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- 保存条件:
低温
- 库存:
大量
- 供应商:
上海善然生物科技有限公司
- 规格:
5mg
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. [2] 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. [2]
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文献和实验相关实验
感染。这些细胞可以转录沉默的原病毒,因此设计出诱导病毒基因表达的策略,以便宿主免疫反应可以介导感染细胞的清除或者使细胞经历病毒诱导的细胞死亡,这引起了科学家们的极大兴趣 3。在世界卫生组织 2016 年版的《使用抗逆转录病毒药物治疗和预防艾滋病毒感染综合指南》中,纳入了新的替代性抗逆转录病毒药物选用方案。将度鲁特韦(dolutegravir)和低剂量依法韦仑(efavirenz)作为一线疗法,而拉替拉韦(raltegravir)和达芦那韦(darunavir)/利托那韦(ritonavir)作为二线疗法
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Dolutegravir (GSK1349572)S2667
¥2211









