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Dolutegravir,GSK1349572 1051375-16-6德罗特韦(GSK-1349

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Dolutegravir,GSK1349572 1051375-16-6德罗特韦(GSK-1349572,DTG)
上海一基实业有限公司是主要从事57配套试剂的生产和销售的企业,产品用途:科研实验,标准对照品研究中心代理的作为一种衡量标准Dolutegravir,GSK1349572

Dolutegravir,GSK1349572  1051375-16-6德罗特韦(GSK-1349572,DTG)

 

德罗特韦(GSK-1349572,DTG)
分子式:C20H19F2N3O5    分子量:419.38
 
产品描述
S/GSK1349572 (GSK1349572) 是HIV integrase抑制剂,IC50为2.7 nM, 适度有效作用于抗Raltegravir的显著突变体Y143R, Q148K, N155H, 和 G140S/Q148H。
靶点
HIV integrase
         
IC50
2.7 nM
         
体外研究
S/GSK1349572 shows the potent inhibitory effect on nine clinical isolates from integrase inhibitor-na?ve HIV-2-infected patients with EC50 ranging from 0.2 nM -1.4 nM. [1] In vitro, S/GSK1349572 inhibits recombinant HIV-1 integrase-catalyzed strand transfer with IC50 of 2.7 nM. Furthermore, S/GSK1349572 potently inhibits HIV replication in cells such as peripheral blood mononuclear cells (PBMCs), MT-4 cells and CIP4 cells infected with a self-inactivating PHIV lentiviral vector with EC50 of 0,51 nM, 0.71 nM and 2.2 nM, respectively.In vitro, S/GSK1349572 exhibits potent activity against five different nonnucleoside reverse transcription inhibitor--resistant or nucleoside reverse transcription inhibitor--resistant viruses with EC50 ranging from 1.3 nM -2.1 nM. Similarly to that against wild-type virus, S/GSK1349572 shows equivalent activity against two protease inhibitor-resistant viruses with EC50 of 0.36 nM and 0.37 nM, respectively.
体内研究
 
溶解性
DMSO 84 mg/mL,水 <1 mg/mL,乙醇 <1 mg/mL
稳定性
2年 -20°C粉状,6月-80°C溶于DMSO
特征
S/GSK1349572 (GSK1349572) is a next-generation and two-metal-binding HIV integrase strand transfer inhibitor.

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