Tizoxanide

Tizoxanide
Names

IUPAC name 2-Hydroxy-N-(5-nitro-2-thiazolyl)benzamide
Other names Desacetyl-nitazoxanide
Identifiers
CAS Number	173903-47-4^N
3D model (JSmol)	Interactive image
ChemSpider	349588^Y
PubChem CID	394397
InChI InChI=1S/C10H7N3O4S/c14-7-4-2-1-3-6(7)9(15)12-10-11-5-8(18-10)13(16)17/h1-5,14H,(H,11,12,15)^Y Key: FDTZUTSGGSRHQF-UHFFFAOYSA-N^Y InChI=1/C10H7N3O4S/c14-7-4-2-1-3-6(7)9(15)12-10-11-5-8(18-10)13(16)17/h1-5,14H,(H,11,12,15) Key: FDTZUTSGGSRHQF-UHFFFAOYAR
SMILES O=C(Nc1ncc(s1)[N+]([O-])=O)c2ccccc2O
Properties
Chemical formula	C₁₀H₇N₃O₄S
Molar mass	265.25 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references

Tizoxanide, also known as desacetyl-nitazoxanide, is a thiazolide and an antiparasitic agent that occurs as a metabolite of nitazoxanide in humans through hydrolysis.^[1] Tizoxanide may undergo further metabolism via conjugation into tizoxanide glucuronide.^[2]^[3]

References

↑ Korba BE, Montero AB, Farrar K, et al. (January 2008). "Nitazoxanide, tizoxanide and other thiazolides are potent inhibitors of hepatitis B virus and hepatitis C virus replication". Antiviral Res. 77 (1): 56–63. PMID 17888524. doi:10.1016/j.antiviral.2007.08.005.
↑ "Nitazoxanide Prescribing Information" (PDF). Romark Pharmaceuticals. August 2013. pp. 1–5. Retrieved 3 January 2016.
↑ Stockis A, Allemon AM, De Bruyn S, Gengler C (May 2002). "Nitazoxanide pharmacokinetics and tolerability in man using single ascending oral doses". Int J Clin Pharmacol Ther. 40 (5): 213–220. PMID 12051573. doi:10.5414/cpp40213.

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