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102-65-8

中文名称 磺胺氯吡嗪钠
英文名称 N-(5-CHLORO-3-PYRAZINE)-4-AMINOBENZENESULFONAININO
CAS 102-65-8
分子式 C10H9ClN4O2S
分子量 284.72
MOL 文件 102-65-8.mol
更新日期 2024/04/16 15:32:55
102-65-8 结构式 102-65-8 结构式

基本信息

中文别名
磺胺氯吡嗪
磺胺氯毗嗪钠
磺胺氯吡嗪鈉
磺胺氯吡嗪钠一水合物
磺胺氯吡嗪(标准品)
磺胺氯吡嗪钠 100MG
磺胺氯吡嗪溶液, 100PPM
N-(5-氯-3-吡嗪基)-4-氨基苯磺酰胺
英文别名
SPZ
102-65-8
sulfaclozine
Sulfalozine sodiu
Sulfalozine sodium
SULFACLOZINE SODIUM
SODIUM SULFACLOZINE
Sulfachloropyrazine
sulfachlorpyrazin sodium
SULFACHLORPYRAZINE SODIUM

物理化学性质

熔点234.8-235.4 °C
沸点495.7±55.0 °C(Predicted)
密度1.588±0.06 g/cm3(Predicted)
储存条件2-8°C(protect from light)
酸度系数(pKa)4.83±0.10(Predicted)

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302-H315-H319-H335

应用领域

用途1
磺胺氯吡嗪钠为抗球虫的专用磺胺药,广泛用于畜禽球虫病。本品可争夺二氢叶酸合成酶影响二氢叶酸的合成,从而抑制细菌和球虫的生长繁殖。本品对家禽球虫的作用特点与磺胺喹沙啉相似,但具更强的抗菌作用,甚至可治疗禽霍乱及鸡伤寒因此最适合球虫病爆发时治疗用。
用途2
磺胺类抗菌药,用于禽畜大肠杆菌和巴式杆菌感染,与甲氧苄啶与蔗糖配置而成复方磺胺氯哒嗪钠盐效果更加,对磺胺类药过敏者忌用,肾功能减退者慎用。
用途3
本品为抗球虫的专用磺胺药,广泛用于畜禽球虫病。本品可争夺二氢叶酸合成酶影响二氢叶酸的合成,从而抑制细菌和球虫的生长繁殖。本品对家禽球虫的作用特点与磺胺喹沙啉相似,但具更强的抗菌作用,甚至可治疗禽霍乱及鸡伤寒因此最适合球虫病爆发时治疗用。

常见问题列表

生物活性
Sulfalozine sodium (Sulfaclozine sodium, Sulfachlopryrazine sodium) 是一种抗原生动物药,用于球虫病的研究。
靶点

Bacterial; Parasite

体外研究

The elimination of Sulfaclozine in the three systems: UV/TiO 2 , UV/K 2 S 2 O 8 , and UV/TiO 2 /K 2 S 2 O 8 . Sulfaclozine is weakly adsorbed on the surface of TiO 2 at pH 7 (< 5%) but efficiently eliminated with the following three systems: UV/TiO 2 , UV/K 2 S 2 O 8 , and UV/TiO 2 /K 2 S 2 O 8 in ultra pure water. Moreover, 12 of Sulfaclozine by-products are identified and reaction pathways show that, in addition of OH and SO 4 •− radicals, the conduction-band electrons are responsible for the formation of some main by-products either directly or by the formation of superoxide radicals.

体内研究

Sulfaclozine (60 mg/kg; intravenous injection or oral administration; male broiler chickens) can be used primarily for the treatment of parasitic and microbial infections of the digestive tract rather than for the treatment of systemic infections.

Animal Model: 14 male broiler chickens (30-day-old)
Dosage: 60 mg/kg
Administration: Intravenous injection or oral administration (Pharmacokinetic Analysis)
Result: Serum drug concentrations at 0.083, 0.50, 2, 6, 24 and 72h were determined to be 99.62, 83.50, 72.68, 58.43, 38.66 and 13.14 μg/mL, respectively, by intravenous injection. By oral administration were determined as 4.33, 7.95, 16.46, 22.88, 16.03 and 5.74 μg/mL, respectively.
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