CAS NO: | 95233-18-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | Atovaquone (Atavaquone) is a potent, selective and orally active inhibitor of theparasite’s mitochondrial cytochrome bc1 complex. Atovaquone is against human and P. falciparum cytochrome bc1 activity withIC50values of 460 nM and 2.0 nM, respectively. Atovaquone is anantimalarial agentand has the potential for the investigation of neumocystis pneumonia, toxoplasmosis, malaria, and babesia[1][2]. | ||||||||||||||||
IC50& Target |
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体外研究 (In Vitro) | Atovaquone targets to the Qo site of the Plasmodium cytochrome bc1 complex of the mitochondrial electron transport chain[1].Atovaquone is against the development in the mosquito from gamete production, through fertilization, zygote formation and finally, to the development of the mature ookinete, and demonstrates an IC50 of 67 nM providing further evidence of the transmission blocking potential of this molecule[1]. | ||||||||||||||||
体内研究 (In Vivo) | Atovaquone (oral administration; 100 mg/kg; once daily) is against survival rates of mice, mice treated orally died within 22 days after discontinuation of sulfadiazine,while the control group died at day 14[2].
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Clinical Trial | |||||||||||||||||
分子量 | 366.84 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C22H19ClO3 | ||||||||||||||||
CAS 号 | 95233-18-4 | ||||||||||||||||
中文名称 | 阿托伐醌 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 8.33 mg/mL(22.71 mM;Need ultrasonic) 配制储备液
* 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;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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