Abstract
Villocarines A-D (1-4), four new indole alkaloids have been isolated from the leaves of Uncaria villosa (Rubiaceae) and their structures were elucidated by 2D NMR methods and chemical correlations. Villocarine A (1) showed vasorelaxation activity against rat aortic ring and showed inhibition effect on vasocontraction of depolarized aorta with high concentration potassium, and also inhibition effect on phenylephrine (PE)-induced contraction in the presence of nicardipine in a Ca2+ concentration-dependent manner. The vasorelaxant effect by 1 might be attributed mainly to inhibition of calcium influx from extracellular space through voltage-dependent calcium channels (VDC) and/or receptor-operated Ca2+-channels (ROC), and also partly mediated through the increased release of NO from endothelial cells and opening of voltage-gated K+-channels. © 2011 Elsevier Ltd. All rights reserved.
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Matsuo, H., Okamoto, R., Zaima, K., Hirasawa, Y., Ismail, I. S., Lajis, N. H., & Morita, H. (2011). New vasorelaxant indole alkaloids, villocarines A-D from Uncaria villosa. Bioorganic and Medicinal Chemistry, 19(13), 4075–4079. https://doi.org/10.1016/j.bmc.2011.05.014
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