Article citationsMore>>

Stoll, V., Qin, W.Y., Stewart, K.D., Jakob, C., Park, C., Walter, K., Simmer, R.L., Helfrich, R., Bussiere, D., Kao, J., Kempf, D., Sham, H.L. and Norbeck, D.W. (2002) X-Ray Crystallographic Structure of ABT-378 (Lopinavir) Bound to HIV-1 Protease. Bioorganic & Medicinal Chemistry, 10, 2803-2806.
https://doi.org/10.1016/S0968-0896(02)00051-2

has been cited by the following article:

• TITLE: In Situ Characterization of Lopinavir by ATR-FTIR Biospectroscopy

  AUTHORS: Alireza Heidari

  KEYWORDS: ATR-FTIR Biospectroscopy, Simulation, Lopinavir, Breakdown, Coronavirus Disease-2019, COVID-19, Infection, Protective and Therapeutic Effect, Potent Drug

  JOURNAL NAME: Computational Chemistry, Vol.8 No.3, July 14, 2020

  ABSTRACT: Lopinavir is an antiretroviral of the protease inhibitor class (Figure 1 and Figure 2). It is used against HIV infections as a fixed-dose combination with another protease inhibitor, ritonavir (lopinavir/ritonavir). In the current research, the stimulated ATR-FTIR biospectroscopy of liquid sample of Lopinavir was investigated. The stimulated ATR-FTIR diffractions emitted through focusing the second harmonic laser beam Nd:YAG into the sample were recorded by Echelle spectrometer and ICCD detector. Increasing the energy of laser beam from 2.6 (mJ) to 16 (mJ) led to increase in stimulated ATR-FTIR signal but after breakdown threshold of liquid sample, further increasing energy led to the decrease in stimulating ATR-FTIR signals and for energies higher than 20 (mJ), they were disappeared.