化合物 Chloroquinoxaline sulfonamide T14953
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
1 mL | 97919-22-7 | ¥1,480.00 | 询底价 |
25 mg | 97919-22-7 | ¥3,630.00 | 询底价 |
1 mg | 97919-22-7 | ¥596.00 | 询底价 |
100 mg | 97919-22-7 | ¥7,390.00 | 询底价 |
10 mg | 97919-22-7 | ¥2,150.00 | 询底价 |
5 mg | 97919-22-7 | ¥1,360.00 | 询底价 |
50 mg | 97919-22-7 | ¥5,230.00 | 询底价 |
500 mg | 97919-22-7 | ¥14,800.00 | 询底价 |
Product Introduction
Bioactivity
英文名: Chloroquinoxaline sulfonamide
描述: Chloroquinoxaline sulfonamide is a topoisomerase II alpha/beta poison. It is used to control coccidiosis in poultry, rabbit, sheep, and cattle.
体外活性: Chloroquinoxaline sulfonamide causes dose-dependent protein-DNA cross-links to CV-1 monkey kidney cell chromosomal DNA when drug treatment was terminated by lysis with GuHCl. The Chloroquinoxaline sulfonamide IC50 for CV-1cells, obtained using an MTT cytotoxicity assay, was 1.8 mM. Chloroquinoxaline sulfonamide-induced protein-DNA cross-links in CV-1 cells. Chloroquinoxaline sulfonamide-induced topoisomerase II-DNA cross-links [1]. Chloroquinoxaline sulfonamide inhibits the proliferation of murine B16 melanoma cells, but only when relatively high drug concentrations (1 mM) are used [2].
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
关键字: NSC 339004 | NSC339004 | Chloroquinoxaline sulfonamide
相关产品: IndiMitecan | Daniquidone | 1,4-Naphthoquinone | Irinotecan | Topovale | (±)-10-Hydroxycamptothecin | Idarubicin hydrochloride | Isosteviol | Ellipticine hydrochloride | Phenoxodiol
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途