School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou 510006, China.
Mar Drugs. 2022 Mar 17;20(3):211. doi: 10.3390/md20030211.
Four new benzodipyran racemates, namely (±)-aspergiletals A-D (-), representing a rare pyrano[4,3-]chromene scaffold were isolated together with eurotiumide G () and eurotiumide F () from the soft-coral-derived fungus sp. EGF 15-0-3. All the corresponding optically pure enantiomers were successfully separated by a chiral HPLC column. The structures and configurations of all the compounds were elucidated based on the combination of NMR and HRESIMS data, chiral separation, single-crystal X-ray diffraction, quantum chemical C NMR, and electronic circular dichroism calculations. Meanwhile, the structure of eurotiumide G was also revised. The TDP1 inhibitor activities and photophysical properties of the obtained compounds were evaluated. In the TDP1 inhibition assay, as a result of synergy between (+)- and (-)-, (±)- displayed strong inhibitory activity to TDP1 with IC values of 6.50 ± 0.73 μM. All compounds had a large Stokes shift and could be utilized for elucidating the mode of bioactivities by fluorescence imaging.
从软珊瑚来源真菌 sp. EGF 15-0-3 中分离得到了四个新的苯并二吡喃外消旋体,即(±)-aspergiletals A-D (-),代表了一种罕见的吡喃并[4,3-]色烯骨架,同时还分离得到了 eurotiumide G () 和 eurotiumide F ()。所有相应的光学纯对映异构体都通过手性 HPLC 柱成功分离。基于 NMR 和 HRESIMS 数据、手性分离、单晶 X 射线衍射、量子化学 C NMR 和电子圆二色性计算的组合,阐明了所有化合物的结构和构型。同时,还修订了 eurotiumide G 的结构。评估了所获得化合物的 TDP1 抑制剂活性和光物理性质。在 TDP1 抑制测定中,由于 (+)-和 (-)-之间的协同作用,(±)-对 TDP1 表现出强烈的抑制活性,IC 值为 6.50 ± 0.73 μM。所有化合物都具有较大的斯托克斯位移,可用于通过荧光成像阐明生物活性模式。