【摘 要】
：
A series of furoxan-based nitric oxide-releasing chrysin and luteolin derivatives were synthesized.Pharmacological assays indicated that all chrysin and luteolin derivatives exhibited in vitro inhibit
【机 构】
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Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, Coll
【出 处】
：
中国化学会第十届全国天然有机化学学术会议
论文部分内容阅读
A series of furoxan-based nitric oxide-releasing chrysin and luteolin derivatives were synthesized.Pharmacological assays indicated that all chrysin and luteolin derivatives exhibited in vitro inhibitory activities against aldose reductase and advanced glycation end-product formation.
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