Li Da-Hong, Li Jian-Yong, Xue Chun-Mei, Han Tong, Sai Chun-Mei, Wang Kai-Bo, Lu Jin-Cai, Jing Yong-Kui, Hua Hui-Ming, Li Zhan-Lin
Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, and ‡School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University , Shenyang 110016, People's Republic of China.
J Nat Prod. 2017 Nov 22;80(11):2893-2904. doi: 10.1021/acs.jnatprod.7b00387. Epub 2017 Nov 13.
Inspired by the intriguing structures and bioactivities of dimeric alkaloids, 11 new thalifaberine-type aporphine-benzylisoquinoline alkaloids, thalicultratines A-K, a tetrahydroprotoberberine-aporphine alkaloid, thalicultratine L, and five known ones were isolated from the roots of Thalictrum cultratum. Their structures were defined on the basis of NMR and HRESIMS data. The antiproliferative activities of compounds 1-17 were evaluated against human leukemia HL-60 and prostate cancer PC-3 cells. Most alkaloids showed potent cytotoxicity against selected cancer cells. Preliminary SARs are discussed. The most active new compound (3), with an IC value of 1.06 μM against HL-60 cells, was selected for mechanism of action studies. The results revealed that compound 3 induced apoptosis and arrested the HL-60 cell cycle at the S phase with the loss of mitochondria membrane potential. The nuclear morphological Hoechst 33258 staining assay was also carried out, and the results confirmed apoptosis.
受二聚体生物碱的有趣结构和生物活性启发,从唐松草的根中分离出11种新的thalifaberine型阿朴啡-苄基异喹啉生物碱(thalicultratines A-K)、1种四氢原小檗碱-阿朴啡生物碱(thalicultratine L)以及5种已知生物碱。它们的结构通过核磁共振(NMR)和高分辨电喷雾电离质谱(HRESIMS)数据确定。评估了化合物1-17对人白血病HL-60细胞和前列腺癌PC-3细胞的抗增殖活性。大多数生物碱对所选癌细胞显示出强大的细胞毒性。讨论了初步的构效关系。选择对HL-60细胞的半数抑制浓度(IC)值为1.06 μM的最具活性的新化合物(3)进行作用机制研究。结果表明,化合物3诱导细胞凋亡,并使HL-60细胞周期停滞于S期,同时线粒体膜电位丧失。还进行了核形态学Hoechst 33258染色试验,结果证实了细胞凋亡。