
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)






Size | Price / USD | Stock | Quantity |
200MG | 28 | In Stock |
![]() ![]() |
500MG | 41 | In Stock |
![]() ![]() |
1G | 48 | In Stock |
![]() ![]() |
Biological Information
-
Product NameClioquinol
-
NoteResearch use only, not for human use.
-
Brief DescriptionClioquinol(Iodochlorhydroxyquin) is an antifungal drug and antiprotozoal compound.
-
DescriptionClioquinol(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 VitroClioquinol (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——
-
SynonymsIodochlorohydroxyquin | NSC 3531 | NSC 74938
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research AreaNeurological Disease
-
Indication——
Chemical Information
-
CAS Number130-26-7
-
Formula Weight305.5
-
Molecular FormulaC9H5ClINO
-
Purity>98% (HPLC)
-
SolubilityChloroform: 15mg/mL
-
SMILESOC1=C2N=CC=CC2=C(Cl)C=C1I
-
Chemical Name5-chloro-7-iodoquinolin-8-ol
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith 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.