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红厚壳提取物成分的库中具有细胞毒性和葡萄糖转运抑制作用。

Constituents of an extract of Cryptocarya rubra housed in a repository with cytotoxic and glucose transport inhibitory effects.

机构信息

Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University , Columbus, Ohio 43210, United States.

出版信息

J Nat Prod. 2014 Mar 28;77(3):550-6. doi: 10.1021/np400809w. Epub 2013 Dec 17.

Abstract

A new alkylated chalcone (1), a new 1,16-hexadecanediol diester (2), and eight known compounds were isolated from a dichloromethane-soluble repository extract of the leaves and twigs of Cryptocarya rubra collected in Hawaii. The structures of the new compounds were determined by interpretation of their spectroscopic data, and the absolute configurations of the two known cryptocaryanone-type flavonoid dimers, (+)-bicaryanone A (3) and (+)-chalcocaryanone C (4), were ascertained by analysis of their electronic circular dichroism and NOESY NMR spectra. All compounds isolated were evaluated against HT-29 human colon cancer cells, and, of these, (+)-cryptocaryone (5) was found to be potently cytotoxic toward this cancer cell line, with an IC50 value of 0.32 μM. This compound also exhibited glucose transport inhibitory activity when tested in a glucose uptake assay.

摘要

从夏威夷采集的Cryptocarya rubra 的叶和小枝的二氯甲烷可溶部分提取物中分离得到一种新的烷基化查尔酮(1)、一种新的 1,16-十六烷二醇二酯(2)和八种已知化合物。新化合物的结构通过其光谱数据的解释来确定,并且通过分析它们的电子圆二色性和 NOESY NMR 光谱确定了两种已知的 cryptocaryanone 型类黄酮二聚体(+)-bicaryanone A(3)和(+)-chalcocaryanone C(4)的绝对构型。分离得到的所有化合物均针对 HT-29 人结肠癌细胞进行了评估,其中(+)-cryptocaryone(5)对该癌细胞系表现出很强的细胞毒性,IC50 值为 0.32 μM。该化合物在葡萄糖摄取测定中还表现出葡萄糖转运抑制活性。

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