ChemicalBook--->CAS DataBase List--->529-49-7

529-49-7

529-49-7 Structure

529-49-7 Structure
IdentificationBack Directory
[Name]

GENTISEIN
[CAS]

529-49-7
[Synonyms]

NSC329491
NSC-329491
NSC 329491
Gentisein(NSC 329491)
1,3,7-trihydroxyxanthen-9-one
1,3,7-Trihydroxy-9H-xanthen-9-one
9H-Xanthen-9-one,1,3,7-trihydroxy-
[Molecular Formula]

C13H8O5
[MDL Number]

MFCD00210571
[MOL File]

529-49-7.mol
[Molecular Weight]

244.2
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[solubility ]

DMF: 30 mg/ml,DMSO: 30 mg/ml,DMSO:PBS (pH 7.2) (1:2): 0.33 mg/ml,Ethanol: 20 mg/ml
[form ]

A solid
[color ]

Light yellow to yellow
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P330-P302+P352-P321-P304+P340-P305+P351+P338-P332+P313-P362+P364-P337+P313-P403+P233-P405-P501
Hazard InformationBack Directory
[Uses]

Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2].
[Definition]

ChEBI: A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3 and 7.
[storage]

-20°C
[References]

[1] Wang H, et al. Identification and determination of four metabolites of mangiferin in rat urine. J Pharm Biomed Anal. 2007;45(5):793-798. DOI:10.1016/j.jpba.2007.07.019
[2] Tzankova, Virginia et al. (2010). Inhibition of 5-HT uptake by some constituents of Hypericum annulatum in rat brain in vitro. Pharmacologyonline. 2.
Spectrum DetailBack Directory
[Spectrum Detail]

GENTISEIN(529-49-7)1HNMR
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