Aeruginosin Analogs and Other Compounds with Rigid Bicyclic Structure as Potential Antithrombotic Agents

Author(s): Guijun Wang, Navneet Goyal

Journal Name: Cardiovascular & Hematological Agents in Medicinal Chemistry
Formerly Current Medicinal Chemistry - Cardiovascular & Hematological Agents

Volume 7 , Issue 2 , 2009

Become EABM
Become Reviewer
Call for Editor


Direct inhibition of blood coagulation factors such as thrombin, factor VIIa, and factor Xa has shown great promise for treating thrombosis disorders. Inhibitors of these serine proteases have been designed, synthesized, and evaluated. Small molecule thrombin inhibitors typically contain P1-P2-P3 components targeting the active binding site. Structure optimizations on the P1 position and the P3 position have been done extensively, but the P2 position has not been as thoroughly studied as the other positions. Thrombin inhibitors with a rigid bicyclic P2 unit are interesting compounds with a more defined conformation. Aeruginosins are a family of naturally occurring small molecules that exhibit serine protease inhibition activities; their structures are typically tetrapeptides with an unusual bicyclic amino acid core structure occupying the P2 position. About 21 compounds sharing the same core structure have been isolated and identified so far, and their analogs have also been synthesized. In this review, the Structure Activity Relationship (SAR) of these compounds against thrombin and other serine proteases and their potential as antithrombotic agents will be discussed. The binding modes to thrombin and other factors of the coagulation cascade and the preparation of the aeruginosin core structure will be summarized. Besides the aeruginosin family, the SAR of other small molecule serine protease inhibitors with a rigid bicyclic P2 unit will also be covered.

Keywords: Aeruginosin, Thrombin Inhibitor, Bicyclic Amino acids

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2009
Page: [147 - 165]
Pages: 19
DOI: 10.2174/187152509787847092
Price: $65

Article Metrics

PDF: 6