产品
编 号：F620489
分子式：C39H32ClF10N7O5S2
分子量：968.28
分子式：C39H32ClF10N7O5S2
分子量：968.28
产品类型
规格
价格
是否有货
1mg
询价
询价
5mg
询价
询价
10mg
询价
询价
25mg
询价
询价
50mg
询价
询价
100mg
询价
询价
结构图
CAS No: 2189684-44-2
产品详情
生物活性：
Lenacapavir (GS-6207) is a HIV-1 capsid inhibitor. Lenacapavir shows anti-HIV activity with an EC50 of 100 pM in MT-4 cells. Lenacapavir displays a mean EC50 of 50 pM (20-160 pM) against 23 HIV-1 clinical isolates from different subtypes in peripheral blood mononuclear cells (PBMCs). Lenacapavir is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
体外研究：
Lenacapavir (GS-6207) 是一种有效的衣壳靶向 HIV 复制抑制剂。Lenacapavir 在靶细胞 (EC50=23 pM)、全周期测定 (EC50=25 pM) 和生产细胞 (EC 50=439 下午)。Lenacapavir 会干扰 HIV-1 复制的早期和晚期阶段，但对早期阶段表现出更强的效力。
Lenacapavir (GS-6207) is a HIV-1 capsid inhibitor. Lenacapavir shows anti-HIV activity with an EC50 of 100 pM in MT-4 cells. Lenacapavir displays a mean EC50 of 50 pM (20-160 pM) against 23 HIV-1 clinical isolates from different subtypes in peripheral blood mononuclear cells (PBMCs). Lenacapavir is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
体外研究：
Lenacapavir (GS-6207) 是一种有效的衣壳靶向 HIV 复制抑制剂。Lenacapavir 在靶细胞 (EC50=23 pM)、全周期测定 (EC50=25 pM) 和生产细胞 (EC 50=439 下午)。Lenacapavir 会干扰 HIV-1 复制的早期和晚期阶段，但对早期阶段表现出更强的效力。
产品资料
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