Emivirine
CAS No. 149950-60-7
Emivirine ( —— )
产品货号. M34240 CAS No. 149950-60-7
Emivirine (MKC-442) 是有效的非核苷逆转录酶的抑制剂 (NNRTIs),对dTTP 和 dGTP 依赖性 DNA 或 RNA 聚合酶活性的 Ki 值分别为 0.20 和 0.01 μM。Emivirine 具有有效且选择性的抗 HIV-1 活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥388 | 有现货 |
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| 5MG | ¥589 | 有现货 |
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| 10MG | ¥953 | 有现货 |
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| 25MG | ¥1548 | 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Emivirine
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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Emivirine (MKC-442) 是有效的非核苷逆转录酶的抑制剂 (NNRTIs),对dTTP 和 dGTP 依赖性 DNA 或 RNA 聚合酶活性的 Ki 值分别为 0.20 和 0.01 μM。Emivirine 具有有效且选择性的抗 HIV-1 活性。
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产品描述Emivirine (MKC-442) is a non-nucleoside reverse transcriptase inhibitors (NNRTIs) with Ki values of 0.20 and 0.01 μM for dTTP- and dGTP-dependent DNA or RNA polymerase activity, respectively. Emivirine displays potent and selective anti-human immunodeficiency virus type 1 (HIV-1) activity.
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体外实验Emivirine (EMV) is also specific for HIV-1 RT and was without effect on HIV-2.Emivirine (EMV) has no obvious toxicity for human healthy cells.:Cell Viability Assay Cell Line:Human bone marrow cells collected from normal healthy volunteers.Concentration:0, 0.1, 1, 10, or 100 μM.Incubation Time:14 days.Result:At concentrations of 0.1 to 10 μM, no effect on cell growth, lactic acid production, mitochondrial DNA synthesis, or mitochondrial structure was seen compared to what occurred with untreated HepG2 cells.
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体内实验Tthe approximate lethal oral dose of Emivirine (EMV) for rats was ≥3 g/kg for males and 2.5 g/kg for females.Animal Model:Male Sprague-Dawley rats.Dosage:50 mg/kg.Administration:Gavage.Result:The oral absorption was 68%.
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同义词——
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通路Microbiology/Virology
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靶点HIV
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受体HIV Protease
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研究领域——
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适应症——
化学信息
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CAS Number149950-60-7
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分子量302.37
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分子式C17H22N2O3
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : 100 mg/mL (330.72 mM; 超声助溶 )
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SMILESC(C1=C(C(C)C)C(=O)NC(=O)N1COCC)C2=CC=CC=C2
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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. Panita Decha, et al. Theoretical studies on the molecular basis of HIV-1RT/NNRTIs interactions. J Enzyme Inhib Med Chem. 2011 Feb;26(1):29-36.?
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