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提供药架潜在药效团的多功能方法:独活属植物三叶独活(Velen.)Brummitt 亚种。

Multifunctional approaches to provide potential pharmacophores for the pharmacy shelf: Heracleum sphondylium L. subsp. ternatum (Velen.) Brummitt.

机构信息

Department of Medicinal Laboratory, Vocational School of Health Services, Selcuk University, Konya-Turkey.

Department of Medicinal Laboratory, Vocational School of Health Services, Selcuk University, Konya-Turkey.

出版信息

Comput Biol Chem. 2019 Feb;78:64-73. doi: 10.1016/j.compbiolchem.2018.11.018. Epub 2018 Nov 20.

Abstract

Heracleum sphondylium L. subsp. ternatum (Velen.) Brummitt. commonly known as "hogweed" is traditionally used to manage several human ailments. This investigation assessed, for the first time, the enzyme inhibitory properties, antioxidant activity, phytochemical profile, antimutagenic, and antimicrobial potential of the ethyl acetate, methanol, and water extracts of H. sphondylium. We also established the possible interactions of identified phenolic compounds with cholinesterases, amylase, glucosidase, and tyrosinase using in silico docking studies. Chlorogenic acid was found in high amounts in the methanol extract of H. sphondylium. The methanol extract was an effective inhibitor of acetylcholinesterase (1.70 mg galantamine equivalent (GALAE)/g extract) while the ethyl acetate extract showed pronounced inhibitory action against butyrylcholinesterase (1.77 mg GALAE/g extract). The extracts exhibited low inhibition against amylase (0.12-0.84 mmol acarbose equivalent (ACAE)/g extract) and a more pronounced inhibition against glucosidase (2.29-3.65 mmol ACAE/g extract). In silico results showed that rutin and quercetin (-70.4 and -72.2 Kcal/mol, for rutin and quercetin respectively) docked to the enzymatic cavity of acetylcholinesterase but these phenolic compounds showed less affinity with butyrylcholinesterase (-15.0 and -5.2 Kcal/mol, for rutin and quercetin respectively). The extracts did not induce any mutations on the bacterial strains, while they have excellent antimutagenic capacity against well-known mutagens (inhibition values 98%, 97% and 96%). The methanol extract (0.78 mg/ml) showed moderate antifungal activity while the ethyl acetate extract (0.78-3.12 mg/ml) showed weak to moderate antimicrobial activity. This study provides valuable baseline data which might serve for the development of future pharmacophores for the management of human ailments.

摘要

欧洲山梗菜的亚种绵果山梗菜(Velen.)Brummitt.俗称“猪毛蒿”,传统上用于治疗多种人类疾病。本研究首次评估了欧洲山梗菜的乙酸乙酯、甲醇和水提取物的酶抑制特性、抗氧化活性、植物化学谱、抗突变和抗菌潜力。我们还通过计算机对接研究确定了鉴定出的酚类化合物与胆碱酯酶、淀粉酶、葡萄糖苷酶和酪氨酸酶的可能相互作用。在欧洲山梗菜的甲醇提取物中发现了大量的绿原酸。甲醇提取物是乙酰胆碱酯酶的有效抑制剂(1.70mg 加兰他敏当量(GALAE)/g 提取物),而乙酸乙酯提取物对丁酰胆碱酯酶表现出明显的抑制作用(1.77mg GALAE/g 提取物)。提取物对淀粉酶的抑制作用较弱(0.12-0.84mmol阿卡波糖当量(ACAE)/g 提取物),对葡萄糖苷酶的抑制作用更为明显(2.29-3.65mmol ACAE/g 提取物)。计算机模拟结果表明,芦丁和槲皮素(分别为-70.4 和-72.2Kcal/mol)与乙酰胆碱酯酶的酶腔结合,但这些酚类化合物与丁酰胆碱酯酶的亲和力较低(分别为-15.0 和-5.2Kcal/mol)。提取物在细菌菌株上没有诱导任何突变,而它们对已知诱变剂具有极好的抗突变能力(抑制值为 98%、97%和 96%)。甲醇提取物(0.78mg/ml)显示出中等的抗真菌活性,而乙酸乙酯提取物(0.78-3.12mg/ml)显示出弱至中等的抗菌活性。本研究提供了有价值的基线数据,可用于开发未来用于治疗人类疾病的药理学。

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