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噻菌灵

产品号 T8904 公司名称 Sigma Aldrich
CAS号 148-79-8 公司网站 http://www.sigmaaldrich.com
分子式 C10H7N3S 电 话 1-800-521-8956
分子量 201.24768 传 真
纯 度 ≥99% 电子邮件
保 存 Chembase数据库ID: 611

产品价格信息

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产品别名

标题
Thiabendazole
IUPAC标准名
2-(1,3-thiazol-4-yl)-1H-1,3-benzodiazole
IUPAC传统名
testo
别名
2-(4-噻唑基)苯并咪唑

产品登记号

Beilstein号 611403
MDL号 MFCD00005587
PubChem SID 24900571
EC号 205-725-8
CAS号 148-79-8

产品性质

纯度 ≥99%
适用性 suitable for 1694 per US EPA
相关基因信息 human ... CYP2C9(1559)
外观 light yellow powder
GHS危险品标识 GHS09
GHS警示词 Warning
GHS危险声明 H410
欧盟危险性物质标志 环境危害性(Nature polluting) 环境危害性(Nature polluting) (N)
个人保护装置 Eyeshields, Gloves
GHS警示性声明 P273-P501
RID/ADR UN 3077 9/PG 3
危险公开号 50/53
RTECS编号 DE0700000
安全公开号 60-61
联合国危险货物等级 9
联合国危险货物编号 3077
联合国危险货物包装类别(PG) 3
德国WGK号 2

产品详细信息

详细说明 (English)
Application
Thiabendazole (TBZ) is a broad-spectrum antihelminthic and is used to treat parasitic infections in humans. It is used as an agricultural fungicide and as a food preservative1. Thiabendazole has been used as a heavy metal chelating detoxification agent. It is used clinically to treat threadworm, cutaneous larva migrans, visceral larva migrans, and trichinosis2.
Biochem/physiol Actions
Thiabendazole inhibits anaerobic respiration at the level of mitochondrial helminth-specific enzyme. It acts as a quinol-fumarate reductase (QFR) inhibitor in ,C. jejuni and H. pylori, blocking quinol oxidation to quinone. Thiabendazole suppresses egg and larval production and may inhibit the subsequent development of eggs and larvae which are passed in feces2. A proposed route of biotransformation of thiabendazole is the CYP1A2-catalyzed hydroxylation to 5-hydroxythiabendazole, which is metabolized to glucuronide and sulfate conjugates1.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information

参考文献