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• W3134643545 abstract "The binding affinity of the beta-cyclodextrin (β-CyD) derivatives with Doxorubicin (Dox) is evaluated by means of the 3D-RISM/KH theory combined with the molecular dynamics simulation in order to screen the compounds for suppressing a side-effect of the cancer drug. A protocol revised for the external and conformational entropies of the host-guest system is employed to calculate the binding free energy. It is found that the direct interactions of CyD with Dox and the desolvation free-energies of the both compounds largely cancel out to leave moderate contributions to the affinity, which are comparable to those from the entropies. The results shed light on the entropy terms for determining the binding affinity, although the external-entropy terms are essentially constant over all the compounds examined and do not affect the screening. The theoretical result is compared with the experimental data of the association constant for a CyD derivative which was predicted to be the best compound by the preliminary calculation without the entropy terms." @default.
• W3134643545 created "2021-03-15" @default.
• W3134643545 creator A5013321826 @default.
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• W3134643545 date "2021-03-01" @default.
• W3134643545 modified "2023-10-17" @default.
• W3134643545 title "Computational Screening of a Functional Cyclodextrin Derivative for Suppressing a Side Effect of Doxorubicin" @default.
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• W3134643545 doi "https://doi.org/10.1021/acs.jpcb.1c00373" @default.
• W3134643545 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33646771" @default.
• W3134643545 hasPublicationYear "2021" @default.
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