RCAI-56, a carbocyclic analogue of KRN7000: its synthesis and potent activity for natural killer (NK) T cells to preferentially produce interferon-γ

Abstract

RCAI-56 ( 3), a carbocyclic analogue of KRN7000 ( 1) was synthesized through an efficient coupling of a carba-α- d-galactose derivative 11 with cyclic sulfamidate derivative 13 of phytosphingosine to give 15. Carbasugar derivative 11 was prepared by starting from methyl α- d-galactopyranoside ( 4), employing Pd(II)-catalyzed Ferrier rearrangement as the key step. RCAI-56 ( 3) is a potent stimulant of NKT cells in vivo to induce the production of Th1 biased cytokines such as interferon-γ in mice. According to the docking model of CD1d- 3 complex, its stabilization energy is approximately at the same level as that of the CD1d- 1 complex.