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从紫穗槐中分离并合成一种新型苯并呋喃化合物,以及几种抑制组胺H1受体基因表达的相关衍生物的合成。

The isolation and synthesis of a novel benzofuran compound from Tephrosia purpurea, and the synthesis of several related derivatives, which suppress histamine H1 receptor gene expression.

作者信息

Shill Manik Chandra, Das Asish Kumar, Itou Tomohiro, Karmakar Sanmoy, Mukherjee Pulok K, Mizuguchi Hiroyuki, Kashiwada Yoshiki, Fukui Hiroyuki, Nemoto Hisao

机构信息

Department of Molecular Pharmacology, Institute of Biomedical Sciences, Tokushima University Graduate School, 1-78-1 Sho-machi, Tokushima 770-8505, Japan.

Pharmacy Discipline, Khulna University, Khulna 9208, Bangladesh.

出版信息

Bioorg Med Chem. 2015 Nov 1;23(21):6869-74. doi: 10.1016/j.bmc.2015.09.049. Epub 2015 Oct 21.

Abstract

A novel naturally occurring compound with a benzofuran skeleton was isolated from a plant, Tephrosia purpurea collected in Bangladesh. The chemical synthesis of this compound confirmed its structure, and preliminary biological results showed its suppressive activity towards histamine H1 gene expression. One isomer and four derivatives were also synthesized, and their suppression activity was investigated. Although only small quantities of this compound can be isolated from its natural source, a 10 g scale synthesis was demonstrated by the newly developed method.

摘要

从孟加拉国采集的植物紫穗槐中分离出一种具有苯并呋喃骨架的新型天然化合物。该化合物的化学合成确定了其结构,初步生物学结果表明其对组胺H1基因表达具有抑制活性。还合成了一种异构体和四种衍生物,并研究了它们的抑制活性。尽管从其天然来源只能分离出少量这种化合物,但新开发的方法实现了10克规模的合成。

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