Mallavadhani Uppuluri V, Mahapatra Anita, Raja S Sabitha, Manjula C
Forest and Marine Products Department, Natural Resources Division, Regional Research Laboratory (CSIR), Bhubaneswar-751 013, Orissa, India.
J Agric Food Chem. 2003 Mar 26;51(7):1952-5. doi: 10.1021/jf020691d.
The 3-O-fatty acid ester derivatives (C(12)-C(18)) of two pentacyclic triterpenic acids, ursolic acid and oleanolic acid, were synthesized under mild esterification conditions in excellent yields (80-85%) and screened for their antifeedant activity, together with the parent acids, against the agricultural pest tobacco caterpillar larvae (Spodoptera litura F) in a no-choice laboratory study. The Urs-12-ene-28-carboxy-3beta-octadecanoate and olean-12-ene-28-carboxy-3beta-hexadecanoate were found to exhibit exceptionally potent antifeedant activities at 50 microg/cm(2) concentration, even after 48 h.
在温和的酯化条件下,以高产率(80 - 85%)合成了两种五环三萜酸——熊果酸和齐墩果酸的3 - O - 脂肪酸酯衍生物(C(12)-C(18)),并在一项无选择的实验室研究中,与母体酸一起针对农业害虫烟草夜蛾幼虫(斜纹夜蛾F)进行了拒食活性筛选。结果发现,熊果 - 12 - 烯 - 28 - 羧基 - 3β - 十八烷酸酯和齐墩果 - 12 - 烯 - 28 - 羧基 - 3β - 十六烷酸酯即使在48小时后,在50微克/平方厘米的浓度下仍表现出极强的拒食活性。