• Product NamePomegranate Extract Ellagic acid
  • CasNo. 476-66-4
  • MFC14H6O8
  • MW302.197
  • Purity
  • Appearancecream to light yellow crystalline solid
  • Packing
  • Contact usInquiry

Product Details

CasNo: 476-66-4

MF: C14H6O8

Appearance: cream to light yellow crystalline solid

Factory Export Top Purity Pomegranate Extract Ellagic acid 476-66-4 In Stock

  • Molecular Formula:C14H6O8
  • Molecular Weight:302.197
  • Appearance/Colour:cream to light yellow crystalline solid 
  • Vapor Pressure:2.32E-26mmHg at 25°C 
  • Melting Point:≥350 °C 
  • Refractive Index:1.894 
  • Boiling Point:796.5 °C at 760 mmHg 
  • Flash Point:310.1 °C 
  • PSA:141.34000 
  • Density:2.066 g/cm3 
  • LogP:1.31280 

Ellagic acid(Cas 476-66-4) Usage

Application

Ellagic acid is used in medicine and cosmetics, as an antioxidant, and has anti-cancer and anti-viral effects.Ellagic acid, a common plant polyphenol, is an inhibitor of glutathione S-transferase with Exhibits antitumor activity. It can be used for the determination of factor XIIa in plasma. Contact activation can occur in blood coagulation. It is also used as selective, ATP-competitive inhibitor of casein kinase 2 and a Topo I and II, FGR, GSK, and PKA inhibitor.

Definition

ChEBI: Ellagic acid is an organic heterotetracyclic compound resulting from the formal dimerisation of gallic acid by oxidative aromatic coupling with intramolecular lactonisation of both carboxylic acid groups of the resulting biaryl. It is found in many fruits and vegetables, including raspberries, strawberries, cranberries, and pomegranates. It has a role as an antioxidant, a food additive, a plant metabolite, an EC 5.99.1.2 (DNA topoisomerase) inhibitor, an EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor, an EC 1.14.18.1 (tyrosinase) inhibitor, an EC 2.3.1.5 (arylamine N-acetyltransferase) inhibitor, an EC 2.4.1.1 (glycogen phosphorylase) inhibitor, an EC 2.5.1.18 (glutathione transferase) inhibitor, an EC 2.7.1.127 (inositol-trisphosphate 3-kinase) inhibitor, an EC 2.7.1.151 (inositol-polyphosphate multikinase) inhibitor, an EC 2.7.4.6 (nucleoside-diphosphate kinase) inhibitor, a skin lightening agent, a fungal metabolite, an EC 2.7.7.7 (DNA-directed DNA polymerase) inhibitor and a geroprotector. It is an organic heterotetracyclic compound, a cyclic ketone, a lactone, a member of catechols and a polyphenol. It is functionally related to a gallic acid.

Preparation

Ellagic acid is mainly extracted from plants, and it is present in several fruits such as cranberries, strawberries, raspberries, and pomegranates. Usually, the raw materials are degreasing and then extracted with an alkaline aqueous solution or extracted with ethanol. Then, after removing water-soluble proteins and gliadins, the sugar ligands can be decomposed by enzymes to obtain purer ellagic acid.

General Description

Cream-colored needles (from pyridine) or yellow powder. Odorless.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Ellagic acid reacts as a weak acid. Incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated. Heat is also generated by the acid-base reaction between phenols and bases. May be sulfonated exothermically very readily (for example, by concentrated sulfuric acid at room temperature). May be nitrated very rapidly, even by dilute nitric acid.

Fire Hazard

Flash point data for Ellagic acid are not available; however, Ellagic acid is probably combustible.

Biological Activity

Selective, ATP-competitive inhibitor of casein kinase 2 (CK2) (IC 50 values are 40, 2900, 3500, 4300 and 9400 nM for CK2, Lyn, PKA, Syk? and FGR respectively). Exhibits antioxidant, antitumor and anticarcinogenic activity and also inhibits glutathione S-transferase.

Biochem/physiol Actions

Commonly occurring plant polyphenol, inhibitor of glutathione S-transferase. Used for the assay of factor XIIa in plasma. Contact activation in blood coagulation.

Anticancer Research

Ellagic acid is a naturally occurring phenolic constituent present in natural productsand nuts, most elevated amounts of which are found in raspberries (Daniel et al.1990). EA is considered as a potent anticarcinogenic and antimutagenic compound.EA shows anti-angiogenic property by repressing PDGF-R movement and phosphorylationof its substrate. It can intrude with endothelial cell-associated VEGR-2phosphorylation bringing about the restraint of the downstream signaling activatedby this receptor and in the hindrance of two key events fundamental in angiogenesis,i.e., EC movement and morphogenic separation into capillary-like structure. In parallel,EA indicated robust inhibitory activity against perivascular cells through itsrestraint of PDGF-R action and signaling prompting hindrance of VSMC relocation(Labrecque et al. 2005).It is a phenolic compound extracted from pomegranate. It is an antiproliferative andantioxidant compound (Murakami et al. 1996). It induces apoptosis in cancer cellsof the prostate and breast and prevents the process of metastasis in different cancers(Singh et al. 2016b).

Purification Methods

This antioxidant crystallises from pyridine. It forms a dark green solution in aqueous N NaOH. The tetraactetate dilactone crystallises from Ac2O, with m 340o. [Beilstein 19 H 261, 19 III/IV 3164, 19/7 V 108.]

InChI:InChI=1/C14H6O8/c15-5-1-3-7-8-4(14(20)22-11(7)9(5)17)2-6(16)10(18)12(8)21-13(3)19/h1-2,15-18H

476-66-4 Relevant articles

Stability and oxidation products of hydrolysable tannins in basic conditions detected by HPLC/DAD-ESI/QTOF/MS

Tuominen, Anu,Sundman, Terhi

, p. 424 - 435 (2013)

Introduction Hydrolysable tannins occur ...

The biomimetic synthesis of balsaminone A and ellagic acid via oxidative dimerization

Daley, Sharna-Kay,Downer-Riley, Nadale

, p. 2026 - 2031 (2020)

The application of oxidative dimerizatio...

Sono-transformation of tannic acid into biofunctional ellagic acid micro/nanocrystals with distinct morphologies

Bhangu, Sukhvir Kaur,Singla, Ritu,Colombo, Enrico,Ashokkumar, Muthupandian,Cavalieri, Francesca

, p. 816 - 821 (2018)

A sustainable, reagent-less and one-pot ...

-

Nierenstein,Spiers,Hatcher

, p. 846 (1925)

-

Rhoipteleanins A and E, Dimeric Ellagitannins formed by Intermolecular C-C Oxidative Coupling from Rhoiptelea chiliantha

Jiang, Zhi-Hong,Tanaka, Takashi,Kouno, Isao

, p. 1467 - 1468 (1995)

The first dimeric ellagitannins, rhoipte...

Isoterchebulin and 4,6-O-isoterchebuloyl-D-glucose, novel hydrolyzable tannins from Terminalia macroptera

Conrad,Vogler,Reeb,Klaiber,Papajewski,Roos,Vasquez,Setzer,Kraus

, p. 294 - 299 (2001)

Two new hydrolyzable tannins, isotercheb...

Ellagic acid formation from galloylglucoses by a crude enzyme of Cornus capitata adventitious roots

Tanaka, Norie,Shimomura, Koichiro,Ishimaru, Kanji

, p. 1869 - 1871 (2001)

The aqueous extract of acetone powder, w...

New Ellagic Acid Glycosides from Punica granatum

Olennikov,Kashchenko,Vennos

, p. 878 - 882 (2019)

Two new ellagic acid glycosides were iso...

Ellagitannins and oligomeric proanthocyanidins of three polygonaceous plants

Huang, Yong-Lin,Jiang, Zhi-Hong,Kitaoka, Masako,Li, Dian-Peng,Li, Yun-Qiu,Matsuo, Yosuke,Nonaka, Gen-Ichiro,Saito, Yoshinori,Takayoshi, Juri,Tanaka, Takashi,Wang, Ya-Feng

, (2021/06/28)

The aim of this study was to characteriz...

Synthetic Ellagic Acid Glycosides Inhibit Early Stage Adhesion of Streptococcus agalactiae Biofilms as Observed by Scanning Electron Microscopy

Chambers, Schuyler A.,Gaddy, Jennifer A.,Townsend, Steven D.

, p. 9923 - 9928 (2020/04/28)

Ellagic acid derivatives possess antimic...

Production of ellagitannin hexahydroxydiphenoyl ester by spontaneous reduction of dehydrohexa-hydroxydiphenoyl ester

Era, Manami,Matsuo, Yosuke,Saito, Yoshinori,Tanaka, Takashi

, (2020/03/17)

Amariin is an ellagitannin with two dehy...

476-66-4 Process route

5-O-galloyl-3,4-(S)-hexahydroxydiphenoyl proto-quercitol
91432-03-0

5-O-galloyl-3,4-(S)-hexahydroxydiphenoyl proto-quercitol

(+)-proto-quercitol
488-73-3

(+)-proto-quercitol

3,4,5-trihydroxybenzoic acid
149-91-7

3,4,5-trihydroxybenzoic acid

ellagic acid
476-66-4

ellagic acid

Conditions
Conditions Yield
With sulfuric acid; at 90 ℃; for 12h;
 
1,5-di-O-galloyl-3,4-(S)-hexahydroxydiphenoyl proto-quercitol
91432-02-9,91686-11-2,107794-85-4

1,5-di-O-galloyl-3,4-(S)-hexahydroxydiphenoyl proto-quercitol

(+)-proto-quercitol
488-73-3

(+)-proto-quercitol

3,4,5-trihydroxybenzoic acid
149-91-7

3,4,5-trihydroxybenzoic acid

ellagic acid
476-66-4

ellagic acid

Conditions
Conditions Yield
With sulfuric acid; at 90 ℃; for 12h;
 

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