Kijjoa Anake, Santos Sonia, Dethoup Tida, Manoch Leka, Almeida Ana Paula, Vasconcelos Maria Helena, Silva Artur, Gales Luís, Herz Werner
ICBAS- Instituto de Ciêncas Biomédicas de Abel Salazar and CIIMAR, Universidade do Porto, 4099-003 Porto, Portugal.
Nat Prod Commun. 2011 Jun;6(6):807-12.
Chemical investigation of a collection of the fungus Neosartorya glabra from Thailand furnished sartoryglabins A-C (1a, 1b and 2) which are analogs of the reverse prenylated indole alkaloids known as (-) ardeemins. Structures of these compounds were established by NMR spectrometry and an X-ray analysis. Sartoryglabins A-C were evaluated for their in vitro growth inhibitory activity on three human tumor cell lines: MCF-7 (breast adenocarcinoma), NCI-H460 (non-small cell lung cancer) and A375-C5 (melanoma). All the compounds exhibited strong to moderate activity against the MCF-7 cell line but weak or no activity against the NCI-H460 and A375-C5 cell lines. Sartoryglabin B was found to exhibit selectivity towards the MCF-7 cell line.
对采自泰国的真菌光滑新萨托菌进行化学研究,得到了萨托菌素A - C(1a、1b和2),它们是被称为(-)ardeemins的反向异戊烯基化吲哚生物碱的类似物。这些化合物的结构通过核磁共振光谱法和X射线分析得以确定。对萨托菌素A - C进行了体外对三种人类肿瘤细胞系的生长抑制活性评估:MCF - 7(乳腺腺癌)、NCI - H460(非小细胞肺癌)和A375 - C5(黑色素瘤)。所有化合物对MCF - 7细胞系均表现出强至中度活性,但对NCI - H460和A375 - C5细胞系活性较弱或无活性。发现萨托菌素B对MCF - 7细胞系具有选择性。