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• W2016285619 abstract "The synthesis of branched and conformationally restricted analogs of the anticancer nucleosides 3'-C-ethynyluridine (EUrd) and 3'-C-ethynylcytidine (ECyd) is presented. Molecular modeling and (1)H NMR coupling constant analysis revealed that the furanose rings of all analogs except the LNA analog are conformationally biased towards South conformation, and are thus mimicking the structure of ECyd. All target nucleosides were devoid of anti-HIV or anticancer activity." @default.
• W2016285619 created "2016-06-24" @default.
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• W2016285619 date "2005-04-01" @default.
• W2016285619 modified "2023-09-27" @default.
• W2016285619 title "Synthesis and biological evaluation of branched and conformationally restricted analogs of the anticancer compounds 3′-C-ethynyluridine (EUrd) and 3′-C-ethynylcytidine (ECyd)" @default.
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• W2016285619 doi "https://doi.org/10.1016/j.bmc.2005.01.029" @default.
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