Enfuvirtide (T20; DP178) acetate is an anti-HIV-1 fusion inhibitor peptide.
性状
Solid
IC50 & Target[1][2]
HIV fusion
体外研究(In Vitro)
A cell-cell fusion assay reveals that the effective concentration for achieving 50% inhibition (IC50) of Enfuvirtide is 23 ± 6 nM. IFN-λs (1, 2, or 3) or the antiretrovirals (AZT, Efavirenz, Indinavir, and Enfuvirtide) significantly inhibita the expression of HIV p24 antigen and Gag gene in macrophages. IFN-λs (1, 2, or 3) also enhanced the anti-HIV (Bal) effect of AZT, Efavirenz, Indinavir, and Enfuvirtide. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Enfuvirtide has a T 1/2 of 3.8 h. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Sealed storage, away from moisturePowder -80°C 2 years;-20°C 1 year
[1]. Figueira TN, et al. Quantitative analysis of molecular partition towards lipid membranes using surface plasmon resonance. Sci Rep. 2017 Mar 30;7:45647.[2]. Cao P, et al. The improved efficacy of Sifuvirtide compared with Enfuvirtide might be related to its selectivity for the rigid biomembrane, as determined through surface plasmon resonance. PLoS One. 2017 Feb 16;12(2):e0171567.
溶解度数据
In Vitro: DMSO : 100 mg/mL (21.97 mM; Need ultrasonic)H2O : 2 mg/mL (0.44 mM; Need ultrasonic)配制储备液