WR99210,98.72%
产品编号:Bellancom-116387| CAS NO:47326-86-3| 分子式:C14H18Cl3N5O2| 分子量:394.68
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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。 | ||||||||||||||||
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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. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability Assay
Cell Cytotoxicity Assay
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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.
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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.
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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.
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性状 | Solid | ||||||||||||||||
溶解性数据 |
In Vitro:
DMSO : 5 mg/mL (12.67 mM; Need ultrasonic) 配制储备液
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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 |
*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 |
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