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使用固定化环氧化酶-2进行磁性配体垂钓以从……中鉴定和筛选抗冠心病配体

Magnetic Ligand Fishing Using Immobilized Cyclooxygenase-2 for Identification and Screening of Anticoronary Heart Disease Ligands From .

作者信息

Chi Miaomiao, Wang Hongsen, Yan Zhankuan, Cao Lei, Gao Xun, Qin Kunming

机构信息

Jiangsu Key Laboratory of Marine Pharmaceutical Compound Screening, Jiangsu Ocean University, Lianyungang, China.

Jiangsu Original Drug Research and Development Co., Ltd., Lianyungang, China.

出版信息

Front Nutr. 2022 Jan 31;8:794193. doi: 10.3389/fnut.2021.794193. eCollection 2021.

Abstract

Inhibition of cyclooxygenase-2 (COX-2) activity is an effective way for treatment of coronary heart disease. And as an important source of COX-2 inhibitors, bioactive compounds of and pharmacological mechanisms remained lacking in prospective researches. Therefore, for the purpose of accelerating the discovery of natural products targeting designed inhibitors, the COX-2 microreactor composed of functionalized microspheres and magnetic ligand fishing was developed and applied in , and the physicochemical properties of the COX-2 functionalized microspheres were characterized using Fourier transform infrared spectroscopy (FT-IR), vibrating sample magnetometer (VSM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Furthermore, the bioactive compounds singled out from ethanol decoction without prepurification were dissociated and identified by ultraperformance liquid chromatography plus Q-Exactive Orbitrap tandem mass spectrometry (UPLC-Q-Exactive Orbitrap-MS/MS). Consequently, 21 bioactive compounds consisting of 6 organic acids, 8 flavonoids, and 7 others were separated and characterized from , which were reported to participate in the COX-2 inhibitory pathway to varying degrees. Therefore, this method could provide a prospective solution for the extraction and identification of active pharmaceutical ingredients and the rapid screening of some enzyme inhibitors in the complex mixtures.

摘要

抑制环氧化酶-2(COX-2)活性是治疗冠心病的有效方法。作为COX-2抑制剂的重要来源,其生物活性化合物及药理机制在前瞻性研究中仍较为缺乏。因此,为了加速发现靶向设计抑制剂的天然产物,开发了由功能化微球和磁性配体垂钓组成的COX-2微反应器并将其应用于[具体内容缺失],并使用傅里叶变换红外光谱(FT-IR)、振动样品磁强计(VSM)、扫描电子显微镜(SEM)和透射电子显微镜(TEM)对COX-2功能化微球的物理化学性质进行了表征。此外,通过超高效液相色谱联用Q-Exactive Orbitrap串联质谱(UPLC-Q-Exactive Orbitrap-MS/MS)对未经预纯化的乙醇煎剂中筛选出的生物活性化合物进行了解离和鉴定。结果,从[具体内容缺失]中分离并鉴定出21种生物活性化合物,包括6种有机酸、8种黄酮类化合物和7种其他化合物,据报道它们在不同程度上参与了COX-2抑制途径。因此,该方法可为复杂混合物中活性药物成分的提取和鉴定以及某些酶抑制剂的快速筛选提供一种前瞻性解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11da/8841743/d2f763da0121/fnut-08-794193-g0001.jpg

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