153345-74-5Relevant articles and documents
An efficient synthesis of cyclic RGD peptides as antithrombotic agents
Zhang, Lin-Hua,Pesti,Costello,Sheeran,Uyeda,Ma,Kauffman,Ward,McMillan
, p. 5180 - 5185 (2007/10/03)
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Template-constrained cyclic peptides: Design of high-affinity ligands for GPIIb/IIIa
Jackson, Sharon,DeGrado, William,Dwivedi, Anil,Parthasarathy, Anju,Higley, Anne,Krywko, James,Rockwell, Arlene,Markwalder, Jay,Wells, Greg,Wexler, Ruth,Mousa, Shaker,Harlow, Richard
, p. 3220 - 3230 (2007/10/02)
Although peptides adopt a large ensemble of conformations in aqueous solution, they are generally believed to bind to a receptor in a unique conformation. Thus, there is considerable interest in devising methods to restrict the conformational freedom of peptides. One such approach involves tying the amino and carboxy terminal ends of the peptide onto a semirigid template that will lock the intervening peptide backbone into a single conformer or a family of related conformers. This general strategy has been tested using the tripeptide sequence Arg-Gly-Asp (RGD), which binds with low affinity to the platelet glycoprotein IIb/IIIa (GPIIb/IIIa or α(IIb)β3). Mimics of RGD are of interest as antithrombotics because of their ability to inhibit the aggregation of platelets. Prior to this study, other workers (Samanen et al. J. Med. Chem. 1991, 34, 3114-3125) prepared a disulfide- containing cyclic pentapeptide that bound to GPIIb/IIIa with an affinity of approximately 0.1 μM. NMR analysis of the solution conformation of this peptide suggested that replacing the disulfide-containing portion of the cycle with the amino acid m-(aminomethyl)benzoic acid would lead to a more rigid structure. Indeed, introduction of this template into a cyclic RGD- containing peptide resulted in compounds with high affinity for the receptor. Further, systematic inclusion of additional conformational constraints in the form of N(α)- and C(α)-alkyl groups led to a peptide with an affinity of approximately 100 pM for binding to the receptor. This peptide also showed good activity in the platelet aggregation assay at oral doses as low as 0.1 mg/kg.
