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Chemical Structure
Chemical Structure
Chemical Structure

Ellagic acid [476-66-4]

Research Use Only
CDX-E0232
Chemodex
CAS Number476-66-4
Product group Chemicals
Estimated Purity>95%
Molecular Weight302.19
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    Ellagic acid [476-66-4]
  • Delivery Days Customer
    10
  • CAS Number
    476-66-4
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Molecular Formula
    C14H6O8
  • Molecular Weight
    302.19
  • Scientific Description
    Chemical. CAS: 476-66-4. Formula: C14H6O8. MW: 302.19. Ellagic acid is a polyphenolic antioxidant that is abundant in many fruits, vegetables, plant bark and peels. It has antioxidant, anticancer, neuroprotective, antimutagenic, anti-inflammatory and organ-preserving properties. It alters cytochrome P450 activity and improvea metabolism and clearance of xenobiotics, as well as altera immune function. Selective, ATP-competitive inhibitor of casein kinase 2 (CK2). Ellagic acid also blocks methylation of arginine 17 of histone 3 (H3R17) by coactivator-associated arginine methyltransferase 1 (CARM1) without significantly altering histone acetylase or DNA methyltransferase activity. It acts as a scavenger of oxygen species produced by hydrogen peroxide treatment and as a protector of the DNA double helix from alkylating agent injury. Also reported to inhibit topoisomerases I and II and gyrase and glutathione S-transferase. - Ellagic acid is a polyphenolic antioxidant that is abundant in many fruits, vegetables, plant bark and peels. It has antioxidant, anticancer, neuroprotective, antimutagenic, anti-inflammatory and organ-preserving properties. It alters cytochrome P450 activity and improvea metabolism and clearance of xenobiotics, as well as altera immune function. Selective, ATP-competitive inhibitor of casein kinase 2 (CK2). Ellagic acid also blocks methylation of arginine 17 of histone 3 (H3R17) by coactivator-associated arginine methyltransferase 1 (CARM1) without significantly altering histone acetylase or DNA methyltransferase activity. It acts as a scavenger of oxygen species produced by hydrogen peroxide treatment and as a protector of the DNA double helix from alkylating agent injury. Also reported to inhibit topoisomerases I and II and gyrase and glutathione S-transferase.
  • SMILES
    OC1=CC2=C3C(OC(C4=C3C(OC2=O)=C(O)C(O)=C4)=O)=C1O
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352200