ChemicalBook--->CAS DataBase List--->493-36-7

493-36-7

493-36-7 Structure

493-36-7 Structure
IdentificationBack Directory
[Name]

2-[(3,4-Dihydroxyphenyl)methyl]-2,4,6-trihydroxy-3(2H)-benzofuranone
[CAS]

493-36-7
[Synonyms]

Alphitonin
2-[(3,4-Dihydroxyphenyl)methyl]-2,4,6-trihydroxy-3(2H)-benzofuranone
3(2H)-Benzofuranone, 2-[(3,4-dihydroxyphenyl)methyl]-2,4,6-trihydroxy-
[Molecular Formula]

C15H12O7
[MDL Number]

MFCD28335979
[MOL File]

493-36-7.mol
[Molecular Weight]

304.25
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble
[form ]

A solid
Hazard InformationBack Directory
[Description]

Alphitonin is a flavonoid that has been found in L. leptolepis wood. It is also a metabolic intermediate that is formed during the catabolism of quercetin by the human gut bacteria E. ramulus.
[Uses]

Alphitonin is a flavonoid and is also a metabolic intermediate that is formed during the catabolism of Quercetin (HY-18085) by the human gut bacteria E. ramulus.
[Definition]

ChEBI: Alphitonin is a hydroxyaurone that is aurone substituted by hydroxy groups at positions 2, 4, 6, 3' and 4' respectively. It has been isolated from Alphitonia excelsa. It has a role as a plant metabolite. It is functionally related to an aurone.
[storage]

Store at -20°C
[References]

[1] K. CHEN . Termite feeding deterrent from Japanese larch wood[J]. Bioresource Technology, 2004, 95 2: Pages 129-134. DOI: 10.1016/j.biortech.2004.02.014
[2] A. BRAUNE. Degradation of Quercetin and Luteolin byEubacterium ramulus[J]. Applied and Environmental Microbiology, 2001, 67 1: 5558-5567. DOI: 10.1128/aem.67.12.5558-5567.2001
[3] INDU B. JAGANATH . In vitro catabolism of rutin by human fecal bacteria and the antioxidant capacity of its catabolites[J]. Free Radical Biology and Medicine, 2009, 47 8: Pages 1180-1189. DOI: 10.1016/j.freeradbiomed.2009.07.031
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