CAS NO: | 1611493-60-7 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
1mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Bictegravir (GS-9883) is a potent inhibitor ofHIV-1integrasewith anIC50of 7.5 nM. | ||||||||||||||||
IC50& Target | IC50: 7.5 nM (HIV-1 integrase)[1] | ||||||||||||||||
体外研究 (In Vitro) | Bictegravir (BIC) inhibits the strand transfer activity with an IC50of 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 IN, with an IC50of 241±51 nM. Bictegravir enhances the accumulation of 2-LTR circles ~5-fold relative to the mock-treated control and reduces the amount of authentic integration products in infected cells by 100-fold. Bictegravir potently inhibits HIV-1 replication in both MT-2 and MT-4 cells with EC50s of 1.5 and 2.4 nM, respectively. Bictegravir exhibits potent antiviral effects in both primary CD4+T lymphocytes and monocyte-derived macrophages, with EC50s of 1.5±0.3 nM and 6.6±4.1 nM, respectively, which are comparable to values obtained in T-cell lines[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 449.38 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C21H18F3N3O5 | ||||||||||||||||
CAS 号 | 1611493-60-7 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, sealed storage, away from moisture and light *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 83.3 mg/mL(185.37 mM;Need ultrasonic and warming) 配制储备液
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