Name: |
Naringin |
Synonyms: |
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Trade name: |
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Chemical name: |
2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one[1]
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Molecular Weight: |
580 g/mol[2]
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Source: |
It is one of the citrus flavanoids[1], It is also a component of grape fruit[3]
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Structure: |
[4],[5]
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Chemical Nature: |
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Actions & Indications: |
Pharmcological Action-
Therapeutic indications:
Preclinical study-
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Notes: |
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REFERENCES |
1. |
Plant Products with Hypocholesterolemic Potentials by Mukherjee PK; In : Advances in Food and Nutrition Research, Volume 47, by Taylor S, Gulf Professional Publishing, 2003, page no. 294.
https://books.google.co.in/books?id=lW3XXVeYBNkC&pg=PA294 |
2. |
6. Sugars and their Derivatives; In :Phytochemical Methods: A Guide to Modern Techniques of Plant Analysis, Second Edition by Harborne JB, Springer Science & Business Media, 2012, page no. 236.
https://books.google.co.in/books?id=Q2N-BgAAQBAJ&pg=PA236 |
3. |
Foods & Nutrition Encyclopedia, Two Volume Set, by Ensminger ME, Ensminger AH, CRC Press, 1993, page no. 1099.
https://books.google.co.in/books?id=XMA9gYIj-C4C&pg=PA1099 |
4. |
10. Grapefruits, Lemons and Limes by Kimball D; In : Processing Fruits, edited by Somogyi L, Barrett DM, Hui YH, CRC Press, 1996, page no. 319.
https://books.google.co.in/books?id=kNQG8AXT6tAC&pg=PA319 |
5. |
Manna K et al, Naringin inhibits gamma radiation-induced oxidative DNA damage and inflammation, by modulating p53 and NF-κB signaling pathways in murine splenocytes. Free Radic Res. 2015;49(4):422-39.
http://dx.doi.org/10.3109/10715762.2015.1016018 |