https://ouci.dntb.gov.ua/works/4EBWjBxl/
High-throughput modular click chemistry synthesis of catechol derivatives as covalent inhibitors of...
The 3C-like protease (3CLpro) is a crucial target in anti-Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) drug design. Herein, we performed...
high throughputclick chemistrycatechol derivativesmodularsynthesis
https://pubmed.ncbi.nlm.nih.gov/24890653/
Catechol-rhodanine derivatives: Specific and promiscuous inhibitors of Escherichia coli...
To develop more effective inhibitors than fosmidomycin, a natural compound which inhibits the deoxyxylulose 5-phosphate reductoisomerase (DXR), the second...
escherichia coliderivativesspecificpromiscuousinhibitors