[CAS NO. 476-66-4]  Ellagicacid

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PRODUCTS SPECIFICATIONS [476-66-4]

Distributor
Catalog
HY-B0183
Brand
MCE
CAS
476-66-4

DESCRIPTION [476-66-4]

Overview

MDLMFCD00006914
Molecular Weight302.19
Molecular FormulaC14H6O8
SMILESO=C1C2=CC(O)=C(O)C(O3)=C2C4=C(C3=O)C=C(O)C(O)=C4O1

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


Summary

Ellagic acid is a natural antioxidant, and acts as a potent and ATP-competitive CK2 inhibitor, with an IC 50 of 40 nM and a K i of 20 nM.


IC50 & Target

CK2

40 nM (IC 50 )


In Vitro

Ellagic acid is a potent CK2 inhibitor, with an IC 50 of 40 nM and a K i of 20 nM. Ellagic acid also blocks other kinases such as LYN, PKA, SYK, GSK3, FGR and CK1, with IC 50 s of 2.9, 3.5, 4.3, 7.5, 9.4 and 13.0 μM, respectively, and shows no obvious effects on DYRK1a, CSK, NPM-ALK, RET and FLT3 (IC 50 s > 40 μM). Ellagic acid (5-100 μM) shows inhibitory activities against Karpas299, SUDHL1, SR786, and FE-PD cell lines [1] . Ellagic acid (10 μM) exhibits cytotoxic effects on MCF-7 cells after treatment of radiation. Ellagic acid (10 μM) in combination with Irradiation (IR) significantly abridges the capacity of MCF-7 cells to form colonies equated with individual treatments. Ellagic acid with IR also induces cell apoptosis, and facilitates the upregulation of pro-apopttotic Bax and downregulation of Bcl-2 in MCF-7 cells [3] .

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


In Vivo

Ellagic acid (EA; 10 mg/kg/day; p.o., 14 days) strongly decreases MDA brain content by 17%, and reduces the levels of brain TNF-α by 42% in rats. Ellagic acid markedly increases the reduced brain contents of 5-HT (39%), dopamine (DA, 71%), and norepinephrine (NE, 77%). Ellagic acid (10 mg/kg, p.o., 14 days) causes decreased histopathological changes induced by Doxorubicin in rats [2] .

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


Clinical Trial

NCT Number Sponsor Condition Start Date Phase
NCT03713164 University of California, Los Angeles
Healthy
February 22, 2018 Not Applicable
NCT02263378 University of Messina
HPV Infection
September 2014 Not Applicable
NCT04011618 University of Guadalajara|National Council of Science and Technology, Mexico
Metabolic Syndrome
September 17, 2019 Phase 2

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 : ≥ 2.5 mg/mL ( 8.27 mM )

Ethanol : < 1 mg/mL (insoluble)

H 2 O : < 0.1 mg/mL (insoluble)

* "≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.3092 mL 16.5459 mL 33.0918 mL
5 mM 0.6618 mL 3.3092 mL 6.6184 mL
10 mM --- --- ---
* Please refer to the solubility information to select the appropriate solvent.


Synonyms

[1]Benzopyrano[5,4,3-cde][1]benzopyran-5,10-dione, 2,3,7,8-tetrahydroxy-
2,3,7,8-Tetrahydroxy[1]benzopyrano[5,4,3-cde][1]benzopyran-5,10-dione
C.I. 55005
C.I. 75270
Alizarine Yellow
Benzoaric acid
Ellagic acid
Gallogen (astringent)
[1,1′-Biphenyl]-2,2′-dicarboxylic acid, 4,4′,5,5′,6,6′-hexahydroxy-, di-δ-lactone
Eleagic acid
Gallogen
Elagostasine
Lagistase
Alizarin yellow
G 91006
LDN 0097519
Ellagic acid LT
2,3,7,8-Tetrahydroxy-chromeno[5,4,3-cde]chromene-5,10-dione