Ellagic acid

Ellagic acid Basic information
Product Name:Ellagic acid
Synonyms:gallogen(astringent);lagistase;TIMTEC-BB SBB006501;2,3,7,8-tetrahydroxy(1)benzopyrano(5,4,3-cde)(1)benzopyran-5,10-dione;ELLAGIC ACID;BENZOARIC ACID;AKOS NCG1-0028;4,4',5,5',6,6'-HEXAHYDROXYDIPHENIC ACID 2,6,2',6'-DILACTONE
CAS:476-66-4
MF:C14H6O8
MW:302.19
EINECS:207-508-3
Product Categories:Anthraquinones, Hydroquinones and Quinones;Natural Plant Extract;Antioxidant;Biochemistry;plant extract;Inhibitors;Building block;Herb extract;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Food additive;Plant extracts;476-66-4
Mol File:476-66-4.mol
Ellagic acid Structure
Ellagic acid Chemical Properties
Melting point ≥350 °C
Boiling point 363.24°C (rough estimate)
density 1.667
refractive index 1.5800 (estimate)
storage temp. 2-8°C
solubility 1 M NaOH: 10 mg/mL, dark green
form powder
pka5.02±0.20(Predicted)
color tan to gray
Water Solubility <0.1 g/100 mL at 21 ºC
Sensitive Air & Light Sensitive
Merck 14,3547
BRN 47549
Stability:Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKeyAFSDNFLWKVMVRB-UHFFFAOYSA-N
LogP0.239 (est)
CAS DataBase Reference476-66-4(CAS DataBase Reference)
EPA Substance Registry SystemEllagic acid (476-66-4)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-36/37
WGK Germany 3
RTECS DJ2620000
8-10-23
HS Code 29322090
Hazardous Substances Data476-66-4(Hazardous Substances Data)
ToxicityLD50 oral in rat: > 20gm/kg
MSDS Information
Ellagic acid Usage And Synthesis
Chemical Propertiescream to light yellow crystalline solid, soluble in methanol, ethanol, DMSO and other organic solvents, derived from Mangiferaindica, Eucalyptuscitriodora, Lythrumsalicaria, Geranium sibiricum, Agrimoniapilosavar.japonica.
UsesEllagic Acid is a phenol antioxidant found naturally in various fruits and vegetables. Ellagic Acid was shown to exhibit high levels of hemostatic, antineoplastic, antimutagenic, antiproliferative and antioxidant properties in studies, which suggests its potential health benefits following ellagic acid consumption.
ApplicationEllagic 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.
DefinitionChEBI: 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.
PreparationEllagic 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 DescriptionCream-colored needles (from pyridine) or yellow powder. Odorless.
Air & Water ReactionsInsoluble in water.
Reactivity ProfileEllagic 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 HazardFlash point data for Ellagic acid are not available; however, Ellagic acid is probably combustible.
Biological ActivitySelective, 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 ActionsCommonly occurring plant polyphenol, inhibitor of glutathione S-transferase. Used for the assay of factor XIIa in plasma. Contact activation in blood coagulation.
Anticancer ResearchEllagic 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).
storageRoom temperature
Purification MethodsThis 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.]
Ellagic acid Preparation Products And Raw materials
Preparation ProductsL-Arabinose-->alpha-L-Rhamnose
FructussSophoraeExtract PomegranateP.E. ELLAGIC ACID(P) RED RASPBERRY PLANT EXTRACT ELLAGIC ACID 20% BY HPLC ELLAGIC ACID HYDRATE TECH. ELLAGIC ACID DIHYDRATE,ELLAGIC ACID HYDRATE Ethyl 2-(Chlorosulfonyl)acetate Ascoric Acid 3,3'-di-O-methylellagic acid Centchroman Punicalagin Pomegranate Extract Ellagic acid 40% HPLC 3’-O-Methyl-ellagic acid-4- O-β-D-xylopyranoside punicalin DIELLAGILACTONE ellagic acid 3,3'-dimethylether ELLAGIC ACID(PRIMARY STANDARD) ELLAGIC ACID(REAGENT / STANDARD GRADE)

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