Korea Bioactive Natural Material Bank, College of Pharmacy, Chosun University, 375 Seosuk-dong, Dong-gu, Gwangju 501-759, Republic of Korea.
Bioorg Med Chem. 2012 Nov 1;20(21):6459-64. doi: 10.1016/j.bmc.2012.08.024. Epub 2012 Sep 7.
Bioassay-guided fractionation of the EtOAc extract of the root of Erythrina addisoniae (Leguminosae) resulted in the isolation of four new (1-4), along with 2 known prenylated isoflavonoids (5-6). The structures of the isolates were assigned on the basis of spectroscopic data analysis, focusing on interpretation of 1D and 2D NMR, and MS data. All the isolates were evaluated for their inhibitory effects on protein tyrosine phosphatase 1B (PTP1B), as well as their growth inhibition on MCF7, adriamycin-resistant MCF7 (MCF7/ADR), and MDA-MB-231 breast cancer cell lines. Compounds which exhibited PTP1B inhibitory activity (IC(50) values ranging from 4.6 ± 0.3 to 24.2 ± 2.1 μM) showed potential cytotoxic activity (IC(50) values ranging from 3.97 ± 0.17 to 11.4 ± 1.9 μM). Taken together, our data suggest that prenylated isoflavonoids, especially the isoflavone-type skeleton could be considered as new lead compounds against breast cancer via PTP1B inhibition.
从夹竹桃科(Apocynaceae)猪屎豆属植物(Erythrina addisoniae)根的乙酸乙酯提取物中进行生物活性导向分离,得到了 4 个新的(1-4)化合物,以及 2 个已知的异戊烯基异黄酮(5-6)。根据光谱数据分析确定了这些分离物的结构,重点是对 1D 和 2D NMR 以及 MS 数据的解释。所有分离物均针对其对蛋白酪氨酸磷酸酶 1B(PTP1B)的抑制作用以及对 MCF7、阿霉素耐药 MCF7(MCF7/ADR)和 MDA-MB-231 乳腺癌细胞系的生长抑制作用进行了评估。表现出 PTP1B 抑制活性(IC50 值范围为 4.6 ± 0.3 至 24.2 ± 2.1 μM)的化合物显示出潜在的细胞毒性活性(IC50 值范围为 3.97 ± 0.17 至 11.4 ± 1.9 μM)。总之,我们的数据表明,异戊烯基异黄酮,尤其是异黄酮型骨架,可通过抑制 PTP1B 被视为针对乳腺癌的新型先导化合物。