Synthesis, Characterization, Cytotoxicity, Cellular Imaging, Molecular Docking, and ADMET Studies of Piperazine-Linked 1,8-Naphthalimide-Arylsulfonyl Derivatives.
Ashanul HaqueKhalaf M AleneziAhmed Al-OtaibiAbdulmohsen Khalaf Dhahi AlsukaibiAtaur RahmanMing Fa HsiehMei-Wen TsengWai Yeung WongPublished in: International journal of molecular sciences (2024)
To reduce the mortality and morbidity associated with cancer, new cancer theranostics are in high demand and are an emerging area of research. To achieve this goal, we report the synthesis and characterization of piperazine-linked 1,8-naphthalimide-arylsulfonyl derivatives (SA1-SA7). These compounds were synthesized in good yields following a two-step protocol and characterized using multiple analytical techniques. In vitro cytotoxicity and fluorescent cellular imaging of the compounds were assessed against non-cancerous fibroblast (3T3) and breast cancer (4T1) cell lines. Although the former study indicated the safe nature of the compounds (viability = 82-95% at 1 μg/mL), imaging studies revealed that the designed probes had good membrane permeability and could disperse in the whole cell cytoplasm. In silico studies, including molecular docking, molecular dynamics (MD) simulation, and ADME/Tox results, indicated that the compounds had the ability to target CAIX-expressing cancers. These findings suggest that piperazine-linked 1,8-naphthalimide-arylsulfonyl derivatives are potential candidates for cancer theranostics and a valuable backbone for future research.
Keyphrases
- molecular docking
- molecular dynamics
- papillary thyroid
- molecular dynamics simulations
- high resolution
- squamous cell
- fluorescent probe
- randomized controlled trial
- single cell
- childhood cancer
- case control
- lymph node metastasis
- living cells
- type diabetes
- fluorescence imaging
- stem cells
- small molecule
- quantum dots
- squamous cell carcinoma
- coronary artery disease
- cardiovascular disease
- single molecule
- risk factors
- current status
- photodynamic therapy
- structure activity relationship
- risk assessment
- breast cancer risk
- wild type