化学
蛋白酶抑制剂(药理学)
酶抑制剂
酶
蛋白酶
药理学
药物发现
生物化学
病毒学
生物活性
结构-活动关系
病毒
药品
抗病毒药物
体外
作者
Malla Reddy Gannarapu,Divakar Reddy Indukuri,Cameron Holberg,Kiira Ratia,O L Ramos,Savio Cardoza,Ganga Reddy Velma,Soumya Reddy Musku,Zuohuang Qi,Steve N. Slilaty,Zuomei Li,Lijun Rong,Gregory R. J. Thatcher,Rui Xiong
标识
DOI:10.1021/acs.jmedchem.5c03846
摘要
High Resolution Image Download MS PowerPoint Slide The SARS-CoV-2 papain-like protease (PLpro) is a critical target for antiviral intervention. Here, we report the discovery of MR1–114 (compound 15 ), a potent, noncovalent PLpro inhibitor. Guided by structure-based design, we incorporated a strategic alkyne linker hypothesized to access the cryptic Val70 Ub pocket, a modification that proved critical for driving cellular potency. Multiparameter optimization yielded MR1–114, which displays a desirable ADME profile characterized by high solubility, permeability, and hepatocyte stability, translating to high oral bioavailability in mice and rats. Notably, the compound exhibits preferential lung enrichment in mice and rats while maintaining broad-spectrum activity against variants, including Delta and Omicron BA.5 with nanomolar potency in vitro . In the K18-hACE2 mouse model, oral administration of MR1–114 matched the therapeutic efficacy of nirmatrelvir, significantly suppressing pulmonary viral replication and preventing disease-associated weight loss.
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