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Bictegravir

    
10mM in DMSO

Bictegravir

源叶(MedMol)
T92292 一键复制产品信息
1611493-60-7
C21H18F3N3O5
449.38
GS-9883
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
T92292-1ml促销
10mM in DMSO

¥206.00 ¥185.00

10 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: ;COVID-19 InhibitorsInformationBictegravir (GS-9883) is a novel, potent, once-daily, unboosted inhibitor ofHIV-1 integrase.TargetsHIV-1 integraseIn vitroBictegravir exhibits potent and selective in vitro antiretroviral activity in both T-cell lines and primary human T lymphocytes, with 50% effective concentrations ranging from 1.5 to 2.4 nM and selectivity indices up to 8,700 relative to cytotoxicity. Bictegravir inhibits the strand transfer activity with an IC50 of 7.5 ± 0.3 nM. Relative to its inhibition of strand transfer activity, Bictegravir is a much weaker inhibitor of 3\'-processing activity of HIV-1 integrase, with an IC50 of 241 ± 51 nM. Bictegravir potently inhibits HIV-1 replication in both MT-2 and MT-4 cells with EC50s of 1.5 and 2.4 nM, respectively, and selectivity indices (50% cytotoxic concentration [CC50]/EC50) of ∼6,800 in MT-2 cells and ∼1,500 in MT-4 cells.
参考文献: 1. Tsiang M, et al. Antiviral Activity of Bictegravir (GS-9883), a Novel Potent HIV-1 Integrase Strand Transfer Inhibitor with an Improved Resistance Profile. Antimicrob Agents Chemother. 2016 Nov 21;60(12):7086-7097.
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.225 ml 11.126 ml 22.253 ml
5 mM 0.445 ml 2.225 ml 4.451 ml
10 mM 0.223 ml 1.113 ml 2.225 ml
50 mM 0.045 ml 0.223 ml 0.445 ml
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参考文献

质检证书(COA)

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摩尔浓度计算器

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