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从Euphorbia cornigera 中分离和鉴定新型生物活性化合物:细胞毒性 ingenol 酯。

Isolation and characterisation of new bio-active compounds from Euphorbia cornigera: cytotoxic ingenol esters.

机构信息

Department of Chemistry, Gomal University, Dera Ismail Khan, Pakistan.

出版信息

Nat Prod Res. 2012;26(20):1857-63. doi: 10.1080/14786419.2011.616507. Epub 2011 Oct 19.

Abstract

The aerial parts of Euphorbia cornigera Boiss., on extraction with MeOH, yielded new bio-active constituents (1, 2) and known compounds (3 and 4) after MTT cytotoxicity assay-guided fractionation and chromatographic separation were conducted. From the aerial parts of E. cornigera Boiss., new bio-active constituents were extracted in methanol. The extract was partitioned in different organic solvents and the ethylacetate-soluble portion was subjected to Craig's distribution. The MTT cytotoxicity assay-guided chromatographic separation yielded four (1-4), out of which two (1, 2) were new and two known (3, 4) bio-active compounds, and they are reported for the first time from this source. Their structure and relative stereochemistry were established by analysing spectroscopic and mass measurement data. The isolates were named as: 13-O-[(2Z ,4 E ,6 Z)]-deca-2,4,6-trienoylingenol (1), 13-O-( 2 Z ,4 E ,6 Z)-deca-2,4,6-trienoyl-20-O-angeloylingenol (2), 13-O-dodecanoyl-20-O-hexanoylingenol (3) and 3-O-(2,3-dimethylbutanoyl)-13-O-dodecanoyl-20-O-hexadecanoylingenol (4). Literature revealed that compounds 1 and 2 are new metabolites, while 3 and 4 are known, and are reported for the first time from this source. Cytotoxicities of isolates were evaluated in terms of IC(50) against RAW and HT-29 cell lines through MTT assay using ambrucin hydrochloride as a control. Compound 3 showed more activity than control, while 1, 2 and 4 were moderate.

摘要

Euphorbia cornigera Boiss. 的地上部分用甲醇提取后,经过 MTT 细胞毒性测定指导的分步提取和色谱分离,得到了新的生物活性成分(1、2)和已知化合物(3、4)。从 Euphorbia cornigera Boiss. 的地上部分用甲醇提取新的生物活性成分。提取物在不同有机溶剂中进行分配,乙酸乙酯可溶部分进行 Craig 分配。MTT 细胞毒性测定指导的色谱分离得到了四个(1-4)化合物,其中两个(1、2)是新的生物活性化合物,两个已知(3、4)化合物,它们是首次从该来源报道的。通过分析光谱和质谱数据确定了它们的结构和相对立体化学。分离物被命名为:13-O-[(2Z,4E,6Z)]-deca-2,4,6-trienoylingenol(1),13-O-(2Z,4E,6Z)-deca-2,4,6-trienoyl-20-O-angeloylingenol(2),13-O-dodecanoyl-20-O-hexanoylingenol(3)和 3-O-(2,3-二甲基丁酰基)-13-O-dodecanoyl-20-O-hexadecanoylingenol(4)。文献表明,化合物 1 和 2 是新的代谢物,而 3 和 4 是已知的,并且是首次从该来源报道的。通过 MTT 法测定 RAW 和 HT-29 细胞系的 IC(50)值,评价分离物的细胞毒性,以盐酸 ambrucin 作为对照。化合物 3 的活性比对照物强,而 1、2 和 4 则为中度。

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