norathyriol CAS 3542-72-1

Introduction:Basic information about norathyriol CAS 3542-72-1, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

norathyriol Basic information

Product Name:norathyriol
Synonyms:norathyriol;1,3,6,7-Tetrahydroxy-9H-xanthen-9-one;1,3,6,7-Tetrahydroxyxanthone;Mangiferitin;rathyriol;9H-Xanthen-9-one, 1,3,6,7-tetrahydroxy-;Norathyriol, 10 mM in DMSO
CAS:3542-72-1
MF:C13H8O6
MW:260.2
EINECS:
Product Categories:
Mol File:3542-72-1.mol

norathyriol Chemical Properties

Melting point 320 °C
Boiling point 595.1±50.0 °C(Predicted)
density 1.766±0.06 g/cm3(Predicted)
solubility DMSO : 100 mg/mL (384.32 mM; Need ultrasonic)
form Solid
pka6.68±0.20(Predicted)
color White to off-white
InChIInChI=1S/C13H8O6/c14-5-1-9(17)12-11(2-5)19-10-4-8(16)7(15)3-6(10)13(12)18/h1-4,14-17H
InChIKeyZHTQCPCDXKMMLU-UHFFFAOYSA-N
SMILESC1(=O)C2=C(C=C(O)C(O)=C2)OC2=C1C(O)=CC(O)=C2

Safety Information

norathyriol Usage And Synthesis

UsesNorathyriol (Mangiferitin) is a natural metabolite of Mangifera. Norathyriol inhibits α-glucosidase in a noncompetitive manner with an IC50 of 3.12?μM[1]. Norathyriol inhibits PPARα, PPARβ, and PPARγ with IC50s of 92.8 μM, 102.4 μM, and 153.5 μM, respectively[2]. Antioxidant, anticancer, antimicrobial, anti-inflammatory, anti-bacterial activities.
DefinitionChEBI: A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3, 6 and 7. Isolated from Garcinia mangostana and Maclura pomifera, it exhibits inhibitory activity againt protein kinase C.
in vivo

Norathyriol is a natural metabolite of Mangifera in the human intestine with the oral availability and safety[1].
Norathyriol (0.92, 1.85 and 3.7?mg/kg) dose dependently decreased the serum urate levels by 27.0, 33.6 and 37.4%, respectively[4].

Animal Model:Adult Kunming mice weighing 18-22?g[4]
Dosage:0.92, 1.85 and 3.7?mg/kg
Administration:Administered intragastrically; twice daily for five times
Result:The serum uric acid levels were decreased by 27.0%, 33.6% and 37.4%.
IC 50PPARα: 92.8 μM (IC50); PPARβ: 102.4 μM (IC50); PPARγ: 153.5 μM (IC50)
References[1] Zhi-Long Shi, et al. In Vitro and In Vivo Effects of Norathyriol and Mangiferin on α-Glucosidase. Biochem Res Int. 2017;2017:1206015. DOI:10.1155/2017/1206015
[2] Ashley S Wilkinson,et al. Effects of the mango components mangiferin and quercetin and the putative mangiferin metabolite norathyriol on the transactivation of peroxisome proliferator-activated receptor isoforms. J Agric Food Chem. 2008 May 14;56(9):3037-42. DOI:10.1021/jf800046n
[3] Jixia Li, et al. Norathyriol suppresses skin cancers induced by solar ultraviolet radiation by targeting ERK kinases. Cancer Res. 2012 Jan 1;72(1):260-70. DOI:10.1158/0008-5472.CAN-11-2596
[4] Yanfen Niu, et al. Hypouricaemic action of mangiferin results from metabolite norathyriol via inhibiting xanthine oxidase activity. Pharm Biol. 2016 Sep;54(9):1680-6. DOI:10.3109/13880209.2015.1120322

norathyriol Preparation Products And Raw materials

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