Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Natural Products >  Chalcones >  SULFURETIN

SULFURETIN

Basic information Safety Supplier Related

SULFURETIN Basic information

Product Name:
SULFURETIN
Synonyms:
  • SULFURETIN
  • 6,3',4'-TRIHYDROXYAURONE
  • 3',4',6-TRIHYDROXYAURONE
  • 2-(3,4-dihydroxybenzylidene)-6-hydroxy-2H-benzofuran-3-one
  • (Z)-2-[(3,4-dihydroxyphenyl)methylene]-6-hydroxy-2H-benzofuran-3-one
  • SULPHURETIN
  • SULFURETIN WITH HPLC
  • SULFURETIN hplc
CAS:
120-05-8
MF:
C15H10O5
MW:
270.24
EINECS:
204-366-4
Product Categories:
  • Aurones
Mol File:
120-05-8.mol
More
Less

SULFURETIN Chemical Properties

Melting point:
295°C
storage temp. 
2-8°C
solubility 
Acetone: Soluble
Chloroform: Soluble
Dichloromethane: Soluble
DMSO: SolubleEthyl Acetate: Soluble
form 
Solid
color 
Yellow to orange
LogP
1.980 (est)
More
Less

SULFURETIN Usage And Synthesis

Uses

Sulfuretin inhibits the inflammatory response by suppressing the NF-κB pathway. Sulfuretin can be used for the research of allergic airway inflammation. Sulfuretin reduces oxidative stress, platelet aggregation, and mutagenesis[1]. Sulfuretin is a competitive and potent inhibitor of monophenolase and diphenolase activities with the IC50 of 13.64 μM[2].

Definition

ChEBI: Sulfuretin is a member of 1-benzofurans.

Biological Activity

Anti-adipogenic, antineoplastic activity, antioxidative stress, Anti-Inflammatory

in vivo

Sulfuretin inhibits the inflammatory responses by suppressing the NF-κB pathway in type 1 diabetes models. Sulfuretin (40 μg/kg; single intraperitoneal injection 2 h after the last OVA challenge) suppresses ovalbumin (OVA)-induced chemotaxis and airway inflammation[1].

Animal Model:Pathogen-free male BALB/c mice (7-8 weeks old)[1]
Dosage:40 μg/kg
Administration:A single intraperitoneal injection was administered 2 h after the last OVA challenge
Result:Suppressed OVA-induced chemotaxis and airway inflammation.

References

[1] Mi-Young Song, et al. Sulfuretin attenuates allergic airway inflammation in mice. Biochem Biophys Res Commun. 2010 Sep 10;400(1):83-8. DOI:10.1016/j.bbrc.2010.08.014
[2] Chen, H., et al. Isolation of sulfuretin and butin from Rhus verniciflua Stokes using medium-pressure liquid chromatography and their tyrosinase inhibitory effects. BioRes. 11(1), 759-771.
[3] SO YOUNG KANG  Myung J O  Ji Young Kang. Antiviral activities of flavonoids isolated from the bark of Rhus verniciflua stokes against fish pathogenic viruses In Vitro.[J]. Journal of Microbiology, 2012, 50 2: 293-300. DOI: 10.1007/s12275-012-2068-7

SULFURETINSupplier

Chembest Research Laboratories Limited
Tel
+86-21-20908456
Email
sales@BioChemBest.com
Nanjing Chemlin Chemical Co., Ltd
Tel
025-83697070
Email
info@chemlin.com.cn
BioBioPha Co., Ltd.
Tel
0871-65217109 13211707573;
Email
y.liu@mail.biobiopha.com
Chengdu Biopurify Phytochemicals Ltd.
Tel
+86-028-82633397 18982077548
Email
cwb1@biopurify.cn
Shanghai Winherb Medical Technology Co., Ltd.
Tel
021-38218169 13341702378
Email
winherb@126.com