Home - Products - Others - Other Targets - 3-(4-prop-2-en-1-ylpiperazin-1-yl)quinox

3-(4-prop-2-en-1-ylpiperazin-1-yl)quinox

CAS No. 149685-89-2

3-(4-prop-2-en-1-ylpiperazin-1-yl)quinox( —— )

Catalog No. M21944 CAS No. 149685-89-2

3-(4-prop-2-en-1-ylpiperazin-1-yl)quinox Antagonism to 2-methyl-5-HT induced contractions in guinea pig ileum

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 45 Get Quote
10MG 68 Get Quote
25MG 122 Get Quote
50MG 184 Get Quote
100MG 275 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    3-(4-prop-2-en-1-ylpiperazin-1-yl)quinox
  • Note
    Research use only, not for human use.
  • Brief Description
    3-(4-prop-2-en-1-ylpiperazin-1-yl)quinox Antagonism to 2-methyl-5-HT induced contractions in guinea pig ileum
  • Description
    3-(4-prop-2-en-1-ylpiperazin-1-yl)quinox Antagonism to 2-methyl-5-HT induced contractions in guinea pig ileum.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    149685-89-2
  • Formula Weight
    279.34
  • Molecular Formula
    C16H17N5
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    C=CCN1CCN(CC1)c1nc2ccccc2nc1C#N
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • Nortrachelogenin-8'-...

    Nortrachelogenin-8'-O-beta-glucoside is a lignan with a diarylhydroxybutyrolactone skeleton which isolated from the leaves and stems of Trachelospermum jasminoides (Lindl.) Lem.

  • Murrangatin

    Murrangatin may be a valuable anti-tumor-promoting agent, it can significantly inhibit Epstein-Barr virus early antigen (EBV-EA) activation, and preserve the high viability of Raji cells, it also exhibits cytotoxicity against cholangiocarcinoma cell line, KKU-100.

  • AGX51

    AGX51 is an antagonist of inhibitor of DNA binding (ID) proteins. AGX51 treatment lead to pan-Id degradation, cell cycle arrest, and cell death.