Kaki Shiva Shanker, Kunduru Konda Reddy, Kanjilal Sanjit, Narayana Prasad Rachapudi Badari
Centre for Lipid Research, CSIR-Indian Institute of Chemical Technology.
J Oleo Sci. 2015;64(8):845-52. doi: 10.5650/jos.ess15035. Epub 2015 Jul 15.
Ferulic acid was modified to produce a novel phenolipid containing butyl chains. Ferulic acid was esterified with butanol to produce butyl ferulate which was further dihydroxylated followed by esterification with butyric anhydride to produce the phenolipid containing butyric acid. IR, NMR and MS techniques confirmed the structure of the synthesized structured lipophilic phenolic compound. The synthesized compound was tested for in vitro antioxidant and antimicrobial activities. The produced phenolipid showed moderate antioxidant activity in DPPH (2, 2-diphenyl-1-picrylhydrazyl) radical scavenging assay but in linoleic acid oxidation method, it exhibited good activity compared with the parent compound and the reference compounds. The prepared derivative could find applications as antioxidant in lipophilic systems and also as a potential prodrug of butyric acid. It also showed antibacterial effect against the four bacterial strains studied. The drug-likeness properties of the prepared molecule calculated were in the acceptable ranges according to Lipinski's rule of 5 and suggest that it has potential to cross the blood-brain barrier.
阿魏酸经过修饰以生成一种含有丁基链的新型酚脂质。阿魏酸与丁醇酯化生成丁基阿魏酸酯,后者进一步进行二羟基化,然后与丁酸酐酯化以生成含有丁酸的酚脂质。红外光谱、核磁共振和质谱技术证实了合成的结构化亲脂性酚类化合物的结构。对合成的化合物进行了体外抗氧化和抗菌活性测试。所制备的酚脂质在二苯基苦味酰基自由基清除试验(DPPH)中表现出中等抗氧化活性,但在亚油酸氧化法中,与母体化合物和参考化合物相比,它表现出良好的活性。所制备的衍生物可作为亲脂性系统中的抗氧化剂以及丁酸的潜在前药。它还对所研究的四种细菌菌株显示出抗菌作用。根据Lipinski的五规则计算,所制备分子的类药性质在可接受范围内,表明它有穿过血脑屏障的潜力。