Menu  → Metabolism information on chemical compounds  → 
Naringenin
Naringenin

Compound Naringenin 
Animal species rat 
Metabolism parameters Intravenous administration
Intravenous administration
Metabolites (2R)-Naringenin
(2S)-Naringenin
Crude drug Immature Orange 
References 1) Jaime A. Yàñez, Connie M. Remsberg, Nicole D. Miranda, Karina R. Vega-Villa, Preston K. Andrews and Neal M. Davies, Pharmacokinetics of selected chiral flavonoids: hesperetin, naringenin and eriodictyol in rats and their content in fruit juices. Biopharm. Drug Dispos. 29: 63–82 (2008). 
Remarks The majority of pharmacokinetic studies of individual flavonoids or after ingestion of foodstuffs have overlooked the chirality of some of these xenobiotics. In order to characterize for the first time the stereoselective pharmacokinetics of three flavonoids, hesperetin, naringenin and eriodictyol were intravenously administered (20 mg/kg) to male Sprague-Dawley rats, and their stereospecific content was assessed in various fruit juices. Concentrations in serum, urine and fruit juices were characterized via HPLC and verified by LC/MS. [Yàñez et al., Biopharm. Drug Dispos., 29: 63–82 (2008)]

Stereospecific pharmacokinetics of eriodictyol in serum after i.v. administration in rats (20 mg/kg) (mean±SEM, n=6)
Stereospecific pharmacokinetics of hesperetin, and naringenin in serum after i.v. administration in rats (20 mg/kg) (mean±SEM, n=6) 
 

TOPICS

Information on genetic analysis

Information of bioassay

Metabolism information on chemical compounds included in crude drugs

Traditional Medical & Pharmaceutical Database


Section of Pharmacognosy,
Division of Medicinal Resources,
Department of Research and Development,
Institute of Natural Medicine,
University of Toyama
2630 Sugitani, Toyama 930-0194 Japan
TEL: +81-76-434-7601
FAX: +81-76-434-5064