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Methyl-Hesperidin

Catalog No. S2323 Name Selleck Chemicals
CAS Number 11013-97-1 Website http://www.selleckchem.com
M. F. C29H36O15 Telephone (877) 796-6397
M. W. 624.58714 Fax (832) 582-8590
Purity Email sales@selleckchem.com
Storage -20°C Chembase ID: 72958

SYNONYMS

IUPAC name
(2S)-2-(3-hydroxy-4-methoxyphenyl)-5-methoxy-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,4-dihydro-2H-1-benzopyran-4-one
IUPAC Traditional name
(2S)-2-(3-hydroxy-4-methoxyphenyl)-5-methoxy-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-2,3-dihydro-1-benzopyran-4-one

DATABASE IDS

CAS Number 11013-97-1

PROPERTIES

Salt Data Free Base
Storage Condition -20°C

DETAILS

Description (English)
Research Area: Cardiovascular Disease , Inflammation
Biological Activity:
Methyl-Hesperidin is a flavanone glycoside (flavonoid) (C28H34O15) found abundantly in citrus fruits. Its aglycone form is called hesperetin. Its name is derived from the Hesperides nymphs of Greek mythology. Hesperidin is believed to play a role in plant defense. Hesperidin reduced cholesterol and blood pressure in rats. Hesperidin has anti-inflammatory effects. Hesperidin is also a potential sedative, possibly acting through opioid or adenosine receptors.Some in vitro results applied only to the aglycone form. Hesperidin also showed the ability to penetrate the blood-brain barrier in an in vitro model. [1]

REFERENCES

  • http://en.wikipedia.org/wiki/Hesperidin