Salvianolic acid H

CAS No. 444179-57-1

Salvianolic acid H( ——— )

Catalog No. M38680 CAS No. 444179-57-1

Salvianolic acid H is a potent acetylcholinesterase (AChE) inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG Get Quote Get Quote
50MG Get Quote Get Quote
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Salvianolic acid H
  • Note
    Research use only, not for human use.
  • Brief Description
    Salvianolic acid H is a potent acetylcholinesterase (AChE) inhibitor.
  • Description
    Salvianolic acid H is a potent acetylcholinesterase (AChE) inhibitor.
  • In Vitro
    ———
  • In Vivo
    ———
  • Synonyms
    ———
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ———
  • Research Area
    ———
  • Indication
    ———

Chemical Information

  • CAS Number
    444179-57-1
  • Formula Weight
    538.456
  • Molecular Formula
    C27H22O12
  • Purity
    >98% (HPLC)
  • Solubility
    ———
  • SMILES
    ———
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Peng WB, et al. Multiple on-line HPLC coupled with biochemical detection methods to evaluate bioactive compounds in Danshen injection. Biomed Chromatogr. 2016 Nov;30(11):1854-1860.?
molnova catalog
related products
  • Kaempferol-3-O-β-D-g...

    Kaempferol-3-O-β-D-glucosyl(1-2)rhamnoside is a natural peoduct isolated from Arabian jasmine.

  • FG 7142

    FG 7142?also modulates GABA-induced chloride flux at GABAA receptors expressing the α1 subunit (EC50= 137 nM).?FG 7142?can increase tyrosine hydroxylation and cause upregulation of β-adrenoceptors in mouse cerebral cortex.?FG 7142 , a non-selectively benzodiazepine inverse agonist, has high affinity for the α1 subunit-containing GABAA receptor (Ki=91 nM).?

  • CTP Synthetase-IN-1

    CTP Synthetase-IN-1 is an orally active and potent cytidine 5'-triphosphate synthetase (CTPS) inhibitor with potential antitumour activity, shows anti-inflammatory activity in animal models of inflammation, inhibits human CTPS1 and human CTPS2, and can be used in studies of arthritis and rheumatoid arthritis.