Phytochemical Analysis of Cinnamomum zeylanicum Bark and Molecular Docking of Procyanidin B2 against the Transcription Factor Nf- κB

B. Varalakshmi, V. Anand, T. Karpagam, A. Shanmugapriya, S. Gomathi, J. Sugunabai, V. Suganya, S. Geetha, S. Sathianachiyar
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引用次数: 3

Abstract

Introduction: Identification of novel natural antioxidant compounds is a highly demanding avenue of therapy for oxidative stress induced diseases. The bark of Cinnamomum zeylanicum commonly known as Ceylon cinnamon is commonly used in Ayurvedic medicine. Method: In this study, the methanolic extract of bark was subjected to GC-MS, UV absorption and TLC techniques to analyze the presence and to elucidate the structure of proanthocyanidins present in the bark. In the latter part of the study, chemdraw structure of the identified procyanidin B2 was subjected to in silico molecular drug docking analysis using GOLD to find out its inhibiting efficacy against NF-κB (1NFI). Results: The phytochemical analysis supported the presence of a proanthocyanidin compound, procyanidin B2. The constitutive or aberrant activation of the transcription factor, NF-κB pathway is often noticed in many cancers, autoimmune disorders, pulmonary, cardiovascular, neurodegenerative and skin diseases. The docking of procyanidin B2 with NF-κB revealed its inhibiting efficacy by binding to active site of NF-κB and thus could inhibited the nuclear translocation and DNA binding of p50/p65 heterodimer to κB DNA sequences. Conclusions: Thus, procyanidin B2 can act as the inhibitor for NF-κB. So, procyanidin B2 present in C. zeylanicum bark can be used as a potential lead compound for drug development against cancer and other oxidative stress disorders.
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肉桂树皮的植物化学分析及原花青素B2对转录因子Nf- κB的分子对接
新型天然抗氧化化合物的鉴定是氧化应激诱导疾病治疗的一个非常重要的途径。肉桂的树皮通常被称为锡兰肉桂,通常用于阿育吠陀医学。方法:采用气相色谱-质谱、紫外吸收、薄层色谱等方法分析树皮甲醇提取物中原花青素的存在并阐明其结构。在研究的后半部分,利用GOLD对鉴定的原花青素B2的化学结构进行硅分子药物对接分析,以确定其对NF-κB (1NFI)的抑制作用。结果:植物化学分析支持原花青素化合物原花青素B2的存在。转录因子NF-κB通路的本构性或异常激活在许多癌症、自身免疫性疾病、肺病、心血管病、神经退行性疾病和皮肤病中都经常被发现。原花青素B2与NF-κB对接,通过结合NF-κB活性位点显示其抑制作用,从而抑制p50/p65异二聚体与κB DNA序列的核易位和DNA结合。结论:原花青素B2具有抑制NF-κB的作用。因此,zezelanum树皮中的原花青素B2可以作为抗癌症和其他氧化应激障碍药物开发的潜在先导化合物。
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