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Oroxylin A

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Oroxylin A manufacturers

  • Oroxylin A
  • Oroxylin A pictures
  • 2026-08-25
  • CAS:480-11-5
  • Min. Order: 10g
  • Purity: 99%
  • Supply Ability: 20kg
  • Oroxylin A
  • Oroxylin A pictures
  • $1.00
  • 2026-08-07
  • CAS:480-11-5
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 200000KG
  • Oroxylin A
  • Oroxylin A pictures
  • $80.00
  • 2026-05-11
  • CAS:480-11-5
  • Purity: 99.98%
  • Supply Ability: 10g
Oroxylin A Basic information
Product Name:Oroxylin A
Synonyms:5,7-Dihydroxy-6-methoxy-2-phenyl-4H-1-benzopyran-4-one;Oroxylia A;6-Methoxybaicalein;Baicalein 6-methyl ether;OLOXYLINA;oxoxylin A;4H-1-Benzopyran-4-one, 5,7-dihydroxy-6-methoxy-2-phenyl-;Autophagy,HIF-PH,HIFs,Inhibitor,HIF/HIF Prolyl-Hydroxylase,inhibit,Oroxylin A,Hypoxia-inducible factors,Virus Protease
CAS:480-11-5
MF:C16H12O5
MW:284.26
EINECS:
Product Categories:Miscellaneous Natural Products;Herbal extracts
Mol File:480-11-5.mol
Oroxylin A Structure
Oroxylin A Chemical Properties
Melting point 195-197℃
Boiling point 346.76°C (rough estimate)
density 1.420
refractive index 1.6200 (estimate)
storage temp. Sealed in dry,2-8°C
solubility DMF: 30 mg/ml; DMSO: 30 mg/ml; DMSO:PBS (pH 7.2) (1:4): 0.20 mg/ml
pka6.48±0.40(Predicted)
form powder
color Yellow
Major Applicationfood and beverages
InChIInChI=1S/C16H12O5/c1-20-16-11(18)8-13-14(15(16)19)10(17)7-12(21-13)9-5-3-2-4-6-9/h2-8,18-19H,1H3
InChIKeyLKOJGSWUMISDOF-UHFFFAOYSA-N
SMILESC1(C2=CC=CC=C2)OC2=CC(O)=C(OC)C(O)=C2C(=O)C=1
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany WGK 3
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
Oroxylin A Usage And Synthesis
Chemical PropertiesYellow needle-shaped crystals, soluble in organic solvents such as methanol, ethanol, and DMSO, mainly derived from Scutellaria baicalensis and Melaleuca alternifolia.
Usesfood and beverages
DefinitionChEBI: A dihydroxy- and monomethoxy-flavone in which the hydroxy groups are positioned at C-5 and C-7 and the methoxy group is at C-6.
Biological ActivityOroxylin A is a flavonoid isolated from Scutellaria baicalensis, which is one of the most important medicinal herbs in traditional Korean/Chinese/Japanese medicine. The amelioration of Abeta(25-35) peptide-induced memory impairment by oroxylin A is believed to be mediated via the GABAergic neurotransmitter system after a single administration, or by reductions in Abeta(25-35) peptide-induced astrocyte and microglia activations, iNOS expression, lipid peroxidation, and increased cholinergic neurotransmission after subchronic administration.
Synthesis
5,6,7-TRIMETHOXYFLAVONE

973-67-1

Oroxylin A

480-11-5

The general procedure for the synthesis of 5,7-dihydroxy-6-methoxy-2-phenyl-4H-benzopyran-4-one from 5,6,7-trimethoxy-2-phenyl-4H-benzopyran-4-one was as follows: 5,6,7-trimethoxy-2-phenyl-4H-benzopyran-4-one (0.20 g, 0.64 mmol) was dissolved in a mixture of 47% hydrobromic acid (5 mL) and glacial acetic acid (10 mL) in a mixed solution and the reaction was refluxed for 2 hours. Upon completion of the reaction, the reaction solution was quenched by carefully pouring it into crushed ice (200 g). The resulting yellow precipitate was collected by filtration and recrystallized from ethanol to afford 5,7-dihydroxy-6-methoxy-2-phenyl-4H-benzopyran-4-one (160 mg, 88% yield) with a melting point of 203-204 °C. The product structure was determined by 1H-NMR. The structure of the product was confirmed by 1H-NMR (DMSO-d6), IR, UV and MS analysis: 1H-NMR (DMSO-d6) δ: 3.91 (3H, s), 6.94 (1H, s), 6.98 (1H, s), 7.59 (3H, m), 8.10 (2H, d, J = 6.3 Hz), 8.77 (1H, s), 12.49 (1H, s); IR (KBr) cm-1: 3435, 1667; UV λmax (EtOH) nm (log ε): 322 (4.12), 278 (4.35), 216 (4.42); MS m/z: 285 (MH+).

References[1] Chemical and pharmaceutical bulletin, 2003, vol. 51, # 3, p. 339 - 340
[2] Patent: US2004/242907, 2004, A1. Location in patent: Page 3
[3] Chemistry and Biodiversity, 2015, vol. 12, # 2, p. 259 - 272
[4] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 7, p. 2534 - 2535
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