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二甲氧苄啶盐酸盐 /Diaveridine HCl {[allProObj[0].p_purity_real_show]}

货号:A287796

Diaveridine HCl is a coccidiostat and inhibits dihydrofolate reductase. It can prevente folic acid synthesis in species of Pneumocystis. Diaveridine also has genotoxicity.

Diaveridine HCl 化学结构 CAS号:2507-23-5
Diaveridine HCl 化学结构
CAS号:2507-23-5
Diaveridine HCl 3D分子结构
CAS号:2507-23-5
Diaveridine HCl 化学结构 CAS号:2507-23-5
Diaveridine HCl 3D分子结构 CAS号:2507-23-5
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Diaveridine HCl 纯度/质量文件 产品仅供科研

货号:A287796 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 DHFR 其他靶点 纯度
Pralatrexate 99%+
Pemetrexed disodium ++++

DHFR, Ki: 7.2 nM

99.9%
Pyrimethamine ++

DHFR, IC50: 15.4 nM

98% HPLC
Pemetrexed ++++

DHFR , Ki: 7.2 nM

99+%
Methotrexate +

hDHFR, IC50: 24 nM

99% (contain ~10%water)
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Diaveridine HCl 生物活性

描述 Diaveridine (DVD) HCl is a popular antibacterial synergist that is widely used in combination with sulfonamide[1]. Thirty healthy chickens were orally administered with sulphachloropyrazine-diaveridine (SPZ-DVD) suspension in water of 300 mg/l (SPZ) per day for seven successive days. The withdrawal period of DVD was 4.77, 4.94, 6.74 and 4.58 days in muscle, liver, kidney and skin with fat, respectively. Therefore, the suggested withdrawal period for SPZ-DVD suspension should be 7 days after dosing for seven successive days[2]. Diaveridine, a developed dihydrofolate reductase inhibitor, has been widely used as anticoccidial drug and antibacterial synergist. Calculated LD50 was 2330 mg/kg b.w. in females and 3100 mg/kg b.w. in males, and chromodacryorrhea was noted in some females before their death[3].

Diaveridine HCl 参考文献

[1]Wang H, Yuan B, Zeng Z, He L, Ding H, Guo C, Kong X, Wang W, Huang X. Identification and elucidation of the structure of in vivo metabolites of diaveridine in chicken. J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Aug 15;965:91-9

[2]Li Y, Bu S. Determination of sulphachloropyrazine-diaveridine residues by high performance liquid chromatography in broiler edible tissues. J Vet Med Sci. 2016 Jan;77(12):1555-63

[3]Wang X, Su S, Ihsan A, Huang Q, Chen D, Cheng G, Liu Z, Wang Y, Yuan Z. Acute and sub-chronic toxicity study of diaveridine in Wistar rats. Regul Toxicol Pharmacol. 2015 Oct;73(1):232-40

Diaveridine HCl 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.37mL

0.67mL

0.34mL

16.85mL

3.37mL

1.68mL

33.70mL

6.74mL

3.37mL

Diaveridine HCl 技术信息

CAS号2507-23-5
分子式C13H17ClN4O2
分子量 296.753
别名
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Keep in dark place,Inert atmosphere,Room temperature

溶解度
动物实验配方
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