Viroallosecurinine

CAS No. 1857-30-3

Viroallosecurinine( (+)-Viroallosecurinine )

Catalog No. M21491 CAS No. 1857-30-3

(+)-Viroallosecurinine is a natural alkaloid with antibacterial activity. It exhibits a MIC of 0.48 μg/mL for Ps. Aeruginosa and Staph. aureus.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 486 Get Quote
10MG 701 Get Quote
25MG 1062 Get Quote
50MG 1458 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
    Viroallosecurinine
  • Note
    Research use only, not for human use.
  • Brief Description
    (+)-Viroallosecurinine is a natural alkaloid with antibacterial activity. It exhibits a MIC of 0.48 μg/mL for Ps. Aeruginosa and Staph. aureus.
  • Description
    (+)-Viroallosecurinine is a natural alkaloid with antibacterial activity. It exhibits a MIC of 0.48 μg/mL for Ps. Aeruginosa and Staph. aureus.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    (+)-Viroallosecurinine
  • Pathway
    GPCR/G Protein
  • Target
    Antibacterial
  • Recptor
    Bacterial
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1857-30-3
  • Formula Weight
    217.26
  • Molecular Formula
    C13H15NO2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C1O[C@@](C2)([C@@H](CCCC3)N3[C@H]2C=C2)C2=C1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Mensah JL et al. Antibacterial activity of the leaves of Phyllanthus discoideus. J Ethnopharmacol. 1990 Feb;28(1):129-33.
molnova catalog
related products
  • 6-Amino-5-azacytidin...

    6-Amino-5-azacytidine has an inhibitory of the growth of E. coli.

  • F1063-0967

    F1063-0967 is a Dual-specificity phosphatase 26 (DUSP26) inhibitor with an IC50 of 11.62 μM.

  • Caerulomycin A

    Caerulomycin A (Cerulomycin; Caerulomycin) is an antifungal compound. Which induces generation of T cells, enhances TGF-β-Smad3 protein signaling via suppressing interferon-γ-induced STAT1 signaling.