| 中文名称： |
2'-C-甲基胞嘧啶核苷 |
| 英文名称: |
NM107 |
| 产品分类： |
核酸及衍生物 |
| CAS号： |
20724-73-6 |
| 分子式： |
C10H15N3O5 |
| 分子量： |
257.24 |
*产品基础信息：
【产品中文名称】2'-C-甲基胞嘧啶核苷;
【产品英文名称】NM107;
【纯度指标】97.85%;
【品牌】TargetMol;
【CAS号】20724-73-6;
【浓度】;
Product Introduction
Bioactivity
| 名称 | NM107 |
| 描述 | NM107 (2'-C-Methylcytidine) is a ribonucleoside with broad-spectrum antiviral activity, is an nucleoside inhibitor of the hepatitis C virus (HCV) NS5B polymerase, NM 107 in the wild-type replicon cells with the EC50 of 1.85 μM |
| 动物实验 | For all experiments, age- and sex-matched mice 8 to 12 weeks of age were infected by oral gavage with 10^6 CCID50 (50% cell culture infective doses) of CR6. At 7 days postinfection (p.i.), mice were left untreated (n = 9) or were treated with 100 mg/kg daily of 2'-C-Methylcytidine(2CMC) subcutaneously for 5 (n = 4), 7 (n = 4), or 11 (n = 4) days. Two more rounds of a 14-day treatment (with an ～4-week interval in between) with 2CMC (n = 10) or favipiravir (200 mg/kg daily by oral gavage [n = 5]) were given. On each day after infection, the general condition and weight of treated and untreated mice were assessed, individual stool samples were collected (whenever possible during one daily period of observation), and levels of MNV RNA were quantified by reverse transcriptase quantitative PCR (RT-qPCR)[2]. |
| 体外活性 | NM107 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. NM107 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 corona virus (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)[1]. |
| 体内活性 | Prolonged norovirus shedding may occur in certain patients, such as organ transplant recipients. Established a mouse model for persistent norovirus infection (using the mouse norovirus MNV.CR6 strain). The nucleoside viral polymerase inhibitor 2′-C-methylcytidine (2CMC), but not favipiravir (T-705), reduced viral shedding to undetectable levels. Viral rebound was observed after stopping treatment, which was again effectively controlled by treatment with 2CMC. No drug-resistant variants emerged[2]. |
| 存储条件 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | H2O : 50 mg/mL (194.37 mM), Sonication is recommended.
10% DMSO+40% PEG300+5% Tween 80+45% Saline : 2 mg/mL (7.77 mM), Sonication is recommended.
|
| 关键字 | NM107 | NM 107 | Inhibitor | inhibit | Hepatitis C virus | HCVProtease | HCV Protease | HCV |
| 相关产品 | Resiquimod | Chlorcyclizine | RO8191 | Honokiol | Artemisinin | EIDD-1931 | Methyl 2-amino-5-bromobenzoate | Deferiprone | (Tetrahydro-2H-pyran-4-yl)methanol | Ribavirin | HCV-IN-29 | Sofosbuvir |
| 相关库 | Inhibitor Library | Bioactive Compound Library | Bioactive Compounds Library Max | ReFRAME Related Library | Anti-Infection Compound Library | NO PAINS Compound Library | Anti-Viral Compound Library | Immunology/Inflammation Compound Library | Human Metabolite Library | Bioactive Compound Library Plus |
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