Synthesis of partial nonpeptidic peptide mimetics as potential neurotensin agonists and antagonists

Abstract

The synthesis of partially nonpeptidic peptides as mimetics of neurotensin (8–13)[NT(8–13)] is described. The sequence Arg⁸Arg⁹Pro¹⁰ of NT(8–13) was replaced by substituted indole-2-carboxylates as non-peptidic equivalents. For the NT(8–13) fragment, a range of dimensions was calculated with the aid of computer modelling of which a subset was translated synthetically into two structures (1 and 2) containing indole-2-carboxylates substituted with guanidines containing appendages at C-3/C-5 and C-3/C-7, respectively. Regioisomeric C-5 and C-7 substituted indole intermediates 4 and 5 were obtained from a single indole precursor 3via thermally induced nitrene insertion. The readily separable indoles 4 and 5 were isolated as a ∼1 : 1 mixture. In turn, these indoles were functionalized individually in seven steps to give the Pmc-protected bisguanidino indole-2-carboxylic acids 14a and 14b, respectively. The carboxylic acids were coupled to the resin-bound tripeptide fragment NT(11–13), and the resulting products were cleaved from the resin using a trifluoroacetic acid cocktail to give NT mimetics 1 and 2. Functional evaluation of 1 and 2 on neuroblastoma N1E-115 cells showed mimetic 1 to be an NT antagonist, while mimetic 2 was found to be an NT antagonist at low concentrations and an NT agonist at higher concentrations in the 10–100 µmol dm^–3 range.