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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Two neolignans from Perilla frutescens and their inhibition of nitric oxide synthase and tumor necrosis factor-alpha expression in murine macrophage cell line RAW 264.7.
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Two neolignans from Perilla frutescens and their inhibition of nitric oxide synthase and tumor necrosis factor-alpha expression in murine macrophage cell line RAW 264.7.

机译:紫苏中的两种新木脂素及其对小鼠巨噬细胞RAW 264.7细胞中一氧化氮合酶和肿瘤坏死因子-α表达的抑制作用。

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摘要

Two neolignans were isolated from leaves of Perilla frutescens (Labiatae) as inhibitors of nitric oxide syntheses (IC50 5.9 microM and 53.5 microM, respectively) and tumor necrosis factor-alpha in lipopolysaccharide-activated RAW 264.7 cells. Their structures were identified as 1beta,2alpha,3beta,4alpha-1,2-dimethyl-3,4-bis-(2,4,5-trimethoxyphenyl)-cyclobutane (magnosalin), and 1alpha,2beta,3beta,4alpha-1,2-dimethyl-3,4-bis-(2,4,5-trimethoxyphenyl)-cyclobutane (andamanicin), and their activities were confirmed as resulted from the suppressed expression of inducible nitric oxide synthase enzyme and from the secretion of tumor necrosis factor-alpha from activated macrophages.
机译:从紫苏叶中分离出两种新木脂素,作为一氧化氮合成抑制剂(分别为IC50 5.9 microM和53.5 microM)和脂多糖激活的RAW 264.7细胞中的肿瘤坏死因子-α。他们的结构被确定为1beta,2alpha,3beta,4alpha-1,2-二甲基-3,4-双-(2,4,5-三甲氧基苯基)-环丁烷(木兰素)和1alpha,2beta,3beta,4alpha-1 ,2-二甲基-3,4-双-(2,4,5-三甲氧基苯基)-环丁烷(安达曼霉素),其活性被证实是由于诱导型一氧化氮合酶表达受到抑制和肿瘤坏死的分泌所致活化的巨噬细胞中的α因子。

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