Pharmaceutical Research and Technology Institute, Kinki University, 3-4-1 Kowakae, Higashi-osaka, Osaka 577-8502, Japan.
Bioorg Med Chem. 2012 Aug 15;20(16):4968-77. doi: 10.1016/j.bmc.2012.06.031. Epub 2012 Jul 6.
A methanol extract of the flowers of Mammea siamensis (Calophyllaceae) was found to inhibit nitric oxide (NO) production in lipopolysaccharide-activated RAW264.7 cells. From the extract, two new geranylated coumarins, mammeasins A (1) and B (2), were isolated together with 17 known compounds including 15 coumarins. The structures of 1 and 2 were determined on the basis of their spectroscopic properties as well as of their chemical evidence. Among the isolates, 1 (IC(50) = 1.8 μM), 2 (6.4 μM), surangins B (3, 5.0 μM), C (4, 6.8 μM), and D (5, 6.2 μM), kayeassamins E (7, 6.1 μM), F (8, 6.0 μM), and G (9, 0.8 μM), mammea A/AD (11, 1.3 μM), and mammea E/BB (16, 7.9 μM) showed NO production inhibitory activity. Compounds 1, 9, and 11 were found to inhibit induction of inducible nitric oxide synthase (iNOS). With regard to mechanism of action of these active constituents (1, 9, and 11), suppression of STAT1 activation is suggested to be mainly involved in their suppression of iNOS induction.
从暹罗蜡梅花(藤黄科)的花的甲醇提取物中发现其抑制脂多糖激活的 RAW264.7 细胞中的一氧化氮(NO)的产生。从提取物中,分离出两种新的香叶基化香豆素,mammeasins A(1)和 B(2),以及 17 种已知化合物,包括 15 种香豆素。1 和 2 的结构是根据其光谱特性以及化学证据确定的。在分离的化合物中,1(IC50 = 1.8 μM),2(6.4 μM),surangins B(3,5.0 μM),C(4,6.8 μM)和 D(5,6.2 μM),kayeassamins E(7,6.1 μM),F(8,6.0 μM)和 G(9,0.8 μM),mammea A/AD(11,1.3 μM)和 mammea E/BB(16,7.9 μM)显示出对 NO 产生的抑制活性。发现化合物 1、9 和 11 抑制诱导型一氧化氮合酶(iNOS)的诱导。关于这些活性成分(1、9 和 11)的作用机制,认为抑制 STAT1 的激活主要涉及它们对 iNOS 诱导的抑制。