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1
Published in 2022 at "Journal of medicinal chemistry"
DOI: 10.1021/acs.jmedchem.2c01659
Abstract: In this work, we utilized the proteolysis targeting chimera (PROTAC) technology to achieve the chemical knock-down of histone deacetylase 6 (HDAC6). Two series of cereblon-recruiting PROTACs were synthesized via a solid-phase parallel synthesis approach, which…
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Keywords:
solid phase;
hdac6;
cereblon recruiting;
histone deacetylase ... See more keywords
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3
Published in 2023 at "Pharmaceutics"
DOI: 10.3390/pharmaceutics15030812
Abstract: The classical low-molecular-weight drugs are designed to bind with high affinity to the biological targets endowed with receptor or enzymatic activity, and inhibit their function. However, there are many non-receptor or non-enzymatic disease proteins that…
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Keywords:
new drugs;
drugs face;
protacs new;
ubiquitin ligase ... See more keywords