Wächter G A, Hoffmann J J, Furbacher T, Blake M E, Timmermann B N
Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson 85706, USA.
Phytochemistry. 1999 Dec;52(8):1469-71. doi: 10.1016/s0031-9422(99)00221-6.
An activity-guided fractionation of a methanol-dichloromethane extract obtained from the aerial parts of Eysenhardtia texana led to the isolation of two novel antibacterial and antifungal flavanones together with a known flavanone. Their structures were established as 4',5,7-trihydroxy-8-methyl-6-(3-methyl-[2-butenyl])-(2S)-flavanone, 4',5,7-trihydroxy-6-methyl-8-(3-methyl-[2-butenyl])-(2S)-flavanone and 4',5-dihydroxy-7-methoxy-6-(3-methyl-[2-butenyl])-(2S)-flavanone on the basis of their UV, 1D and 2D-NMR spectra.
对得克萨斯州艾森豪蒂亚(Eysenhardtia texana)地上部分的甲醇 - 二氯甲烷提取物进行活性导向分级分离,得到了两种新型抗菌和抗真菌黄烷酮以及一种已知黄烷酮。根据它们的紫外光谱、一维和二维核磁共振谱,确定它们的结构分别为4',5,7 - 三羟基 - 8 - 甲基 - 6 - (3 - 甲基 - [2 - 丁烯基]) - (2S) - 黄烷酮、4',5,7 - 三羟基 - 6 - 甲基 - 8 - (3 - 甲基 - [2 - 丁烯基]) - (2S) - 黄烷酮和4',5 - 二羟基 - 7 - 甲氧基 - 6 - (3 - 甲基 - [2 - 丁烯基]) - (2S) - 黄烷酮。