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Updated: Oct 19, 2026

Chemiluminescence-based Assays for Detection of Nitric Oxide and its Derivatives from Autoxidation and Nitrosated Compounds
Published on: February 16, 2022
Targeting nitric oxide to cancer cells: cytotoxicity studies of glyco-S-nitrosothiols
1Department of Chemistry, Wayne State University, Detroit, MI 48201, USA.
Abstract:
Glyco-S-nitrosothiols, fructose-2-SNAP and glucose-2-SNAP, were synthesized and found to be much more cytotoxic than SNAP in killing DU-145 human prostate cancer cells in vitro.
Insights
New glyco-S-nitrosothiols, including fructose-2-SNAP and glucose-2-SNAP, show enhanced cytotoxicity against prostate cancer cells. These compounds are more effective than SNAP in killing DU-145 cells in vitro.
Area of Science:
- Biochemistry
- Organic Chemistry
- Cancer Biology
Background:
- S-nitrosothiols (SNPs) are compounds that release nitric oxide (NO), a signaling molecule with diverse biological roles.
- Nitric oxide plays a role in cancer progression and cell death.
- Developing novel SNP derivatives can offer new therapeutic strategies.
Purpose of the Study:
- To synthesize novel glyco-S-nitrosothiols, specifically fructose-2-SNAP and glucose-2-SNAP.
- To evaluate the in vitro cytotoxicity of these novel compounds against human prostate cancer cells.
- To compare their efficacy with the parent compound, SNAP.
Main Methods:
- Chemical synthesis of fructose-2-SNAP and glucose-2-SNAP.
- In vitro cytotoxicity assays using DU-145 human prostate cancer cell line.
- Comparison of cell viability after treatment with synthesized compounds and SNAP.
Main Results:
- Fructose-2-SNAP and glucose-2-SNAP were successfully synthesized.
- Both novel glyco-S-nitrosothiols demonstrated significantly higher cytotoxicity compared to SNAP.
- The compounds effectively reduced the viability of DU-145 prostate cancer cells in vitro.
Conclusions:
- Glyco-S-nitrosothiols represent a promising class of compounds for prostate cancer therapy.
- Fructose-2-SNAP and glucose-2-SNAP exhibit superior cytotoxic effects against prostate cancer cells than SNAP.
- Further investigation into the mechanisms and in vivo efficacy of these compounds is warranted.
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