1986
DOI: 10.1055/s-2007-969356
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5-Lipoxygenase-Inhibitors from Medicinal Plants

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1989
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“…This agrees with our findings that wedelolactone (8) (IC50: 2.5 piM), isolated by us from Eclipta alba and Wedelia calendulacea, has nearly the same inhibitory activity as the most potent lipoxygenase inhibitor so far reported, i.e. nordihydroguaretic acid (NDGA; IC50: 1.5 liNt) (32). Chemiluminescence due to oxygen radicals is inhibited in a concentration-dependent manner by wedelolactone in the concentration range 3 x 10 to 3 x i0 .tM.…”
Section: Lipophific Substituents Enhance the Inhibitory Propertiessupporting
confidence: 92%
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“…This agrees with our findings that wedelolactone (8) (IC50: 2.5 piM), isolated by us from Eclipta alba and Wedelia calendulacea, has nearly the same inhibitory activity as the most potent lipoxygenase inhibitor so far reported, i.e. nordihydroguaretic acid (NDGA; IC50: 1.5 liNt) (32). Chemiluminescence due to oxygen radicals is inhibited in a concentration-dependent manner by wedelolactone in the concentration range 3 x 10 to 3 x i0 .tM.…”
Section: Lipophific Substituents Enhance the Inhibitory Propertiessupporting
confidence: 92%
“…Chemiluminescence due to oxygen radicals is inhibited in a concentration-dependent manner by wedelolactone in the concentration range 3 x 10 to 3 x i0 .tM. Since similar inhibitory behaviour is displayed by NDGA, the radical scavenger properties of this class of compound appear to be confirmed (32). Investigations of the structure-activity relationships of the coumestan series, however, show that strong inhibitory properties are displayed only by derivatives with catechol-type substitution in ring B and an OHgroup or OH-group together with a second lipophilic group (OCH3, 0C2H5) in ring A (33).…”
Section: Lipophific Substituents Enhance the Inhibitory Propertiesmentioning
confidence: 71%