Likhitwitayawuid Kittisak, Sritularak Boonchoo, Benchanak Kanokwan, Lipipun Vimolmas, Mathew Judy, Schinazi Raymond F
Department of Pharmacognosy, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok 10330, Thailand.
Nat Prod Res. 2005 Feb;19(2):177-82. doi: 10.1080/14786410410001704813.
From the leaves of Millettia erythrocalyx, a new flavone named 3',5'-dimethoxy-[2",3": 7,8]-furanoflavone and three known compounds were isolated. Assays for anti-herpes simplex virus activity (HSV-1 and HSV-2) were performed on 24 phenolic compounds obtained from M. erythrocalyx and Artocarpus lakoocha. It was found that the flavones ovalifolin, pongol methyl ether and millettocalyxin A, and the stilbene oxyresveratrol possessed moderate activity against both types of HSV. In addition, oxyresveratrol was evaluated for potential anti-HIV activity against a wild-type human immunodeficiency virus type 1 (HIV-1/LAI) isolate and was found to be a modest inhibitor of HIV (EC50 28.2 microM), showing no toxicity in PBM, CEM and Vero cells at 100 microM. The heartwood of A. lakoocha, which contains a large amount of oxyresveratrol, could be considered as a source of starting material for the development of new natural product-based anti-HSV and anti-HIV agents.
从红萼崖豆藤的叶子中分离出一种名为3',5'-二甲氧基-[2",3": 7,8]-呋喃黄酮的新黄酮和三种已知化合物。对从红萼崖豆藤和大叶桂木中获得的24种酚类化合物进行了抗单纯疱疹病毒活性(HSV-1和HSV-2)测定。结果发现,黄酮类化合物椭圆叶豆素、庞戈醇甲醚和红萼崖豆藤素A以及芪类化合物氧化白藜芦醇对两种类型的HSV均具有中等活性。此外,对氧化白藜芦醇针对野生型人类免疫缺陷病毒1型(HIV-1/LAI)分离株的潜在抗HIV活性进行了评估,发现其为HIV的适度抑制剂(EC50为28.2 microM),在100 microM浓度下对PBM、CEM和Vero细胞无毒性。大叶桂木的心材含有大量氧化白藜芦醇,可被视为开发新型天然产物抗HSV和抗HIV药物的起始原料来源。