Furoxan nitric oxide donor coupled chrysin derivatives: synthesis and vasculoprotection |
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Authors: | Zou Xiao-Qing Peng Sheng-Ming Hu Chang-Ping Tan Li-Feng Deng Han-Wu Li Yuan-Jian |
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Affiliation: | a Department of Pharmacology, School of Pharmaceutical Sciences, Central South University, Changsha 410078, China b Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University, Xiangtan 411105, China |
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Abstract: | A series of furoxan-based nitric oxide-releasing chrysin derivatives were synthesized. Pharmacological assays indicated that all chrysin derivatives exhibited in vitro inhibitory activities against aldose reductase and advanced glycation end-product formation. Some chrysin derivatives were also found to increase the glucose consumption of HepG2 cells. Furthermore, the compounds released a low amount of NO in the presence of l-cysteine (range from 0.20% to 1.89%). These hybrid furoxan-based NO donor chrysin derivatives offer a mutual prodrug design concept for the development of therapeutic or preventive agents for vascular complications due to diabetes. |
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Keywords: | Hybrid Furoxan NO donor Chrysin derivatives Vasculoprotection |
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