IKZF2 Degradation: It′s Time to Take into Account it When Designing Cereblon‐Based PROTACs
Proteolysis‐targeting chimera (PROTAC) has become a very important means of protein degradation and a new way of disease treatment. In particular, PROTACs constructed with ligands for E3 ligase cereblon account for more than 90 % of the PROTACs currently in clinical research. Notably, CRBN ligands t...
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Veröffentlicht in: | Chembiochem : a European journal of chemical biology 2024-08, Vol.25 (16) |
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description | Proteolysis‐targeting chimera (PROTAC) has become a very important means of protein degradation and a new way of disease treatment. In particular, PROTACs constructed with ligands for E3 ligase cereblon account for more than 90 % of the PROTACs currently in clinical research. Notably, CRBN ligands themselves are a class of molecular glue compounds capable of degrading neo‐substrate proteins. Compared to the target proteins degradation, the degradation of neo‐substrates, especially IKZF2, has not received enough attention. Therefore, this review summarizes the currently published IKZF2 degraders derived from articles and patents, which are conducive to the design of PROTACs with desired IKZF2 degradation from the perspective of medicinal chemistry. |
doi_str_mv | 10.1002/cbic.202400365 |
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In particular, PROTACs constructed with ligands for E3 ligase cereblon account for more than 90 % of the PROTACs currently in clinical research. Notably, CRBN ligands themselves are a class of molecular glue compounds capable of degrading neo‐substrate proteins. Compared to the target proteins degradation, the degradation of neo‐substrates, especially IKZF2, has not received enough attention. 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Therefore, this review summarizes the currently published IKZF2 degraders derived from articles and patents, which are conducive to the design of PROTACs with desired IKZF2 degradation from the perspective of medicinal chemistry.</description><subject>Biodegradation</subject><subject>Chimeras</subject><subject>Degradation</subject><subject>Ligands</subject><subject>Medical treatment</subject><subject>Proteins</subject><subject>Proteolysis</subject><subject>Substrates</subject><subject>Ubiquitin-protein ligase</subject><issn>1439-4227</issn><issn>1439-7633</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kMtOAjEYhRujiYhuXTdxPdjLTEvdIYoSSTBmjIkLJ532HyxCB9th4Y5H8Fl8JJ7EMRBX5yzOJfkQOqekRwlhl6Z0pscISwnhIjtAHZpylUjB-eHep4zJY3QS45wQogSnHfQ2fngdMXwDs6Ctblztr_C42W5-Is7dEnBT41x_AHa-dQNj6rVvsGvwyzv4thXdzDs_w0MIUC5qv918X-sIFj8-TfPBMJ6io0ovIpzttYueR7f58D6ZTO_Gw8EkMTRjTUKB8D7XSkkQkjGqAJjKmOGlBiulrEQFWvCsT6hQBCxkGSemTAWx2kpreRdd7HZXof5cQ2yKeb0Ovr0sOFFpmkrWVrqot0uZUMcYoCpWwS11-CooKf4YFn8Mi3-G_BeEY2Sv</recordid><startdate>20240819</startdate><enddate>20240819</enddate><creator>Li, Minglei</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><orcidid>https://orcid.org/0000-0002-8381-2455</orcidid></search><sort><creationdate>20240819</creationdate><title>IKZF2 Degradation: It′s Time to Take into Account it When Designing Cereblon‐Based PROTACs</title><author>Li, Minglei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c152t-1e0383a997e672219ee2952c3baed777f6fea635801690ede5530cb460dad7dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Biodegradation</topic><topic>Chimeras</topic><topic>Degradation</topic><topic>Ligands</topic><topic>Medical treatment</topic><topic>Proteins</topic><topic>Proteolysis</topic><topic>Substrates</topic><topic>Ubiquitin-protein ligase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Minglei</creatorcontrib><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Chembiochem : a European journal of chemical biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Minglei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>IKZF2 Degradation: It′s Time to Take into Account it When Designing Cereblon‐Based PROTACs</atitle><jtitle>Chembiochem : a European journal of chemical biology</jtitle><date>2024-08-19</date><risdate>2024</risdate><volume>25</volume><issue>16</issue><issn>1439-4227</issn><eissn>1439-7633</eissn><abstract>Proteolysis‐targeting chimera (PROTAC) has become a very important means of protein degradation and a new way of disease treatment. 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subjects | Biodegradation Chimeras Degradation Ligands Medical treatment Proteins Proteolysis Substrates Ubiquitin-protein ligase |
title | IKZF2 Degradation: It′s Time to Take into Account it When Designing Cereblon‐Based PROTACs |
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