Department of Medicinal Chemistry and Pharmacognosy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid 22110, Jordan.
Department of Medicinal Chemistry and Pharmacognosy, Faculty of Pharmacy, Jordan University of Science and Technology, Irbid 22110, Jordan.
Fitoterapia. 2020 Oct;146:104706. doi: 10.1016/j.fitote.2020.104706. Epub 2020 Aug 21.
Thirteen compounds were isolated from the methanolic extract of the leaves of Androcymbium palaestinum Baker (Colchicaceae). Of these, three were new, two were new natural products, and eight were known. The new isolated compounds were (+)-1-demethylandrocine (5), (-)-andropalaestine (8), and (+)-2-demethyl-β-lumicolchicone (10), while the new natural products were (+)-O-methylkreysigine-N-oxide (3) and (+)-O,O-dimethylautumnaline (9). Moreover, two known compounds are reported for the first time from this species, specifically (-)-colchicine (11) and (-)-3-demethyldemecolcine (13). The structures of the isolated compounds were elucidated using a series of spectroscopic and spectrometric techniques, principally HRESIMS, 1D-NMR (H and C NMR) and 2D-NMR (COSY, edited-HSQC, and HMBC). ECD spectroscopy was used for assigning the absolute configurations of compounds 3, 5, and 10. The cytotoxic activities of the isolated compounds were evaluated using the MDA-MB-435 (melanoma), MDA-MB-231 (breast), and OVCAR3 (ovary) cancer cell lines. Compound 11 was the most potent against all tested cell lines, with IC values of 12, 95 and 23 nM, respectively.
从Palestinian 安第茱萸(Colchicaceae)的甲醇提取物中分离得到了 13 种化合物。其中,有 3 种是新化合物,2 种是新的天然产物,8 种是已知化合物。新分离得到的化合物为 (+)-1-去甲基安第林(5)、(-)-andro palaestine(8)和 (+)-2-去甲基-β-lumicolchicone(10),而新的天然产物为 (+)-O-甲基 kreysigine-N-氧化物(3)和 (+)-O,O-二甲基 autumnaline(9)。此外,两种已知化合物首次从该物种中报道,分别为 (-)-秋水仙碱(11)和 (-)-3-去甲基 demecolcine(13)。利用一系列光谱和光谱技术,主要是 HRESIMS、1D-NMR(H 和 C NMR)和 2D-NMR(COSY、编辑-HSQC 和 HMBC),阐明了分离化合物的结构。ECD 光谱用于确定化合物 3、5 和 10 的绝对构型。通过 MDA-MB-435(黑色素瘤)、MDA-MB-231(乳腺癌)和 OVCAR3(卵巢)癌细胞系评估了分离化合物的细胞毒性活性。化合物 11 对所有测试的细胞系均具有最强的活性,其 IC 值分别为 12、95 和 23 nM。