SARS-CoV-2 Mpro-IN-2
CAS No. 2768834-39-3
SARS-CoV-2 Mpro-IN-2 ( —— )
产品货号. M35696 CAS No. 2768834-39-3
SARS-CoV-2 Mpro-IN-2 (化合物 GC-14) 是一种选择性的、低细胞毒性的非共价 Mpro 抑制剂(IC50=0.40 μM),具有良好的抗 SARS-CoV-2 活性 (EC50=1.1 μM)。SARS-CoV-2 Mpro-IN-2 可用于 COVID-19 的研究。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥3924 | 有现货 |
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| 10MG | ¥5586 | 有现货 |
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| 25MG | ¥8138 | 有现货 |
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| 50MG | ¥10974 | 有现货 |
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| 100MG | ¥14310 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称SARS-CoV-2 Mpro-IN-2
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述SARS-CoV-2 Mpro-IN-2 (化合物 GC-14) 是一种选择性的、低细胞毒性的非共价 Mpro 抑制剂(IC50=0.40 μM),具有良好的抗 SARS-CoV-2 活性 (EC50=1.1 μM)。SARS-CoV-2 Mpro-IN-2 可用于 COVID-19 的研究。
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产品描述SARS-CoV-2 Mpro-IN-2 (compound GC-14) is a selective, low cytotoxic and non-covalent Mpro inhibitor (IC50=0.40 μM) with good anti-SARS-CoV-2 activity (EC50=1.1 μM). SARS-CoV-2 Mpro-IN-2 can be used in COVID-19 studies.
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体外实验SARS-CoV-2 Mpro-IN-2 (0.01-100 μM; 4 h) shows low cytotoxicity in Vero E6 cells.Cell Cytotoxicity Assay Cell Line:Vero E6 cells Concentration:0.01-100 μM Incubation Time:4 h Result:Exhibited low cytotoxicity with a CC50 value of more than 100 μM.
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体内实验SARS-CoV-2 Mpro-IN-2 (2 mg/kg; i.v.; single) exhibits clearance rate (CL), mean residence time (MRT), and half-life (t1/2) are 3140 mL/h/kg, 0.40 h, and 0.36 h, respectively.SARS-CoV-2 Mpro-IN-2 (10 mg/kg; p.o.; single) is rapidly absorbed, with a time-to-maximum concentration (Tmax) of 0.5 h, and shows a moderate pharmacokinetic profile including a favorable t1/2 (1.73 h), a maximum concentration (Cmax) 74.6 ng/mL, and an area under curve (AUC0-t) of 235 ng h/mL.Animal Model:Male Sprague-Dawley rats.Dosage:2 mg/kg (for i.v.); 10 mg/kg (for p.o.).Administration:Intravenous injection or oral administration; single.
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同义词——
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通路Others
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靶点Other Targets
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受体SARS-CoV
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研究领域——
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适应症——
化学信息
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CAS Number2768834-39-3
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分子量475.39
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分子式C22H20Cl2N4O2S
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纯度>98% (HPLC)
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溶解度——
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SMILESC(NCC1=CC=CS1)(=O)[C@H]2N(CCN(C(=O)C=3C=CC=NC3)C2)C4=CC(Cl)=C(Cl)C=C4
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Gao S, et al. Discovery and Crystallographic Studies of Trisubstituted Piperazine Derivatives as Non-Covalent SARS-CoV-2 Main Protease Inhibitors with High Target Specificity and Low Toxicity. J Med Chem. 2022 Sep 15:acs.jmedchem.2c01146. ?
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