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球孢白僵菌中2-吡啶酮生物碱和咯嗪的分离与鉴定

Isolation and characterization of 2-pyridone alkaloids and alloxazines from Beauveria bassiana.

作者信息

Andrioli W J, Lopes A A, Cavalcanti B C, Pessoa C, Nanayakkara N P D, Bastos J K

机构信息

a Faculdade de Ciências Farmacêuticas de Ribeirão Preto , Universidade de São Paulo , Ribeirão Preto , Brazil.

d Laboratório de Produtos Bioativos , Universidade Federal do Rio de Janeiro , Macaé , Brazil.

出版信息

Nat Prod Res. 2017 Aug;31(16):1920-1929. doi: 10.1080/14786419.2016.1269091. Epub 2016 Dec 29.

Abstract

Two novel compounds bearing heterocyclic nitrogen, 2-pyridone alkaloid (1) and alloxazine derivative (2), along with the known pretenellin B (3), pyridovericin (4) and lumichrome (5) were isolated from a culture of the entomopathogenic fungal strain Beauveria bassiana. The chemical structures of 2-pyridone alkaloid and alloxazine derivative were established on the basis of the interpretation of spectroscopic data. The isolated compounds were evaluated in a panel of five cancer cell lines and pyridovericin exhibited cytotoxicity (IC, μM) against cancer cell lines: HL-60 (25.9 ± 0.3), HCT8 (34.6 ± 3.6), MDA-MB435 (34.8 ± 3.8) and SF295 (31.1 ± 0.6). Considering that other pyridone compounds display good cytotoxic activity, it would be suggested to obtain new semi synthetic derivatives of pyridovericin, for the development of new cytotoxic chemical entities.

摘要

从昆虫病原真菌球孢白僵菌的培养物中分离出两种带有杂环氮的新型化合物,即2-吡啶酮生物碱(1)和咯嗪衍生物(2),以及已知的前青霉烯素B(3)、吡啶霉素(4)和核黄素(5)。基于光谱数据的解析确定了2-吡啶酮生物碱和咯嗪衍生物的化学结构。对分离出的化合物在五种癌细胞系中进行了评估,吡啶霉素对癌细胞系HL-60(25.9±0.3)、HCT8(34.6±3.6)、MDA-MB435(34.8±3.8)和SF295(31.1±0.6)表现出细胞毒性(IC,μM)。鉴于其他吡啶酮化合物显示出良好的细胞毒性活性,建议获得吡啶霉素的新半合成衍生物,以开发新的细胞毒性化学实体。

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