产品说明书

Raltegravir

Print
Chemical Structure| 518048-05-0 同义名 : 雷特格韦 (MK-0518) ;MK-0518
CAS号 : 518048-05-0
货号 : A121488
分子式 : C20H21FN6O5
纯度 : 98%
分子量 : 444.416
MDL号 : MFCD10698872
存储条件:

粉末 Sealed in dry,Store in freezer, under -20°C

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 105 mg/mL(236.26 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方:

2% DMSO+40% PEG 300+2% Tween 80+water 8 mg/mL

生物活性
描述 Raltegravir is the first approved clinical used inhibitor of integrase which can inhibit different kind of INs with alternative IC50 values, for example, the IC50 for the wild type and S217Q prototype foamy virus(PFV) IN are 90 nM and 40 nM respectively, while it’s 3.3 nM for HIV IN. In human MT-4 cells, the IC50 for raltegravir to inhibit overall IN activity was 9nM while it inhibited strand transfer step at 6.8nM. Besides, this compound could reduce HIV-1-induced CPE by 50% at the concentration of 1.4nM. At the concentration of >18 μM, MT-4 cells viability could be inhibited, suggesting a good antiviral activity for HIV. While MT-4 cells infected with SIVmac251, Raltegravir could inhibit SIVmac251 replication with a lower EC50 value (< 1nM) compared with HIV-1/HIV-2 infected MT-4 cells. In SIVmac251 infected CEMx174 cells, Raltegravir displayed reproducible anti-SIVmac251 activity by using of syncytia counts which could be still produced in the presence of this compound, while the syncytia formation induced apoptotic and necrotic cell death in MT-4 cells. In human CD4+ T cells, Raltegravir also showed inhibitory effect when the cell fraction showed expression of the CD4 antigen >94%. In one phase 2 study, 198 HIV-1 infected participants with the HIV-1 RNA level at >5000 copies/mL and the CD4 cell count >100 cells/μL were treated with 400 mg Raltegravir twice daily from 48 week. The result showed that the proportions of patients with an HIV-1 RNA level at <50 copies/mL were 83%. While in another phase 2 study, the 201 HIV-1 infected participants with the same RNA and CD4 levels were treated with gradient concentrations of Raltegravir twice daily showed a quicker reduction on RNA levels at week 48 that ranges in 83%-88% in a dose-independent manner.
细胞研究
细胞系 浓度 检测类型 检测时间 活动说明 数据源
human HeLa cells Function assay 48 h Antiviral activity against VSV-G pseudotyped HIV1 lentiviral particles infected in human HeLa cells incubated for 48 hrs by spectrofluorometry, IC50=10 nM 22858300
human HOS cells Function assay Antiviral activity against HIV1 harboring wild-type integrase infected in human HOS cells, EC50=4 nM 21493066
human MT2 cells Function assay 5 days Antiviral activity against HIV1 3B infected in human MT2 cells after 5 days by chemiluminescence in presence of fetal bovine serum, EC50=4 nM 19285389
临床研究
NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT01270802 HIV Phase 4 Completed - United States, Indiana ... 展开 >> Indiana University School of Medicine Indianapolis, Indiana, United States, 46202 收起 <<
NCT00654147 HIV Infections Phase 2 Completed - United States, Florida ... 展开 >> University of Miami AIDS Clinical Research Unit Miami, Florida, United States, 33136 收起 <<
NCT01270802 - Completed - -
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

2.25mL

0.45mL

0.23mL

11.25mL

2.25mL

1.13mL

22.50mL

4.50mL

2.25mL

参考文献

[1]Zhang X, Huang H, et al. Raltegravir Attenuates Experimental Pulmonary Fibrosis In Vitro and In Vivo. Front Pharmacol. 2019 Aug 20;10:903.

[2]Raltegravir