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Chemical Structure
Chemical Structure
Chemical Structure

Andrographolide [5508-58-7]

Research Use Only
CDX-A0576
Chemodex
CAS Number5508-58-7
Product group Chemicals
Estimated Purity>98%
Molecular Weight350.455
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    Andrographolide [5508-58-7]
  • Delivery Days Customer
    10
  • CAS Number
    5508-58-7
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Hazard Information
    Non-hazardous,Warning
  • Molecular Formula
    C20H30O5
  • Molecular Weight
    350.455
  • Scientific Description
    Andrographolide, a bioactive diterpene lactone, is the main constituent of Andrographis paniculata, a plant used in traditional medicines. It is known to have different biological properties such as anti-inflammatory, immunosuppressive, antidiabetic, antihyperglycemic, antibacterial, antioxidant, antinoniceptive, antimalarial, anticancer and hepatoprotective activity. It also shows potent anti-viral effect against dengue virus. It blocks T-cell proliferation and the proliferation of several cancer cell lines in vitro. It acts as an irreversible antagonist of NF-kappa and AP-1 (IC50 < 15 microM) activation, and prevents in vitro and in vivo T cell activation. - Chemical. CAS: 5508-58-7. Formula: C20H30O5. MW: 350.455. Andrographolide, a bioactive diterpene lactone, is the main constituent of Andrographis paniculata, a plant used in traditional medicines. It is known to have different biological properties such as anti-inflammatory, immunosuppressive, antidiabetic, antihyperglycemic, antibacterial, antioxidant, antinoniceptive, antimalarial, anticancer and hepatoprotective activity. It also shows potent anti-viral effect against dengue virus. It blocks T-cell proliferation and the proliferation of several cancer cell lines in vitro. It acts as an irreversible antagonist of NF-kappa and AP-1 (IC50 < 15 microM) activation, and prevents in vitro and in vivo T cell activation.
  • SMILES
    C=C1CC[C@@]([C@@](CO)(C)[C@H](O)CC2)([H])[C@]2(C)[C@@H]1C/C=C3C(OC[C@H]/3O)=O
  • Storage Instruction
    -20°C
  • UNSPSC
    12352200