Novel Cytotoxic Phenanthro-triazine-3-thiol Derivatives as Potential DNA Intercalators and Bcl-2 Inhibitors
| Author | Mehdi Khoshneviszadeh | en |
| Author | Omidreza Firuzi | en |
| Author | Malihe Aminsafaee | en |
| Author | Masoud Kashefizadeh | en |
| Author | Sara Ranjbar | en |
| Author | Zahra Rezaei | en |
| Author | Hossein Sadeghpour | en |
| Author | Farshid Zargari | en |
| Author | Ramin Miri | en |
| Author | Najmeh Edraki | en |
| Issued Date | 2021-07-31 | en |
| Abstract | Novel phenanthro-triazine-3-thiol derivatives were designed as potential DNA intercalators and Bcl-2 inhibitors. After being synthesized, the compounds were evaluated for their cytotoxic activity against MOLT-4 (human acute lymphoblastic leukemia) and MCF-7 (human breast adenocarcinoma) cells by MTT assay. P1 (bearing hydrogen substitution) was the most potent derivative against MOLT-4 with an IC50 value of 7.1 ± 1.1 μM, whereas P11 (bearing phenyl substitution) demonstrated considerable cytotoxicity against MCF-7 with an IC50 value of 15.4 ± 2.9 μM. Compounds P7, P8, P14 and P15 exhibited moderate cytotoxic effects. Furthermore, to confirm the potential DNA intercalation and Bcl-2 inhibitory activities of phenanthro-triazine scaffolds, molecular docking analysis was performed. Molecular docking studies indicated that these compounds not only bind to DNA by intercalation mainly through stacking interactions but also are well accommodated in the active site of Bcl-2. Therefore, P1 and P11 having phenanthro-triazine-3-thiol scaffold could be presented as cytotoxic agents with dual DNA intercalation and Bcl-2 inhibitory activities. | en |
| DOI | https://doi.org/10.22037/ijpr.2020.113902.14553 | en |
| Keyword | Triazine | en |
| Keyword | Phenanthrene | en |
| Keyword | Cancer | en |
| Keyword | Antiproliferative effect | en |
| Keyword | Molecular docking | en |
| Publisher | Brieflands | en |
| Title | Novel Cytotoxic Phenanthro-triazine-3-thiol Derivatives as Potential DNA Intercalators and Bcl-2 Inhibitors | en |
| Type | Original Article | en |