Small Molecular Inactivators of HIV

我们已经开发和研究了我们的分子，无论是作为活性形式还是作为前药。我们已经开发了这些分子的大规模合成，并合作研究它们的抗病毒活性和评估它们的临床前毒性。总的来说，这些分子在人类PBMCs的HIV-1临床分离物中显示出广泛的活性，与其他fda批准的HIV药物表现出协同抗病毒相互作用的添加剂，并且在14次传代后不允许产生HIV抗性菌株。我们的分子没有明显的毒性。我们的分子也已成功地发展成为应用于杀微生物剂的平台。我们目前正在研究这些分子的详细机制，进行体内研究，并探索这些分子是否对SARS-CoV-2具有抗病毒活性。

We have developed and studied our molecule both in the active form and as a prodrug. We have developed large-scale syntheses for these molecules and worked in collaboration to study their antiviral activity and evaluate their preclinical toxicity. Overall, the molecules show broad range of activity across a panel of HIV-1 clinical isolates in human PBMCs, demonstrate additive to synergistic antiviral interactions with other FDA-approved HIV drugs, and fail to allow the generation of HIV resistant strains after 14 passages. There is no observable toxicity with our molecules. Our molecules have also been successfully developed into platforms for application as a microbicide. We are currently examining the detailed mechanism of these molecules, performing an in vivo study, and exploring whether these molecules have antiviral activity against SARS-CoV-2.