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Theoretical Study of the Radical Scavenging Activity of Shikonin and Its Derivatives
Author(s) -
Jin Ruifa,
Li Jie
Publication year - 2012
Publication title -
chinese journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 1001-604X
DOI - 10.1002/cjoc.201100044
Subject(s) - chemistry , scavenging , molecule , computational chemistry , hydrogen bond , derivative (finance) , radical ion , electron transfer , photochemistry , combinatorial chemistry , organic chemistry , antioxidant , ion , financial economics , economics
A series of shikonin derivatives have been designed and their radical scavenging activity has been characterized by the B3LYP/6‐31+G(d) approach. The hydrogen bond properties of the studied structures were investigated using the atoms in molecules (AIM) theory. The calculated results reveal that the hydrogen bond is important for good scavenging activity. The introduction of electron‐drawing (electron‐donating) groups increases (decreases) the scavenging activities of radical and radical cations of shikonin derivatives. Shikonin derivatives appear to be good candidates for the single‐electron‐transfer mechanism, particularly for N(CH 3 ) 2 derivative. Taking this system as an example, we present an efficient method for the investigation of radical scavenging activity from theoretical point of view. With the current work, we hope to highlight the radical scavenging activity of hydroxynaphthoquinones derivatives and stimulate the interest for further studies and exploitation in pharmaceutical industry.