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AbstractAbstract
[en] The antifungal leaves extract from Piper scutifolium was submitted to bioactivity-guided chromatographic separation against Cladosporium cladosporioides and C. sphaerospermum yielding piperine, piperlonguminine and corcovadine as the active principles which displayed a detection limit of 1 μg. Structure-activity relationships were investigated with the preparation of twelve analogs having differences in the number of unsaturations, aromatic ring substituents and in the amide moiety. Analogs having a single double-bond and no substituent in the aromatic ring displayed higher activity, while N,N,-diethyl analogs displayed higher dose-dependent activity. (author)
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Available from http://www.scielo.br/pdf/jbchs/v21n10/a03v2110.pdf
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Journal Article
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ADSORBENTS, ALCOHOLS, ALKYL RADICALS, AMIDES, AMINES, AZINES, CARBON ISOTOPES, CHEMICAL REACTIONS, CHROMATOGRAPHY, DECOMPOSITION, EVEN-ODD NUCLEI, HETEROCYCLIC COMPOUNDS, HYDROGEN ISOTOPES, HYDROXY COMPOUNDS, ISOTOPES, LIGHT NUCLEI, LYSIS, NUCLEI, ODD-EVEN NUCLEI, ORGANIC COMPOUNDS, ORGANIC NITROGEN COMPOUNDS, PYRIDINES, RADICALS, SEPARATION PROCESSES, SOLVOLYSIS, SPECTRA, STABLE ISOTOPES
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