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Details

Stereochemistry ABSOLUTE
Molecular Formula C28H34O15.H3O4P
Molecular Weight 708.5557
Optical Activity UNSPECIFIED
Defined Stereocenters 11 / 11
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Hesperidin phosphate

SMILES

OP(O)(O)=O.COC1=C(O)C=C(C=C1)[C@@H]2CC(=O)C3=C(O)C=C(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)C=C3O2

InChI

InChIKey=AQQZZBLCTUPEBH-QTTJGSJSSA-N
InChI=1S/C28H34O15.H3O4P/c1-10-21(32)23(34)25(36)27(40-10)39-9-19-22(33)24(35)26(37)28(43-19)41-12-6-14(30)20-15(31)8-17(42-18(20)7-12)11-3-4-16(38-2)13(29)5-11;1-5(2,3)4/h3-7,10,17,19,21-30,32-37H,8-9H2,1-2H3;(H3,1,2,3,4)/t10-,17-,19+,21-,22+,23+,24-,25+,26+,27+,28+;/m0./s1

HIDE SMILES / InChI

Molecular Formula H3O4P
Molecular Weight 97.9952
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C28H34O15
Molecular Weight 610.5606
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 11 / 11
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including: https://en.wikipedia.org/wiki/Hesperidin http://www.bimsifram.fr/hesperidin/indications_and_usage_of_hesperidin.htm

Hesperidin is a flavanone glycoside found in citrus fruits. Its aglycone form is called hesperetin. Its name is derived from the word "hesperidium", for fruit produced by citrus trees. Hesperidin was first isolated in 1828 by French chemist Lebreton from the white inner layer of citrus peels (mesocarp, albedo). As a flavanone found in citrus fruits (such as oranges, lemons or pummelo fruits), hesperidin is under laboratory research for possible biological properties. One area of research is focused on the possible chemopreventive effects of hesperidin, but there is no current proof that hesperidin has this role in human cancer mechanisms. Hesperidin was effective in an animal model of Alzheimer's, alleviating pathological changes induced by aluminum. Early research suggests that taking one tablet of a specific product (Daflon 500, Les Laboratoires Servier) containing hesperidin and diosmin by mouth for 45 days decreases blood sugar levels and improves blood sugarcontrol in women with type 2 diabetes. For Rheumatoid arthritis (RA): early research suggests that drinking a beverage containing alpha-glucosyl hesperidin for 12 weeks improves symptoms of RA. Orally, hesperidin can cause gastrointestinal side effects, including abdominal pain, diarrhea, and gastritis. Headache can also occur in some patients. The possible anti-inflammatory action of hesperidin is probably due to the possible anti-inflammatory action of its aglycone hesperetin. Hesperetin appears to interfere with the metabolism of arachidonic acid as well as with histamine release. Hesperetin appears to inhibit phospholipase A2, lipoxygenase and cyclo-oxygenase. There is evidence that hesperetin inhibits histamine release from mast cells, which would account for the possible anti-allergic activity of hesperidin. The possible hypolipidemic effect of hesperidin is probably due to hesperetin's possible action in lipid lowering. Hesperetin may reduce plasma cholesterol levels by inhibition of 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase, as well as acyl coenzyme A: cholesterol acytransferase (ACAT). Inhibition of these enzymes by hesperetin has been demonstrated in rats fed a high cholesterol diet. The mechanism of hesperidin's possible vasoprotective action is unclear. Animal studies have shown that hesperidin decreases microvascular permeability. Hesperidin, itself or via hesperetin, may protect endothelial cells from hypoxia by stimulating certain mitochondrial enzymes, such as succinate dehydrogenase. The mechanism of hesperidin's possible anticarcinogenic action is also unclear. One explanation may be the inhibition of polyamine synthesis. Inhibition of lipoxygenase and cyclo-oxygenase is another possibility.

CNS Activity

Curator's Comment: Hesperidin (HESP), a flavanone glycoside, shows high antioxidant properties and posses ability to go through the blood–brain barrier. Therefore, it could be a potential drug molecule against aggregation based diseases such as Alzheimer’s, Parkinson’s, and systemic amyloidoses.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
FRUIT ALLERGEN MIX

Approved Use

For the temporary relief of symptoms related to allergies to Vitamin C in foods and supplements, including fatigue, upper respiratory, gastrointestinal, musculoskeletal, and urinary symptoms.
Inactive ingredient
Volu-Firm Eye Renewal Cream

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Preventing
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Anti-AIDS agents, 10. Acacetin-7-O-beta-D-galactopyranoside, an anti-HIV principle from Chrysanthemum morifolium and a structure-activity correlation with some related flavonoids.
1994 Jan
Inhibition of HIV activation in latently infected cells by flavonoid compounds.
1996 Jan 1
Flavanone glycosides from Citrus junos and their anti-influenza virus activity.
2001 Aug
Flavonoids and nitric oxide synthase.
2002 Dec
Kinetics of radical-scavenging activity of hesperetin and hesperidin and their inhibitory activity on COX-2 expression.
2005 Sep-Oct
Effect of constituents from Fructus Aurantii Immaturus and Radix Paeoniae Alba on gastrointestinal movement.
2009 Jan
The inhibitory effect of hesperidin on tumor cell invasiveness occurs via suppression of activator protein 1 and nuclear factor-kappaB in human hepatocellular carcinoma cells.
2010 Apr 15
Effect of citrus polyphenol- and curcumin-supplemented diet on inflammatory state in obese cats.
2011 Oct
Mangiferin has an additive effect on the apoptotic properties of hesperidin in Cyclopia sp. tea extracts.
2014
Hesperidin blunts streptozotocin-isoproternol induced myocardial toxicity in rats by altering of PPAR-γ receptor.
2014 Aug 5
Investigation of the effects of some phenolic compounds on the activities of glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase from human erythrocytes.
2014 Nov
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: There is not enough evidence concerning doses of hesperidin used alone. Most studies describe the use of hesperidin in combination products that also contain other ingredients.
For arthritis: beverages containing 3 grams of a hesperidin derivative have been used every morning for 12 weeks. For blood vessel disorders (easily damaged capillary blood vessels): one tablet of Daflon ( 90% diosmin and 10% other flavonoids expressed as hesperidin.) has been used twice daily.
Route of Administration: Oral
In Vitro Use Guide
in vitro assay, a concentration of 200 μg/ml of hesperidin resulted in the mortality of 100% adult worms of Schistosoma (S.) mansoni within 72 h and a partial tegumental alteration in 10% of worms.
Substance Class Chemical
Created
by admin
on Sat Dec 16 18:42:59 UTC 2023
Edited
by admin
on Sat Dec 16 18:42:59 UTC 2023
Record UNII
8HDT8GA9UW
Record Status Validated (UNII)
Record Version
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Name Type Language
Hesperidin phosphate
Common Name English
Hesperidin phosphate [WHO-DD]
Common Name English
Hesperidin, phosphate
Common Name English
4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-, monophosphate, (2S)-
Systematic Name English
Code System Code Type Description
CAS
121708-83-6
Created by admin on Sat Dec 16 18:43:00 UTC 2023 , Edited by admin on Sat Dec 16 18:43:00 UTC 2023
PRIMARY
FDA UNII
8HDT8GA9UW
Created by admin on Sat Dec 16 18:43:00 UTC 2023 , Edited by admin on Sat Dec 16 18:43:00 UTC 2023
PRIMARY
PUBCHEM
164888941
Created by admin on Sat Dec 16 18:43:00 UTC 2023 , Edited by admin on Sat Dec 16 18:43:00 UTC 2023
PRIMARY
SMS_ID
100000077920
Created by admin on Sat Dec 16 18:43:00 UTC 2023 , Edited by admin on Sat Dec 16 18:43:00 UTC 2023
PRIMARY
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