482-36-0

482-36-0 structure

Name: Hyperoside
Chemical Name: quercetin 3-O-β-D-galactopyranoside
CAS Number: 482-36-0
Molecular Formula: C₂₁H₂₀O₁₂
Molecular Weight: 464.376
Catalog: Natural product Flavonoids
Create Date: 2018-02-08 08:00:00
Modify Date: 2024-01-02 12:49:25
Hyperoside, a natural flavonoid, isolated from Camptotheca acuminate, possesses antifungal, anti-inflammatory, anti-viral, anti-oxidative and anti-apoptotic activities[1].

Name	quercetin 3-O-β-D-galactopyranoside
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 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3-(β-D-galactopyranosyloxy)-5,7-dihydroxy- 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

Description	Hyperoside, a natural flavonoid, isolated from Camptotheca acuminate, possesses antifungal, anti-inflammatory, anti-viral, anti-oxidative and anti-apoptotic activities[1].
Related Catalog	Research Areas >> Infection Signaling Pathways >> Others >> Others
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.

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
Storage condition	-20°C Freezer, Under Inert Atmosphere

CHEMICAL NAME :: 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3-(beta-D-galactopyranosyloxy )-5,7-dihydroxy-

WISWESSER LINE NOTATION :: T66 BO EVJ CR CQ DQ& GQ IQ DO- BT6OTJ CQ DQ EQ F1Q

REFERENCE :: ENMUDM Environmental Mutagenesis. (New York, NY) V.1-9, 1979-87. For publisher information, see EMMUEG. Volume(issue)/page/year: 3,401,1981

Symbol	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

161126-00-7

~78%

482-36-0

117-39-5

482-36-0

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

357194-03-7

482-36-0

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

742062-20-0

482-36-0

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

53209-27-1

482-36-0

149-91-7

Literature: Yazaki, Kazufumi; Shida, Shoko; Okuda, Takuo Phytochemistry (Elsevier), 1989 , vol. 28, # 2 p. 607 - 610

53171-28-1

482-36-0

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