ABSTRACT
In the present study, we identified that two representative compounds (7c and 9f) of our newly synthesized coumarin-tagged bis-triazoles induced apoptosis in human pancreatic cells (PANC-1) by caspase 3/7mediated pathway. Both 7c and 9f (IC50 = 7.15 ± 1.19 and 6.09 ± 0.79 µM, respectively) were found to be ~100 times superior against PANC-1 as compared to the standard drug Gemcitabine (IC50 = >500 µM), without showing any toxicity to the normal pancreatic epithelial cells (H6C7). Molecular docking studies further endorsed them as potential pancreatic cancer therapeutics due to their strong hydrogen bonding interactions with the epidermal growth factor receptor (EGFR) enzyme, which is overexpressed in cancerous cells including pancreatic cancer. Additionally, these compounds also showed moderate inhibitory activity against a panel of microbial strains. Overall, our findings reveal that the coumarin hybrids 7c and 9f are viable chemotypes to be adopted as templates for the development of new anticancer drugs, particularly against pancreatic cancer.
ABSTRACT
In this work, a novel stand-alone multi-axial loading test setup was developed to test miniature samples under uniaxial tension, uniaxial compression, in-plane biaxial tension, and biaxial compression stress states. Good agreement in stress-strain responses was observed between the uniaxial experiments carried out using the miniature sample geometry in the custom-built setup and the uniaxial standard geometry in a universal testing machine. With regard to biaxial experiments, the full-field strain captured using digital image correlation for the biaxial specimens revealed strain homogeneity in the central gage section of the sample. Furthermore, the in situ capability of the setup was demonstrated by integrating it with a commercial laboratory x-ray diffractometer, and good agreement was found between the calculated stress values from the load sensor and the stress obtained using x-ray diffraction.
