An EtOAc extract from the roots of Sophora flavescens (Kushen) potentiated γ-aminobutyric acid (GABA)-induced chloride influx in Xenopus oocytes transiently expressing GABAA receptors with subunit composition, α 1 β 2 γ 2S. HPLC-based activity profiling of the extract led to the identification of 8-lavandulyl flavonoids, kushenol I, sophoraflavanone G, (−)-kurarinone, and kuraridine as GABAA receptor modulators. In addition, a series of inactive structurally related flavonoids were characterized. Among these, kushenol Y (4) was identified as a new natural product. The 8-lavandulyl flavonoids are first representatives of a novel scaffold for the targe
Classical benzodiazepines (BZs) are the most widely prescribed drugs acting on the central nervous s...
AbstractTo establish a quantitative structure-activity relationship model of the binding affinity co...
Nine compounds, including two undescribed withanolides, withasomniferolides A and B (1 and 2), three...
An EtOAc extract of Casearia corymbosa leaves led to an allosteric potentiation of the GABA signal i...
Gamma-aminobutyric acid type A (GABAA) receptors are major inhibitory neurotransmitter receptors in ...
GABAA receptors (GABAARs) are a class of physiologically and therapeutically important ligand-gated ...
Purpose: To study the in vivo metabolism of kurarinone, a lavandulyl flavanone which is a major cons...
Benzodiazepines are the most widely prescribed class of psychoactive drugs in current therapeutic us...
Aims: Melissa officinalis (Mo) and Lavandula angustifolia (La) essential oils and their major consti...
In a two-microelectrode voltage clamp assay with <i>Xenopus laevis</i> oocytes, a dichloromethane ex...
Prenylated flavonoids derived from Hops (Humulus lupulus) activate the γ-aminobutyric acid (GABA) ty...
This study focused on the effects of the methanol crude extract of Zizyphus mauritiana leaves and th...
Context: Discovery of pharmacologically active natural products as starting points for drug developm...
Context: Discovery of pharmacologically active natural products as starting points for drug developm...
Nine compounds, including two undescribed withanolides, withasomniferolides A and B (1 and 2), three...
Classical benzodiazepines (BZs) are the most widely prescribed drugs acting on the central nervous s...
AbstractTo establish a quantitative structure-activity relationship model of the binding affinity co...
Nine compounds, including two undescribed withanolides, withasomniferolides A and B (1 and 2), three...
An EtOAc extract of Casearia corymbosa leaves led to an allosteric potentiation of the GABA signal i...
Gamma-aminobutyric acid type A (GABAA) receptors are major inhibitory neurotransmitter receptors in ...
GABAA receptors (GABAARs) are a class of physiologically and therapeutically important ligand-gated ...
Purpose: To study the in vivo metabolism of kurarinone, a lavandulyl flavanone which is a major cons...
Benzodiazepines are the most widely prescribed class of psychoactive drugs in current therapeutic us...
Aims: Melissa officinalis (Mo) and Lavandula angustifolia (La) essential oils and their major consti...
In a two-microelectrode voltage clamp assay with <i>Xenopus laevis</i> oocytes, a dichloromethane ex...
Prenylated flavonoids derived from Hops (Humulus lupulus) activate the γ-aminobutyric acid (GABA) ty...
This study focused on the effects of the methanol crude extract of Zizyphus mauritiana leaves and th...
Context: Discovery of pharmacologically active natural products as starting points for drug developm...
Context: Discovery of pharmacologically active natural products as starting points for drug developm...
Nine compounds, including two undescribed withanolides, withasomniferolides A and B (1 and 2), three...
Classical benzodiazepines (BZs) are the most widely prescribed drugs acting on the central nervous s...
AbstractTo establish a quantitative structure-activity relationship model of the binding affinity co...
Nine compounds, including two undescribed withanolides, withasomniferolides A and B (1 and 2), three...