Studies on the antioxidant effect of (polyhydroxy-benzylidene)-(hydroxy-phenyl)amines

碩士 === 嘉南藥理科技大學 === 化妝品科技研究所 === 93 === Abstract In this study we aim to originally systhesize a series of highly productive (polyhydroxy-benzylidene)-(hydroxyl-phenyl)amines and observe their antioxidant capacity estimated in four different systems. 1. The effect on DPPH radical savenging 2. The ef...

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Main Authors: Hsiao-Ching Lin, 林小菁
Other Authors: Chau-Chen Yang
Format: Others
Language:zh-TW
Published: 2005
Online Access:http://ndltd.ncl.edu.tw/handle/57097823436056331855
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spelling ndltd-TW-093CNUP57930022015-12-23T04:08:16Z http://ndltd.ncl.edu.tw/handle/57097823436056331855 Studies on the antioxidant effect of (polyhydroxy-benzylidene)-(hydroxy-phenyl)amines (多羥基苯亞甲基)-(羥基苯)胺化合物抗氧化之研究 Hsiao-Ching Lin 林小菁 碩士 嘉南藥理科技大學 化妝品科技研究所 93 Abstract In this study we aim to originally systhesize a series of highly productive (polyhydroxy-benzylidene)-(hydroxyl-phenyl)amines and observe their antioxidant capacity estimated in four different systems. 1. The effect on DPPH radical savenging 2. The effect on trolox equivalent antioxidant capacity 3. The effect on scavenge nitric oxide. 4. The effect on liposome assay. The results of the study shows : the estimations of both the capture of DPPH and TEAC assay are similar, as the indicator in the two systems are the reduction of free radicals. The results show that A ring has obvious influence on the type, number and position of substituent. However, B ring is decisive only in the positions of substituents and have little to do with the types and existence of substituent. As a whole, A ring has greater effect than B ring, and substituents at the ortho and para position are best effective on antioxidant: DPPH assay IC 50 (2.90~3.40ppm) is 2.5 times better than trolox(7.5~8ppm), TEAC assay IC 50 (0.91~1.02ppm) is about 5-6 times better than trolox(5.56ppm). In liposome and NO assay systems, they are found that in low density of A ring monohydroxyl substituent at A ring are better than dihydroxy or trihydroxy substituents. But, in higher density the suppressive effect in these three composites are about the same. However, the more hydroxy groups of benzylidene phenyl amines are methylated to be methoxy groups at A ring, while the less effect on the antioxidant capacity. But, the methoxy group or not substituent at B ring are not poor effects than hydroxy groups at B ring. This results indicate that the type, number and positions of subtituents, in benzylidene-phenyl amines to play a critical role in exerting the antioxidant Chau-Chen Yang 楊朝成 2005 學位論文 ; thesis 102 zh-TW
collection NDLTD
language zh-TW
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description 碩士 === 嘉南藥理科技大學 === 化妝品科技研究所 === 93 === Abstract In this study we aim to originally systhesize a series of highly productive (polyhydroxy-benzylidene)-(hydroxyl-phenyl)amines and observe their antioxidant capacity estimated in four different systems. 1. The effect on DPPH radical savenging 2. The effect on trolox equivalent antioxidant capacity 3. The effect on scavenge nitric oxide. 4. The effect on liposome assay. The results of the study shows : the estimations of both the capture of DPPH and TEAC assay are similar, as the indicator in the two systems are the reduction of free radicals. The results show that A ring has obvious influence on the type, number and position of substituent. However, B ring is decisive only in the positions of substituents and have little to do with the types and existence of substituent. As a whole, A ring has greater effect than B ring, and substituents at the ortho and para position are best effective on antioxidant: DPPH assay IC 50 (2.90~3.40ppm) is 2.5 times better than trolox(7.5~8ppm), TEAC assay IC 50 (0.91~1.02ppm) is about 5-6 times better than trolox(5.56ppm). In liposome and NO assay systems, they are found that in low density of A ring monohydroxyl substituent at A ring are better than dihydroxy or trihydroxy substituents. But, in higher density the suppressive effect in these three composites are about the same. However, the more hydroxy groups of benzylidene phenyl amines are methylated to be methoxy groups at A ring, while the less effect on the antioxidant capacity. But, the methoxy group or not substituent at B ring are not poor effects than hydroxy groups at B ring. This results indicate that the type, number and positions of subtituents, in benzylidene-phenyl amines to play a critical role in exerting the antioxidant
author2 Chau-Chen Yang
author_facet Chau-Chen Yang
Hsiao-Ching Lin
林小菁
author Hsiao-Ching Lin
林小菁
spellingShingle Hsiao-Ching Lin
林小菁
Studies on the antioxidant effect of (polyhydroxy-benzylidene)-(hydroxy-phenyl)amines
author_sort Hsiao-Ching Lin
title Studies on the antioxidant effect of (polyhydroxy-benzylidene)-(hydroxy-phenyl)amines
title_short Studies on the antioxidant effect of (polyhydroxy-benzylidene)-(hydroxy-phenyl)amines
title_full Studies on the antioxidant effect of (polyhydroxy-benzylidene)-(hydroxy-phenyl)amines
title_fullStr Studies on the antioxidant effect of (polyhydroxy-benzylidene)-(hydroxy-phenyl)amines
title_full_unstemmed Studies on the antioxidant effect of (polyhydroxy-benzylidene)-(hydroxy-phenyl)amines
title_sort studies on the antioxidant effect of (polyhydroxy-benzylidene)-(hydroxy-phenyl)amines
publishDate 2005
url http://ndltd.ncl.edu.tw/handle/57097823436056331855
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