74071-59-3Relevant articles and documents
Conformationally constrained peptides and semipeptides derived from RGD as potent inhibitors of the platelet fibrinogen receptor and platelet aggregation
Ali,Bennett,Calvo,Elliott,Hwang,Ku,Lago,Nichols,Romoff,Shah,Vasko,Wong,Yellin,Yuan,Samanen
, p. 769 - 780 (2007/10/02)
Structure-activity studies have been pursued on cyclo-S,S-[Ac-Cys-(N(α)- Me)Arg-Gly-Asp-Pen]-NH2, 2 (SK and F 106760), a potent inhibitor of platelet aggregation, in an effort to improve potency and affinity for the GPIIb/IIIa receptor. Modific
Development of a Small RGD Peptide Fibrinogen Receptor Antagonist with Potent Antiaggregatory Activity in Vitro
Samanen, J.,Ali, F.,Romoff, T.,Calvo, R.,Sorenson, E.,et al.
, p. 3114 - 3125 (2007/10/02)
The development of potent antithrombotic agents from the fibrinogen platelet receptor binding sequences Fg-α 572-575 -Arg-Gly-Asp-Ser- and Fg-γ 400-411 -HHLGGAKQAGDV, believed to be a cryptic RGD-type sequence, is described.The tetrapeptide Ac-RGDS-NH2 it