阿魏酸
咖啡酸
肉桂酸
香豆酸
化学
对香豆酸
酚酸
有机化学
生物化学
抗氧化剂
作者
Hisashi Katsuragi,Kei Shimoda,Naoji Kubota,Nobuyoshi Nakajima,Hatsuyuki Hamada,Hiroki Hamada
摘要
Biotransformations of phenylpropanoids such as cinnamic acid, p-coumaric acid, caffeic acid, and ferulic acid were investigated with plant-cultured cells of Eucalyptus perriniana. The plant-cultured cells of E. perriniana converted cinnamic acid into cinnamic acid β-d-glucopyranosyl ester, p-coumaric acid, and 4-O-β-d-glucopyranosylcoumaric acid. p-Coumaric acid was converted into 4-O-β-d-glucopyranosylcoumaric acid, p-coumaric acid β-d-glucopyranosyl ester, 4-O-β-d-glucopyranosylcoumaric acid β-d-glucopyranosyl ester, a new compound, caffeic acid, and 3-O-β-d-glucopyranosylcaffeic acid. On the other hand, incubation of caffeic acid with cultured E. perriniana cells gave 3-O-β-d-glucopyranosylcaffeic acid, 3-O-(6-O-β-d-glucopyranosyl)-β-d-glucopyranosylcaffeic acid, a new compound, 3-O-β-d-glucopyranosylcaffeic acid β-d-glucopyranosyl ester, 4-O-β-d-glucopyranosylcaffeic acid, 4-O-β-d-glucopyranosylcaffeic acid β-d-glucopyranosyl ester, ferulic acid, and 4-O-β-d-glucopyranosylferulic acid. 4-O-β-d-Glucopyranosylferulic acid, ferulic acid β-d-glucopyranosyl ester, and 4-O-β-d-glucopyranosylferulic acid β-d-glucopyranosyl ester were isolated from E. perriniana cells treated with ferulic acid.
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