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• W3131677514 abstract "The androgen receptor (AR), a family of nuclear receptor proteins, stimulates the transcription of androgen-responsive genes. As its abnormal activation can cause the progression of prostate cancer, numerous types of ligands for AR have been developed as promising antagonists for the treatment of prostate cancer. We previously investigated the specific interactions between AR and nine types of existing non-steroidal ligands, using molecular simulations based on molecular mechanics and ab initio fragment molecular orbital methods. The results were confirmed to be comparable to the binding affinities of these ligands observed in experiments. We here propose novel ligands as potent inhibitors against AR and investigate their binding properties to AR, using the same molecular simulations. The results indicate that the most promising ligand binds stronger to AR than the existing non-steroidal ligands, and that our proposed ligand binds strongly to a mutant-type AR, which has drug resistance to the existing non-steroidal ligands." @default.
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• W3131677514 date "2021-06-01" @default.
• W3131677514 modified "2023-09-26" @default.
• W3131677514 title "Proposal of novel potent inhibitors against androgen receptor based on ab initio molecular orbital calculations" @default.
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• W3131677514 doi "https://doi.org/10.1016/j.jmgm.2021.107873" @default.
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