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Design and modular parallel synthesis of a MCR derived α-helix mimetic protein–protein interaction inhibitor scaffold |
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AbstractA terphenyl α-helix mimetic scaffold recognized to be capable of disrupting protein–protein interactions was structurally morphed into an easily amenable and versatile multicomponent reaction (MCR) backbone. The design, modular in-parallel library synthesis, initial cell based biological data, and preliminary in vitro screening for the disruption of the Bcl-w/Bak protein–protein interaction by representatives of the MCR derived scaffold are presented.
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