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Hyperoside

Hyperoside structure

CAS No:
482-36-0
Formula:
C21H20O12
Chemical Name:
Hyperoside
Synonyms:
4H-1-Benzopyran-4-one,2-(3,4-dihydroxyphenyl)-3-(β-D-galactopyranosyloxy)-5,7-dihydroxy-;Hyperin;2-(3,4-Dihydroxyphenyl)-3-(β-D-galactopyranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one;Hyperoside;Hyperosid;Quercetin 3-galactoside;Quercetin 3-O-galactoside;Quercetin 3-O-β-D-galactopyranoside;Quercetin 3-O-β-D-galactoside;Quercetin 3-β-D-galactoside;Quercetin 3-β-galactoside;3,3′,4′,5,7-Pentahydroxyflavone 3-O-β-D-galactopyranoside;3-O-β-D-galactopyranosylquercetin;Quercetin 3-O-β-galactoside;3-O-β-D-Galactopyranosyl quercetin;Quercetin 3-O-β-galactopyranoside;NSC 407304;Quercetin 3-O-galactopyranoside;3-D-Galactosylquercetin;112457-37-1;26857-03-4;28986-85-8;29224-70-2;31710-72-2;56552-81-9;61277-37-0;63003-36-1;71184-39-9;158560-10-2
Categories:
Natural Products > Flavonoids

Description

Hyperoside, a natural flavonoid, isolated from Camptotheca acuminate, possesses antifungal, anti-inflammatory, anti-viral, anti-oxidative and anti-apoptotic activities[1].

Solid

Quercetin 3-O-beta-D-galactopyranoside is a quercetin O-glycoside that is quercetin with a beta-D-galactosyl residue attached at position 3. Isolated from Artemisia capillaris, it exhibits hepatoprotective activity. It has a role as a hepatoprotective agent and a plant metabolite. It is a tetrahydroxyflavone, a monosaccharide derivative, a beta-D-galactoside and a quercetin O-glycoside.

Hyperoside Basic Attributes

Molecular Weight：

464.37600

Exact Mass：

464.38

EC Number：

207-580-6

UNII：

8O1CR18L82

HScode：

29389090

Characteristics

PSA：

210.51000

XLogP3：

0.4

Appearance：

Solid

Density：

1.87 g/cm3

Melting Point：

236 °C

Boiling Point：

872.6ºC at 760 mmHg

Flash Point：

307.4ºC

Refractive Index：

1.803

Water Solubility：

2.782e+004 mg/L @ 25 °C (est)

Storage Conditions：

-20ºC Freezer, Under Inert Atmosphere

Vapor Pressure：

0mmHg at 25°C

Safety Information

Transport codes：

NONH for all modes of transport

wgk germany：

hazard class code：

R22

safety instructions：

S22; S45

RTECS Number：

DJ3009200

Marks：

Precautionary statement(s)：

P301 + P312 + P330

Hazard Statements：

H302

Drug Information

MeSH Entry Terms：

hyperin

Hyperoside Use and Manufacturing

Hyperin has the effects of protecting the liver, cardiovascular and cerebrovascular protection, nervous system protection, anti-inflammatory, antispasmodic and analgesic, lowering blood lipids, enhancing immune function, and anti-depression. 1. Hyperoside has a significant local analgesic effect. The analgesic effect is weaker than morphine and stronger than aspirin, and it is not dependent. It is a new type of local analgesic. 2. It has a good protective effect on myocardial ischemia reperfusion, cerebral ischemia reperfusion and cerebral infarction. 3. Hyperoside has obvious anti-inflammatory effect: After the rat is implanted with wool ball, 20mg/Kg is injected intraperitoneally for 7 days every day, which can significantly inhibit the inflammation process. 4. It has a strong antitussive effect. 5. It has a strong inhibitory effect on ocular aldose reductase, which may be beneficial to the prevention of diabetic cataract. Obvious anti-inflammatory effect

Computed Properties

Molecular Weight:464.4
XLogP3:0.4
Hydrogen Bond Donor Count:8
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:4
Exact Mass:464.09547607
Monoisotopic Mass:464.09547607
Topological Polar Surface Area:207
Heavy Atom Count:33
Complexity:758
Defined Atom Stereocenter Count:5
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Drug Function and Efficacy

anti-inflammatory, antioxidant

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

SENECIO AUREUS- packera aurea_liquid
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Guide of Hyperoside

Description
Basic Attributes
Characteristics
Safety Information
Drug Information
Use and Manufacturing
Computed Properties
Drug Function and Efficacy
Related Drugs
Recommended Suppliers
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