<Suppliers Price>

Chrysoeriol

Names

[ CAS No. ]:
491-71-4

[ Name ]:
Chrysoeriol

[Synonym ]:
Chrysoeriol
Luteolin 3'-methyl ether
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-chromen-4-one
3'-Methoxyapigenin
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one
3'-Methoxy-4',5,7-trihydroxyflavone
Chryseriol
Chrysoriol
3'-O-Methyluteolin
4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-
Scoparol
4',5,7-trihydroxy-3'-methoxyflavone
EINECS 207-742-6
3'-O-Methylluteolin

Biological Activity

[Description]:

Chrysoeriol, a natural flavonoid extracted from the tropical plant Coronopus didymus, exhibits potent antioxidant activity. Chrysoeriol shows significant inhibition of lipid peroxidation[1].

[Related Catalog]:

Signaling Pathways >> Others >> Others
Research Areas >> Metabolic Disease

[References]

[1]. Beena Mishra, et al. Effect of O-glycosilation on the Antioxidant Activity and Free Radical Reactions of a Plant Flavonoid, Chrysoeriol. Bioorg Med Chem. 2003 Jul 3;11(13):2677-85.

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
574.3±50.0 °C at 760 mmHg

[ Melting Point ]:
>300ºC (dec.)

[ Molecular Formula ]:
C16H12O6

[ Molecular Weight ]:
300.263

[ Flash Point ]:
219.4±23.6 °C

[ Exact Mass ]:
300.063385

[ PSA ]:
100.13000

[ LogP ]:
1.81

[ Vapour Pressure ]:
0.0±1.6 mmHg at 25°C

[ Index of Refraction ]:
1.697

[ Storage condition ]:
2-8C

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
LK9278000
CHEMICAL NAME :
Flavone, 4',5,7-trihydroxy-3'-methoxy-
CAS REGISTRY NUMBER :
491-71-4
BEILSTEIN REFERENCE NO. :
0295004
LAST UPDATED :
199709
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C16-H12-O6
MOLECULAR WEIGHT :
300.28
WISWESSER LINE NOTATION :
T66 BO EVJ CR DQ CO1& GQ IQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
Mutation in microorganisms
TEST SYSTEM :
Bacteria - Salmonella typhimurium
DOSE/DURATION :
100 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

Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.