| Weight | 580.539 g/mol |
|---|---|
| Formula | C27H32O14 |
| Hydrogen Acceptors | 14 |
| Hydrogen Donors | 8 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 6 |
naringin (10236-47-2)
naringin dihydrochalcone · 4',5,7-trihydroxyflavanone 7-rhamnoglucoside · Cyclorel
Score:
#1660 in Biochemistry
,
#3739 in Biology
,
#4707 in Chemistry
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- Flavanone absorption after naringin, hesperidin, and citrus administration (Clinical Pharmacology & Therapeutics, 1996)
- Grapefruit juicefelodipine interaction: Mechanism, predictability, and effect of naringin (Clinical Pharmacology & Therapeutics, 1993)
- Quantitative survey of narirutin, naringin, hesperidin, and neohesperidin in citrus (Journal of Agricultural and Food Chemistry, 1987)
- Naringin is a Major and Selective Clinical Inhibitor of Organic AnionTransporting Polypeptide 1A2 (OATP1A2) in Grapefruit Juice (Clinical Pharmacology & Therapeutics, 2007)
- The Hypoglycemic Effects of Hesperidin and Naringin Are Partly Mediated by Hepatic Glucose-Regulating Enzymes in C57BL/KsJ-db/db Mice (Journal of Nutrition, 2004)
- Effect of grapefruit juice and naringin on nisoldipine pharmacokinetics (Clinical Pharmacology & Therapeutics, 1993)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - naringin dihydrochalcone
- 4',5,7-trihydroxyflavanone 7-rhamnoglucoside
- Cyclorel
- naringin sodium
- naringenin-7-hesperidoside
- aurantiin
-
SMILESCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O
-
InChIKeyDFPMSGMNTNDNHN-UHFFFAOYSA-N
- Pubchem - naringin
- Wikipedia - naringin
Naringin is a flavanone-7-O-glycoside between the flavanone naringenin and the disaccharide neohesperidose. The flavonoid naringenin occurs naturally in citrus fruits, especially in grapefruit, where naringin is responsible for the fruit's bitter taste. In commercial grapefruit juice production, the enzyme naringinase can be used to remove the bitterness created by naringin.
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