Synthesis of Low‐Molecular‐Weight Fucoidan Analogue and Its Inhibitory Activities against Heparanase and SARS‐CoV‐2 Infection

Abstract Heparan sulfate (HS) is ubiquitous on cell surfaces and is used as a receptor by many viruses including SARS‐CoV‐2. However, increased activity of the inflammatory enzyme heparanase (HPSE), which hydrolyses HS, in patients with COVID‐19 not only increases the severity of symptoms but also may facilitate the spread of the virus by degrading HS on the cell surface. Therefore, synthetic HPSE blockades, which can bind to SARS‐CoV‐2 spike protein (SARS‐CoV‐2‐S) and inhibit viral entry, have attracted much attention. This study investigated the development of a new dual‐targeting antiviral agent against HPSE and SARS‐CoV‐2‐S using fucoidan as a structural motif. It was found that all‐sulfated fucoidan derivative 10 , which exhibited the highest binding affinity to SARS‐CoV‐2‐S among 13 derivatives, also showed the highest inhibitory activity against HPSE. Based on this, a newly designed and synthesized fucoidan analogue 16 , in which the octyl group of 10 was changed to a cholestanyl group, was found to show approximately 3 times higher activity than 10 but did not inhibit factor Xa associated with undesired anticoagulant effects. The binding affinity of 16 to SARS‐CoV‐2‐S was significantly increased approximately 400‐fold over that of 10 . The binding of 16 to SARS‐CoV‐2‐S inhibited the binding between SARS‐CoV‐2‐S and heparin and between SARS‐CoV‐2‐S and ACE2. Furthermore, 16 effectively inhibited infection by the SARS‐CoV‐2 Wuhan strain and two Omicron subvariants.