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希氏千里光属(菊科)地上部分的次生代谢产物及其生物评价。

Secondary Metabolites and Their Biological Evaluation from the Aerial Parts of Sibth. & Sm. (Asteraceae).

机构信息

Laboratory of Pharmacognosy, Faculty of Health Sciences, School of Pharmacy, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.

Department of Chemistry, Division of Organic Chemistry, University of Crete, 71003 Heraklion, Greece.

出版信息

Int J Mol Sci. 2024 Oct 1;25(19):10586. doi: 10.3390/ijms251910586.

Abstract

Phytochemical investigation of Sibth. & Sm. resulted in the isolation of twenty-two natural products: eleven sesquiterpene lactones, artemorin (), tamirin (), tanachin (), reynosin (), baynol C (), desacetyl-β-cyclopyrethrosin (), 1β-hydroxy-4α-methoxy-5α,7α,6β-eudesm-11(13)-en-6,12-olide (), 1β,4α,6α-trihydroxyeudesm-11-en-8α,12-olide (), 1β-hydroxy-arbusculin A (), methyl-1β,4α,6α-trihydroxy-5α,7αH-eudesm-11(13)-en-12-oate () and methyl-1β,6α,8α-trihydroxy-5α,7αH-eudesma-4(15),11(13)-dien-12-oate (); one lignan, pinoresinol (); one norisoprenoid, loliolide (); six flavonoids (four genins and two glycosides), hispidulin (), nepetin (), jaceosidin (), eriodictyol (), eriodictyol-3'-O-β-D-glucoside () and eriodictyol-7-O-β-D-glucuronide (); and three phenolic derivatives (one phenolic acid and two phenolic glucosides), protocatechuic acid (), arbutin () and nebrodenside A (). From the isolated compounds, only nepetin () has been reported previously from the genus and, to the best of our knowledge, it is the first time that compound () has been identified in Asteraceae. A number of these substances were tested for (a) inhibition of lipoxygenase and acetylocholinesterase, (b) their antioxidant activity using the DPPH (1,1-Diphenyl-2-picrylhydrazyl) method or/and (c) inhibition of lipid peroxidation. The tested components exhibited low antioxidant activity with the exception of and , while the effectiveness of these compounds in the inhibition of acetylocholinesterase is limited. Furthermore, Molinspiration, an online computer tool, was used to determine the bioactivity ratings of the isolated secondary metabolites. The compounds' bioactivity ratings for potential therapeutic targets were very promising.

摘要

对 Sibth. & Sm. 的植物化学研究导致了二十二种天然产物的分离:十一种倍半萜内酯,芹黄素()、塔米林()、丹参酮()、雷诺辛()、巴尼奥尔 C()、去乙酰基-β-环戊内酯()、1β-羟基-4α-甲氧基-5α,7α,6β-桉叶烷-11(13)-烯-6,12-内酯()、1β,4α,6α-三羟基-5α,7αH-桉叶烷-11-烯-8α,12-内酯()、1β-羟基-阿布斯枯林 A()、甲基-1β,4α,6α-三羟基-5α,7αH-桉叶烷-11(13)-烯-12-酸酯()和甲基-1β,6α,8α-三羟基-5α,7αH-桉叶-4(15),11(13)-二烯-12-酸酯();一种木脂素,松柏醇();一种异戊二烯,丁香酸();六种类黄酮(四种苷元和两种糖苷),芹菜素()、新橙皮苷()、芹菜苷()、圣草酚()、圣草酚-3'-O-β-D-葡萄糖苷()和圣草酚-7-O-β-D-葡萄糖醛酸苷();以及三种酚类衍生物(一种酚酸和两种酚糖苷),原儿茶酸()、熊果苷()和尼伯苷 A()。在所分离的化合物中,只有新橙皮苷()以前曾在 Asteraceae 属中报道过,据我们所知,化合物()是首次在菊科中鉴定出来的。这些物质中的许多物质都进行了(a)抑制脂氧合酶和乙酰胆碱酯酶、(b)使用 DPPH(1,1-二苯基-2-苦基肼)法测定其抗氧化活性和/或(c)抑制脂质过氧化。除了()和()之外,测试的成分表现出低抗氧化活性,而这些化合物在抑制乙酰胆碱酯酶方面的有效性是有限的。此外,还使用在线计算机工具 Molinspiration 来确定分离的次生代谢物的生物活性评分。这些化合物对潜在治疗靶点的生物活性评分非常有希望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/796c/11476517/c5cbad5c3000/ijms-25-10586-g001.jpg

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