CAS NO: | 143491-57-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
50mg | 电议 |
100mg | 电议 |
500mg | 电议 |
1 g | 电议 |
5 g | 电议 |
生物活性 |
Emtricitabine is a nucleosidereverse transcriptase inhibitor(NRTI) with anEC50of 0.01 μM in PBMC cell. It is an antiviral drug for the treatment ofHIVinfection. |
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IC50& Target |
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体外研究 (In Vitro) |
Emtricitabine hasin vitroactivity against both laboratory strains of HIV-1 and HIV-2 and clinical isolates of HIV-1. The 50% effective concentration (EC50) ranges from 0.002 to 1.5 μ mol/L, depending on the viral isolate and cell line used. Emtricitabine demonstratesin vitrosynergy with zidovudine and stavudine and additivein vitroactivity when combines with zalcitabine or didanosine[1].
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体内研究 (In Vivo) |
Reproductive and developmental toxicology studies are conducted with emtricitabine. Oral doses up to 1000 mg/kg/day provided daily area under the curve (AUC0→24) exposure to pregnant animals approximately 60- (mice) to 120-fold (rabbits) higher than that in humans at the recommended dose of 200 mg given once per day. In a mouse fertility study, emtricitabine had no effect on fertility, sperm count, or early embryonic development. There is no increased incidence of malformations in mouse and rabbit embryofetal toxicology studies. The development and fertility of F1 progeny are unaffected by emtricitabine in a mouse pre- and post-natal study. These data demonstrate a favorable pre-clinical reproductive safety profile for emtricitabine[2].
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Clinical Trial |
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分子量 |
247.25 |
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性状 |
Solid |
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Formula |
C8H10FN3O3S |
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CAS 号 |
143491-57-0 |
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中文名称 |
恩曲他滨 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : ≥ 100 mg/mL(404.45 mM) H2O : ≥ 25 mg/mL(101.11 mM) *"≥" means soluble, but saturation unknown.
配制储备液
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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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