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Phthalimide derivatives as a new class of papain‐like protease inhibitors in SARS‐CoV‐2
Fischer, Thomas ; Frasson, David ; Sievers, Martin , et al. Arch. Pharm.,2024,e2400714. DOI: 10.1002/ardp.202400714 PubMed ID: 39648568
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Abstract: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) papain-like cysteine protease (PLpro) represents one of only two essential cysteine proteases involved in the regulation of viral replication. It, therefore, qualifies as a promising therapeutic target for the development of antiviral agents. We identified a previously synthesized protease inhibitor, resulting from an earlier project, as a PLpro inhibitor and crafted a structure-activity relationship around the hit, leading to the more potent inhibitors ZHAWOC6941 (17h) and ZHAWOC25153 (17o) displaying IC50 values of 8 and 7 μM, respectively. The two compounds represent a new class of PLpro inhibitors and, with single‐digit micromolar IC50 values, are comparable to inhibitors found in the literature.
Keywords: Inhibitor ; papain-like protease ; SARS-CoV-2 ; structure-activity relationship
Purchased from AmBeed: 42058-59-3 ; 2564-83-2 ; 14199-15-6 ; 534-17-8
CAS No. : | 42058-59-3 | MDL No. : | MFCD00017660 |
Formula : | C9H10O3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | AMDDOQIUPAINLH-UHFFFAOYSA-N |
M.W : | 166.17 | Pubchem ID : | 39129 |
Synonyms : |
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Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P273 | UN#: | N/A |
Hazard Statements: | H302-H412 | Packing Group: | N/A |
GHS Pictogram: |
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