A nitrofuran antibiotic
Related Products
Labeled Version(s)
33382Nifuroxazide-d4
Technical Support & Resources

Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

Nifuroxazide

Item No. 18163

Technical Information
Formal Name
4-hydroxy-benzoic acid, 2-[(5-nitro-2-furanyl)methylene]hydrazide
CAS Number
965-52-6
Molecular Formula
C12H9N3O5
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/mlDMSO:PBS (pH7.2) (1:1): 0.5 mg/ml
λmax
285, 365 nm
SMILES
OC1=CC=C(C(N/N=C/C2=CC=C([N+]([O-])=O)O2)=O)C=C1
InChi Code
InChI=1S/C12H9N3O5/c16-9-3-1-8(2-4-9)12(17)14-13-7-10-5-6-11(20-10)15(18)19/h1-7,16H,(H,14,17)/b13-7+
InChi Key
YCWSUKQGVSGXJO-NTUHNPAUSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Add

    Add

    Cayman Chemical
    Visit Our Cancer Resource Center
    Find Tools & Resources to Study the Hallmarks of Cancer
    • Cancer cell signaling & regulation
    • Cancer metabolism
    • Tumor microenvironment
    EXPLORE NOW
    Product Description

    Nifuroxazide is a nitrofuran antibiotic.1 It is active against strains of the enteropathogenic bacteria C. jejuni, Salmonella, Y. enterocolitica, Shigella, and E. coli.1 It inhibits quorum sensing and virulence factor production in P. aeruginosa.2 Nifuroxazide inhibits STAT3 activity in a reporter assay (IC50 = ~3 µM) and decreases viability of U266 and INA-6 myeloma cells, which have constitutive STAT3 phosphorylation, with EC50 values of approximately 4.5 µM for both.3 It also decreases viability, migration, and invasion of, and induces apoptosis in, MCF-7, 4T1, and MDA-MB-231 breast cancer cells.4 Nifuroxazide (50 mg/kg per day) reduces tumor growth and prevents pulmonary metastasis in a 4T1 murine mammary carcinoma model. It also reduces diarrhea, weight loss, and colon inflammation in a rat model of acetic acid-induced ulcerative colitis.5

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Vanhoof, R., Coignau, H., Stas, G., et alEvaluation of the in vitro activity of nifuroxazide on enteropathogenic microorganisms: Determination of bacteriostatic and bactericidal concentrations and disk susceptibility. Acta Clin. Belg. 36(3), 126-129 (1981).

    2. Yang, L., Rybtke, M.T., Jakobsen, T.H., et alComputer-aided identification of recognized drugs as Pseudomonas aeruginosa quorum-sensing inhibitors. Antimicrob. Agents Chemother. 53(6), 2432-2443 (2009).

    3. Nelson, E.A., Walker, S.R., Kepich, A., et alNifuroxazide inhibits survival of multiple myeloma cells by directly inhibiting STAT3. Blood 112(13), 5095-5102 (2008).

    4. Yang, F., Hu, M., Lei, Q., et alNifuroxazide induces apoptosis and impairs pulmonary metastasis in breast cancer model. Cell Death Dis. 6(3), e1701 (2015).

    5. El-Far, Y.M., Elsherbiny, N.M., El-Shafey, M., et alThe interplay of the inhibitory effect of nifuroxazide on NF-κB/STAT3 signaling attenuates acetic acid-induced ulcerative colitis in rats. Environ. Toxicol. Pharmacol. 79, 103433 (2020).