15-Dicaffeoylquinic acid

CAS No. 30964-13-7

15-Dicaffeoylquinic acid( Cynarine )

Catalog No. M20177 CAS No. 30964-13-7

15-Dicaffeoylquinic acid has neuroprotective and antioxidant effects it can inhibition of GSK3β as well as the modulation of Bcl-2/Bax.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 47 In Stock
5MG 61 In Stock
10MG 102 In Stock
25MG 192 In Stock
50MG 290 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
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Biological Information

  • Product Name
    15-Dicaffeoylquinic acid
  • Note
    Research use only, not for human use.
  • Brief Description
    15-Dicaffeoylquinic acid has neuroprotective and antioxidant effects it can inhibition of GSK3β as well as the modulation of Bcl-2/Bax.
  • Description
    15-Dicaffeoylquinic acid has neuroprotective and antioxidant effects it can inhibition of GSK3β as well as the modulation of Bcl-2/Bax.(In Vitro):Cynarin inhibits taste receptors, making water to be sweet. It has been shown to have some pharmacological properties including hypocholesterolemic, hepatoprotective, antiviral, antibacterial, and antihistamic effects. Cynarin has marked antioxidant, anticholinergic, reducing ability, radical-scavenging, and metal-binding activities. Cynarin demonstrates 87.72% inhibition of linoleic acid lipid peroxidation at 30 mg/mL concentration. Cynarin exhibits effective DMPD+, ABTS+, O2-, DPPH1, and H2O2 scavenging effects, reducing capabilities and Fe2+ chelating effects. IC50 and Ki of cynarin for acetylcholinesterase enzyme inhibition are 243.67nM and 39.34±13.88 nM, respectively. Cynarin is a potential immunosuppressant that blocks the interaction between the CD28 of T-cell receptor and CD80 of antigen presenting cells. Cynarin blocks about 87% of the CD28-dependent "signal 2" pathway of T-cell activation under the condition of one to one ratio of T-cell and B-cell. Cynarin binds to the "G-pocket" of CD28 and thus interrupts the site of interaction between CD28 and CD80.
  • In Vitro
    Cynarin inhibits taste receptors, making water to be sweet. It has been shown to have some pharmacological properties including hypocholesterolemic, hepatoprotective, antiviral, antibacterial, and antihistamic effects. Cynarin has marked antioxidant, anticholinergic, reducing ability, radical-scavenging, and metal-binding activities. Cynarin demonstrates 87.72% inhibition of linoleic acid lipid peroxidation at 30 mg/mL concentration. Cynarin exhibits effective DMPD+, ABTS+, O2-, DPPH1, and H2O2 scavenging effects, reducing capabilities and Fe2+ chelating effects. IC50 and Ki of cynarin for acetylcholinesterase enzyme inhibition are 243.67nM and 39.34±13.88 nM, respectively. Cynarin is a potential immunosuppressant that blocks the interaction between the CD28 of T-cell receptor and CD80 of antigen presenting cells. Cynarin blocks about 87% of the CD28-dependent "signal 2" pathway of T-cell activation under the condition of one to one ratio of T-cell and B-cell. Cynarin binds to the "G-pocket" of CD28 and thus interrupts the site of interaction between CD28 and CD80.
  • In Vivo
    ——
  • Synonyms
    Cynarine
  • Pathway
    Immunology/Inflammation
  • Target
    Antiviral
  • Recptor
    Antiviral|Antioxidant
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    30964-13-7
  • Formula Weight
    516.45
  • Molecular Formula
    C25H24O12
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:23 mg/mL?(44.53 mM)
  • SMILES
    O[C@@H]1C[C@](C[C@@H](OC(=O)\C=C\c2ccc(O)c(O)c2)[C@H]1O)(OC(=O)\C=C\c1ccc(O)c(O)c1)C(O)=O
  • Chemical Name
    (1R3R4S5R)-13-Bis[[3-(34-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-45-dihydroxycyclohexanecarboxylic acid

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Cao X et al. 1 5-Dicaffeoylquinic acid-mediated glutathione synthesis through activation of Nrf2 protects against OGD/reperfusion-induced oxidative stress in astrocytes.Brain Res. 2010 Aug 6;1347:142-8
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