Synthesis and LTB4 receptor antagonist activities of the naturally occurring LTB4 receptor antagonist Leucettamine A and related analogues

Article abstract of DOI:10.1021/jm00074a014

The isolation and structure determination of the naturally occurring LTB₄ receptor antagonist Leucettamine A (1) was recently reported. Herein we describe the synthesis of this natural product, the preparation of several analogues, and their effectiveness as antagonists of [³H]LTB₄ binding to intact human U-937 cells. Total synthesis of Leucettamine A (1) is achieved by a convergent route which takes advantage of the elements of symmetry within the molecule. Syntheses of analogues of 1, which lacked the same degree of symmetry, are achieved by a different approach starting from α- amino acids. The natural product 1 inhibits [³H]LTB₄ binding to its receptors on intact human U-937 cells with a K(i) = 3.5 ± 0.8 μM and is devoid of measurable agonist activity at the concentrations tested. 2-Amino imidazole analogues of 1 lacking the dioxolane groups were prepared. Generally these are significantly less potent than 1. However, one (26), designed on the basis of a putative structural overlay with LTB₄, demonstrated potency comparable to that of the natural product (K(i) = 2.4 ± 0.2 μM).