物质信息

ID:220

名称和标识
商标名
Actin-NAlfucinBecafurazoneChemofuranChixinCocafurinFurazymeIbiofuralMonafuracinNefcoNitrofurolSanfuranNitrozoneOtofuralVabrocidFurazoneFurosemFuvacillinMastofuranNifuridNifuzonNitrofuraneFuracinFuracin-EFuracyclineFurametralFuraseptylFurazilineSpray-ForalAmifurBabrocidCoxistatFuracillinFurfurinHemofuranMonafuracisNifucinNitrofuranOtofuranNitrofuralSpray-DermisVadrocidYatrocinFurazinFurazol WFuresolMammexMonofuracinNF-7NFSFuracoccidFuraldonFuraloneFuraplastFuratsilinFurazinaBiofureaDymazoneFedacinFuracin Soluble DressingFuracin Topical SolutionFuracineFuracin Topical CreamFuracin-HCFuracinettenFuradermFuran-OftenoAldomycinFuralcynFuraskinBiofuracinaDynazoneFlavazoneFuracilinDermofuralEldezolEldezol F-6FracineFuracortFuragent
IUPAC标准名
[(E)-[(5-nitrofuran-2-yl)methylidene]amino]urea
别名
NitrofurazanNitrofurazoneNFZNF
IUPAC传统名
nitrofurazone
数据登录号
PubChem CID
PubChem SID
CAS号
化合物性质
理化性质
疏水性(logP)
0.2
溶解度
210 mg/L (Approximately 50%)
描述信息
Drug Groups
approved
Description
A topical anti-infective agent effective against gram-negative and gram-positive bacteria. It is used for superficial wounds, burns, ulcers, and skin infections. Nitrofurazone has also been administered orally in the treatment of trypanosomiasis. [PubChem]
Indication
For the treatement of bacterial skin infections including pyodermas, infected dermatoses and infections of cuts, wounds, burns and ulcers due to susceptible organisms.
Pharmacology
Nitrofurazone is a topical antibacterial agent indicated as an adjunctive therapy for second and third degree burns when resistance to other agents is a real or potential problem. Nitrofurazone is also indicated in skin grafting when bacterial contamination may cause graft rejection or donor site infection, especially in hospitals with a history of resistant bacteria.
Toxicity
Rat LD50 = 590 mg/kg; Allergic contact dermatitis is the most frequently reported adverse effect, occurring in approximately 1 % of patients treated.
Affected Organisms
Gram negative and gram positive bacteria
Biotransformation
Nitrofurans, including nitrofural, undergo metabolic reduction at the nitro group to generate reactive species which can covalently bind to cellular macromolecules (Polnaszek et al., 1984; Kutcher & McCalla, 1984; McCalla 1979; McCalla et al., 1975).
Absorption
Well absorbed.
Half Life
5 hours
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