Removing skin-cancer damaging based on destroying thymine dimer complexes

Abstract

Cyclobutane pyrimidine dimers including thymine or uracil have been studied and characterized through several spectroscopic methods. The azetidin intermediates are generated when the 3’-end bases are cytosine group, through cycloaddition of the 4-imino functional of the latter pyrimidin base. Spontaneous rearrangement of the oxetan or azetidin yields rises to the pyrimidin (6-4) pyrimidon adducts. Chemical shifts, isotropies, anisotropies, spans, asymmetries, and other properties are all the integrals of those current densities that can be explained through magnetic criteria and are the trustworthy accounts of the currents induced via external magnetic field capabilities.