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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.
1. Evaluation 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. Computer-
3. Nifuroxazide inhibits survival of multiple myeloma cells by directly inhibiting STAT3. Blood 112(13), 5095-5102 (2008).
4. Nifuroxazide induces apoptosis and impairs pulmonary metastasis in breast cancer model. Cell Death Dis. 6(3), e1701 (2015).
5. The interplay of the inhibitory effect of nifuroxazide on NF-