Hyperoside

Modify Date: 2025-08-21 14:32:32

Hyperoside Structure
Hyperoside structure
 Common Name Hyperoside
CAS Number 482-36-0 Molecular Weight 464.376
Density 1.9±0.1 g/cm3 Boiling Point 872.6±65.0 °C at 760 mmHg
Molecular Formula C21H20O12 Melting Point 225-226ºC
MSDS Chinese USA Flash Point 307.5±27.8 °C
Symbol GHS07
GHS07		 Signal Word Warning

 Use of Hyperoside


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

 Names

Name quercetin 3-O-β-D-galactopyranoside
Synonym More Synonyms

 Hyperoside Biological Activity

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

[1]. Li S, et al. Antifungal activity of camptothecin, trifolin, and hyperoside isolated from Camptotheca acuminata. J Agric Food Chem. 2005 Jan 12;53(1):32-7.

 Chemical & Physical Properties

Density 1.9±0.1 g/cm3
Boiling Point 872.6±65.0 °C at 760 mmHg
Melting Point 225-226ºC
Molecular Formula C21H20O12
Molecular Weight 464.376
Flash Point 307.5±27.8 °C
Exact Mass 464.095490
PSA 210.51000
LogP 1.75
Vapour Pressure 0.0±0.3 mmHg at 25°C
Index of Refraction 1.803
InChIKey OVSQVDMCBVZWGM-DTGCRPNFSA-N
SMILES O=c1c(OC2OC(CO)C(O)C(O)C2O)c(-c2ccc(O)c(O)c2)oc2cc(O)cc(O)c12
Storage condition -20°C Freezer, Under Inert Atmosphere

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
DJ3009200
CHEMICAL NAME :
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3-(beta-D-galactopyranosyloxy )-5,7-dihydroxy-
CAS REGISTRY NUMBER :
482-36-0
LAST UPDATED :
199410
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C21-H20-O12
MOLECULAR WEIGHT :
464.41
WISWESSER LINE NOTATION :
T66 BO EVJ CR CQ DQ& GQ IQ DO- BT6OTJ CQ DQ EQ F1Q

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
Mutation in microorganisms
TEST SYSTEM :
Bacteria - Salmonella typhimurium
DOSE/DURATION :
20 ug/plate
REFERENCE :
ENMUDM Environmental Mutagenesis. (New York, NY) V.1-9, 1979-87. For publisher information, see EMMUEG. Volume(issue)/page/year: 3,401,1981

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302
Precautionary Statements P301 + P312 + P330
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xn:Harmful;
Risk Phrases R22
Safety Phrases 22-45
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS DJ3009200

 Synthetic Route

2-(3',4'-dihydroxyphenyl)-5,7-dihydroxy-3-β-D-tetraacetylgalactosyl-4H-chromen-4-one structure

2-(3',4'-dihydr...

CAS#:161126-00-7

~78%

Hyperoside Structure

Hyperoside

CAS#:482-36-0

Literature: Chen, Lili; Li, Jian; Luo, Cheng; Liu, Hong; Xu, Weijun; Chen, Gang; Liew, Oi Wah; Zhu, Weiliang; Puah, Chum Mok; Shen, Xu; Jiang, Hualiang Bioorganic and Medicinal Chemistry, 2006 , vol. 14, # 24 p. 8295 - 8306
Quercetin structure

Quercetin

CAS#:117-39-5

~%

Hyperoside Structure

Hyperoside

CAS#:482-36-0

Literature: Chen, Zhiwei; Hu, Yongzhou; Wu, Haohao; Jiang, Huidi Bioorganic and Medicinal Chemistry Letters, 2004 , vol. 14, # 15 p. 3949 - 3952
2-(2,2-diphenylbenzo[d][1,3]dioxol-5-yl)-3,5,7-trihydroxy-4H-chroMen-4-one structure

2-(2,2-diphenyl...

CAS#:357194-03-7

~%

Hyperoside Structure

Hyperoside

CAS#:482-36-0

Literature: Chen, Zhiwei; Hu, Yongzhou; Wu, Haohao; Jiang, Huidi Bioorganic and Medicinal Chemistry Letters, 2004 , vol. 14, # 15 p. 3949 - 3952
2-(2,2-diphenylbenzo[d][1,3]dioxol-5-yl)-5,7-dihydroxy-3-(2,3,4,6-tetraacetyl-β-D-galactopyranosyl)-4H-chromen-4-one structure

2-(2,2-diphenyl...

CAS#:742062-20-0

~%

Hyperoside Structure

Hyperoside

CAS#:482-36-0

Literature: Chen, Zhiwei; Hu, Yongzhou; Wu, Haohao; Jiang, Huidi Bioorganic and Medicinal Chemistry Letters, 2004 , vol. 14, # 15 p. 3949 - 3952
2''-O-Galloylhyperin structure

2''-O-Galloylhyperin

CAS#:53209-27-1

~%

Hyperoside Structure

Hyperoside

CAS#:482-36-0

Gallic acid structure

Gallic acid

CAS#:149-91-7

Literature: Yazaki, Kazufumi; Shida, Shoko; Okuda, Takuo Phytochemistry (Elsevier), 1989 , vol. 28, # 2 p. 607 - 610
Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside structure

Quercetin 3-O-(...

CAS#:53171-28-1

~%

Hyperoside Structure

Hyperoside

CAS#:482-36-0

Literature: Masuda; Iritani; Yonemori; Oyama; Takeda Bioscience, biotechnology, and biochemistry, 2001 , vol. 65, # 6 p. 1302 - 1309

 Articles48

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 HyperosideBioassay

View more

Name: HepG2 viability counterscreen (readout 2: ATP content) against the NCATS DSHEA and TC...
Source: NCGC
Target: N/A
External Id: DSHEA-v1-HepG2-viability-CTG-ATP
Name: Antiviral activity against Dengue virus assessed as inhibition of viral replication
Source: ChEMBL
Target: Dengue virus
External Id: CHEMBL3384587
Name: Antibacterial activity against Staphylococcus aureus MRSA ATCC 43300 (CO-ADD:GP_020);...
Source: ChEMBL
Target: Staphylococcus aureus
External Id: CHEMBL4296184
Name: Inhibition of human OATP2B1 expressed in Flp-In-CHO cells assessed as inhibition of O...
Source: ChEMBL
Target: Solute carrier organic anion transporter family member 2B1
External Id: CHEMBL5260630
Name: Inhibition of human OATP2B1 expressed in Flp-In-CHO cells assessed as inhibition of O...
Source: ChEMBL
Target: Solute carrier organic anion transporter family member 2B1
External Id: CHEMBL5260629
Name: Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
Source: ChEMBL
Target: Klebsiella pneumoniae
External Id: CHEMBL4296186
Name: Antibacterial activity against Escherichia coli ATCC 25922 (CO-ADD:GN_001); MIC in CA...
Source: ChEMBL
Target: Escherichia coli
External Id: CHEMBL4296185
Name: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
Name: Inhibition of human OATP2B1 expressed in Flp-In-CHO cells assessed as inhibition of O...
Source: ChEMBL
Target: Solute carrier organic anion transporter family member 2B1
External Id: CHEMBL5260631
Name: Inhibition of PTP1B (unknown origin) at 20 ug/ml using pNPP substrate measured after ...
Source: ChEMBL
Target: Tyrosine-protein phosphatase non-receptor type 1
External Id: CHEMBL3405964
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 Synonyms

2-(3,4-Dihydroxyphenyl)-3-(β-D-galactopyranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one
Quercetin 3-O-β-D-galactoside
quercetin-3-O-galactoside
Hyperin
Quercetin 3-O-galactoside
Quercetin 3-β-D-galactopyranoside
Hyperoside
Quercetin 3-O-β-D-galactopyranoside
Quercetin-3-O-β-D-galactoside
MFCD00016933
Hyperasid
Hyperosid
quercetin-3-β-O-galactoside
Quercetin 3-galactoside
quercetin 3-O-beta-D-galactopyranoside
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl β-D-galactopyranoside
hyperozide
Quercetin 3-D-galactoside
EINECS 207-580-6
quercetin-3-galactoside
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Chemsrc provides Hyperoside(CAS#:482-36-0) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of Hyperoside are included as well.>> amp version: Hyperoside

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