Hesperetin
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IUPAC name
(2S)-3′,5,7-Trihydroxy-4′-methoxyflavan-4-one
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Preferred IUPAC name
(2S)-5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-2,3-dihydro-4H-1-benzopyran-4-one | |
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3D model (JSmol)
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DrugBank | |
ECHA InfoCard | 100.007.538 |
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CompTox Dashboard (EPA)
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Properties | |
C16H14O6 | |
Molar mass | 302.282 g·mol−1 |
Melting point | 226–228 °C (439–442 °F; 499–501 K) |
Solubility in other solvents | Sol. EtOH, alkalis |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
what is ?) | (|
Infobox references | |
Hesperetin is the 4'-methoxy derivative of eriodictyol, a flavanone. Hesperetin's 7-O-glycoside, hesperidin, is a naturally occurring flavanon-glycoside, the main flavonoid in lemons and sweet oranges.[1] Hesperetin (and naringenin, the parent flavanone of naringin) are not found to a significant extent in Citrus spp.[2]
Glycosides[]
A variety of glycosides of hesperetin are known, including:
- Hesperidin (hesperetin-7-O-rutinoside) is a water-insoluble flavonoid glycoside whose solubility is below 5 μg/ml in water.[3] Hesperidin is found in citrus fruits and upon ingestion it releases its aglycone, hesperetin.
- Neohesperidin is the 7-O-neohesperidoside of hesperetin.
- Hesperetin-7-O-α-L-Rhamnopyranoside (CAS 66513-83-5) is found in the roots of clammy cherry[4] (Cordia obliqua a.k.a. Cordia obliqua var. wallichii[5]).
Metabolism[]
Hesperidin 6-O-α-L-rhamnosyl-β-D-glucosidase is an enzyme that uses hesperidin and H2O to produce hesperetin and rutinose. It is found in the hyphomycetes species Stilbella fimetaria.
Effects[]
Hesperetin was found to be affecting the slow inactivation phase of inward sodium current channels (INa) and therefore could be used as a template to develop drugs against lethal cardiac arrhythmias in LQT3.[6] Hesperetin also inhibits TRPM3 channels.[7]
References[]
- ^ "Hesperetin".
- ^ Lewinsohn, E; Britsch, L; Mazur, Y; Gressel, J (1989). "Flavanone Glycoside Biosynthesis in Citrus: Chalcone Synthase, UDP-Glucose:Flavanone-7-O-Glucosyl-Transferase and -Rhamnosyl-Transferase Activities in Cell-Free Extracts". Plant Physiology. 91 (4): 1323–1328. doi:10.1104/pp.91.4.1323. PMC 1062186. PMID 16667183.
- ^ Majumdar S.; Srirangam, R. (2009). "Solubility, stability, physicochemical characteristics and in vitro ocular tissue permeability of hesperidin: a natural bioflavonoid". Pharm. Res. 26 (5): 1217–1225. doi:10.1007/s11095-008-9729-6. PMC 2664388. PMID 18810327.
- ^ http://ccd.chemnetbase.com/AAA00.entry?parentCHNumber=CNB06-R:CNB07-S[full citation needed]
- ^ http://www.newcropslisting.info/listing/species_pages_C/Cordia_obliqua.htm[full citation needed]
- ^ Alvarez‐Collazo, Julio; López‐Requena, Alejandro; Galán, Loipa; Talavera, Ariel; Alvarez, Julio L.; Talavera, Karel (27 March 2019). "The citrus flavanone hesperetin preferentially inhibits slow‐inactivating currents of a long QT syndrome type 3 syndrome Na+ channel mutation". British Journal of Pharmacology. 176 (8): 1090–1105. doi:10.1111/bph.14577. PMC 6451064. PMID 30650182.
- ^ Straub, Isabelle; Krügel, Ute; Mohr, Florian; Teichert, Jens; Rizun, Oleksandr; Konrad, Maik; Oberwinkler, Johannes; Schaefer, Michael (November 2013). "Flavanones that selectively inhibit TRPM3 attenuate thermal nociception in vivo". Molecular Pharmacology. 84 (5): 736–750. doi:10.1124/mol.113.086843. ISSN 1521-0111. PMID 24006495.
- Aromatase inhibitors
- O-Methylated flavanones
- Flavonoids found in Rutaceae
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