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海洋来源放线菌 Streptomyces sp. ZZ735 中抗神经胶质瘤细胞的增殖代谢产物。

Antiproliferative metabolites against glioma cells from the marine-associated actinomycete Streptomyces sp. ZZ735.

机构信息

Ocean College, Zhoushan Campus, Zhejiang University, Zhoushan 316021, China.

Zhejiang Marine Development Research Institute, Zhoushan 316000, China.

出版信息

Fitoterapia. 2024 Oct;178:106176. doi: 10.1016/j.fitote.2024.106176. Epub 2024 Aug 8.

DOI:10.1016/j.fitote.2024.106176
PMID:39127306
Abstract

Metabolites produced by the genus Streptomyces are the most important resource for discovering bioactive compounds. In this study, chemical investigation on the metabolites produced by the marine-derived Streptomyces sp. ZZ735 in rice solid medium led to the isolation of eighteen compounds (1-18). Chemical structures of the isolated compounds were determined based on their HRESIMS data and the extensive NMR spectral analyses. Streptonaphthothiazines A (1), B (2), 2-(2-hydroxy-2-methylpropanoylamino)-benzoic acid (7), and streptomycinoic acids A (17), B (18) are characterized as five previously undescribed compounds. The structural backbones of streptonaphthothiazines A (1), B (2) and streptomycinoic acids A (17), B (18) are found from a natural resource for the first time. It is also the first report of 2-(2-methylpropanoylamino)-benzoic acid (3), 2-(2-methylpropanoylamino)-benzamide (4), methyl 2-(3-hydroxypropanoylamino)-benzoate (5), 2-propionylaminobenzamide (6), and (2E)-3-(3-hydroxy-4,5-dimethoxyphenyl)-2-propenoic acid (15) as natural products. Streptonaphthothiazines A (1), B (2) and streptomycinoic acids A (17), B (18) have antiproliferative activity against human glioma U87MG or U251 cells with IC values ranging from 31.8 to 37.9 μM.

摘要

由链霉菌属产生的代谢产物是发现生物活性化合物的最重要资源。在这项研究中,对海洋来源的链霉菌属 sp. ZZ735 在大米固体培养基中产生的代谢产物进行了化学研究,分离得到了 18 种化合物(1-18)。根据它们的 HRESIMS 数据和广泛的 NMR 光谱分析确定了分离化合物的化学结构。Streptonaphthothiazines A(1)、B(2)、2-(2-羟基-2-甲基丙酰氨基)-苯甲酸(7)和 streptomycinoic acids A(17)、B(18)被鉴定为五种以前未描述的化合物。Streptonaphthothiazines A(1)、B(2)和 streptomycinoic acids A(17)、B(18)的结构骨架首次从天然资源中发现。这也是 2-(2-甲基丙酰氨基)-苯甲酸(3)、2-(2-甲基丙酰氨基)-苯甲酰胺(4)、甲基 2-(3-羟基丙酰氨基)-苯甲酸(5)、2-丙酰氨基苯甲酰胺(6)和(2E)-3-(3-羟基-4,5-二甲氧基苯基)-2-丙烯酸(15)首次作为天然产物报道。Streptonaphthothiazines A(1)、B(2)和 streptomycinoic acids A(17)、B(18)对人神经胶质瘤 U87MG 或 U251 细胞具有抗增殖活性,IC 值范围为 31.8-37.9 μM。

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