Article ID Journal Published Year Pages File Type
5230323 Tetrahedron 2006 11 Pages PDF
Abstract
A series of multi-β-substituted cationic porphyrins have been synthesized. Their photooxidative abilities and interactions with DNA were investigated. Substituents at β-position of the porphyrins have significant effect on the interactions and binding modes of the porphyrins with DNA compared to the β-unsubstituted one. Increasing positive charges in porphyrins strengthen their interactions with DNA.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
, , , , , , ,