Chemodex

Florfenicol

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Product Details
Synonyms Sch 25298; (-)-Florfenicol; Aquafen; 2,2-Dichloro-N-[(1S,2R)-1-(fluoromethyl)-2-hydroxy-2-[4-(methylsulfonyl)phenyl]ethyl]acetamide
Product Type Chemical
Properties
Formula C12H14Cl2FNO4S
MW 358.21
CAS 73231-34-2
Source/Host Chemicals Synthetic
Purity Chemicals ≥98% (Assay)
Appearance White to off white crystalline.
Solubility Soluble in DMSO (30mg/ml), DMF (20mg/ml) or ethanol (10mg/ml).
Identity Determined by IR.
Declaration Manufactured by Chemodex.
Other Product Data

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Our product description may differ slightly from the original manufacturer's product datasheet.

InChi Key AYIRNRDRBQJXIF-NXEZZACHSA-N
Smiles [C@@H]([C@H](NC(C(Cl)Cl)=O)CF)(O)C1=CC=C(S(C)(=O)=O)C=C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
Product Specification Sheet
Datasheet Download PDF
Description
Florfenicol is a broad-spectrum fluorinated antibiotic and a derivative of thiamphenicol and analog of chloramphenicol. Florfenicol inhibits bacterial protein synthesis by binding to the A site of the 23S rRNA in the 50S subunit of the 70S ribosome, blocking peptidyl transferase activity, and thereby preventing peptide bond formation, which makes it effective against various bacteria. It is primarily used in veterinary medicine to treat respiratory infections in cattle and swine, and to prevent Salmonella infection in poultry. Although florfenicol is primarily known for its antimicrobial activity, it also shows immunomodulatory properties, including anti-inflammatory activity, downregulating pro-inflammatory cytokines such as TNF-α, IL-1β, and IL-6, suppression of innate immune responses, affect lymphocyte proliferation and immunoglobulin production, and influence TLR expression in immune cells.
Product References
(1) H.C. Neu & K.P. Fu; Antimicrob. Agents Chemother. 18, 311 (1980) | (2) V.P. Syriopoulou, et al.; Antimicrob. Agents Chemother. 19, 294 (1981) | (3) R. Graham, et al.; Eur. J. Clin. Microbiol. Infect. Dis. 7, 691 (1988) | (4) M. Cannon, et al.; J. Antimicrob. Chemother. 26, 307 (1990) | (5) Y. Ueda & I. Suenaga; J. Vet. Med. Sci. 57, 363 (1995) | (6) S. Priebe & S. Schwarz; Antimicrob. Agents Chemother. 47, 2703 (2003) | (7) G. Shuang, et al.; Immunol. Invest. 40, 356 (2011) | (8) X. Guo, et al.; Environ. Res. 244, 117934 (2024) (Review)
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