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Chemical Structure
Chemical Structure
Chemical Structure

Asiaticoside [16830-15-2]

Research Use Only
CDX-A0575
Chemodex
CAS Number16830-15-2
Product group Chemicals
Estimated Purity>95%
Molecular Weight959.133
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Overview

  • Supplier
    Chemodex
  • Product Name
    Asiaticoside [16830-15-2]
  • Delivery Days Customer
    10
  • CAS Number
    16830-15-2
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Molecular Formula
    C48H78O19
  • Molecular Weight
    959.133
  • Scientific Description
    Asiaticoside is the main saponin constituent of C. asiatica, a plant long used in the Ayurvedic system of medicine to treat dermatitis, diabetes, cough, cataract, hypertension, as well as for wound healing and improving memory. It is a human collagen I synthesis inducer with anti-wrinkle activity. It shows wound healing activity, enhancing normal human skin cell migration, attachment and growth. Asiaticoside is an anti-inflammatory compound that inibits MAPKs, NF-kappa, COX-2 and iNOS expression, and production of TNF-alpha and IL-6. Also shown to induce apoptosis and autophagy in cancer cells. Described to have also antibacterial, antioxidant, anxiolytic, antidepressant-like, hepatoprotective, neuroprotective and antileishmanial activity. - Chemical. CAS: 16830-15-2. Formula: C48H78O19. MW: 959.133. Asiaticoside is the main saponin constituent of C. asiatica, a plant long used in the Ayurvedic system of medicine to treat dermatitis, diabetes, cough, cataract, hypertension, as well as for wound healing and improving memory. It is a human collagen I synthesis inducer with anti-wrinkle activity. It shows wound healing activity, enhancing normal human skin cell migration, attachment and growth. Asiaticoside is an anti-inflammatory compound that inibits MAPKs, NF-kappa, COX-2 and iNOS expression, and production of TNF-alpha and IL-6. Also shown to induce apoptosis and autophagy in cancer cells. Described to have also antibacterial, antioxidant, anxiolytic, antidepressant-like, hepatoprotective, neuroprotective and antileishmanial activity.
  • SMILES
    O[C@H]1[C@H](O)[C@@](C)(CO)C(CC[C@]2(C)[C@]3([H])CC=C4[C@@]2(C)CC[C@]5(C(O[C@@H]6O[C@H](CO[C@@H]7O[C@H](CO)[C@@H](OC8O[C@H](C)[C@H](O)[C@@H](O)[C@@H]8O)[C@H](O)[C@H]7O)[C@@H](O)[C@H](O)[C@H]6O)=O)C4[C@@H](C)[C@H](C)CC5)[C@]3(C)C1
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352200

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