Novel and Efficient Method for Solid Phase Synthesis of Urea-Containing Peptides Targeting Prostate Specific Membrane Antigen (PSMA) in Comparison with Current Methods

AuthorMona Mosayebniaen
AuthorSedigheh Rezaeianpouren
AuthorPedram Rikhtechien
AuthorZahra Hajimahdien
AuthorDavood Beikien
AuthorFarzad Kobarfarden
AuthorOmid sabzevarien
AuthorMohsen Aminien
AuthorKhosrou Abdien
AuthorSoraya Shahhosseinien
Issued Date2018-07-31en
AbstractThe basic chemical structure of most prostate specific membrane antigen (PSMA) inhibitors which are now in pre-clinical and clinical studies is Glu-Ureido-based peptides. Synthesis of urea-based PSMA inhibitors includes two steps: 1- isocyanate intermediate formation and 2- urea bond formation. In current methods, isocyanate is formed in liquid phase and then reacts with amine existing in liquid phase or bound to solid phase for urea bond formation. In this study, we developed a new facile method for formation of both isocyanate and urea on solid phase under standard peptide coupling conditions. The solid phase-bound isocyanate served as intermediate to form urea bond. To monitor reaction progress qualitative test (Kaiser Test) and On-Bead FT-IR spectroscopy were used. The structure of Glutamate-Urea-Lysine (EUK) was confirmed using LC-Mass and 1H-NMR. This novel method successfully was applied to synthesize of another urea-based peptide containing a sequence of Glu-Urea-Lys (OMe)-GABA-Tyr-Tyr-GABA and the bifunctional linker hydrazinonicotinamide (HYNIC) as well.en
DOIhttps://doi.org/10.22037/ijpr.2018.2276en
KeywordPSMAen
KeywordGlutamate-Urea-Lysineen
Keywordurea bonden
Keywordsolid phaseen
KeywordIsocyanateen
PublisherBrieflandsen
TitleNovel and Efficient Method for Solid Phase Synthesis of Urea-Containing Peptides Targeting Prostate Specific Membrane Antigen (PSMA) in Comparison with Current Methodsen
TypeOriginal Articleen

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