NM107 (2'-C-Methylcytidine)
(Synonyms: 2'-C-甲基胞嘧啶核苷,2'-C-Methylcytidine; NM-107) 目录号 : GC33936A ribonucleoside with broad-spectrum antiviral activity
Cas No.:20724-73-6
Sample solution is provided at 25 µL, 10mM.
2'-C-Methylcytidine (2CMC) is a ribonucleoside with broad-spectrum antiviral activity.1 It reduces the number of viral plaques in BHK-21 cells infected with dengue type 2, reovirus type 1, West Nile, and yellow fever RNA viruses with EC50 values of 95, 26, 80, and 75 μM, respectively. 2CMC inhibits hepatitis C virus (HCV) replication (EC50 = 2.2 μM in a replicon assay) and protects MDBK cells from infection with bovine virus diarrhea virus (BVDV; EC50 = 2.2 μM) and human coronavirus (HCoV; EC50 = 90 μM). It also reduces infectious virus yield in BHK-21 cells infected with foot-and-mouth disease virus (FMDV; EC50 = 6.4 μM) and swine vesicular disease virus (SVDV; EC50 = 45.2 μM).2 In vivo, 2CMC reduces viral shedding to undetectable levels in a mouse model of persistent norovirus infection.3
1.Benzaria, S., Bardiot, D., Bouisset, T., et al.2′-C-Methyl branched pyrimidine ribonucleoside analogues: Potent inhibitors of RNA virus replicationAntivir. Chem. Chemother.18(4)225-242(2007) 2.Goris, N., De Palma, A., Toussaint, J.F., et al.2'-C-methylcytidine as a potent and selective inhibitor of the replication of foot-and-mouth disease virusAntiviral Res.73(3)161-168(2007) 3.Rocha-Pereira, J., Van Dycke, J., and Neyts, J.Treatment with a nucleoside polymerase inhibitor reduces shedding of murine norovirus in stool to undetectable levels without emergence of drug-resistant variantsAntimicrob. Agents Chemother.60(3)1907-1911(2015)
Cas No. | 20724-73-6 | SDF | |
别名 | 2'-C-甲基胞嘧啶核苷,2'-C-Methylcytidine; NM-107 | ||
Canonical SMILES | NC(C=CN1[C@@H]2O[C@H](CO)[C@@H](O)[C@@]2(C)O)=NC1=O | ||
分子式 | C10H15N3O5 | 分子量 | 257.24 |
溶解度 | Water : ≥ 50 mg/mL (194.37 mM) | 储存条件 | Store at -20°C |
General tips | 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。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
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Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 |
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 3.8874 mL | 19.4371 mL | 38.8742 mL |
5 mM | 0.7775 mL | 3.8874 mL | 7.7748 mL |
10 mM | 0.3887 mL | 1.9437 mL | 3.8874 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Quality Control & SDS
- View current batch:
- Purity: >98.50%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet