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呋喃妥因

产品号 N7878 公司名称 Sigma Aldrich
CAS号 67-20-9 公司网站 http://www.sigmaaldrich.com
分子式 C8H6N4O5 电 话 1-800-521-8956
分子量 238.15704 传 真
纯 度 电子邮件
保 存 Chembase数据库ID: 104426

产品价格信息

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产品别名

标题
Nitrofurantoin
IUPAC标准名
1-[(E)-[(5-nitrofuran-2-yl)methylidene]amino]imidazolidine-2,4-dione
IUPAC传统名
nitrofurantoin sodium
别名
硝基呋喃妥因
呋喃坦啶
N-(5-硝基-2-呋喃亚甲基)-1-氨基海因

产品登记号

MDL号 MFCD00003224
CAS号 67-20-9
PubChem SID 24897842
Beilstein号 893207
EC号 200-646-5

产品性质

外观 yellow crystalline
GHS危险品标识 GHS07
GHS危险品标识 GHS08
GHS警示词 Danger
GHS危险声明 H302-H317-H334
欧盟危险性物质标志 有害性(Harmful) 有害性(Harmful) (Xn)
个人保护装置 dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS警示性声明 P261-P280-P342 + P311
危险公开号 22-42/43
RTECS编号 MU2800000
安全公开号 22-36/37-45
德国WGK号 3

产品详细信息

详细说明 (English)
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 1 and antiobiotic resistance2.
Biochem/physiol Actions
Nitrofurantoin is activated by bacterial flavoproteins (nitrofuran reductase) to active reduced 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 death3. 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 2O 2. 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 stress1.

参考文献