Abstract
From a methanol extract of Artemisia caruifolia, which showed a moderate inhibitory activity on HIV-1 protease in a preliminary screening, N1,N5,N10-tri-p-coumaroylspermidine and three dicaffeoylquinic acids were isolated. The former compound was found to appreciably inhibit HIV-1 protease. Of related amides which were chemically synthesized, N1,N5,N10,N14-tetra -p-coumaroylspermine and N1,N4,N7,N10,N 13-penta-p-coumaroyltetraethylenepentamine inhibited HIV-1 protease more potently than N1,N5,N10-tri-p-coumaroylspermidine.
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CITATION STYLE
Ma, C. M., Nakamura, N., & Hattori, M. (2001). Inhibitory effects on HIV-1 protease of tri-p-coumaroylspermidine from Artemisia caruifolia and related amides. Chemical and Pharmaceutical Bulletin, 49(7), 915–917. https://doi.org/10.1248/cpb.49.915
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