TIZOXANIDE Chemical Properties

Melting point:

279-281°(dec)

Density 

1.644±0.06 g/cm3(Predicted)

storage temp. 

Sealed in dry,Room Temperature

solubility 

DMSO (Slightly), Methanol (Slightly, Heated)

form 

Solid

pka

6.70±0.50(Predicted)

color 

Off-White to Pale Yellow

Safety Information

HS Code 

2934.10.1000

TIZOXANIDE Usage And Synthesis

Description

Tizoxanide is an active metabolite of the antiparasitic nitazoxanide . Tizoxanide is formed from nitazoxanide via deacetylation of nitazoxanide in the stomach. It is active against M. tuberculosis (MIC = 16 μg/ml). It also reduces the growth of the disease-causing parasites L. mexicana and T. cruzi in vitro (IC₅₀s = 6.2 and 17.5 μM, respectively), inhibits influenza A replication (EC₅₀s = 0.3-1 μM), and inhibits hepatitis B and hepatitis C virus replication (EC₅₀ = 0.15 μM for both).

Chemical Properties

Light Yellow Powder

Uses

A metabolite of Nitazoxanide; a potent inhibitor of hepatitis B virus and hepatitis C virus.

Uses

A metabolite of Nitazoxanide (N490100); a potent inhibitor of hepatitis B virus and hepatitis C virus. Kills Mycobacterium tuberculosis.

Definition

ChEBI: Desacetyl-nitazoxanide is a member of salicylamides.

in vitro

previous study found that tizoxanide showed potent inhibition of both hbv and hcv replication. tizoxanide also exhibited selective inhibition of intracellular hbv replication and extracellular virus production by 2.2.15 cells. tizoxanide could selectively reduce intracellular hcv replication in ava5 cells. moreover, the combination of tizoxanide with either recombinant human interferon alpha 2b (ifnα), or an ns5b (hcv polymerase) inhibitor, 2′-c-methyl cytidine, resulted in synergistic interactions against hcv replication. in addition, antiviral activities of tizoxanide against a full-length genotype 1a replicon were equivalent to that observed for ava5 cells [1].

in vivo

animal study in an immunosuppressed rat model suggested that relapses were less frequent after treatment with nitazoxanide, the parent drug of tizoxanide, than with the non-absorbable sinefungin and paromomycin [2].

IC 50

0.17 to 0.21 μm for civs

References

[1] korba be,montero ab,farrar k,gaye k,mukerjee s,ayers ms,rossignol jf. nitazoxanide, tizoxanide and other thiazolides are potent inhibitors of hepatitis b virus and hepatitis c virus replication. antiviral res.2008 jan;77(1):56-63.
[2] gargala g,delaunay a,li x,brasseur p,favennec l,ballet jj. efficacy of nitazoxanide, tizoxanide and tizoxanide glucuronide against cryptosporidium parvum development in sporozoite-infected hct-8 enterocytic cells. j antimicrob chemother.2000 jul;46(1):57-60.

TIZOXANIDE(173903-47-4)Related Product Information

• Nitazoxanide
• 2-Amino-5-nitrothiazole
• Nitazoxanide Impurity 2
• Thiacloprid
• Thiamethoxam