A series of novel N-substituted tyramine (2-p-hydroxyphenylethylamine) derivatives (1-11) were synthesized and evaluated for their inhibitory activity against pig kidney aldose reductase (EC 1, 1, 1, 21). Of these compounds, N-2-p-hydroxyphenylethyl maleamic acid (10) exhibits the strongest aldose reductase inhibitory activity, which is 22 times more potent than that of YUA0011).
CITATION STYLE
Sun, W. S., Lee, H. S., Park, J. M., Kim, S. H., Yu, J. H., & Kim, J. H. (2001). YUA001, a novel aldose reductase inhibitor isolated from alkalophilic Corynebacterium sp. YUA25 II. Chemical modification and biological activity. Journal of Antibiotics, 54(10), 827–830. https://doi.org/10.7164/antibiotics.54.827
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