Nitrofurantoin, crystalline

Code: n7878-25g D2-231

Not available outside of the UK & Ireland.

Application

Nitrofurantoin is a nitrofuran antibiotic that is used as a substrate of bacterial nitrofuran reductase to study the interactions of active metabolites with DNA, ...


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Your Price
£57.60 25G

Not available outside of the UK & Ireland.

Application

Nitrofurantoin is a nitrofuran antibiotic that is used as a substrate of bacterial nitrofuran reductase to study the interactions of active metabolites with DNA, ribosomal proteins and metabolic and pro-oxidant processes. It is used to study nitrofurantoin-induced toxicity and antibiotic resistance.Nitrofurantoin is suitable for killing L. monocytogenes-persisters in vitro. Studies has described the use of antioxidants to mitigate the toxic effects of nitrofurantoin on human WI-38 fibroblasts in culture. Alterations to the in vitro morphologic features, viability, and phagocytic activity of isolated bovine mammary polymorphonuclear leukocytes caused by various antibiotics, including nitrofurantoin, have been reported.

Biochem/physiol Actions

Nitrofurantoin is an antibactericidal compound that has been historically prepared by the reaction of 1-aminohydantoin sulfate and 5-nitro-2-furaldehyde diacetate. It shows activity against many Gram-positive and Gram-negative bacteria. Nitrofurantoin is effective against enterococci, staphylococci, streptococci, corneybacteria, many strains of Escherichia coli. Most strains of Proteus spp. and Pseudomonas aeurginosa are more resistant to this compound. Nitrofurantoin is activated by bacterial flavoproteins (nitrofuran reductase) to actively reduce reactive intermediates that modulate and damage ribosomal proteins or other macromolecules, such as DNA. This inhibits DNA, RNA, protein, and cell wall synthesis which causes cell death. Nitrofurantoin has a low resistance potential that is rapidly metabolized by mammals and is active against both Gram-positive and Gram-negative bacteria. It is also a pro-oxidant that is cytotoxic due to the generation of intracellular H 2O2. It is an inhibitor of glutathione reductase. Nitrofurantoin produces hepatotoxicity caused by the redox cycling of the nitro group and its radical anion which leads to oxidative stress.

Other Notes

Keep container tightly closed in a dry and well-ventilated place.Light sensitive.

Packaging

10, 25, 100, 250 g in glass bottle

antibiotic activity spectrumGram-positive bacteria, Gram-negative bacteria
assay98.0-102.0% (EP, UV)
coloryellow
form(Crystalline Powder or crystals)
InChI keyNXFQHRVNIOXGAQ-YCRREMRBSA-N
InChI1S/C8H6N4O5/c13-6-4-11(8(14)10-6)9-3-5-1-2-7(17-5)12(15)16/h1-3H,4H2,(H,10,13,14)/b9-3+
mode of actioncell wall synthesis | interferes, protein synthesis | interferes, DNA synthesis | interferes
Quality Level200
SMILES string[O-][N+](=O)c1ccc(C=NN2CC(=O)NC2=O)o1
solubilityDMF: soluble 50 mg/mL
Code
Description
Unit Size
List Price
Qty
N7878-10G
Unit:10G
List Price: £28.90
Source:List Price
ADD
N7878-100G
Unit:100G
List Price: £173.00
Source:List Price
ADD
Cas Number67-20-9
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