School of Pharmacy, Taipei Medical University , Taipei, Taiwan 110.
J Nat Prod. 2013 Sep 27;76(9):1796-800. doi: 10.1021/np400192q. Epub 2013 Aug 21.
Four previously unreported chemical entities, boydone A (1), boydone B (2), botryorhodine F (3), and botryorhodine G (4), along with five known compounds, fusidilactone A (5), (R)-(-)-mevalonolactone (6), (R)-(-)-lactic acid (7), ovalicin (8), and botryorhodine C (9), were isolated from the ethyl acetate extracts of the fermented broths of the fungal strain Pseudallescheria boydii NTOU2362. The structures of 1-9 were characterized on the basis of their spectroscopic data analyses. The absolute configurations of 1 and 2 were established by comparison with the literature and the modified Mosher's method. The growth inhibitory activities of 1-9 against the A549 non-small-cell lung cancer cell line were evaluated, and 2 and 8 exhibited moderate to potent bioactivities with GI₅₀ values of 41.3 and 4.1 μM, respectively, in comparison with fluorouracil (GI₅₀ = 3.6 μM).
从真菌假丝酵母(Pseudallescheria boydii)NTOU2362 的发酵液的乙酸乙酯提取物中分离得到了四个以前未报道的化学实体,即博伊酮 A(1)、博伊酮 B(2)、博曲红定 F(3)和博曲红定 G(4),以及五个已知化合物,fusidilactone A(5)、(R)-(-)-甲羟戊酸内酯(6)、(R)-(-)-乳酸(7)、ovalicin(8)和博曲红定 C(9)。基于光谱数据分析,对 1-9 的结构进行了表征。通过与文献和改进的 Mosher 法进行比较,确定了 1 和 2 的绝对构型。对 1-9 对 A549 非小细胞肺癌细胞系的生长抑制活性进行了评价,与氟尿嘧啶(GI₅₀ = 3.6 μM)相比,化合物 2 和 8 表现出中等至较强的生物活性,GI₅₀ 值分别为 41.3 和 4.1 μM。