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生物活性测定指导下的构树抗口腔微生物黄酮类化合物

Anti-oral Microbial Flavanes from Broussonetia papyrifera Under the Guidance of Bioassay.

作者信息

Geng Chang-An, Yan Meng-Hong, Zhang Xue-Mei, Chen Ji-Jun

机构信息

State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, 132# Lanhei Road, Kunming, 650201, Yunnan, People's Republic of China.

Yunnan Key Laboratory of Natural Medicinal Chemistry, Kunming, 650201, People's Republic of China.

出版信息

Nat Prod Bioprospect. 2019 Apr;9(2):139-144. doi: 10.1007/s13659-019-0197-y. Epub 2019 Jan 16.

Abstract

A new flavane, bropapyriferol (1), and eleven known ones were isolated from the EtOAc part of Broussonetia papyrifera under the guidance of bioassay. The structure of compound 1 was determined by extensive 1D and 2D NMR, [α] spectroscopic data and quantum computation. Daphnegiravan F (2) and 5,7,3',4'-tetrahydroxy-3-methoxy-8,5'-diprenylflavone (3) showed significantly anti-oral microbial activity against five Gram-positive strains and three Gram-negative strains in vitro. Especially, compound 3 was more potent in suppressing Actinomyces naeslundii and Porphyromonas gingivalis (MIC = 1.95 ppm) than the positive control, triclosan.

摘要

在生物活性测定的指导下,从构树的乙酸乙酯部位分离得到一种新的黄烷类化合物——溴帕皮甾醇(1)和11种已知化合物。通过广泛的一维和二维核磁共振、旋光光谱数据以及量子计算确定了化合物1的结构。瑞香黄烷F(2)和5,7,3',4'-四羟基-3-甲氧基-8,5'-二异戊烯基黄酮(3)在体外对5种革兰氏阳性菌和3种革兰氏阴性菌显示出显著的抗口腔微生物活性。特别是,化合物3在抑制内氏放线菌和牙龈卟啉单胞菌方面(最低抑菌浓度=1.95 ppm)比阳性对照三氯生更有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96c3/6426910/37b8ae748aa4/13659_2019_197_Fig1_HTML.jpg

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