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Chemical Structure
Chemical Structure
Chemical Structure

Astragaloside IV [84687-43-4]

Research Use Only
CDX-A0577
Chemodex
CAS Number84687-43-4
Product group Chemicals
Estimated Purity>98%
Molecular Weight784.98
Price on request
Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    Astragaloside IV [84687-43-4]
  • Delivery Days Customer
    10
  • CAS Number
    84687-43-4
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Molecular Formula
    C41H68O14
  • Molecular Weight
    784.98
  • Scientific Description
    Astragaloside IV (AS-IV) is a bioactive saponin and constituent of the traditional chinese medicine plant Astragali radix. AS-IV has multiple pharmacologic effects, including anti-inflammatory, antioxidative, anti-asthma, antidiabetes, anticancer, immunoregulation, neuroprotective and cardioprotective properties via numerous signaling pathways. This includes inhibition of NF-kappaB, inducing hypoxia-inducible factor-1alpha accumulation via PI3K/Akt pathway, reducing Abeta production in Alzheimers disease through inhibition of BACE1, working as a natural PPARgamma agonist, improving lipid metabolism in obese mice, enhancing chemosensitivity through CD276 (B7-H3)-pathway inhibition, and suppressing glucose-induced NLRP3 inflammasome activation. - Chemical. CAS: 84687-43-4. Formula: C41H68O14. MW: 784.98. Astragaloside IV (AS-IV) is a bioactive saponin and constituent of the traditional chinese medicine plant Astragali radix. AS-IV has multiple pharmacologic effects, including anti-inflammatory, antioxidative, anti-asthma, antidiabetes, anticancer, immunoregulation, neuroprotective and cardioprotective properties via numerous signaling pathways. This includes inhibition of NF-kappaB, inducing hypoxia-inducible factor-1alpha accumulation via PI3K/Akt pathway, reducing Abeta production in Alzheimers disease through inhibition of BACE1, working as a natural PPARgamma agonist, improving lipid metabolism in obese mice, enhancing chemosensitivity through B7-H3 inhibition, and suppressing glucose-induced NLRP3 inflammasome activation.
  • SMILES
    O[C@H]1C[C@@]2(C)[C@]3([H])C[C@H](O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@@]5([H])C(C)(C)[C@@H](O[C@H]6OC[C@@H](O)[C@H](O)[C@H]6O)CC[C@]57[C@]3(C7)CC[C@]2(C)[C@H]1[C@]8(C)O[C@H](C(C)(O)C)CC8
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352200