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别名 | NSC-163039, RTCA, Tribavirin | 储存条件 (自收到货起) |
3年 / -20°C / 粉状 1年 / -80°C / 溶于溶剂 |
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| 化学式 | C8H12N4O5 |
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| 分子量 | 244.20864 | CAS号 | 36791-04-5 | ||||||||||||
| Solubility (25°C)* | 体外 | DMSO | 49 mg/mL (200.64 mM) | ||||||||||||
| Water | 49 mg/mL (200.64 mM) | ||||||||||||||
| Ethanol | Insoluble | ||||||||||||||
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* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
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| 产品描述 | Ribavirin (NSC-163039, ICN-1229, RTCA, Tribavirin)是一种抗病毒剂,用于治疗重症RSV感染,丙型肝炎病毒感染和其他病毒感染。 |
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| 体外研究 | Ribavirin显著降低了亚基因组复制子转染细胞的复制系统的效率,尽管Ribavirin对HCV复制的水平几乎没有影响。Ribavirin增加丙型肝炎病毒的突变频率,NS5A编码区的突变率最高。Ribavirin增强TH1,同时抑制T2细胞因子产生刺激的T细胞。 Ribavirin显示了抗病毒活性,抗多种RNA病毒,并结合使用α-干扰素来治疗丙型肝炎病毒感染。Ribavirin减少感染的脊髓灰质炎病毒的产生,少到细胞培养物的0.00001%。 Ribavirin的抗病毒活性是通过病毒的遗传物质的致死突变直接作用。 Ribavirin在生理浓度(高达500毫克/毫升)显着降低病毒引起的巨噬细胞的活化。Ribavirin抑制Th2细胞产生IL-4,而这并不会抹杀Th1细胞产生IFN-γ。 Ribavirin在体外表现出对DNA和RNA病毒广泛的抗病毒活性。Ribavirin是一种细胞生长抑制剂,导致DNA,RNA和蛋白质合成的的减少。Ribavirin能诱导辅助性T细胞表型从从2型转变为1型。 |

, Cancer Lett, 2016, 375(1):31-8.

数据来源于[Data independently produced by , , J Virol, 2015, 89(20):10512-23.]

数据来源于[Data independently produced by , , Antiviral Res, 2017, 143:237-245]
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如果需要长期保存,请于零下二十度低温保存。禁止用于人体及治疗!
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