Design, synthesis, and anticancer properties of isocorydine derivatives

Bioorganic & Medicinal Chemistry
Qian YanDuolong Di

Abstract

Isocorydine (ICD), an aporphine alkaloid, is widely distributed in nature. Its ability to target side population (SP) cells found in human hepatocellular carcinoma (HCC) makes it and its derivative 8-amino-isocorydine (NICD) promising chemotherapeutic agents for the treatment of HCC. To improve the anticancer activity of isocorydine derivatives, twenty derivatives of NICD were designed and synthesized through chemical structure modifications of the aromatic amino group at C-8. The anti-proliferative activities of all synthesized compounds against human hepatocellular (HepG2), cervical (HeLa), and gastric (MGC-803) cancer cell lines were evaluated using an MTT assay. The results showed that all the synthetic compounds had some tumor cell growth inhibitory activity. The compound COM33 (24) was the most active with IC50 values under 10 μM (IC50 for HepG2 = 7.51 µM; IC50 for HeLa = 6.32 μM). FICD (12) and COM33 (24) were selected for further investigation of their in vitro and in vivo activities due to their relatively good antiproliferative properties. These two compounds significantly downregulated the expression of four key proteins (C-Myc, β-Catenin, CylinD1, and Ki67) in HepG2 cells. The tumor inhibition rate of COM33 (24) in ...Continue Reading

Citations

Jun 7, 2019·Molecules : a Journal of Synthetic Chemistry and Natural Product Chemistry·Chuanming ZhangChun Hu
Jul 27, 2021·Current Therapeutic Research, Clinical and Experimental·Lei SongJunxi Liu
Jul 13, 2019·Journal of Medicinal Chemistry·Xuefeng ZhouLan Tang

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