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Molnupiravir {[allProObj[0].p_purity_real_show]}

货号:A1463646

Molnupiravir是一种口服生物可用的高效核糖核苷类类似物,能抑制多种RNA病毒的复制,包括SARS-CoV-2(COVID-19的致病因子)。

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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+
Molnupiravir 化学结构 CAS号:2492423-29-5
Molnupiravir 化学结构
CAS号:2492423-29-5
Molnupiravir 3D分子结构
CAS号:2492423-29-5
Molnupiravir 化学结构 CAS号:2492423-29-5
Molnupiravir 3D分子结构 CAS号:2492423-29-5
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Molnupiravir 纯度/质量文件 产品仅供科研

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Molnupiravir 生物活性

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].

Molnupiravir 细胞实验

Cell Line
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

Molnupiravir 动物实验

Species
Animal Model
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

Molnupiravir 参考文献

[1]Sheahan TP, Sims AC, Zhou S, et al. An orally bioavailable broad-spectrum antiviral inhibits SARS-CoV-2 in human airway epithelial cell cultures and multiple coronaviruses in mice. Sci Transl Med. 2020;12(541):eabb5883.

[2]Toots M, Yoon JJ, Cox RM, et al. Characterization of orally efficacious influenza drug with high resistance barrier in ferrets and human airway epithelia. Sci Transl Med. 2019;11(515):eaax5866.

[3]Singh AK, Singh A, Singh R, Misra A. Molnupiravir in COVID-19: A systematic review of literature. Diabetes Metab Syndr. 2021;15(6):102329.

Molnupiravir 实验方案

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

Molnupiravir 技术信息

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

请根据您的动物给药指南选择适当的溶解方案。
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
方案 一
方案 二
方案 三
配制的工作液建议现用现配,短期内尽快用完。 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
方案 一
方案 二
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