Department of Biochemistry, School of Bioengineering and Biosciences, Lovely Professional University (LPU), Jalandhar- Delhi G.T. Road, Phagwara, Punjab 144411, India
Department of Pharmaceutical Sciences, Lovely Professional University, Phagwara, India
Curr Drug Discov Technol. 2020;17(5):619-630. doi: 10.2174/1570163816666190321142826.
Fenchone is a natural monoterpene abundantly present in fennel essential oil. It is known for its wound healing properties but its other biological activities are less explored.
We used an in silico structural similarity searching approache to identify various biological activities of fenchone. The identified biological activities of fenchone (purchased from Sigma Aldrich) were validated by conducting DPPH free radical scavenging assay, MTT assay, well diffusion assay for antimicrobial activity and enzymatic assays to analyze the activity of different antioxidant enzymes.
Camphor was found to possess maximum structural similarity with fenchone (similarityindex 100). Molecular docking demonstrated that the binding modes of fenchone were also similar to camphor against protein Cytochrome CYP101D1 (PDB ID: 4C9K). Fenchone also demonstrated to possess an antioxidant activity (IC50: 3.32±0.008mM), an antimicrobial activity (MIC: 0.49mM) and a very strong antifungal activity. Fenchone protects yeast cells from H2O2 induced cytotoxicity and is cytotoxic to cancerous Hela cells (IC50: 12.63±0.12 μM). Fenchone treatment also showed the reduced activity of antioxidant enzymes i.e glutathione-S-transferase, catalase and lipid peroxidase.
To the best of our knowledge, this is the first report that used structural similarity searching to explore the biological activities of fenchone.
葎草酮是一种天然单萜,大量存在于茴香精油中。它以其伤口愈合特性而闻名,但它的其他生物活性尚未得到充分探索。
我们使用一种基于结构相似性的计算机搜索方法来确定葎草酮的各种生物活性。从西格玛奥德里奇购买的葎草酮的已识别生物活性通过 DPPH 自由基清除测定、MTT 测定、抗菌活性的孔扩散测定和分析不同抗氧化酶活性的酶测定来验证。
发现樟脑与葎草酮具有最大的结构相似性(相似度指数 100)。分子对接表明,葎草酮的结合模式也与樟脑类似,针对蛋白质细胞色素 CYP101D1(PDB ID:4C9K)。葎草酮还表现出抗氧化活性(IC50:3.32±0.008mM)、抗菌活性(MIC:0.49mM)和很强的抗真菌活性。葎草酮可保护酵母细胞免受 H2O2 诱导的细胞毒性,并对癌细胞 Hela 细胞具有细胞毒性(IC50:12.63±0.12μM)。葎草酮处理还显示抗氧化酶即谷胱甘肽-S-转移酶、过氧化氢酶和脂质过氧化物酶的活性降低。
据我们所知,这是首次使用结构相似性搜索来探索葎草酮的生物活性的报告。