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靶向特定白血病细胞系的极端环境真菌来源的半胱天冬酶-1 抑制剂。

Caspase-1 inhibitors from an extremophilic fungus that target specific leukemia cell lines.

机构信息

Department of Biomedical and Pharmaceutical Sciences, The University of Montana, Missoula, Montana 59812, United States.

出版信息

J Nat Prod. 2012 Mar 23;75(3):344-50. doi: 10.1021/np200414c. Epub 2012 Feb 1.

Abstract

Berkeley Pit Lake, Butte, Montana, is a 540 m deep abandoned open-pit copper mine filled with over 140 billion liters of acidic, metal-sulfate-contaminated water. This harsh environment has yielded several microorganisms that produce interesting biologically active compounds. Several polyketide metabolites including the new berkazaphilones A (1) and B (2) and octadienoic acid derivatives berkedienoic acid (13) and berkedienolactone (15), as well as previously reported azaphilone 4, vermistatin (6), dihydrovermistatin (7), penisimplicissin (8), aldehyde 9, and methylparaconic acid (11), were isolated from a culture broth of Penicillium rubrum taken from a depth of 270 m. The structures of these compounds were deduced by interpretation of spectroscopic data. The compounds were isolated either for their inhibition of the signal transduction enzyme caspase-1 or because of their structural similarity to these inhibitors. Selected compounds were further evaluated for their ability to inhibit interleukin-1β production by inflammasomes in induced THP-1 cells. Berkazaphilones B (2) and C (4) and vermistatin analogue penisimplicissin (8) exhibited selective activity against leukemia cancer cell lines in the National Cancer Institute 60 human cell line assay.

摘要

伯克利坑湖,比尤特,蒙大拿州,是一个 540 米深的废弃露天铜矿,里面充满了超过 1400 亿升的酸性、含金属硫酸盐的水。这个恶劣的环境产生了几种能够产生有趣的生物活性化合物的微生物。从取自 270 米深处的红色青霉培养物中分离到了几种聚酮代谢物,包括新的伯克沙菲酮 A(1)和 B(2)以及辛二烯酸衍生物伯克烯酸(13)和伯克烯内酯(15),以及以前报道过的氮杂菲酮 4、vermistatin(6)、二氢 vermistatin(7)、penisimplicissin(8)、醛 9 和甲基巴豆酸(11)。这些化合物的结构通过光谱数据分析推断得出。这些化合物的分离要么是因为它们抑制信号转导酶 caspase-1,要么是因为它们的结构与这些抑制剂相似。选择的化合物进一步评估了它们抑制诱导的 THP-1 细胞中炎症小体产生白细胞介素-1β的能力。伯克沙菲酮 B(2)和 C(4)以及 vermistatin 类似物 penisimplicissin(8)在国立癌症研究所的 60 个人类细胞系测定中对白血病癌细胞系表现出选择性活性。

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