| Literature DB >> 33560122 |
Yu-Ting Li, Chan Yang, Yan Wu1, Jun-Jiang Lv2, Xiao Feng, Xiaofei Tian3, Zhengzheng Zhou, Xiaoyan Pan1, Shuwen Liu, Li-Wen Tian.
Abstract
A new axial chiral binaphtoquinone, hypocrellone (1), and a new perylenequinone, hypomycin F (2), were isolated from the stromata of Hypocrella bambusae, together with five known compounds, 3-7. The structures of 1 and 2 were assigned by spectroscopic and HRESIMS data analyses. The axial chirality of 1 was determined by electronic circular dichroism data analysis, and the absolute configurations of 2 and 3 were determined by X-ray crystallography. The axial chirality of 7 was determined by UV-induced photooxidation from 4. Compounds 1, 4, and 5 showed inhibitory activity against pseudotyped SARS-CoV-2 infection in 293T-ACE2 cells with IC50 values of 0.17, 0.038, and 0.12 μM. Compounds 4 and 5 were also active against live SARS-CoV-2 infection with EC50 values of 0.22 and 0.21 μM, respectively. Further cell-cell fusion assays, surface plasmon resonance assays, and molecular docking studies revealed that 4 and 5 could bind with the receptor-binding domain of SARS-CoV-2 S protein to prevent its interaction with human angiotensin-converting enzyme II receptor. Our results revealed that 4 and 5 are potential SARS-CoV-2 entry inhibitors.Entities:
Year: 2021 PMID: 33560122 DOI: 10.1021/acs.jnatprod.0c01136
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050