School of Pharmacy, College of Pharmacy, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
Institute of Traditional Medicine, National Yang-Ming University, Taipei 112, Taiwan.
Molecules. 2018 Jan 30;23(2):289. doi: 10.3390/molecules23020289.
The resinous wood of , known as agarwood ( in Chinese), is traditionally used for the treatment of abdominal pain, vomiting, circulatory disorders, and dyspnea. Four new 2-(2-phenylethyl)-4-chromen-4-one derivatives, namely 7-methoxy-2-[2-(4'-hydroxy-phenyl)ethyl]chromone (), 7-hydroxy-2-[2-(4'-methoxyphenyl)ethyl]chromone (), 5,6-dihydroxy- 2-[2-(3'-hydroxy-4'-methoxyphenyl)ethyl]chromone (), and 6-hydroxy-5-methoxy-2-(2-phenyl-ethyl)chromone (), have been isolated from the resinous wood of , together with nine known compounds. The structures of these compounds were determined through spectroscopic and MS analyses. Among the isolated compounds, neopetasan, 7-methoxy-2-(2-phenylethyl)-chromone, 6,7-dimethoxy-2-(2-phenylethyl)chromone, and 6,7-dimethoxy-2-[2-(4'-methoxy-phenyl)ethyl]chromone inhibited NF-κB activation in LPS-stimulated RAW 264.7 macrophages with relative luciferase activity values of 0.55 ± 0.09, 0.54 ± 0.03, 0.31 ± 0.05, and 0.38 ± 0.14, respectively, versus that of vehicle control (1.03 ± 0.02). In addition, 5,6-dihydroxy-2-[2-(3'-hydroxy-4'-methoxyphenyl)ethyl]chromone, 7-methoxy-2-(2-phenylethyl)chromone, 7-dimethoxy-2-(2-phenylethyl)chromone, and 6,7-dimethoxy-2-[2-(4'-methoxyphenyl)ethyl]chromone could suppress LPS-induced NO production in RAW 264.7 cells and did not induce cytotoxicity against RAW 264.7 cells after 24-h treatment.
沉香木的树脂,被称为沉香(在中文中),传统上用于治疗腹痛、呕吐、循环障碍和呼吸困难。从沉香木的树脂中分离得到了四个新的 2-(2-苯乙基)-4-色满酮衍生物,分别为 7-甲氧基-2-[2-(4'-羟基苯基)乙基]色酮()、7-羟基-2-[2-(4'-甲氧基苯基)乙基]色酮()、5,6-二羟基-2-[2-(3'-羟基-4'-甲氧基苯基)乙基]色酮()和 6-羟基-5-甲氧基-2-(2-苯乙基)色酮(),以及九个已知化合物。这些化合物的结构通过光谱和 MS 分析确定。在分离得到的化合物中,neopetasan、7-甲氧基-2-(2-苯乙基)-色酮、6,7-二甲氧基-2-(2-苯乙基)色酮和 6,7-二甲氧基-2-[2-(4'-甲氧基苯基)乙基]色酮在 LPS 刺激的 RAW 264.7 巨噬细胞中抑制 NF-κB 激活,相对荧光素酶活性值分别为 0.55 ± 0.09、0.54 ± 0.03、0.31 ± 0.05 和 0.38 ± 0.14,而载体对照为 1.03 ± 0.02。此外,5,6-二羟基-2-[2-(3'-羟基-4'-甲氧基苯基)乙基]色酮、7-甲氧基-2-(2-苯乙基)色酮、7-二甲氧基-2-(2-苯乙基)色酮和 6,7-二甲氧基-2-[2-(4'-甲氧基苯基)乙基]色酮可抑制 LPS 诱导的 RAW 264.7 细胞中 NO 的产生,并且在 24 小时处理后对 RAW 264.7 细胞没有诱导细胞毒性。