WR99210,98.72%

产品编号:Bellancom-116387| CAS NO:47326-86-3| 分子式:C14H18Cl3N5O2| 分子量:394.68

本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,

货号 包装 价格 库存与货期 购买量 操作
Bellancom-116387
2700.00 杭州 北京(现货)
Bellancom-116387
8950.00 杭州 北京(现货)

增值税发票√顺丰快递√订货电话:18601927057

WR99210

产品介绍 WR99210 是一种口服有效的、低毒的二氢叶酸还原酶 (DHFR) 抑制剂 (IC50<0.075 nM)。WR99210 具有较好的抗寄生虫活性,能有效抑制间日疟原虫和恶性疟原虫株 (包括耐 Pyrimethamine (HY-18062) 的恶性疟原虫株) 以及弓形虫。
生物活性

WR99210 is an orally active and low-toxicity dihydrofolate reductase (DHFR) inhibitor (IC50<0.075 nM). WR99210 shows good antiparasitic activity and is effective against P. falciparum and P. falciparum strains (including Pyrimethamine (HY-18062)-resistant P. falciparum strains) as well as T. gondii.

体外研究

WR99210 (0-100 nM; 92 h) is highly effective against T. gondii tachyzoites in tissue culture.
WR99210 (0-100 nM; 92 h) shows low cytotoxicity to human foreskin fibroblasts.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay

Cell Line: Human foreskin fibroblasts (T. gondii-infected)
Concentration: 0-100 nM
Incubation Time: 92 h
Result: Showed marked inhibition of T. gondii, with an IC50 value of approximately 50 nM.

Cell Cytotoxicity Assay

Cell Line: Human foreskin fibroblasts
Concentration: 0-100 nM
Incubation Time: 92 h
Result: Lacked of toxicity for fibroblasts.
体内研究
(In Vivo)

WR99210 (1.25 mg/kg; i.p.; single daily for 5 days) is highly effective against T. gondii tachyzoites in a mouse model.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male mice (T. gondii-infected).
Dosage: 1.25 mg/kg
Administration: Intraperitoneal injection; single daily for 5 days.
Result: Exhibited intraperitoneal parasite numbers were 2 logs less in mice on the day 5.
体内研究

WR99210 (1.25 mg/kg; i.p.; single daily for 5 days) is highly effective against T. gondii tachyzoites in a mouse model.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male mice (T. gondii-infected).
Dosage: 1.25 mg/kg
Administration: Intraperitoneal injection; single daily for 5 days.
Result: Exhibited intraperitoneal parasite numbers were 2 logs less in mice on the day 5.
体内研究

WR99210 (1.25 mg/kg; i.p.; single daily for 5 days) is highly effective against T. gondii tachyzoites in a mouse model.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male mice (T. gondii-infected).
Dosage: 1.25 mg/kg
Administration: Intraperitoneal injection; single daily for 5 days.
Result: Exhibited intraperitoneal parasite numbers were 2 logs less in mice on the day 5.
性状Solid
溶解性数据
In Vitro: 

DMSO : 5 mg/mL (12.67 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.5337 mL 12.6685 mL 25.3370 mL
5 mM 0.5067 mL 2.5337 mL 5.0674 mL
10 mM 0.2534 mL 1.2668 mL 2.5337 mL
*

请根据产品在不同溶剂中的溶解度,选择合适的溶剂配制储备液;该产品在溶液状态不稳定,建议您现用现配,即刻使用

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years

*该产品在溶液状态不稳定,建议您现用现配,即刻使用。

参考文献

相关文档

化学品安全说明书(MSDS)

下载MSDS

质检证书(COA)

相关产品


服务热线

13911702513
18601927057

微信客服