Weight | 272.256 g/mol |
---|---|
Formula | C15H12O5 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 3 |
Aromatic Rings | 2 |
Rotatable Bonds | 1 |
(R)-naringenin (480-41-1)
naringenin · naringenin-7-sulfate · BE-14348A
Score:
#1580 in Biochemistry
,
#3624 in Biology
,
#4550 in Chemistry
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- Anti-Inflammatory Effects of Flavonoids: Genistein, Kaempferol, Quercetin, and Daidzein Inhibit STAT-1 and NF-B Activations, Whereas Flavone, Isorhamnetin, Naringenin, and Pelargonidin Inhibit only NF-B Activation along with Their Inhibitory Effect on iNOS Expression and NO Production in Activated Macrophages (Mediators of Inflammation, 2007)
- Review of the flavonoids quercetin, hesperetin, and naringenin. Dietary sources, bioactivities, bioavailability, and epidemiology (Nutrition Research, 2004)
- Plasma Kinetics and Urinary Excretion of the Flavanones Naringenin and Hesperetin in Humans after Ingestion of Orange Juice and Grapefruit Juice (Journal of Nutrition, 2001)
- In vitro inhibition of dihydropyridine oxidation and aflatoxin B1 activation in human liver microsomes by naringenin and other flavonoids. (Carcinogenesis, 1990)
- Neuroprotective properties of the natural phenolic antioxidants curcumin and naringenin but not quercetin and fisetin in a 6-OHDA model of Parkinson's disease. (Free Radical Research, 2005)
- Secretion of hepatocyte apoB is inhibited by the flavonoids, naringenin and hesperetin, via reduced activity and expression of ACAT2 and MTP (Journal of Lipid Research, 2001)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - naringenin
- naringenin-7-sulfate
- BE-14348A
- BE 14348A
- 4',5,7-trihydroxyflavanone
-
SMILESC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O
-
InChIKeyFTVWIRXFELQLPI-UHFFFAOYSA-N
- Pubchem - (R)-naringenin
- Wikipedia - naringenin
Naringenin is a bitter, colourless flavanone, a type of flavonoid. It is the predominant flavanone in grapefruit, and is found in a variety of fruits and herbs.
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