In this paper, we report the mechanical relaxation behavior of low molecular weight glass-forming side-chain liquid crystalline compounds with cyclic cores and their linear polymeric analogues near the glass transition temperature. We examined two systems : one based on cyclic and linear siloxane backbones and one based on cyclic (cyclohexane) and linear aliphatic backbones. Dynamic mechanical spectroscopy is used to measure the dynamic shear moduli and the complex viscosity near but above T-g. The temperature dependence of the zero-shear viscosity of the cyclic compounds is well described by the Vogel-Tammann-Fulcher (VTF) equation, The strong temperature dependence of the viscosity along with the values of the fitted parameters of the VTF equation shows that the cyclic LC compounds are "fragile" liquids. All cyclic LC compounds, regardless of chemical structure, show identical relaxation behavior when viscosity is plotted versus normalized temperature (T-g/T), where T-g is the temperature obtained calorimetrically at a heating rate of 10 K/min. All cyclic compounds show lower viscosity than their linear analogues when plotted versus T-g/T. The difference in viscosity between the cyclic and linear siloxane compounds is much more pronounced than the difference observed in the aliphatic compounds. For the cyclic compounds, master curves of G’ and G " can be described by a single Maxwell mode. The linear compounds exhibit much broader mechanical spectra, suggesting a more complex relaxation phenomenon is taking place. Our results show that, while there is little difference in relaxation behavior among low molecular weight cyclic liquid crystalline compounds, the behavior of the linear polymeric systems is quite different.