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Ganga Reddy Velma ; Zhengnan Shen ; Cameron Holberg , et al. JMC,2024,67(16):13681-13702. DOI: 10.1021/acs.jmedchem.4c00378 PubMed ID: 39102360
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Abstract: The SARS-CoV-2 papain-like protease (PLpro), essential for viral processing and immune response disruption, is a promising target for treating acute infection of SARS-CoV-2. To date, there have been no reports of PLpro inhibitors with both submicromolar potency and animal model efficacy. To address the challenge of PLpro’s featureless active site, a noncovalent inhibitor library with over 50 new analogs was developed, targeting the PLpro active site by modulating the BL2-loop and engaging the BL2-groove. Notably, compounds 42 and 10 exhibited strong antiviral effects and were further analyzed pharmacokinetically. 10, in particular, showed a significant lung accumulation, up to 12.9-fold greater than plasma exposure, and was effective in a mouse model of SARS-CoV-2 infection, as well as against several SARS-CoV-2 variants. These findings highlight the potential of 10 as an in vivo chemical probe for studying PLpro inhibition in SARS-CoV-2 infection.
Purchased from AmBeed: 2840-04-2 ; 1310584-14-5 ; 1122-58-3 ; 101623-68-1
CAS No. : | 1310584-14-5 | MDL No. : | MFCD20264878 |
Formula : | C45H59ClNPPd | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | - |
M.W : | 786.80 | Pubchem ID : | - |
Synonyms : |
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Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | Packing Group: | |
GHS Pictogram: |