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首页> 外文期刊>Planta medica: Natural products and medicinal plant research >Inhibition of chitin synthase 2 and antifungal activity of lignans from the stem bark of Lindera erythrocarpa.
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Inhibition of chitin synthase 2 and antifungal activity of lignans from the stem bark of Lindera erythrocarpa.

机译:红果Lindera erythrocarpa茎皮的几丁质合酶2的抑制作用和木脂素的抗真菌活性。

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Potent chitin synthase 2 inhibitors, methyllinderone (1), linderone (2) and kanakugiol (3) were isolated from the stem bark of L. erythrocarpa Makino (Lauraceae). These compounds inhibited chitin synthase 2 with IC(50) values of 23.3, 21.4 and 23.8 microg/mL, respectively. Methyllinderone (1) and linderone (2) exhibited no inhibitory activities for chitin synthases 1 and 3 from S. cerevisiae, and chitin synthase 1 from Candida albicans up to the concentration of 280 microg/mL, while kanakugiol (3) exhibited very weak activity against chitin synthase 1 of C. albicans with an IC(50) of 160 microg/mL. All of the compounds showed moderate to weak antifungal activities against various pathogenic fungi (MIC: 8 - >128 microg/mL) including Cryptococcus neoformans, Aspergillus fumigatus, and Colletotrichum lagenarium. The results indicate that these compounds are specific inhibitors of chitin synthase 2 and can potentially serve as antifungal agents.
机译:从L. erythrocarpa Makino(Lauraceae)的茎皮中分离出有效的几丁质合酶2抑制剂,甲基linderone(1),linderone(2)和kanakugiol(3)。这些化合物抑制几丁质合酶2的IC(50)值分别为23.3、21.4和23.8 microg / mL。甲基linderone(1)和linderone(2)对酿酒酵母的几丁质合酶1和3和白色念珠菌的几丁质合酶1均无抑制活性,直至浓度为280 microg / mL,而Kanakugiol(3)的活性却很弱。抗白色念珠菌的几丁质合酶1,IC(50)为160微克/毫升。所有化合物均对各种致病真菌(MIC:8-> 128 microg / mL)表现出中度至弱的抗真菌活性,其中包括新型隐球菌,烟曲霉和产炭疽菌。结果表明,这些化合物是几丁质合酶2的特异性抑制剂,可以潜在地用作抗真菌剂。

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