GLPBio

Chrysoeriol

Catalog No.: GC60109Purity:>98.00%Synonyms: 3'-methoxy Apigenin, Luteolin 3'-methyl ether
Chrysoeriol is a natural flavonoid found in Coronopus didymus that exerts anti-inflammatory effects by inhibiting the JAK2/STAT3 and NF-κB signaling pathways.

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Chrysoeriol
Cas No.: 491-71-4
10mM (in 1mL DMSO)In Stock
$106.00
1
1mgIn Stock
$40.00
1
5mgIn Stock
$96.00
1
10mgIn Stock
$152.00
1
25mgIn Stock
$256.00
1
50mgIn Stock
$388.00
1

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    183(7):1867-1883 (2020)
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Description

Chrysoeriol is a natural flavonoid found in Coronopus didymus that exerts anti-inflammatory effects by inhibiting the JAK2/STAT3 and NF-κB signaling pathways[1,2]. Chrysoeriol possesses potent antioxidant, anti-inflammatory, and anticancer activities and is commonly used in the treatment and research of acute skin inflammation, diabetes, and cardiovascular diseases[3,4].

In vitro, SH-SY5Y cells were pretreated with Chrysoeriol (5, 10, and 20μM) for 4h, followed by co-incubation with 1mM 1-methyl-4-phenylpyridinium iodide (MPP+) for an additional 24h. Chrysoeriol dose-dependently attenuated MPP+-induced cell death, with 20μM Chrysoeriol significantly increasing cell survival from 50% to approximately 90%[5]. ARPE-19 cells were pretreated with Chrysoeriol (2.5 and 5μM) for 2h, followed by co-incubation with H2O2 (500μM) for an additional 24h. Chrysoeriol pretreatment significantly upregulated the mRNA expression of the mitochondrial transcription factor TFAM and the DNA polymerase subunit gamma-1 (POLG)[6].

In vivo, Chrysoeriol (20mg/kg) was orally administered to streptozotocin (STZ)-induced diabetic rats for 45 days, which significantly reduced the elevated serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST), bringing them back to near-normal levels[7].

References:
[1] PRABHAKAR K R, SRINIVASAN K K, RAO P G M. Chemical investigation, anti-inflammatory and wound healing properties of Coronopus didymus[J]. Pharmaceutical Biology, 2002, 40(7): 490-493.
[2] WU J Y, CHEN Y J, BAI L, et al. Chrysoeriol ameliorates TPA-induced acute skin inflammation in mice and inhibits NF-κB and STAT3 pathways[J]. Phytomedicine, 2020, 68: 153173.
[3] ABOULAGHRAS S, SAHIB N, BAKRIM S, et al. Health benefits and pharmacological aspects of chrysoeriol[J]. Pharmaceuticals, 2022, 15(8): 973.
[4] CHA B Y, SHI W L, YONEZAWA T, et al. An inhibitory effect of chrysoeriol on platelet-derived growth factor (PDGF)-induced proliferation and PDGF receptor signaling in human aortic smooth muscle cells[J]. Journal of Pharmacological Sciences, 2009, 110(1): 105-110.
[5] LIMBOONREUNG T, TUCHINDA P, CHONGTHAMMAKUN S. Chrysoeriol mediates mitochondrial protection via PI3K/Akt pathway in MPP⁺ treated SH-SY5Y cells[J]. Neuroscience Letters, 2020, 714: 134545.
[6] KIM M H, KWON S Y, WOO S Y, et al. Antioxidative effects of chrysoeriol via activation of the Nrf2 signaling pathway and modulation of mitochondrial function[J]. Molecules, 2021, 26(2): 313.
[7] KRISHNAN B, PUGALENDI K V, SARAVANAN R. Ameliorative potential of Chrysoeriol, a bioactive flavonoid on oxidative stress and hepatic marker enzymes in STZ induced diabetic rats[J]. Asian Journal of Pharmacy and Pharmacology, 2019, 5(3): 614-624.

Protocol

Cell experiment [1]:

Cell lines

SH-SY5Y cells

Preparation Method

SH-SY5Y cells were pre-treated with different doses of Chrysoeriol for 4h followed by 1mM MPP+ for 24h, and then subjected to MTT assay for cell viability measurement.

Reaction Conditions

5, 10, and 20μM; 4h

Applications

MPP+-reduced cell viability was partially but significantly attenuated by the treatment of cells with Chrysoeriol in a concentration-dependent manner. Chrysoeriol at the concentration of 20µM significantly reduced the MPP+-induced cell death, and improved the percentage of survival cells from 50% to 90%.
Animal experiment [2]:

Animal models

STZ-induced diabetic rats

Preparation Method

STZ-induced diabetic rats (plasma glucose > 255mg/dl) were orally administered Chrysoeriol (20mg/kg) for 45 days, then serum ALT and AST levels were measured using the Reitman and Frankel method.

Dosage form

20mg/kg; 45 days; p.o.

Applications

Treatment with Chrysoeriol significantly reduced elevated ALT and AST levels in serum, restoring them to near-normal levels.

References:
[1] LIMBOONREUNG T, TUCHINDA P, CHONGTHAMMAKUN S. Chrysoeriol mediates mitochondrial protection via PI3K/Akt pathway in MPP⁺ treated SH-SY5Y cells[J]. Neuroscience Letters, 2020, 714: 134545.
[2] KRISHNAN B, PUGALENDI K V, SARAVANAN R. Ameliorative potential of Chrysoeriol, a bioactive flavonoid on oxidative stress and hepatic marker enzymes in STZ induced diabetic rats[J]. Asian Journal of Pharmacy and Pharmacology, 2019, 5(3): 614-624.

Product Documents

Purity:>98.00%Appearance:A solid

Chemical Properties

CAS No.
491-71-4
Synonyms
3'-methoxy Apigenin, Luteolin 3'-methyl ether
SMILES
O=C1C=C(C2=CC=C(O)C(OC)=C2)OC3=CC(O)=CC(O)=C13
Molecular Formula
C16H12O6
Molecular Weight
300.26
Solubility
DMSO : 100 mg/mL (333.04 mM; Need ultrasonic)
Storage
Store at 2-8°C,protect from light
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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