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索非布韦 /Sofosbuvir {[allProObj[0].p_purity_real_show]}

货号:A298621 同义名: GS-7977;PSI-7977

Sofosbuvir(GS-7977)是一种HCV RNA复制抑制剂,EC50为92 nM。

Sofosbuvir 化学结构 CAS号:1190307-88-0
Sofosbuvir 化学结构
CAS号:1190307-88-0
Sofosbuvir 3D分子结构
CAS号:1190307-88-0
Sofosbuvir 化学结构 CAS号:1190307-88-0
Sofosbuvir 3D分子结构 CAS号:1190307-88-0
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Sofosbuvir 纯度/质量文件 产品仅供科研

货号:A298621 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 DNA synthesis helicase RdRp ribonucleotide reductase tRNA synthetase YB-1 其他靶点 纯度
Fexinidazole 98%
Daptomycin 98%
Blasticidin S·HCl 98%
Metronidazole 98%
Daunorubicin HCl +++

DNA synthesis, Ki: 20 nM

98%
Triglycidyl isocyanurate p53 98+%
Nedaplatin 99%+
Bendamustine 98+%
Trifluridine 98%
Robinetin 99%+
Carboplatin 99%
Cidofovir 99%
Cisplatin 99%
Cytarabine ++++

DNA synthesis, IC50: 16 nM

98%
Acelarin ++++

DNA synthesis, EC50: 0.2 nM

99%+
Oxaliplatin 98%
YK-4-279 99%+
ML216 +

BLM636-1298, IC50: 0.97 μM

BLMfull-length, IC50: 2.98 μM

99%+
RK-33 98%
Brr2-IN-3 99%+
Phen-DC3 Trifluoromethanesulfonate 98%
Favipiravir 99%
Suramin sodium salt ++

RdRp, IC50: 0.26 μM

99%+
Clofarabine ++

Ribonucleotide reductase, IC50: 65 nM

97%
Didox 98%
(E)-3-AP 99%
Halofuginone +++

prolyl-tRNA synthetase, Ki: 18.3nM

99%+
BC-LI-0186 +++

Leucyl-tRNA synthetase, Kd: 42.1 nM

Leucyl-tRNA synthetase, IC50: 46.11 nM

98%
SU056 +

YB-1, IC50: 1.73 μM

98%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Sofosbuvir 生物活性

描述 Sofosbuvir (GS-7977) is an inhibitor of HCV RNA replication, with an EC50 of 92 nM[1].
体外研究

When cathepsin A (CatA) is exposed to PSI-7977 or Sofosbuvir (PSI-7977) for 150 minutes, approximately 18-fold more PSI-352707 is produced compared to PSI-7976 when Sofosbuvir (PSI-7977) is the substrate. Furthermore, the catalytic efficiency of Sofosbuvir (PSI-7977) with CatA is approximately 30-fold higher than that of PSI-7976[1].

The genotype coverage of Sofosbuvir (PSI-7977) is evaluated using replicons derived from GT 1b (Con1), 1a (H77), and 2a (JFH-1), as well as chimeric replicons containing the NS5B region from the J6 GT 2a isolate and from GT 2b and GT 3a patient isolates. Sofosbuvir (PSI-7977) inhibits the replication of these replicons with similar EC50s (between 16 and 48 nM) and is particularly effective against the chimeric replicon containing the J6 NS5B (EC50=4.7 nM). It also inhibits clone A (GT 1b) wild-type and S282T replicons with EC90 values of 0.42 and 7.8 μM, respectively[2].

In the clone A replicon assay, Sofosbuvir (PSI-7977) exhibits anti-HCV activity with EC90 values of 0.42 μM[3].

Sofosbuvir 参考文献

[1]Murakami E, et al. Mechanism of activation of PSI-7851 and its diastereoisomer PSI-7977.J Biol Chem. 2010 Nov 5;285(45):34337-47.

[2]Lam AM, et al. Genotype and subtype profiling of PSI-7977 as a nucleotide inhibitor of hepatitis C virus. Antimicrob Agents Chemother. 2012 Jun;56(6):3359-68.

Sofosbuvir 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.89mL

0.38mL

0.19mL

9.44mL

1.89mL

0.94mL

18.89mL

3.78mL

1.89mL

Sofosbuvir 技术信息

CAS号1190307-88-0
分子式C22H29FN3O9P
分子量 529.452
别名 GS-7977;PSI-7977;Resof;Hepcvir;Hepcinat;Vosevi;Virunon;Sovaldi;GI-7977
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Sealed in dry,Store in freezer, under -20°C

溶解度

DMSO: 50 mg/mL(94.44 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 25 mg/mL(47.22 mM),配合低频超声,并水浴加热至45℃助溶

动物实验配方
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