Clioquinol

CAS No. 130-26-7

Clioquinol( Iodochlorohydroxyquin | NSC 3531 | NSC 74938 )

Catalog No. M11214 CAS No. 130-26-7

Clioquinol(Iodochlorhydroxyquin) is an antifungal drug and antiprotozoal compound.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
200MG 28 In Stock
500MG 41 In Stock
1G 48 In Stock

Biological Information

  • Product Name
    Clioquinol
  • Note
    Research use only, not for human use.
  • Brief Description
    Clioquinol(Iodochlorhydroxyquin) is an antifungal drug and antiprotozoal compound.
  • Description
    Clioquinol(Iodochlorhydroxyquin) is an antifungal drug and antiprotozoal compound that shows effectivity for Alzheimer's disease treatment and induce Y cell death.(In Vitro):Clioquinol (0.01-1000 uM; 72 hours) shows anticancer activity against U251, and MV-4-11 cells.
  • In Vitro
    Clioquinol (0.01-1000 uM; 72 hours) shows anticancer activity against U251, and MV-4-11 cells. Cell Viability Assay Cell Line:The MV-4-11, and U-251 cell lines Concentration:0.01, 0.1, 1, 10, 100, 1000 uM Incubation Time:72 hours Result:The IC50s were 32 and 46 μM in U251 and MV-4-11 cells, respectively.
  • In Vivo
    ——
  • Synonyms
    Iodochlorohydroxyquin | NSC 3531 | NSC 74938
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    130-26-7
  • Formula Weight
    305.5
  • Molecular Formula
    C9H5ClINO
  • Purity
    >98% (HPLC)
  • Solubility
    Chloroform: 15mg/mL
  • SMILES
    OC1=C2N=CC=CC2=C(Cl)C=C1I
  • Chemical Name
    5-chloro-7-iodoquinolin-8-ol

Shipping & Storage Information

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

Reference

1.Rohde W, et al. Antimicrob Agents ChemOthers. 1976 Aug;10(2):234-40.
molnova catalog
related products
  • Cyasterone

    Cyasterone, a natural EGFR inhibitor, can inhibit the growth of A549 and MGC823 cells, via regulating EGFR signaling pathway, it may be a promising anti-cancer agent.

  • VH032-cyclopropane-F

    VH032-cyclopropane-F is a VH032-based VHL ligand. VH032-cyclopropane-F can be connected to the ligand for protein by a linker to form PROTACs. PROTAC 1 is a partial degrader of SMARCA2 and SMARCA4.

  • Ginsenoside Rg5

    Ginsenoside Rg5 could be a beneficial agent for the treatment of Alzheimer's disease.