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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Synthesis and characterization of norbelladine, a precursor of Amaryllidaceae alkaloid, as an anti-inflammatory/anti-COX compound
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Synthesis and characterization of norbelladine, a precursor of Amaryllidaceae alkaloid, as an anti-inflammatory/anti-COX compound

机译:芳樟科生物碱的前体降冰片碱的合成和表征,作为一种抗炎/抗COX化合物

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摘要

Rising ROS and systemic inflammation is often a serious concern in many disease conditions including obesity. Therefore, compounds with both anti-oxidant and anti-inflammatory activities are considered beneficial in preventing/treating several human chronic diseases. Norbelladine is an amine compound, a precursor for Amaryllidaceae alkaloids (e.g., belladine, crinamine, lycorine, and galanthamine) found in plants traditionally used for treating a variety of human diseases. However, little information is available about its potential health effects. Therefore, the amine was first synthesized, and its anti-oxidant and anti-inflammatory activities were investigated in this study. Also, the potential effects of the amine on NF-kappa B activation were investigated due to the critical involvement of ROS in the activation. Norbelladine was synthesized with more than 60% yield, analyzed by a HPLC method, and verified using NMR spectroscopic method. Then, its radical scavenging activity was investigated using DPPH-and superoxide radical assays. At the concentration of 10 mu M, norbelladine was a compound able to quench DPPH-radical by 31% (P < 0.05) and reduce superoxide radicals from xanthine oxidase by 33% (P < 0.05). At the concentration of 0.25 mu M, the amine also inhibited both COX-1 and COX-2 enzymes by 51% and 25% (P < 0.05), respectively. Furthermore, at the concentration of 10 mu M, norbelladine inhibited NF-kappa B activation by 23% (P < 0.05). In summary, the data suggests that norbelladine may be a compound to quench radicals, inhibit COX enzymes as well as suppress NF-kappa B activation at relatively lower concentrations. Published by Elsevier Ltd.
机译:在包括肥胖症在内的许多疾病中,ROS升高和全身性炎症通常是一个严重的问题。因此,具有抗氧化和抗炎活性的化合物被认为有利于预防/治疗几种人类慢性疾病。 Norbelladine是一种胺化合物,是芳基科的生物碱(例如belladine,crinamine,lycorine和galanthamine)的前体,通常用于治疗多种人类疾病。但是,关于其潜在健康影响的信息很少。因此,本研究首先合成了胺,并研究了其抗氧化和抗炎活性。而且,由于ROS在活化中的关键参与,还研究了胺对NF-κB活化的潜在影响。合成诺贝拉定的收率超过60%,通过HPLC方法进行分析,并使用NMR光谱法进行验证。然后,使用DPPH和超氧自由基检测法研究了其自由基清除活性。在浓度为10μM时,去甲苦参碱是能够将DPPH自由基淬灭31%(P <0.05),并能使黄嘌呤氧化酶的超氧自由基减少33%(P <0.05)的化合物。在0.25μM的浓度下,胺还分别抑制COX-1和COX-2酶51%和25%(P <0.05)。此外,在10μM的浓度下,去甲苦参碱可抑制NF-κB活化23%(P <0.05)。总而言之,数据表明降冰片碱可能是在相对较低的浓度下淬灭自由基,抑制COX酶以及抑制NF-κB活化的化合物。由Elsevier Ltd.发布

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