Magalhães Aderbal F, Tozzi Ana Maria G A, Magalhães Eva G, Souza-Neta Lourdes C
Organic Chemistry Department, Chemistry Institute, UNICAMP, Campinas, São Paulo, Brazil.
Planta Med. 2006 Mar;72(4):358-63. doi: 10.1055/s-2005-916232.
The analysis of root extracts from Deguelia longeracemosa (Benth.) A.M.G. Azevedo yielded fifteen prenylated metabolites. Nine of them are novel, and their molecular structures were determined through spectral analyses (UV, IR, MS and NMR) as being five derivatives of 4-hydroxy-3-phenylcoumarin: 4-hydroxy-3-(4'-hydroxyphenyl)-5-methoxy-6-(8',9'-epoxy-9'-methylbutyl)-2'',2''-dimethylpyrano-(5'',6'':8,7)-coumarin; 4-hydroxy-3-(3',4'-methylenedioxyphenyl)-5-methoxy-6-(3,3-dimethylallyl)-2'',2''-dimethypyrano-(5'',6'':8,7)-coumarin; 4-hydroxy-3-(3'-hydroxy-4'-methoxyphenyl)-5-methoxy-6-(3,3-dimethylallyl)-2'',2''-dimethylpyrano-(5'',6'':8,7)-coumarin; 4-hydroxy-3-(3'-hydroxy-4'-methoxyphenyl)-5-methoxy-2'',2''-dimethylpyrano-(5'',6'':6,7)-coumarin and 4-hydroxy-3-[4'-O-(3,3-dimethylallyl)phenyl]-5-methoxy-2'',2''-dimethylpyrano-(5'',6'':6,7)-coumarin, three derivatives of 1,2-diphenyl-1,2-ethanodione (alpha-oxodeoxybenzoin derivatives): 1-[6-hydroxy-2-methoxy-3-(3,3-dimethylallyl)-2'',2''-dimethylpyrano-(5'',6'':5,4)- ]-2-(4'-hydroxyphenyl)-1,2-ethanedione; 1-[6-hydroxy-2-methoxy-2'',2''-dimethylpyrano-(5'',6'':3,4)]-2-(4'-methoxyphenyl)-1,2-ethanedione; 1-[6-hydroxy-2-methoxy-2'',2''-dimethylpyrano-(5'',6'':3,4)]-2-(3',4'-methylenedioxyphenyl)-1,2-ethanedione and one derivative of deoxybenzoin: 2,4'-dimethoxy-6-hydroxy-2'',2''-dimethylpyrano-(5'',6'':3,4)-deoxybenzoin. The antimicrobial activity of roots extracts and some isolated compounds was screened through bioautography against bacteria and fungi.
对长总序德氏豆(Deguelia longeracemosa (Benth.) A.M.G. Azevedo)根提取物的分析得到了15种异戊烯基化代谢产物。其中9种是新化合物,通过光谱分析(紫外、红外、质谱和核磁共振)确定了它们的分子结构,分别为5种4-羟基-3-苯基香豆素衍生物:4-羟基-3-(4'-羟基苯基)-5-甲氧基-6-(8',9'-环氧-9'-甲基丁基)-2'',2''-二甲基吡喃并-(5'',6'':8,7)-香豆素;4-羟基-3-(3',4'-亚甲二氧基苯基)-5-甲氧基-6-(3,3-二甲基烯丙基)-2'',2''-二甲基吡喃并-(5'',6'':8,7)-香豆素;4-羟基-3-(3'-羟基-4'-甲氧基苯基)-5-甲氧基-6-(3,3-二甲基烯丙基)-2'',2''-二甲基吡喃并-(5'',6'':8,7)-香豆素;4-羟基-3-(3'-羟基-4'-甲氧基苯基)-5-甲氧基-2'',2''-二甲基吡喃并-(5'',6'':6,7)-香豆素和4-羟基-3-[4'-O-(3,3-二甲基烯丙基)苯基]-5-甲氧基-2'',2''-二甲基吡喃并-(5'',6'':6,7)-香豆素,3种1,2-二苯基-1,2-乙二酮衍生物(α-氧代脱氧安息香衍生物):1-[6-羟基-2-甲氧基-3-(3,3-二甲基烯丙基)-2'',2''-二甲基吡喃并-(5'',6'':5,4)- ]-2-(4'-羟基苯基)-1,2-乙二酮;1-[6-羟基-2-甲氧基-2'',2''-二甲基吡喃并-(5'',6'':3,4)]-2-(4'-甲氧基苯基)-1,2-乙二酮;1-[6-羟基-2-甲氧基-2'',2''-二甲基吡喃并-(5'',6'':3,4)]-2-(3',4'-亚甲二氧基苯基)-1,2-乙二酮以及1种脱氧安息香衍生物:2,4'-二甲氧基-6-羟基-2'',2''-二甲基吡喃并-(5'',6'':3,4)-脱氧安息香。通过生物自显影法对根提取物和一些分离得到的化合物针对细菌和真菌的抗菌活性进行了筛选。