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EIDD-1931 {[allProObj[0].p_purity_real_show]}

货号:A1241627

EIDD-1931 has a broad-spectrum antiviral activity against multiple coronaviruses, including SARS-CoV2, MERS-CoV, SARS-CoV. and related zoonotic group 2b or 2c Bat-CoVs, as well as increased potency against a coronavirus bearing resistance mutations to another nucleoside analog inhibitor.

HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
EIDD-1931 化学结构 CAS号:3258-02-4
EIDD-1931 化学结构
CAS号:3258-02-4
EIDD-1931 3D分子结构
CAS号:3258-02-4
EIDD-1931 化学结构 CAS号:3258-02-4
EIDD-1931 3D分子结构 CAS号:3258-02-4
规格 价格 会员价 库存 数量
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EIDD-1931 纯度/质量文件 产品仅供科研

货号:A1241627 标准纯度: {[allProObj[0].p_purity_real_show]}
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EIDD-1931 生物活性

描述 Venezuelan equine encephalitis virus (VEEV) can cause widespread epidemics among humans and domestic animals. VEEV infections result in severe meningoencephalitis and long-term sequilae. EIDD-1931 is a very potent antiviral agent which effectively inhibits the replication activity of VEEV, Chikungunya virus (CHIKV) and hepatitis C virus (HCV). EIDD-1931 inhibited VEEV with EC50, EC90, and EC99 of 0.426, 1.036, and 2.5 μM, respectively. EIDD-1931 demonstrated a strong negative effect on replication of VEEV TC-83 in Vero cells. EIDD-1931 at 1 μM and 2.5 μM concentrations reduced titers of released virus progeny by 2 and 4 orders of magnitude, respectively. EIDD-1931 treatment at 2 μM concentration led to at least a 10-fold increase in accumulation of mutations. Notably, VEEV resistance to EIDD-1931 developed very inefficiently[1]. EIDD-1931 inhibited CHIKV replicon activity with an EC50 of 0.8 μM in the Huh-7-CHIKV replicon cell line. CC50 values for NHC were determined to be 30.6, 7.7 and 2.5 μM in PBM, Vero, and CEM cells, respectively[2].

EIDD-1931 参考文献

[1]Urakova N, et al. β-d-N4-Hydroxycytidine Is a Potent Anti-alphavirus Compound That Induces a High Level of Mutations in the Viral Genome. J Virol. 2018 Jan 17;92(3):e01965-17

[2]Ehteshami M, et al. Characterization of β-d-N4-Hydroxycytidine as a Novel Inhibitor of Chikungunya Virus. Antimicrob Agents Chemother. 2017 Mar 24;61(4):e02395-16

EIDD-1931 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.86mL

0.77mL

0.39mL

19.29mL

3.86mL

1.93mL

38.58mL

7.72mL

3.86mL

EIDD-1931 技术信息

CAS号3258-02-4
分子式C9H13N3O6
分子量 259.216
别名
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Inert atmosphere,2-8°C

溶解度

DMSO: 105 mg/mL(405.07 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(96.44 mM)

动物实验配方
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