The coronavirus (CoV) that causes severe acute respiratory syndrome, or SARS, is called SARS-CoV. CoVs, which are enveloped viruses with positive-sense, single-stranded RNA and can target the human respiratory system to spread disease, include not only the SARS virus but also MERS and SARS-CoV-2, which is the source of COVID-19.
The spike (S), membrane (M), envelope (E), and nucleocapsid (N) proteins are the four main structural proteins of CoVs. By binding to a cellular receptor (ACE2 for SARS-CoV and SARS-CoV-2, DPP4 for MERS-CoV), an S protein mediates the CoV entry into host cells, which is followed by the fusion of the virus and host cell membranes. Following entry, a large number of nonstructural proteins, including Mpro (main protease or 3CLpro), PLpro (papain-like protease), and RdRp (RNA-dependent RNA polymerase), participate in genome replication and subgenomic RNA transcription.The structural proteins are then translated, put together into mature virions, and exocytosed to release them via vesicles. It is noteworthy that a protease known as TMPRSS2 (transmembrane protease, serine 2), which cleaves S protein, plays crucial roles throughout the entire life of CoVs (such as attachment, assembling, and release). For the treatment of diseases brought on by CoVs, all the proteins and subcellular structures involved in the life cycle of CoVs are promising targets.
Structure | Cat No. | Product Name | CAS No. | Product Description |
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V76086 | SARS-CoV-2 nsp3-IN-1 | 2892105-43-8 | SARS-CoV-2 nsp3-IN-1 (Compound 15c) is a Mac1 (SARS-CoV-2 nsp3 macrodomain) inhibitor (antagonist) with IC50 of 6.1 μM. |
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V105031 | SARS-CoV-2 PLpro-IN-1 | 3053753-61-7 | SARS-CoV-2 PLpro-IN-1 (Compound 85) is a non-covalent competitive inhibitor of SARS-CoV-2 PLpro with IC50 of 15.06 μM and Ki of 22.93 μM. |
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V54397 | SARS-CoV-2-IN-10 | 2722634-95-7 | SARS-CoV-2-IN-10 is a potent and non-toxic inhibitor of SARS-CoV-2 3CL protease (3CLpro) with IC50 and EC50 of 0.13 and 1.03 nM respectively. |
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V94382 | SARS-CoV-2-IN-100 | 374543-46-1 | SARS-CoV-2-IN-100 (Compound 172) is a SARS-CoV-2 inhibitor that exhibits broad-spectrum antiviral activity against different SARS-CoV-2 variants. |
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V93757 | SARS-CoV-2-IN-101 | SARS-CoV-2-IN-101 (Compound 10O) is a potent, oral SARS-CoV-2 inhibitor with an EC50 value of 0.64 µM against HCoV-229E. | |
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V93274 | SARS-CoV-2-IN-102 | 3055041-73-8 | SARS-CoV-2-IN-102 (Example 58) is a SARS-CoV papain-like protease (SARS-CoV PLpro) inhibitor with IC50 <100 nM. |
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V103983 | SARS-CoV-2-IN-106 | 2863607-73-0 | SARS-CoV-2-IN-106 (Compound 19) is a SARS-CoV-2 papain inhibitor with IC50 values of 0.44 μM and 0.18 μM for papain and viral replication, respectively. |
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V104908 | SARS-CoV-2-IN-107 | SARS-CoV-2-IN-107 (Compound A7) is an inhibitor of SARS-CoV-2 3CLpro with IC50 of 261.3 nM. | |
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V104665 | SARS-CoV-2-IN-108 | SARS-CoV-2-IN-108 (Compound 29) is an inhibitor of SARSCoV-2 papain-like protease with IC50 of 0.14 µM. | |
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V54409 | SARS-CoV-2-IN-11 | 2722635-28-9 | SARS-CoV-2-IN-11 is a potent and nontoxic inhibitor of SARS-CoV-2 3CL protease (3CLpro) with IC50 and EC50 of 0.17 and 1.45 nM, respectively. |
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V77713 | SARS-CoV-2-IN-25 disodium | SARS-CoV-2-IN-25 (Compound CP026) disodium is a potent inhibitor of SARS-CoV-2 spike pseudoparticle transduction with IC50 of 1.6 μM. | |
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V37548 | SARS-CoV-2-IN-31 | 1017691-52-9 | SARS-CoV-2-IN-31 is a potent COVID-19 inhibitor. |
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V37544 | SARS-CoV-2-IN-32 | 96068-42-7 | SARS-CoV-2-IN-32 (compound 3g) is a COVID-19 inhibitor. |
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V37543 | SARS-CoV-2-IN-33 | 299919-79-2 | SARS-CoV-2-IN-33 (compound 3m) is a COVID-19 inhibitor. |
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V81366 | SARS-CoV-2-IN-34 | SARS-CoV-2-IN-34 (S-20-1) is a pan-coronavirus (CoV) fusion inhibitor (antagonist) with broad-spectrum inhibitory activity that can penetrate the BBB (blood-brain barrier). | |
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V54404 | SARS-CoV-2-IN-35 | 2757763-47-4 | SARS-CoV-2-IN-35 is an orally bioactive SARS-CoV-2 M pro inhibitor (antagonist) with a Ki of 12.1 nM. |
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V80058 | SARS-CoV-2-IN-36 | SARS-CoV-2-IN-36 is a potent inhibitor of SARS-CoV-2 Mpro (SARS-CoV) with IC50 of 2.37 μM and a Kd of 1.19 μM in an enzymatic assay. | |
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V54429 | SARS-CoV-2-IN-38 | 2882823-27-8 | SARS-CoV-2-IN-38 (compound 24) is a SARS-CoV-2 inhibitor (antagonist) with good oral bioavailability (F) in mice (F%=39.75%). |
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V54396 | SARS-CoV-2-IN-39 | 2882823-03-0 | SARS-CoV-2-IN-39 (compound 21) is a SARS-CoV-2 inhibitor (antagonist) with EC50 of 1 μM. |
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V78846 | SARS-CoV-2-IN-40 | SARS-CoV-2-IN-40 (Compound 19) is a SARS-CoV-2 inhibitor. |