端锚聚合酶与细胞的癌变和衰老密切相关, 被认为是细胞癌变机制和癌症治疗靶标研究的新热点. 为寻找新型抗肿瘤化合物, 实验采用计算机辅助的虚拟药物筛选, 设计并合成苯并[f][1,4]氧氮杂?酮类化合物12个, 结构经¹H NMR、¹³C NMR、HRMS确证. 对合成化合物进行初步生物活性测试和构效关系阐释, 部分化合物对肿瘤细胞显示抑制作用, 其中3h对Hep-3B具有显著的活性, IC₅₀值为3.5 μmol/L.

The telomere-associated protein tankyrase is a poly(adenosine diphosphate-ribose) polymerase and is considered to be a promising target for cancer therapy, especially selective lethality on breast cancer associated (BRCA) cell lines, including breast cancer as well as malignancies of the ovaries, pancreas, and prostate gland. A variety of drug candidates have been developed and investigated, such as XAV-939, which was identified as a tankyrase inhibitor during screening for a small-mole- cule inhibitor of the Wnt/β-catenin pathway, and it exhibits nanomolar activity in the tankyrase-2 biochemical assay. Coincidentally, almost all compounds which exhibit excellent activity in the tankyrase-2 biochemical assay showed the common structure: lactam ring or amide structure. According to the reported co-crystal structure of inhibitors with tankyrase-2 analysis, it was found that the lactam ring or amide of the compounds forms three conserved hydrogen bonds to Gly1032 and Ser1068 and a π-stacking interaction with Tyr1071. Thus the lactam ring or amide was identified to be a key structure of tankyrase inhibitors. So a new class of structure based on benzo[f][1,4]oxazepinone scaffold was designed through computer-aided virtual drug screening, and 12 new compounds were synthesized via Mannich reactions of aromatic aldehydes with aromatic amines and aromatic ketones, ring expansion, reduction and condensation. The target compound was confirmed by ¹H NMR, ¹³C NMR, HRMS. Followed by the methyl thiazolyl tetrazolium (MTT) assay [A1] to test in vitro anti-tumor activity, part compounds showed potent inhibitory effect on tumor cells. This study culminates in compound 3h, an inhibitor with potent activity against Hep-3B (IC₅₀=3.5 μmol/L). Here, the synthesis and structure-activity relationship (SAR) of this novel series were described. To explore the anti-tumor mechanism of benzo[f][1,4]oxazepinone compounds, we explored the interaction of the compound 3h complex with the Gly1032, Ser1068 and Tyr1071 binding site of tankyrase-2, which confirms the three conserved hydrogen and π-stacking binding mode, as supporting information for the in vitro anti-tumor activity.