Design and synthesis of the novel DNA topoisomerase II inhibitors: Esterification and amination substituted 4'-demethylepipodophyllotoxin derivates exhibiting anti-tumor activity by activating ATM/ATR signaling pathways

摘要

According to the structure-activity relationship, drug combination principle and bioisosterism, a series of the novel esterification and amination 4'-demethylepipodophyllotoxin derivates were rationally designed in order to discover the potential antitumor prodrug. And then these compounds were tested by the drug-topoisomerase II docking models for virtual screening. Thus, twelve target compounds were screened out and synthesized. Most of compounds exhibited promising in vitro anti-tumor activity, particularly 4-N-tris(hydroxymethyl)metylaminomethane-4-deoxy-4'-demethylepipodophyllotoxin (Compound 1). The anti-tumor activity of Compound 1 against the tumor cell lines BGC-823 (i.e., the IC_(50) value of 5.35 ± 0.77 muM), HeLa (i.e., the IC_(50) value of 160.48 ± 14.50 muM), and A549 (i.e., the IC_(50) value of 13.95 ± 5.41 muM) was significantly improved by 706%, 31% and 900% than that of etoposide (i.e., the IC_(50) values of 43.74 ± 5.13, 209.90 ± 13.42, and 139.54 ± 7.05 muM), respectively. Moreover, the IC_(50) value of Compound 1 against the normal human cell line HK-2 (i.e., 16.3 ± 3.77 muM) was 78% lower than that of etoposide (i.e., 9.17 ± 1.58 muM). Compound 1 could diminish the relaxation reaction topoisomerase II DNA decatenation at a concentration of 10 muM and induce BGC-823 apoptosis by breaking DNA double-strand and activating ATM/ATR signaling pathways.