Dynamics and thermodynamics of molecular systems in the vicinity of the boundary between thermodynamically nonequilibrium glassy and metastable supercooled liquid states are still incompletely explored and their theoretical and simulation models are imperfect despite many previous efforts. Among them, the role of total system entropy, configurational entropy, and excess entropy in the temperature-pressure or temperature-density dependence of global molecular dynamics (MD) timescale relevant to the glass transition is an essential topic intensively studied for over half of a century. By exploiting a well-known simple ellipsoidal model recently successfully applied to simulate the supercooled liquid state and the glass transition, we gain a new insight into the different views on the relationship between entropy and relaxation dynamics of glass formers, showing the molecular grounds for the entropy scaling of global MD timescale. Our simulations in the anisotropic model of supercooled liquid, which involves only translational and rotational degrees of freedom, give evidence that the total system entropy is sufficient to scale global MD timescale. It complies with the scaling effect on relaxation dynamics exerted by the configurational entropy defined as the total entropy diminished by vibrational contributions, which was earlier discovered for measurement data collected near the glass transition. Moreover, we argue that such a scaling behavior is not possible to achieve by using the excess entropy that is in excess of the ideal gas entropy, which is contrary to the results earlier suggested within the framework of simple isotropic models of supercooled liquids. Thus, our findings also warn against an excessive reliance on isotropic models in theoretical interpretations of molecular phenomena, despite their simplicity and popularity, because they may reflect improperly various physicochemical properties of glass formers.