6-O-Feruloylglucose - CAS 137887-25-3
Catalog number: 137887-25-3
Not Intended for Therapeutic Use. For research use only.
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6-O-Feruloylglucose isolated from the herbs of Catalpa fargesii f. duclouxii.
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beta-D-Glucopyranose 6-[(2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propenoate];(2R,3R,4S,5R)-2,3,4,5-Tetrahydroxy-6-oxohexyl 3-(4-hydroxy-3-Methoxyphenyl)acrylate
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1.Reaction of hydroxyl radical with phenylpropanoid glycoside and its derivatives by pulse radiolysis.
Shi Y;Wang W;Kang J;Shi Y;Jia Z;Wang Y;Su B;Yao S;Lin N;Zheng R Sci China C Life Sci. 1999 Aug;42(4):420-6. doi: 10.1007/BF02882062.
The reaction of hydroxyl radical with 1 phenylpropanoid glycoside (PPG), cistanoside C, and its 3 derivatives: 1-0-beta-D-2-(p-hydroxyphenyl)-ethanyl-glucose, 6-O-(E)-femloyl-glucose and 6-O-(E)-p-hydroxy-cinnarnoylglucose isolated from folk medicinal herbs was investigated by pulse radiolysis technique respectively. The reaction rate constants were determined by analysis of built-up trace of absorption at lambda(max) of specific transient absorption spectra of PPG and its derivatives upon attacking . OH. All four compounds react with . OH at close to diffusion controlled rate (1. 03 x 10(9)-19.139 x 10(9) L . mol(-1) . s(-1)), suggesting that they are effective . OH scavengers. The results demonstrated that the numbers of phenolic hydroxyl groups of PPG and its derivatives are directly related to their scavenging activities. By comparing the reaction rates of . OH with 1-O-beta-D-2-(p-hydroxyphenyl)-ethanyl-glucose, 6-O-(E)-feruloyl-glucose or 6-O-(E)-p-hydroxy-cinnomoyl-glucose, it is evident that the phenylethyl group is more impofiant than phenylacryloyl group for scavenging . OH.
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CAS 137887-25-3 6-O-Feruloylglucose

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