Neoandrographolide

CAS No. 27215-14-1

Neoandrographolide ( Neoandrographolide )

Catalog No. M18343 CAS No. 27215-14-1

Neoandrographolide has potent hypolipidemic effect and protects the cardiovascular without significant liver damage.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 150 In Stock
10MG 240 In Stock
25MG 408 In Stock
50MG 588 In Stock
100MG 824 In Stock
500MG 1647 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Neoandrographolide
  • Note
    Research use only, not for human use.
  • Brief Description
    Neoandrographolide has potent hypolipidemic effect and protects the cardiovascular without significant liver damage.
  • Description
    Neoandrographolide is one of the principle diterpenoids isolated from A. paniculata, a well-recognized medicinal plant in Asia. Extracts from A. paniculata have been reported to exert a wide range of therapeutic actions, including immunosuppressant, antithrombotic, anti-inflammatory, antineoplastic, anti-viral, anti-bacterial, anti-diabetic, anti-oxidative stress, antipyretic, anti-edematogenic, and anti-nociceptive activities.
  • Synonyms
    Neoandrographolide
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    COX-2; iNOS
  • Research Area
    Others-Field
  • Indication
    ——

Chemical Information

  • CAS Number
    27215-14-1
  • Formula Weight
    480.6
  • Molecular Formula
    C26H40O8
  • Purity
    98%
  • Solubility
    ——
  • SMILES
    O1CC=C(C1=O)CC[C@@H]1C(=C)CC[C@@H]2[C@@](CCC[C@@]12C)(CO[C@@H]1O[C@@H]([C@H]([C@@H]([C@H]1O)O)O)CO)C
  • Chemical Name
    3-(2-((1R,4aS,5R,8aS)-5,8a-dimethyl-2-methylene-5-((((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)methyl)decahydronaphthalen-1-yl)ethyl)furan-2(5H)-one

Shipping & Storage Information

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

Reference

1. Yang T,et al. Hypolipidemic effects of andrographolide and neoandrographolide in mice and rats. Phytother Res. 2013 Apr;27(4):618-23.
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