Author/Authors :
J.C. Califano، نويسنده , , A. Uribe، نويسنده , , J.L. Chang، نويسنده , , C.L. Becker، نويسنده , , J.J. Napier، نويسنده , , V. Kishore Kumar، نويسنده , , D. Zhou، نويسنده , , G. Love، نويسنده , , K. Gernhardt، نويسنده , , J.C. Tolle، نويسنده ,
Abstract :
Oligomers of arginine, such as octa-d-arginine amide, are excellent transporters for active drugs through cell membranes and tissue. The synthesis of octa-d-arginine amide, as the nonahydrochloride salt, was approached via a solution phase synthetic route involving the preparation of an octa-d-ornithine intermediate, which was then converted into the desired octa-d-arginine compound through a guanidinylation step. The multi-step synthesis was carried out at pilot scale, resulting in the preparation of 700 g of the target molecule. No chromatographic purification was needed at any step of the process.
Keywords :
Minimal isolation peptide synthesis , amino acids and derivatives , Guanidinylation , Arginine , Peptide transport , Peptide process development