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norathyriol

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Company Name: Shaanxi Dideu Medichem Co. Ltd
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Email: 1057@dideu.com
Products Intro: Product Name:Norathyriol
CAS:3542-72-1
Purity:98% Package:1Kg;1USD
Company Name: BOC Sciences
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Products Intro: Product Name:Norathyriol
CAS:3542-72-1
Purity:98.5% Package:10 mg Remarks:Please reach out to us for more information about custom solutions.
Company Name: Shaanxi Dideu Medichem Co. Ltd
Tel: +86-29-87569262 +86-15003564040
Email: 1056@dideu.com
Products Intro: Product Name:norathyriol
CAS:3542-72-1
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Company Name: TargetMol Chemicals Inc.
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CAS:3542-72-1
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Company Name: Aktin Chemicals, Inc.
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Products Intro: Product Name:Norathyriol
CAS:3542-72-1
Purity:0.98 Package:10mg;20mg;50mg;100mg;200mg;500mg;1g;10g;100g;可按照客戶要求定制包裝

norathyriol manufacturers

  • Norathyriol
  • Norathyriol pictures
  • $152.00
  • 2026-06-02
  • CAS:3542-72-1
  • Purity: 99.55%
  • Supply Ability: 10g
  • norathyriol
  • norathyriol pictures
  • 2026-02-02
  • CAS:3542-72-1
  • Min. Order: 5mg
  • Purity: 99%HPLC
  • Supply Ability: 2000tons
  • Norathyriol
  • Norathyriol pictures
  • $1.00
  • 2024-07-20
  • CAS:3542-72-1
  • Min. Order: 1Kg
  • Purity: 98%
  • Supply Ability: 20T
norathyriol Basic information
Product Name:norathyriol
Synonyms:norathyriol;1,3,6,7-Tetrahydroxy-9H-xanthen-9-one;rathyriol;9H-Xanthen-9-one, 1,3,6,7-tetrahydroxy-;Norathyriol, 10 mM in DMSO;1,3,6,7-Tetrahydroxyxanthone;Mangiferitin
CAS:3542-72-1
MF:C13H8O6
MW:260.2
EINECS:
Product Categories:
Mol File:3542-72-1.mol
norathyriol Structure
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
MSDS 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 3.12μM[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 again t 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 3.7mg/kg) dose dependently decreased the serum urate levels by 27.0, 33.6 and 37.4%, respectively[4].

Animal Model:Adult Kunming mice weighing 18-22g[4]
Dosage:0.92, 1.85 and 3.7mg/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
Preparation Products2,3',4,4',6-Pentahydroxybenzophenone
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