Riparin III

CAS No. 112356-54-4

Riparin III( —— )

Catalog No. M34132 CAS No. 112356-54-4

Riparin III (Riparin) is a smooth muscle relaxant that inhibits CaCl2-induced contractions.Riparin III has potential antioxidant, anti-inflammatory, and antidepressant properties, and may reverse the most abnormal behavioral and neurochemical changes induced by corticosterone.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 29 In Stock
5MG 45 In Stock
10MG 72 In Stock
25MG 147 In Stock
50MG 221 In Stock
100MG 367 In Stock
200MG 512 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Riparin III
  • Note
    Research use only, not for human use.
  • Brief Description
    Riparin III (Riparin) is a smooth muscle relaxant that inhibits CaCl2-induced contractions.Riparin III has potential antioxidant, anti-inflammatory, and antidepressant properties, and may reverse the most abnormal behavioral and neurochemical changes induced by corticosterone.
  • Description
    Riparin is a nonspecific smooth muscle relaxant. Riparin inhibits CaCl2-induced contractions in a reversible and non-competitive manner and can be used in spasmolytic studies.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Antioxidant
  • Recptor
    Antioxidant | Calcium Channel
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    112356-54-4
  • Formula Weight
    287.31
  • Molecular Formula
    C16H17NO4
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(NCCC1=CC=C(OC)C=C1)C=2C(O)=CC=CC2O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Thomas G, et al. Studies on the mechanism of spasmolytic activity of (O-methyl-)-N-(2,6-dihydroxybenzoyl)tyramine, a constituent of Aniba riparia (Nees) Mez. (Lauraceae), in rat uterus, rabbit aorta and guinea-pig alveolar leucocytes. J Pharm Pharmacol. 1994 Feb;46(2):103-7.?
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