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从 L. 中分离得到的一种新的肼衍生物 Muricazine,具有抗氧化、脂氧合酶和脲酶抑制活性。

Muricazine, a new hydrazine derivative from L. with antioxidant, lipoxygenase and urease inhibitory activities.

机构信息

Department of Pharmacy, Sarhad University of Science and Information Technology, Peshawar, Pakistan.

Department of Pharmacy, University of Peshawar, Peshawar, Pakistan.

出版信息

Nat Prod Res. 2022 Feb;36(4):961-966. doi: 10.1080/14786419.2020.1855169. Epub 2020 Dec 7.

Abstract

L., an important member of family Ranunculaceae upon submission to phytochemical studies, led to the isolation of a novel natural hydrazine derivative, muricazine (). Chemical structure of the compound was established with the aid of advanced spectroscopic techniques. It was evaluated for antioxidant, lipoxygenase, and urease (jack-bean) inhibitory activities. Results suggested that compound could scavenge the DPPH free radical (42.1 ± 0.12 M) to a great extent as compared to the standard (40.6 ± 0.91 M). However, it showed moderate inhibitory potential against lipoxygenase (65.2 ± 0.45 M) and urease (54.8 ± 0.23 M) enzymes.

摘要

L.,毛茛科的重要成员,经过植物化学研究,导致了一种新型天然肼衍生物的分离,即 muricazine()。化合物的化学结构是借助先进的光谱技术确定的。它被评估了抗氧化、脂氧合酶和脲酶(豇豆)抑制活性。结果表明,与标准品(40.6±0.91M)相比,化合物可以极大地清除 DPPH 自由基(42.1±0.12M)。然而,它对脂氧合酶(65.2±0.45M)和脲酶(54.8±0.23M)的抑制活性适中。

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