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从榕葡萄中分离出的内生菌产生的新型紫穗槐烷和二氯间苯二酚衍生物。

New eremophilane and dichlororesorcinol derivatives produced by endophytes isolated from Ficus ampelas.

作者信息

Shiono Yoshihito, Muslihah Niken Istikhari, Suzuki Takuma, Ariefta Nanang Rudianto, Anwar Chairil, Nurjanto Handojo Hadi, Aboshi Takako, Murayama Tetsuya, Tawaraya Keitaro, Koseki Takuya, Yoshida Jun, Usukhbayar Narandulam, Uesugi Shota, Kimura Ken-Ichi

机构信息

Department of Food, Life, and Environmental Science, Faculty of Agriculture, Yamagata University, Yamagata, Japan.

Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Yogyakarta, Indonesia.

出版信息

J Antibiot (Tokyo). 2017 Dec;70(12):1133-1137. doi: 10.1038/ja.2017.125. Epub 2017 Oct 25.

Abstract

The novel compound, 11-O-methylpetasitol (1), was isolated from Penicillium sp. N-175-1, and two new compounds, cosmochlorins D (5) and E (6), were isolated from Phomopsis sp. N-125. In addition, three known eremophilane sesquiterpenes, sporogen-AO1 (2), petasol (3) and 6-dehydropetasol (4), were isolated from Penicillium sp. N-175-1. The structures of 1, 5 and 6 were elucidated by a combination of extensive spectroscopic analyses, including 2D NMR, high-resolution electrospray ionization time-of-flight mass spectrometry (HRESITOFMS) and chemical reactions. Compounds 2, 3, 5 and 6 exhibited cytotoxicity to HL60 and 2 and 3 to HeLa cells. Furthermore, 2 and 3 showed robust growth-restoring activity of a Saccharomyces cerevisiae (cdc2-1 rad9Δ) mutant strain, whereas 5 and 6 exhibited minor growth-restoring activity in this strain. Thus, these compounds may inhibit the growth of HL60 and HeLa cells by blocking the cell cycle, and they may be utilized as new lead compounds that act as inhibitors of survival signal transduction pathways.

摘要

新型化合物11 - O - 甲基佩塔醇(1)是从青霉属菌株N - 175 - 1中分离得到的,而两种新化合物,宇宙绿菌素D(5)和E(6),是从拟茎点霉属菌株N - 125中分离得到的。此外,从青霉属菌株N - 175 - 1中还分离出了三种已知的桉烷倍半萜,即产孢素 - AO1(2)、佩塔醇(3)和6 - 脱氢佩塔醇(4)。通过包括二维核磁共振、高分辨率电喷雾电离飞行时间质谱(HRESI - TOFMS)和化学反应在内的广泛光谱分析相结合的方法,阐明了化合物1、5和6的结构。化合物2、3、5和6对HL60细胞具有细胞毒性,化合物2和3对HeLa细胞具有细胞毒性。此外,化合物2和3对酿酒酵母(cdc2 - 1 rad9Δ)突变株表现出强大的生长恢复活性,而化合物5和6在该菌株中表现出较弱的生长恢复活性。因此,这些化合物可能通过阻断细胞周期来抑制HL60和HeLa细胞的生长,并且它们可以用作新的先导化合物,作为存活信号转导途径的抑制剂。

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