteinase Inhibitors
  • para-Aminobenzoates
  • Tissue Plasminogen Activator
  • Ticlopidine
  • 4-Aminobenzoic Acid
Topics
  • 4-Aminobenzoic Acid (chemical synthesis, chemistry, pharmacology, therapeutic use)
  • Animals
  • Disease Models, Animal
  • Drug Design
  • Female
  • Fibrinolytic Agents (chemical synthesis, chemistry, pharmacology, therapeutic use)
  • Hemorrhage (drug therapy)
  • Humans
  • Macaca fascicularis
  • Male
  • Mice
  • Models, Molecular
  • Molecular Structure
  • Piperazines (chemical synthesis, chemistry, pharmacology, therapeutic use)
  • Plasminogen Activator Inhibitor 1 (chemistry, metabolism)
  • Protein Conformation
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Wistar
  • Serine Proteinase Inhibitors (chemistry, metabolism)
  • Structure-Activity Relationship
  • Thrombosis (drug therapy)
  • Ticlopidine (pharmacology, therapeutic use)
  • Tissue Plasminogen Activator (therapeutic use)
  • para-Aminobenzoates

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