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ProductsBack/(+/-)-Naringenin [67604-48-2]
Chemical Structure
Chemical Structure
Chemical Structure

(+/-)-Naringenin [67604-48-2]

Research Use Only
CDX-N0206
Chemodex
CAS Number67604-48-2
DownloadDatasheet
Product group Chemicals
Estimated Purity>98%
Molecular Weight272.25
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Overview

  • Supplier
    Chemodex
  • Product Name
    (+/-)-Naringenin [67604-48-2]
  • Delivery Days Customer
    10
  • CAS Number
    67604-48-2
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Hazard Information
    Warning
  • Molecular Formula
    C15H12O5
  • Molecular Weight
    272.25
  • Scientific Description
    Chemical. CAS: 67604-48-2. Formula: C15H12O5. MW: 272.25. Naringenin is a citrus-derived flavonoid that inhibits CYP3A4 activity in human liver microsomes. It has a broad panel of properties, including antibacterial, antiviral, antifungal, anti-inflammatory, antioxidant, anticancer, antidiabetic, cardioprotective and neuroprotective activities. Naringenin activity is primarily attributed to its anti-inflammatory (via inhibiting recruitment of cytokines and inflammatory transcription factors) and antioxidant (via scavenging of free radicals, bolstering of endogenous antioxidant defense system and metal ion chelation) effects. Naringenin exerts its anti-diabetic effects by inhibition of gluconeogenesis through upregulations of AMPK, leading to its lipid lowering and insulin-like properties. - Naringenin is a citrus-derived flavonoid that inhibits CYP3A4 activity in human liver microsomes. It has a broad panel of properties, including antibacterial, antiviral, antifungal, anti-inflammatory, antioxidant, anticancer, antidiabetic, cardioprotective and neuroprotective activities. Naringenin activity is primarily attributed to its anti-inflammatory (via inhibiting recruitment of cytokines and inflammatory transcription factors) and antioxidant (via scavenging of free radicals, bolstering of endogenous antioxidant defense system and metal ion chelation) effects. Naringenin exerts its anti-diabetic effects by inhibition of gluconeogenesis through upregulations of AMPK, leading to its lipid lowering and insulin-like properties.
  • SMILES
    OC1=CC(O)=C2C(OC(C3=CC=C(O)C=C3)CC2=O)=C1
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352200