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- W4312114801 abstract "Conformational analysis is central to the design of bioactive molecules. It is particularly challenging for macrocycles due to noncovalent transannular interactions, steric interactions, and ring strain that are often coupled. Herein, we simulated the conformations of five macrocycles designed to express a progression of increasing complexity in environment-dependent intramolecular interactions and verified the results against NMR measurements in chloroform and dimethyl sulfoxide. Molecular dynamics using an explicit solvent model, but not the Monte Carlo method with implicit solvation, handled both solvents correctly. Refinement of conformations at the ab initio level was fundamental to reproducing the experimental observations─standard state-of-the-art molecular mechanics force fields were insufficient. Our simulations correctly predicted the intramolecular interactions between side chains and the macrocycle and revealed an unprecedented solvent-induced conformational switch of the macrocyclic ring. Our results provide a platform for the rational, prospective design of molecular chameleons that adapt to the properties of the environment." @default.
- W4312114801 created "2023-01-04" @default.
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- W4312114801 date "2022-12-23" @default.
- W4312114801 modified "2023-10-06" @default.
- W4312114801 title "Simulation Reveals the Chameleonic Behavior of Macrocycles" @default.
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- W4312114801 doi "https://doi.org/10.1021/acs.jcim.2c01093" @default.
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