Department of Pharmacognosy, Faculty of Pharmacy, Minia University, Minia, Egypt.
Department of Pharmacognosy, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Nat Prod Res. 2024 Jan-Feb;38(2):236-244. doi: 10.1080/14786419.2022.2114474. Epub 2022 Aug 26.
One new iridoid named aureanin () was isolated from the leaves of (Silva Manso) Benth. & Hook.f. ex S.Moore, together with eight known compounds, isoquercetin (), astragalin (), callicoside B (), amphipaniculoside E (), rehmaglutin D (), quercetin-3-sambubioside (), rutin (), kaempferol-3--rutinoside (). The structures of the isolated compounds were elucidated and confirmed by spectroscopic methods, including 1 D and 2 D NMR experiments, as well as HR-ESI-MS. Compounds were evaluated for their cytotoxic activity against three human cancer cell lines (A549, HepG2, and MCF-7) and . Compound showed activity against A549 (IC: 36.8 ± 1.5 μg/mL, etoposide (positive control): 28.1 ± 4.2 μg/mL), however, none of the compounds were active against .
从(Silva Manso)Benth. & Hook.f. ex S.Moore 的叶子中分离得到一种新的环烯醚萜类化合物 aureanin (),此外还分离得到了 8 种已知化合物,分别为 isoquercetin ()、astragalin ()、callicoside B ()、amphipaniculoside E ()、rehmaglutin D ()、quercetin-3-sambubioside ()、rutin ()和 kaempferol-3--rutinoside ()。通过光谱方法,包括 1D 和 2D NMR 实验以及 HR-ESI-MS,对分离得到的化合物的结构进行了阐明和确证。评估了化合物对三种人癌细胞系(A549、HepG2 和 MCF-7)和 的细胞毒性活性。化合物 对 A549 具有活性(IC:36.8±1.5μg/mL,阳性对照依托泊苷:28.1±4.2μg/mL),但没有一种化合物对 具有活性。