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从青霉 G59 衍生的突变株 3-f-31 中分离得到的四种新型抗肿瘤代谢物。

Four new antitumor metabolites isolated from a mutant 3-f-31 strain derived from Penicillium purpurogenum G59.

机构信息

State Key Laboratory of Toxicology and Medical Countermeasures, Institute of Pharmacology and Toxicology, Beijing, 100850, China.

Beijing Institute of Biomedine, Beijing, 100091, China.

出版信息

Eur J Med Chem. 2018 Oct 5;158:548-558. doi: 10.1016/j.ejmech.2018.09.015. Epub 2018 Sep 8.

Abstract

Penicimutanolones A (1) and B (2), penicimutanolone A methyl ether (3), and penicimumide (4), four new antitumor metabolites, were isolated from a neomycin-resistant mutant of the marine-derived fungus Penicillium purpurogenum G59. The structures of the compounds were elucidated by spectroscopic methods, and the absolute configurations were determined by X-ray crystallography and calculated ECD. In MTT and SRB assays, compounds 1-3 showed strong inhibitory effects on 14 human cancer cell lines. Compounds 1 and 2 maybe induce apoptosis of cancer cells mainly due to the inhibition of the expression of survivin, a client protein of HSP90. In addition, in vivo antitumor activity was observed for compound 1 in murine sarcoma HCT116 tumor-bearing Kunming mice, using docetaxel as a positive control.

摘要

Penicimutanolones A (1) 和 B (2)、penicimutanolone A 甲醚 (3) 和 penicimumide (4) 是从海洋来源真菌青霉属 purpurogenum G59 的新霉素抗性突变株中分离得到的四种新型抗肿瘤代谢产物。通过光谱方法阐明了化合物的结构,并通过 X 射线晶体学和计算 ECD 确定了它们的绝对构型。在 MTT 和 SRB 测定中,化合物 1-3 对 14 种人癌细胞系表现出强烈的抑制作用。化合物 1 和 2 可能主要通过抑制 HSP90 的客户蛋白 survivin 的表达诱导癌细胞凋亡。此外,在荷有鼠肉瘤 HCT116 的昆明小鼠中,以多西紫杉醇为阳性对照,观察到化合物 1 的体内抗肿瘤活性。

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