N7878

Nitrofurantoïne

98.0-102.0% (EP, UV)

• Synonyme(s) : N-(5-nitro-2-furfurylidène)-1-aminohydantoïne, Nitrofurantoïne
• Formule empirique (notation de Hill): C₈H₆N₄O₅
• Numéro CAS: 67-20-9
• Poids moléculaire : 238.16
• Numéro Beilstein : 893207
• Numéro CE : 200-646-5
• Numéro MDL: MFCD00003224
• Code UNSPSC : 51102829
• ID de substance PubChem : 24897842
• Nomenclature NACRES : NA.85

Propriétés

• Niveau de qualité: 200
• Pureté: 98.0-102.0% (EP, UV)
• Forme: (Crystalline Powder or crystals)
• Couleur: yellow
• Solubilité: DMF: soluble 50 mg/mL
• Spectre d'activité de l'antibiotique: Gram-negative bacteria; Gram-positive bacteria
• Mode d’action: DNA synthesis | interferes; cell wall synthesis | interferes; protein synthesis | interferes
• Chaîne SMILES: [O-][N+](=O)c1ccc(\C=N\N2CC(=O)NC2=O)o1
• InChI: 1S/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+
• Clé InChI: NXFQHRVNIOXGAQ-YCRREMRBSA-N

Description

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.

Actions biochimiques/physiologiques

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.

Autres remarques

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

Informations sur la sécurité

• Pictogrammes: GHS08,GHS07
• Mention d'avertissement: Danger
• Mentions de danger: H302,H317,H334
• Conseils de prudence: P280 - P301 + P312 + P330 - P302 + P352
• Classification des risques: Acute Tox. 4 Oral - Resp. Sens. 1 - Skin Sens. 1
• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 1
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable
• Équipement de protection individuelle: dust mask type N95 (US), Eyeshields, Faceshields, Gloves