Naringin:Naringoside.(2R)-Isomer of Maringin.:Introduction and Its Benefit Applications.
Article Content:
- .Chemical Info:Naringin.
- .Introduction:Naringin.
- .Natural sources:Naringin.
- .Common Benefits of Naringin.
- .Naringin Safety and Toxicity.
- .Research Update:Naringin.
Products Related:Naringin:Naringoside.(2R)-Isomer of Maringin.
Name:Naringin:Naringoside.(2R)-Isomer of Maringin.
Serie No:Pure04.
Specifications:98%HPLC.
INCI Name:
EINECS/ELINCS No.:233-566-4
CAS:10236-47-2
Chem/IUPAC Name:2R-Naringin,Naringoside,NSC5548;4',5,7-Trihydroxyflavanone 7-rhamnoglucoside.
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Applications and Properties:
Applications:
Protects against toxins in chemotherapy drugs and the environment.
Enhances lipid metabolism.
Enhances ethanol metabolism.
Reduces negative effects of ethanol intake.
Acts as an antioxidant,Acts as a free radical scavenger,Significantly inhibits LDL oxidation.
Reduces cytotoxicity.
Acts as an anti-apoptotic.
Properties:
Naringin is the major flavonoid glycoside in grapefruit and gives grapefruit juice its bitter taste. It is metabolized to the flavanone naringenin in humans. Both naringenin and hesperetin, which are the aglycones of naringin and hesperidin, occur naturally in citrus fruits.
Dosages:100~200 mgs per day.
Safety and Toxicity:
Acute toxicity(LD50):Naringin.LD50-Lethal dose,50 percent kill. Intraperitoneal.Rodent-rat.2 gm(2000 mgs)/kg.Details of toxic effects not reported other than lethal dose value.
Reference:
1.Naringin:Naringoside.(2R)-Isomer of Maringin.:Introduction and Its Benefit Applications.




