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disrupts EGFR stability by dissociating the EGFR-HSP90 complex and recruiting E3 ligase, RNF149. More importantly, the potent and selective PD-L1 and BTK degraders were discovered successfully by utilizing the SiHyT strategy. The development of these innovative SiHyT compounds could broaden the repertoire of HyTs, enhancing the future design of TPD agents.
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Ma Lan
Nankai University
Kun Zhang
Xinyang Normal University
Ziqi Huang
Jinan University
Journal of Medicinal Chemistry
Nankai University
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Lan et al. (Mon,) studied this question.
synapsesocial.com/papers/6a03acc5f6c0e004a6de0649 — DOI: https://doi.org/10.1021/acs.jmedchem.4c02273