Figures & data
Table 1. Complex1' s crystallographic parameters along with refinement details.
Figure 1. (a) 1's basic repetitive unit. (b) The one-dimensional chain-like network within 1. (c) 1's two-dimensional layered network. (d) 1's three-dimensional packing network showing the 1 D channels along the c axis.
![Figure 1. (a) 1's basic repetitive unit. (b) The one-dimensional chain-like network within 1. (c) 1's two-dimensional layered network. (d) 1's three-dimensional packing network showing the 1 D channels along the c axis.](/cms/asset/1d85800b-6c38-446e-a8e7-d8d890b4d0de/tjen_a_1690137_f0001_c.jpg)
Figure 4. Reduced BT474 breast cancer cells survival rate after treating with nano 1. The BT474 breast cancer cells were treated by nano 1 of distinct consistence, cancer cells viability was measured via CCK-8 method and the IC50 value of nano 1 was calculated.
![Figure 4. Reduced BT474 breast cancer cells survival rate after treating with nano 1. The BT474 breast cancer cells were treated by nano 1 of distinct consistence, cancer cells viability was measured via CCK-8 method and the IC50 value of nano 1 was calculated.](/cms/asset/b6f6aab5-2852-4283-8fc6-55bd421decfe/tjen_a_1690137_f0004_b.jpg)
Figure 5. Increased percentage of the apoptotic BT474 breast cancer cell after nano 1 treatment. The BT474 breast cancer cell were inoculated into plates of 6 well and treated by 1 × IC50 as well as 3 × IC50. The apoptosis of cell was measured via Annexin V-FITC/PI method kit in flow cytometry at 488/525 and 625 mm. This experiment was performed at least three times.
![Figure 5. Increased percentage of the apoptotic BT474 breast cancer cell after nano 1 treatment. The BT474 breast cancer cell were inoculated into plates of 6 well and treated by 1 × IC50 as well as 3 × IC50. The apoptosis of cell was measured via Annexin V-FITC/PI method kit in flow cytometry at 488/525 and 625 mm. This experiment was performed at least three times.](/cms/asset/810fb74e-18dc-4ae0-a149-f2e3db7eef4f/tjen_a_1690137_f0005_c.jpg)
Figure 6. Increased ROS accumulation in the BT474 breast cancer cells after nano 1 treatment. The BT474 breast cancer cell were inoculated into plates of 6 well and treated by 1 × IC50 as well as 3 × IC50. The levels of ROS within the cancer cells were determined via DCFH-DA with fluorescence method.
![Figure 6. Increased ROS accumulation in the BT474 breast cancer cells after nano 1 treatment. The BT474 breast cancer cell were inoculated into plates of 6 well and treated by 1 × IC50 as well as 3 × IC50. The levels of ROS within the cancer cells were determined via DCFH-DA with fluorescence method.](/cms/asset/184538c3-503a-4cba-b7a7-fb7afc64f54b/tjen_a_1690137_f0006_c.jpg)
Figure 7. Predicted binding pattern of receptor DNA and synthesized compound. (A&B) Binding pattern holistic view reveals a direct binding potential for the compound to DNA. Compound was cyan rod-like and DNA banded. (C&D) The views of surface binding reveal that compound interacts with the DNA through its multiple functional group.
![Figure 7. Predicted binding pattern of receptor DNA and synthesized compound. (A&B) Binding pattern holistic view reveals a direct binding potential for the compound to DNA. Compound was cyan rod-like and DNA banded. (C&D) The views of surface binding reveal that compound interacts with the DNA through its multiple functional group.](/cms/asset/54602483-194a-4432-a0aa-f845dcc002cf/tjen_a_1690137_f0007_c.jpg)