The ellagitannin trimer rugosin G inhibits recombinant human histidine decarboxylase

The ellagitannin trimer rugosin G inhibits recombinant human histidine decarboxylase
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鞣花单宁三聚体 rugosin G 抑制重组人组氨酸脱羧酶

DOI:
10.1080/09168451.2019.1606695
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发表时间:
2019
期刊:
Bioscience, Biotechnology, and Biochemistry
影响因子:
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通讯作者:
Kikuzaki Hiroe
Kikuzaki Hiroe
中科院分区:
--
文献类型:
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作者:
Nitta Yoko;Ito Hideyuki;Komori Hirohumi;Ueno Hiroshi;Takeshima Daiki;Ito Mikiko;Sakaue Motoyoshi;Kikuzaki Hiroe

文献摘要

相似文献

从红玫瑰花瓣水溶性组分中分离得到鞣花单宁三聚体Rugosin G,研究其对重组人组氨酸脱羧酶的抑制活性。与鞣花单宁单体和具有大环结构的二聚体(oenothein B)相比,Rugosin G显示出有效的抑制作用,表明Rugosin G的有效抑制作用归因于其线性寡聚体构象。
Rugosin G, an ellagitannin trimer, was isolated from the water-soluble fraction of red rose petals, and its inhibitory activity against recombinant human histidine decarboxylase was investigated. Rugosin G showed potent inhibition compared to ellagitannin monomers and a dimer with macrocyclic structure (oenothein B), suggesting the potent inhibition of rugosin G was attributed to its linear oligomeric conformation.Abbreviations:HDC, histidine decarboxylase; Me2CO, acetone; EtOAc, ethyl acetate