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• W2977731985 startingPage "126730" @default.
• W2977731985 abstract "Cyclic peptides combine several favorable properties such as good binding affinity, target selectivity and low toxicity that make them an attractive modality for drug development. In an effort to identify what conformation could be accounting for the bioactive disparity of natural and synthetic cyclic peptides, some structurally-constrained analogs of cyclopeptide Axinastatin 3 were prepared by photo-induced single electron transfer (SET) reaction. Detailed stereochemistry study was performed by experimental electronic circular dichroism combined with theoretical calculations. Our study suggested that the cyclopeptide 1 with βI-turn presented stronger antitumor activity comparing with those without such secondary structures. Moreover, a rare ‘π helix unit’ (compound 3) was realized because of the constrained cyclic structure, which could be considered an important research object for future study of unique helix secondary structures." @default.
• W2977731985 created "2019-10-10" @default.
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• W2977731985 date "2019-11-01" @default.
• W2977731985 modified "2023-10-10" @default.
• W2977731985 title "Photo-induced synthesis of Axinastatin 3 analogs, the secondary structures and their in vitro antitumor activities" @default.
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• W2977731985 doi "https://doi.org/10.1016/j.bmcl.2019.126730" @default.
• W2977731985 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31607609" @default.
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