Inhibition of hiv-1 infection by synthetic peptide analogues derived from the nh2-Terminal extracellular region of gpr1
摘要:
Several shortened peptide analogues of the N-terminal domain of GPR1, an orphan G protein-coupled receptor (GPCR). were prepared and their anti-HIV-1 activities were evaluated. Some of the prepared compounds, especially sulfated derivatives. showed potent inhibitory activity against a broad range of HIV-1, including T cell-tropic, dual cell-tropic and brain-derived (BT) cell-tropic HIV-1 strains. (C) 2001 Elsevier Science Ltd. All rights reserved.
Several shortened peptide analogues of the N-terminal domain of GPR1, an orphan G protein-coupled receptor (GPCR). were prepared and their anti-HIV-1 activities were evaluated. Some of the prepared compounds, especially sulfated derivatives. showed potent inhibitory activity against a broad range of HIV-1, including T cell-tropic, dual cell-tropic and brain-derived (BT) cell-tropic HIV-1 strains. (C) 2001 Elsevier Science Ltd. All rights reserved.