Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5266005 | Tetrahedron Letters | 2011 | 5 Pages |
Abstract
An approach for the solid-phase synthesis of apoptosis-inducing Smac peptidomimetics is presented. Using a Rink linker strategy, tetrapeptides mimicking the N-4-terminal residue of the Smac protein [(N-Me)AVPF sequence] were synthesized on PEGA resin in excellent purities and yields. Following two synthetic routes, a known tetrapeptide, incorporating a substituted proline, previously shown to exhibit excellent biological activity in vitro as well as low toxicity, was synthesized effectively on a solid support.
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Authors
Sebastian T. Le Quement, Mette Ishoey, Mette T. Petersen, Pernille M. Simonsen, Nanna S. Holck, Thomas E. Nielsen,