Lago João Henrique G, Chaves Mariana H, Ayres Mariane Cruz C, Agripino Débora G, Young Maria Cláudia M
Centro de Ciências e Humanidades, Universidade Presbiteriana Mackenzie, São Paulo, SP, Brazil.
Planta Med. 2007 Mar;73(3):292-5. doi: 10.1055/s-2007-967108. Epub 2007 Mar 12.
Bioactivity-guided fractionation of the alkaloidal fractions of the CH2Cl2 extract from branches of Porcelia macrocarpa using mutant yeast strains of Saccharomyces cerevisiae and fungi Cladosporium cladosporioides and C. sphaerospermum led to the isolation of bioactive alkaloids: two tetrahydrobenzylisoquinolines (1 and 2), two aporphines (3 and 4), one proaporphine (5), one oxoaporphine (6), four azantraquinones (7-10) and four azafluorenones (11-14). The alkaloids cleistopholine (7) and 6-methoxycleistopholine (8) showed the highest fungitoxic activity while the mixture of 6- and 7-methoxyonychine (12+13) and 6,7-dimethoxyonychine (14) showed a weak DNA-damaging potential.
使用酿酒酵母突变株以及枝孢菌和球孢枝孢菌对大果泡桐树枝二氯甲烷提取物的生物碱部分进行生物活性导向分离,得到了具有生物活性的生物碱:两种四氢苄基异喹啉(1和2)、两种阿朴啡(3和4)、一种原阿朴啡(5)、一种氧代阿朴啡(6)、四种氮杂蒽醌(7 - 10)和四种氮杂芴酮(11 - 14)。生物碱克莱斯托佛林(7)和6 - 甲氧基克莱斯托佛林(8)表现出最高的杀真菌活性,而6 - 甲氧基和7 - 甲氧基奥尼辛(12 + 13)与6,7 - 二甲氧基奥尼辛(14)的混合物显示出较弱的DNA损伤潜力。