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来自毛泡桐果实的C-香叶基化合物。

C-geranyl compounds from Paulownia tomentosa fruits.

作者信息

Smejkal Karel, Grycová Lenka, Marek Radek, Lemière Filip, Jankovská Dagmar, Forejtníková Hana, Vanco Ján, Suchý Václav

机构信息

Department of Natural Drugs, University of Veterinary and Pharmaceutical Sciences Brno, Palackého 1-3, CZ-612 42 Brno, Czech Republic.

出版信息

J Nat Prod. 2007 Aug;70(8):1244-8. doi: 10.1021/np070063w. Epub 2007 Jul 11.

DOI:10.1021/np070063w
PMID:17625893
Abstract

Five geranylflavonoids, one prenylated flavonoid, and a simple flavanone were isolated from an ethanolic extract of Paulownia tomentosa fruit. Tomentodiplacol (1), 3'-O-methyl-5'-methoxydiplacol (2), 6-isopentenyl-3'-O-methyltaxifolin (3), and dihydrotricin (4) are reported from a natural source for the first time and 3'-O-methyldiplacone (6) for the first time from the genus Paulownia. The structures of the compounds were determined by mass spectrometry, including HRMS, and by 1D and 2D NMR spectroscopy. The cytotoxicity and DPPH (2,2-diphenyl-1-picrylhydrazyl)-quenching activity of some of these compounds were tested, with diplacone proving to be the best antioxidant, although the most cytotoxic compound.

摘要

从毛泡桐果实的乙醇提取物中分离出了五种香叶基黄酮、一种异戊烯基化黄酮和一种简单的黄烷酮。托门托地普拉醇(1)、3'-O-甲基-5'-甲氧基二普拉醇(2)、6-异戊烯基-3'-O-甲基紫杉叶素(3)和二氢曲菌素(4)首次从天然来源报道,3'-O-甲基二普拉酮(6)首次从泡桐属中报道。通过质谱(包括高分辨质谱)以及一维和二维核磁共振光谱确定了这些化合物的结构。测试了其中一些化合物的细胞毒性和DPPH(2,2-二苯基-1-苦基肼)淬灭活性,结果表明二普拉酮是最佳抗氧化剂,不过也是细胞毒性最强的化合物。

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