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+ |


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
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快速发货 顺丰冷链运输,1-2 天到达
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| 描述 | Molnupiravir (EIDD-2801) is an antiviral medication that inhibits the replication of certain RNA viruses. Molnupiravir has broad spectrum antiviral activity against influenza virus and multiple coronaviruses, such as SARS-CoV-2, MERS-CoV, SARS-CoV. Molnupiravir (50-500 mg/kg; p.o.; every 12 hours for 3 days) is robustly antiviral and able to prevent SARS-CoV replication and disease[1]. Molnupiravir (7 mg/kg; p.o.; twice daily for 3.5 days) significantly reduces shed virus load and duration of fever[2]. It has recently been tested in COVID-19. 1600mg daily dose of molnupiravir is safe and tolerable, without any serious adverse events up to 5.5 days, and significantly lower time to clearance (RNA negative) with molnupiravir 800mg twice daily. The study also showed a significant reduction in the risk of hospital admission or death by 50% with the treatment of molnupiravir[3]. |
| Concentration | Treated Time | Description | References | |
| A549-hACE2 cells | 2.8 μM | 48 hours | Evaluate the inhibitory effect of Molnupiravir on SARS-CoV-2 nLUC replication, showing dose-dependent antiviral effects | Sci Transl Med. 2022 May 4;14(643):eabm3410 |
| Calu-3 cells | 10 μM | 48 hours | To validate the antiviral activity of Molnupiravir against SARS-CoV-2 in Calu-3 cells, results showed significant antiviral effects. | Nature. 2022 Apr;604(7904):134-140 |
| human airway organoids (hAOs) | 10 μM | Validate the antiviral activity of Molnupiravir in hAOs. Results showed that 10 μM Molnupiravir reduced viral RNA levels by >90%. | Cell Res. 2022 Mar;32(3):322-324 | |
| human lung epithelial Calu-3 cells | 1 μM, 10 μM | 48 hours | Evaluate the antiviral activity of Molnupiravir against the Omicron variant. Results showed that 1 μM Molnupiravir reduced viral RNA by 70.4%, and complete inhibition was achieved at 10 μM and higher concentrations. | Cell Res. 2022 Mar;32(3):322-324 |
| Administration | Dosage | Frequency | Description | References | ||
| Syrian Gold hamsters | SARS-CoV-2 infection model | Oral | 250 mg/kg | Twice daily for 6 days | Evaluate the inhibitory effect of drug combination on SARS-CoV-2 replication, results showed combination treatment significantly reduced viral load | iScience. 2022 May 20;25(5):104293. |
| Ferrets | Upper respiratory infection model | Oral | 5 mg/kg | Twice daily for 4 days | Assess the therapeutic effect of EIDD-1931 on upper respiratory infection, showing significant reduction in viral shedding and prevention of transmission. | Nat Commun. 2022 Jul 29;13(1):4416. |
| Sprague-Dawley rats | Pregnant rat model | Intravenous injection | 100 mg/kg | Single dose | To investigate the pharmacokinetics and placental transfer of EIDD-1931 in pregnant rats. Results showed that EIDD-1931 rapidly crosses the placental barrier into the fetus, and its concentration in the fetus was higher than the IC50 for SARS-CoV-2. | EBioMedicine. 2023 Sep;95:104748 |
| C57BL/6 mice | SARS-CoV infection model | Oral | 50, 150, 500 mg/kg | Every 12 hours until the end of the study | Evaluate prophylactic and therapeutic efficacy of EIDD-2801 against SARS-CoV, significantly reduced weight loss and lung hemorrhage, decreased virus titer | Sci Transl Med. 2020 Apr 29;12(541):eabb5883 |
| Ferrets | SARS-CoV-2 infection model | Oral gavage | 5 mg/kg or 15 mg/kg | Twice daily, continued until four days after infection | To evaluate the therapeutic effect of oral MK-4482/EIDD-2801 on SARS-CoV-2 infection in ferrets, results showed significant reduction in upper respiratory tract viral load and complete suppression of virus transmission to untreated contact animals. | Nat Microbiol. 2021 Jan;6(1):11-18 |
| Ferrets | Upper respiratory infection model | Oral | 5 mg/kg | Every 12 hours for 4 days | Assess the therapeutic effect of Molnupiravir on upper respiratory infection, showing significant reduction in viral shedding and prevention of transmission. | Nat Commun. 2022 Jul 29;13(1):4416 |
| Syrian hamsters | SARS-CoV-2 infection model | Oral gavage | 250 mg/kg | Dosed every 12 hours for 3 days | To assess the inhibitory effect of MK-4482 on SARS-CoV-2 replication, results showed that MK-4482 significantly reduced viral lung loads and pathology | Nat Commun. 2021 Apr 16;12(1):2295 |
| BALB/C mice | SARS-CoV-2 Beta variant infection model | Oral | 50 mg/kg and 150 mg/kg | Twice daily for 2 days | To evaluate the antiviral efficacy of Molnupiravir in a mouse model of SARS-CoV-2 Beta variant infection, results showed significant reduction in viral titers and lung inflammation. | Nature. 2022 Apr;604(7904):134-140 |
| Balb/c mice | HCoV-OC43 infection model | Oral | 200 mpk | Once daily for 4 days | Evaluate the therapeutic efficacy of Molnupiravir against HCoV-OC43 infection, showing significant reduction in viral load. | Signal Transduct Target Ther. 2023 Sep 22;8(1):360 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
3.04mL 0.61mL 0.30mL |
15.18mL 3.04mL 1.52mL |
30.37mL 6.07mL 3.04mL |
|
| CAS号 | 2492423-29-5 |
| 分子式 | C13H19N3O7 |
| 分子量 | 329.31 |
| SMILES Code | O[C@H]1[C@@](O[C@H](COC(C(C)C)=O)[C@H]1O)(N2C(=O)N/C(=N\O)/C=C2)[H] |
| MDL No. | MFCD32663515 |
| 别名 | |
| 运输 | 蓝冰 |
| InChI Key | HTNPEHXGEKVIHG-QCNRFFRDSA-N |
| Pubchem ID | 145996610 |
| 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 |
| 溶解方案 |
DMSO: 50 mg/mL(151.83 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: 12 mg/mL(36.44 mM),配合低频超声助溶 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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