Aurantiamide

CAS No. 58115-31-4

Aurantiamide( TMC-58B )

Catalog No. M20469 CAS No. 58115-31-4

Aurantiamide has anti-cancer anti-inflammatory and antinociceptive activities it may suppress the growth of malignant gliomas by blocking autophagic flux.Aurantiamide has an anti-neuroinflammatory effect on LPS stimulation through its inhibition of the NF-κB JNK and p38 pathways.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 374 In Stock
10MG 556 In Stock
25MG 887 In Stock
50MG 1197 In Stock
100MG 1611 In Stock
200MG Get Quote In Stock
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Biological Information

  • Product Name
    Aurantiamide
  • Note
    Research use only, not for human use.
  • Brief Description
    Aurantiamide has anti-cancer anti-inflammatory and antinociceptive activities it may suppress the growth of malignant gliomas by blocking autophagic flux.Aurantiamide has an anti-neuroinflammatory effect on LPS stimulation through its inhibition of the NF-κB JNK and p38 pathways.
  • Description
    Aurantiamide has anti-cancer anti-inflammatory and antinociceptive activities it may suppress the growth of malignant gliomas by blocking autophagic flux.Aurantiamide has an anti-neuroinflammatory effect on LPS stimulation through its inhibition of the NF-κB JNK and p38 pathways.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    TMC-58B
  • Pathway
    Apoptosis
  • Target
    NF-κB
  • Recptor
    NF-κB|p38
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    58115-31-4
  • Formula Weight
    402.5
  • Molecular Formula
    C25H26N2O3?
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    OC[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)c1ccccc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Yoon C S Kim D C Lee D S et al. Anti-neuroinflammatory effect of aurantiamide acetate from the marine fungus Aspergillus sp. SF-5921: Inhibition of NF-κB and MAPK pathways in lipopolysaccharide-induced mouse BV2 microglial cells[J]. International Immunopharmacology 2014 23(2):568-574.
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