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Octahydrocurcumin

CAS No. 36062-07-4

Octahydrocurcumin( —— )

Catalog No. M24320 CAS No. 36062-07-4

Octahydrocurcumin has antioxidant and and anti-inflammatory activities, it can inhibit the lipopolysaccharide (LPS)-induced inflammatory response via the mechanism of inhibiting NF-kB translocation to the nucleus.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 103 In Stock
5MG 93 In Stock
10MG 150 In Stock
25MG 275 In Stock
50MG 403 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock
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Biological Information

  • Product Name
    Octahydrocurcumin
  • Note
    Research use only, not for human use.
  • Brief Description
    Octahydrocurcumin has antioxidant and and anti-inflammatory activities, it can inhibit the lipopolysaccharide (LPS)-induced inflammatory response via the mechanism of inhibiting NF-kB translocation to the nucleus.
  • Description
    Octahydrocurcumin has antioxidant and and anti-inflammatory activities, it can inhibit the lipopolysaccharide (LPS)-induced inflammatory response via the mechanism of inhibiting NF-kB translocation to the nucleus. Octahydrocurcumin exhibits potent cytotoxic effect (IC50 =19.46 ug/mL) and shows high antimicrobial activity.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Microbiology/Virology
  • Target
    Antifection
  • Recptor
    Anti-infection|NF-κB|ROS
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    36062-07-4
  • Formula Weight
    376.44
  • Molecular Formula
    C21H28O6
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:100 mg/mL (265.65 mM; Need ultrasonic);Ethanol:10 mg/mL (26.56 mM; Need ultrasonic)
  • SMILES
    COc(cc(CCC(CC(CCc(cc1)cc(OC)c1O)O)O)cc1)c1O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Different Curcuminoids Inhibit T-Lymphocyte Proliferation Independently of Their Radical Scavenging Activities. Pharmaceutical Research,2008, 25,(8):1822-7.
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