| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1987980 | International Journal of Biological Macromolecules | 2009 | 6 Pages |
Abstract
Six low molecular fucoidan (DFPS) derivatives were synthesized successfully, and their potential antioxidant activities were investigated employing various established in vitro systems. All DFPS derivatives possessed considerable antioxidant activity, and had stronger antioxidant ability than DFPS in certain tests. The benzoylated DFPS (PHDF) showed strongest scavenging activity on superoxide, hydroxyl and 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical, however, DFPS exhibited greatest reducing power. Available data suggested that substituted groups of DFPS played an important role on antioxidant activity, and the mechanism on influence the antioxidant activity of samples of substituted group was indicated.
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Authors
Jing Wang, Feng Wang, Quanbin Zhang, Zhongshan Zhang, Xuelian Shi, Pengcheng Li,