Novel quinoline derivatives carrying nitrones/oximes nitric oxide donors: Design, synthesis, antiproliferative and caspase-3 activation activities.
Mahmoud S AbdelbasetMohamed Abdel-AzizGamal El-Din A Abuo-RahmaMostafa H AbdelrahmanMohamed RamadanBahaa G M YoussifPublished in: Archiv der Pharmazie (2018)
Novel quinoline derivatives carrying nitrones and oxime as nitric oxide donors were prepared and characterized using different spectroscopic techniques. Nitrones can release nitric oxide in larger amounts compared to corresponding oximes. Antiproliferative screening results showed that the 2-benzylthioquinoline nitrones 6e and 6f and the 2-methylthio analogues 6g and 6h exhibited promising antiproliferative activity especially against leukemia and colon cancer cell lines. Compounds 6c, 6e, and 6f exhibited higher potency as anticancer agents compared to doxorubicin, with IC50 ranging from 0.45 to 0.91 μM. A remarkable overexpression of caspase-3 protein levels was observed in cells treated with the tested compounds. Compound 6e exhibited more pre-G1 apoptosis and cell cycle arrest at the G2/M phase than in other phases. These results revealed that the tested compounds can cause programmed cell death through overexpression of caspase 3, which may be attributed to the release of nitric oxide.
Keyphrases
- cell cycle arrest
- nitric oxide
- cell death
- molecular docking
- induced apoptosis
- nitric oxide synthase
- pi k akt
- hydrogen peroxide
- cell proliferation
- endoplasmic reticulum stress
- signaling pathway
- oxidative stress
- transcription factor
- structure activity relationship
- bone marrow
- molecular dynamics simulations
- kidney transplantation
- cancer therapy
- binding protein
- newly diagnosed
- amino acid