Shenyang Pharmaceutical University, Shenyang, People's Republic of China.
Nat Prod Res. 2020 Jul;34(13):1884-1890. doi: 10.1080/14786419.2019.1569004. Epub 2019 Feb 13.
(+) Benzomalvins E () and (-) Benzomalvins E (), a pair of epimeric derivatives, together with three known benzomalvins (), were isolated from solid cultures of a interrhizospheric fungus sp. SYPF 8411. The planar structure of (+) Benzomalvins E () has been previously reported. While, the absolute configuration of compound was established by X-ray crystallographic analysis for the first time. The planar structure of the new compound were elucidated by detailed interpretation of their HR ESI-TOF MS and NMR spectroscopic data. The absolute configuration of compound was established by Rh(OCOCF)-induced CD spectral data and the electronic circular dichroic (ECD) method. Furthermore, the epimerization induced by pH, temperature and HO was revealed. Benzomalvins (), a type of indoximod, enhanced the cytotoxic capability of 5-fluorouracil against A549.
(+) 苯并马文素 E () 和 (-) 苯并马文素 E (),一对差向异构体,与三种已知的苯并马文素 () 一起,从 interrhizospheric 真菌 sp. SYPF 8411 的固体培养物中分离得到。(+) 苯并马文素 E () 的平面结构先前已有报道。而化合物的绝对构型是通过 X 射线晶体学分析首次确定的。新化合物的平面结构通过详细解释其高分辨电喷雾飞行时间质谱 (HR ESI-TOF MS) 和核磁共振波谱数据来阐明。通过 Rh(OCOCF)3 诱导的 CD 光谱数据和电子圆二色性 (ECD) 方法确定了化合物的绝对构型。此外,揭示了 pH、温度和 HO 诱导的差向异构化。苯并马文素 (),一种吲哚莫德,增强了 5-氟尿嘧啶对 A549 的细胞毒性作用。