Hong Liu

TL;DR: Two peptidomimetic aldehydes were designed, synthesized, and evaluated as antiviral drug candidates, and both exhibited excellent inhibitory activity and potent anti-SARS-CoV-2 infection activity.

TL;DR: A Ni3S2 nanorods/Ni foam composite electrode is prepared as a high-performance catalyst for the oxygen evolution reaction (OER), which exhibits excellent OER activity with a small overpotential of ∼157 mV based on the onset of catalytic current as discussed by the authors.

TL;DR: This tutorial review introduces the characteristics of 1D TiO2 nanostructures, the design principles for the fabrication of1DTiO2NSHs, and summary of the recent progress in developing synthesis methods and applications of 1Ds in different fields is summarized.

TL;DR: Self-assembled copper-amino acid mercaptide nanoparticles (Cu-Cys NPs) for in situ glutathione-activated and H2O2-reinforced chemodynamic therapy for drug-resistant breast cancer efficiently inhibited drug- resistant breast cancer without causing obvious systemic toxicity.

TL;DR: The 2.7 angstrom–resolution crystal structure of human CCR5 bound to the marketed HIV drug maraviroc reveals a ligand-binding site that is distinct from the proposed major recognition sites for chemokines and the viral glycoprotein gp120, providing insights into the mechanism of allosteric inhibition of chemokine signaling and viral entry.