Ellagic acid (Standard)

cas: 476-66-4 — see every product listed under this CAS number, including other names

Ellagic acid (Standard) (CAS 476-66-4) is a chemical reagent available from Chemat. Available pack sizes: 50 mg, 10 mg, 25 mg. Offered by: MedChemExpress.

brandMedChemExpress
catalog numberHY-B0183R-50 mg
cas476-66-4
size50 mg
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Available pack sizes

brand size price
MedChemExpress 50 mg 598.33 Pln
MedChemExpress 10 mg 291.83 Pln
MedChemExpress 25 mg 435.79 Pln

properties

delivery time over 3 weeks
purityno data
Structural formula: {0} (CAS {1})

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 EC 2.7.7.7 (DNA-directed DNA polymerase) inhibitor, a geroprotector, an antioxidant, 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, a food additive, an EC 2.5.1.18 (glutathione transferase) inhibitor, a plant metabolite, a fungal metabolite, an EC 2.3.1.5 (arylamine N-acetyltransferase) inhibitor, an EC 2.4.1.1 (glycogen phosphorylase) 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 and a skin lightening agent. It is a lactone, a polyphenol, a member of catechols, an organic heterotetracyclic compound and a cyclic ketone. It is functionally related to a gallic acid. It is a conjugate acid of an ellagic acid(2-).

Source: ChEBI

Identity
Molecular formulaC14H6O8
Molecular weight302.19 g/mol
IUPAC name6,7,13,14-tetrahydroxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione
InChIKeyAFSDNFLWKVMVRB-UHFFFAOYSA-N
SMILESC1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O

Computed by PubChem (NCBI)

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