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Front Cover: Development of Fluorophosphoramidate as a Biocompatibly Transformable Functional Group and its Application as a Phosphate Prodrug for Nucleoside Analogs (ChemMedChem 17/2022)

The Front Cover shows a new type of biocompatible phosphate analog, a fluorophosphoramidate (FPA) functional group with characteristic P–F and P–N bonds. The stability of the FPA group was found to vary depending on the number of the amino group substitutions. Taking advantage of this intriguing mol...

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Published in:ChemMedChem 2022-09, Vol.17 (17), p.n/a
Main Authors: Yoshida, Yuki, Zheng, Ti, Tanabe, Wataru, Tomoike, Fumiaki, Hashiya, Fumitaka, Suzuki, Tetsuro, Hirota, Shuto, Saiki, Yuriko, Horii, Akira, Hirayama, Akiyoshi, Soga, Tomoyosi, Kimura, Yasuaki, Abe, Hiroshi
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container_issue 17
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container_title ChemMedChem
container_volume 17
creator Yoshida, Yuki
Zheng, Ti
Tanabe, Wataru
Tomoike, Fumiaki
Hashiya, Fumitaka
Suzuki, Tetsuro
Hirota, Shuto
Saiki, Yuriko
Horii, Akira
Hirayama, Akiyoshi
Soga, Tomoyosi
Kimura, Yasuaki
Abe, Hiroshi
description The Front Cover shows a new type of biocompatible phosphate analog, a fluorophosphoramidate (FPA) functional group with characteristic P–F and P–N bonds. The stability of the FPA group was found to vary depending on the number of the amino group substitutions. Taking advantage of this intriguing molecular profile, gemcitabine FPA‐prodrug, which was designed to be efficiently converted to the corresponding monophosphate in cells, showed superior anticancer activity compared with the parent compound gemcitabine and its ProTide prodrug. More information can be found in the Research Article by Yuki Yoshida, Hiroshi Abe et al.
doi_str_mv 10.1002/cmdc.202200450
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subjects anti-cancer drugs
antiviral drugs
nucleoside analogs
phosphate
prodrugs
title Front Cover: Development of Fluorophosphoramidate as a Biocompatibly Transformable Functional Group and its Application as a Phosphate Prodrug for Nucleoside Analogs (ChemMedChem 17/2022)
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