Tang Shiyun, Shi Jianlian, Liu Chunbo, Jiang Rui, Zhao Wei, Liu Xin, Xiang Nengjun, Chen Yongkuan, Shen Qinpeng, Miao Mingming, Liu Zhihua, Yang Guangyu
a Key Laboratory of Tobacco Chemistry of Yunnan Province , China Tobacco Yunnan Industrial Co., Ltd , Kunming , P.R. China.
b Yunnan Key Laboratory of Pharmacology for Nature Products , School of Pharmaceutical Science , Kunming , P.R. China.
Nat Prod Res. 2017 Jun;31(12):1351-1357. doi: 10.1080/14786419.2016.1247081. Epub 2016 Oct 21.
Three new phenylpropanoids, 3-(3,4-dimethoxy-5-methylphenyl)-3-oxopropyl acetate (1), 3-hydroxy-1-(3,4-dimethoxy-5-methylphenyl)propan-1-one (2), and 3-hydroxy-1-(4-methylbenzo[d][1,3]dioxol-6-yl) propan-1-one (3), together with three known phenylpropanoids (4-6) were isolated from the whole plant of Lavandula angustifolia. Their structures were determined by means of HRESIMS and extensive 1D and 2D NMR spectroscopic studies. Compounds 1-6 were tested for their anti-tobacoo mosaic virus (TMV) activities and cytotoxicity activities. The results revealed that compounds 1-3 showed high anti-TMV activity with inhibition rate of 35.2, 38.4 and 33.9%. These rates are higher than that of positive control. The other compounds also showed potential anti-TMV activities with inhibition rates in the range of 26.8-28.9%, respectively. Compounds 1-6 also showed weak inhibitory activities against some tested human tumour cell lines with IC50 values in the range of 3.8-8.8 μM.
从狭叶薰衣草全株中分离出三种新的苯丙素类化合物,3-(3,4-二甲氧基-5-甲基苯基)-3-氧代丙基乙酸酯(1)、3-羟基-1-(3,4-二甲氧基-5-甲基苯基)丙-1-酮(2)和3-羟基-1-(4-甲基苯并[d][1,3]二氧杂环戊烯-6-基)丙-1-酮(3),以及三种已知的苯丙素类化合物(4-6)。通过高分辨电喷雾电离质谱(HRESIMS)以及广泛的一维和二维核磁共振光谱研究确定了它们的结构。对化合物1-6进行了抗烟草花叶病毒(TMV)活性和细胞毒性活性测试。结果表明,化合物1-3表现出较高的抗TMV活性,抑制率分别为35.2%、38.4%和33.9%。这些抑制率高于阳性对照。其他化合物也表现出潜在的抗TMV活性,抑制率分别在26.8%-28.9%范围内。化合物1-6对一些测试的人类肿瘤细胞系也表现出较弱的抑制活性,IC50值在3.8-8.8 μM范围内。