tetano
Editor, Senior Moderator
Bioorg Med Chem Lett
. 2024 Feb 20:129672.
doi: 10.1016/j.bmcl.2024.129672. Online ahead of print. Discovery of an ellipticine derivative as TLR3 inhibitor against influenza A virus and SARS-CoV-2
Yue Pan[SUP] 1 [/SUP], Qiuyue Fu[SUP] 1 [/SUP], Yinyan Li[SUP] 1 [/SUP], Jie Yang[SUP] 2 [/SUP], Kui Cheng[SUP] 3 [/SUP]
Affiliations
Influenza and COVID-19 continue to pose global threats to public health. Classic antiviral drugs have certain limitations, coupled with frequent viral mutations leading to many drugs being ineffective, the development of new antiviral drugs is urgent. Meanwhile, the invasion of influenza virus can cause an immune response, and an excessive immune response can generate a large number of inflammatory storms, leading to tissue damage. Toll-like receptor 3 (TLR3) recognizes virus dsRNA to ignite the innate immune response, and inhibit TLR3 can block the excess immune response and protect the host tissues. Taking TLR3 as the target, SMU-CX1 was obtained as the specific TLR3 inhibitor by high-throughput screening of 15,700 compounds with IC[SUB]50[/SUB] value of 0.11 µM. Its anti-influenza A virus activity with IC[SUB]50[/SUB] ranged from 0.14 to 0.33 µM against multiple subtypes of influenza A virus and also showed promising anti-SARS-CoV-2 activity with IC[SUB]50[/SUB] at 0.43 µM. Primary antiviral mechanism study indicated that SMU-CX1 significantly inhibited PB2 and NP protein of viruses, it can also inhibit inflammatory factors in host cells including IFN-β, IP-10 and CCL-5. In conclusion, this study demonstrates the potential of SMU-CX1 in inhibiting IAV and SARS-CoV-2 activity, thereby offering a novel approach for designing antiviral drugs against highly pathogenic viruses.
Keywords: Anti-inflammatory; Influenza A virus; SARS-CoV-2; Small molecule; Toll-like receptor 3.
. 2024 Feb 20:129672.
doi: 10.1016/j.bmcl.2024.129672. Online ahead of print. Discovery of an ellipticine derivative as TLR3 inhibitor against influenza A virus and SARS-CoV-2
Yue Pan[SUP] 1 [/SUP], Qiuyue Fu[SUP] 1 [/SUP], Yinyan Li[SUP] 1 [/SUP], Jie Yang[SUP] 2 [/SUP], Kui Cheng[SUP] 3 [/SUP]
Affiliations
- PMID: 38387691
- DOI: 10.1016/j.bmcl.2024.129672
Influenza and COVID-19 continue to pose global threats to public health. Classic antiviral drugs have certain limitations, coupled with frequent viral mutations leading to many drugs being ineffective, the development of new antiviral drugs is urgent. Meanwhile, the invasion of influenza virus can cause an immune response, and an excessive immune response can generate a large number of inflammatory storms, leading to tissue damage. Toll-like receptor 3 (TLR3) recognizes virus dsRNA to ignite the innate immune response, and inhibit TLR3 can block the excess immune response and protect the host tissues. Taking TLR3 as the target, SMU-CX1 was obtained as the specific TLR3 inhibitor by high-throughput screening of 15,700 compounds with IC[SUB]50[/SUB] value of 0.11 µM. Its anti-influenza A virus activity with IC[SUB]50[/SUB] ranged from 0.14 to 0.33 µM against multiple subtypes of influenza A virus and also showed promising anti-SARS-CoV-2 activity with IC[SUB]50[/SUB] at 0.43 µM. Primary antiviral mechanism study indicated that SMU-CX1 significantly inhibited PB2 and NP protein of viruses, it can also inhibit inflammatory factors in host cells including IFN-β, IP-10 and CCL-5. In conclusion, this study demonstrates the potential of SMU-CX1 in inhibiting IAV and SARS-CoV-2 activity, thereby offering a novel approach for designing antiviral drugs against highly pathogenic viruses.
Keywords: Anti-inflammatory; Influenza A virus; SARS-CoV-2; Small molecule; Toll-like receptor 3.