329911-79-7Relevant academic research and scientific papers
Synthesis and antiaggregatory activity of RGD-peptidomimetics based on 4-oxo-4-(piperazine-1-yl)butyric acid as Arg-mimetic
Andronati, Sergei A.,Krysko, Andrei A.,Kabanov, Vladimir M.,Kabanova, Tatyana A.,Karaseva, Tamara L.,Chugunov, Boris M.,Meshkova, Svetlana B.,Topilova, Zoya M.
, p. 375 - 381 (2007/10/03)
A scheme of synthesis of previously obtained RGDF-peptidomimetic-4-oxo- 4-(piperazine-1-yl)butyrylglycyl-D,L-β-phenyl-β-alanine (I), was simplified. The novel RGDF-peptidomimetic - 4-o-xo-4-(piperazine-1-yl) butyryl-glycyl-L-aspartyl-L-phenylalanine (II was synthesized with the use of 4-oxo-4-(piperazine-1-yl)butyric acid as arginyl mimetic. The obtained pseudopeptides were able to inhibit both platelet aggregation in human blood and binding of fibrinogen to its receptor.
Synthesis and antiaggregation activity of a new RGDF peptidomimetic
Krys'ko,Kabanov,Polishchuk,Chugunov,Pavlovskii,Andronati,Mazepa,Kabanova,Karaseva
, p. 948 - 952 (2007/10/03)
A new RGDF peptidomimetic, [4-oxo-4-(pyperazin-1-yl)butyryl]glycyl-D,L-β-phenyl-β-alanine was synthesized. The arginyl mimetic used was the 4-oxo-4-(piperazin-1-yl)butanoic acid residue, and the Asp-Phe chain is replaced by a β-phenyl-β-alanine residue. The synthesized pseudopeptide showed ability to inhibite ADF-induced thrombocyte aggregation in a thrombocyte-rich rat blood plasma (IC50 8.7 × 10-9 M).
Synthesis and properties of peptidomimetics - Inhibitors of platelet aggregation
Andronati,Krysko,Kabanov,Karaseva,Kabanova
, p. 15 - 21 (2007/10/03)
The literature data on effective approaches to the development of the novel peptidomimetics, antagonists of fibrinogen GP IIb/IIIa receptors as potential antithrombotic agents are generalized and systematized in the review. The data obtained by the authors on the synthesis and properties of novel peptidomimetics are reported.
