Siti Fadilah Juhan, Siti Mariam Mohd Nor, Mohd Shukri Mat Ali, Siti Zulaika Md Nor
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引用次数: 0
摘要
利用辣根过氧化物酶(HRP)在香兰素(1)与阿弗酸甲酯(2)或辛酸甲酯(3)之间进行酶偶联反应,合成了5个化合物,包括8- o -4′-新木聚糖(7)、2个芳基萘木聚糖(5,8)、芳基二氢苯并呋喃新木聚糖(4)和木脂素(6)。所有这些化合物以及先前合成的钯催化偶联产物新木聚糖(9)、8- o -4′-新木聚糖(10)、芳基香豆素(11)和木脂素(12)。测定了对双头小蠹2龄幼虫的杀虫活性。研究显示,在接触24小时后,9种合成化合物中有7种的死亡率超过90%。与标准印楝素(LD50 =2.818 mg/L)相比,新木脂素(10)和木脂素(6)的杀虫活性最强,LD50分别为2.218 mg/L和1.678 mg/L。结果表明,所合成的化合物具有较高的防治潜力,可用于开发新的、更有效的杀幼虫化合物。
LARVICIDAL ACTIVITY OF THE SYNTHESISED LIGNANS, NEOLIGNANS, AND COUMARIN AGAINST Crocidolimia binotalis 2nd INSTAR LARVAE
Five compounds comprising 8-O-4’-neolignan (7), two arylnaphthalene lignans (5, 8), aryldihydrobenzofuran neolignan (4), and lignan (6) were synthesised by enzymatic coupling reaction using horseradish peroxidase (HRP) between vanillin (1) with methyl ferulate (2) or methyl sinapate (3). All of these compounds, as well as previously synthesised palladium-catalysed coupling products of neolignan (9), 8-O-4'-neolignan (10), arylcoumarin (11), and lignan (12), were examined for larvicidal activity against Crocidolomia binotalis 2nd instar larvae. It revealed that seven out of nine synthesised compounds had a mortality rate of more than 90% after 24 hours of exposure. Neolignan (10) and lignan (6) demonstrated the strongest larvicidal activity with LD50 = 2.218 mg/L and LD50 = 1.678 mg/L, respectively compared to the standard azadirachtin (LD50 =2.818 mg/L). The results showed that the synthesised compounds have a high potential for use in the control of C. binotalis larvae and could be used in the development of new and more effective compounds as larvicides.