[CAS NO. 4143-62-8]  3',4'-Dimethoxyflavone

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PRODUCTS SPECIFICATIONS [4143-62-8]

Distributor
Catalog
AS522595
Brand
Arctom Scientific
CAS
4143-62-8

DESCRIPTION [4143-62-8]

Overview

MDLMFCD00143009
Molecular Weight282.29
Molecular FormulaC17H14O4
SMILESO=C1C=C(C2=CC=C(OC)C(OC)=C2)OC3=CC=CC=C13

For research use only. We do not sell to patients.

Summary

3',4'-Dimethoxyflavone is a lipophilic flavone, can be isolated from the leaves of Primula veris . 3',4'-Dimethoxyflavone can reduce the synthesis and accumulation of PARP and protect cortical neurones against cell death induced by Parthanatos. 3',4'-Dimethoxyflavone is also an aryl hydrocarbon receptor antagonist in human breast cancer cells. 3',4'-Dimethoxyflavone can promote the proliferation of human hematopoietic stem cells. 3',4'-Dimethoxyflavone has various biological activities, including antioxidant, anti-cancer, anti-inflammatory, anti-atherogenic, hypolipidaemic, and neuroprotective or neurotrophic effects [1] [2] [3] [4] .


IC50 & Target

PARP, Aryl hydrocarbon receptor [1]


In Vitro

3',4'-Dimethoxyflavone (10 and 20 μM) has protection against the reduction in SH-SY5Y viability induced by Methylnitronitrosoguanidine (MNNG) (HY-128612) [2] .
3',4'-Dimethoxyflavone (6.25-25 μM) decreases the levels of PAR induced by MNNG in HeLa cells [2] .
3',4'-Dimethoxyflavone (12.5, 25, 50 and 100 μM; 15-20 h) reduces cortical neuronal death induced by exposure to NMDA (HY-17551) [2] .
3',4'-Dimethoxyflavone (0.1-10 μM; 24 h) exhibits significant inhibition of 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD)-induced EROD activity in MCF-7 and T47D cells [3] .
3',4'-Dimethoxyflavone inhibits AhR-dependent CYP1A1 induction and AhR-mediated inhibition of estrogen-induced gene expression in T47D and MCF-7 breast cancer cells [3] .
3′,4′-Dimethoxyflavone (2.5 μM; 7 days) promotes the proliferation of human hematopoietic stem cells [4] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay [2]

Cell Line: Primary cortical neurones (isolated from fetal CD1 mice, incubated with NMDA)
Concentration: 12.5, 25, 50 and 100 μM
Incubation Time: 15-20 h
Result: Reduced concentration-dependently neuronal death induced by exposure to NMDA.

Cell Proliferation Assay [4]

Cell Line: CD 34+ cells
Concentration: 2.5 μM
Incubation Time: 7 days
Result: Induced a significantly higher amplification of the CD 34+ population under normoxia.

Appearance

Solid



Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month

Solvent & Solubility

In Vitro:

DMSO : ≥ 50 mg/mL ( 177.12 mM )

* "≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.5425 mL 17.7123 mL 35.4246 mL
5 mM 0.7085 mL 3.5425 mL 7.0849 mL
10 mM 0.3542 mL 1.7712 mL 3.5425 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: 10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline

    Solubility: ≥ 2.5 mg/mL (8.86 mM); Clear solution

  • 2.

    Add each solvent one by one: 10% DMSO >> 90% corn oil

    Solubility: ≥ 2.5 mg/mL (8.86 mM); Clear solution

* All of the co-solvents are available by MCE.


Synonyms

4H-1-Benzopyran-4-one, 2-(3,4-dimethoxyphenyl)-
Flavone, 3′,4′-dimethoxy-
2-(3,4-Dimethoxyphenyl)-4H-1-benzopyran-4-one
3′,4′-Dimethoxyflavone
2-(3,4-Dimethoxyphenyl)-4H-chromen-4-one
2-(3,4-Dimethoxyphenyl)chromen-4-one