Loading…
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...
Saved in:
Published in: | ChemMedChem 2022-09, Vol.17 (17), p.n/a |
---|---|
Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | n/a |
container_issue | 17 |
container_start_page | |
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 |
format | article |
fullrecord | <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_cmdc_202200450</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CMDC202200450</sourcerecordid><originalsourceid>FETCH-LOGICAL-c890-2bae6009385cc7550fd4744ad11d59c811b83bad9948475742dc98d6af20b7e53</originalsourceid><addsrcrecordid>eNqFkDFPwzAQhSMEEqWwMt8IQ1s7dWqHraSkILXQoXvk2E5r5MSRnRT1t_HnSCiCkeH0Tnf3PuleENxiNMYIhRNRSjEOURgiRCJ0Fgwwm6ERxYye__Y0vgyuvH_vTgjDbBB8ps5WDST2oNwDLNRBGVuXqhvZAlLTWmfrvfVdOV5qyRsF3AOHR22FLWve6NwcYet45QvrSp4bBWlbiUbbihtYOtvWwCsJuvEwr2ujBe93J8rmG91DN85K1-6gg8BrK4yyXksF8w5idx7ukr0q10r2AphO-jfvr4OLghuvbn50GGzTp23yPFq9LV-S-WokWIxGYc7VDKF4yiIhaBShQhJKCJcYyygWDOOcTXMu45gwQiNKQiliJme8CFFOVTQdBuMTVjjrvVNFVjtdcnfMMMr65LM--ew3-c4Qnwwf2qjjP9dZsl4kf94vbySKeg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><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)</title><source>Wiley-Blackwell Read & Publish Collection</source><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</creator><creatorcontrib>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</creatorcontrib><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.</description><identifier>ISSN: 1860-7179</identifier><identifier>EISSN: 1860-7187</identifier><identifier>DOI: 10.1002/cmdc.202200450</identifier><language>eng</language><subject>anti-cancer drugs ; antiviral drugs ; nucleoside analogs ; phosphate ; prodrugs</subject><ispartof>ChemMedChem, 2022-09, Vol.17 (17), p.n/a</ispartof><rights>2022 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-0440-6820 ; 0000-0002-3967-3291 ; 0000-0002-0663-2792 ; 0000-0002-3754-789X ; 0000-0003-2724-2272 ; 0000-0003-0048-3789 ; 0000-0002-3609-602X ; 0000-0001-9502-2509</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Yoshida, Yuki</creatorcontrib><creatorcontrib>Zheng, Ti</creatorcontrib><creatorcontrib>Tanabe, Wataru</creatorcontrib><creatorcontrib>Tomoike, Fumiaki</creatorcontrib><creatorcontrib>Hashiya, Fumitaka</creatorcontrib><creatorcontrib>Suzuki, Tetsuro</creatorcontrib><creatorcontrib>Hirota, Shuto</creatorcontrib><creatorcontrib>Saiki, Yuriko</creatorcontrib><creatorcontrib>Horii, Akira</creatorcontrib><creatorcontrib>Hirayama, Akiyoshi</creatorcontrib><creatorcontrib>Soga, Tomoyosi</creatorcontrib><creatorcontrib>Kimura, Yasuaki</creatorcontrib><creatorcontrib>Abe, Hiroshi</creatorcontrib><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)</title><title>ChemMedChem</title><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.</description><subject>anti-cancer drugs</subject><subject>antiviral drugs</subject><subject>nucleoside analogs</subject><subject>phosphate</subject><subject>prodrugs</subject><issn>1860-7179</issn><issn>1860-7187</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkDFPwzAQhSMEEqWwMt8IQ1s7dWqHraSkILXQoXvk2E5r5MSRnRT1t_HnSCiCkeH0Tnf3PuleENxiNMYIhRNRSjEOURgiRCJ0Fgwwm6ERxYye__Y0vgyuvH_vTgjDbBB8ps5WDST2oNwDLNRBGVuXqhvZAlLTWmfrvfVdOV5qyRsF3AOHR22FLWve6NwcYet45QvrSp4bBWlbiUbbihtYOtvWwCsJuvEwr2ujBe93J8rmG91DN85K1-6gg8BrK4yyXksF8w5idx7ukr0q10r2AphO-jfvr4OLghuvbn50GGzTp23yPFq9LV-S-WokWIxGYc7VDKF4yiIhaBShQhJKCJcYyygWDOOcTXMu45gwQiNKQiliJme8CFFOVTQdBuMTVjjrvVNFVjtdcnfMMMr65LM--ew3-c4Qnwwf2qjjP9dZsl4kf94vbySKeg</recordid><startdate>20220905</startdate><enddate>20220905</enddate><creator>Yoshida, Yuki</creator><creator>Zheng, Ti</creator><creator>Tanabe, Wataru</creator><creator>Tomoike, Fumiaki</creator><creator>Hashiya, Fumitaka</creator><creator>Suzuki, Tetsuro</creator><creator>Hirota, Shuto</creator><creator>Saiki, Yuriko</creator><creator>Horii, Akira</creator><creator>Hirayama, Akiyoshi</creator><creator>Soga, Tomoyosi</creator><creator>Kimura, Yasuaki</creator><creator>Abe, Hiroshi</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-0440-6820</orcidid><orcidid>https://orcid.org/0000-0002-3967-3291</orcidid><orcidid>https://orcid.org/0000-0002-0663-2792</orcidid><orcidid>https://orcid.org/0000-0002-3754-789X</orcidid><orcidid>https://orcid.org/0000-0003-2724-2272</orcidid><orcidid>https://orcid.org/0000-0003-0048-3789</orcidid><orcidid>https://orcid.org/0000-0002-3609-602X</orcidid><orcidid>https://orcid.org/0000-0001-9502-2509</orcidid></search><sort><creationdate>20220905</creationdate><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)</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c890-2bae6009385cc7550fd4744ad11d59c811b83bad9948475742dc98d6af20b7e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>anti-cancer drugs</topic><topic>antiviral drugs</topic><topic>nucleoside analogs</topic><topic>phosphate</topic><topic>prodrugs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yoshida, Yuki</creatorcontrib><creatorcontrib>Zheng, Ti</creatorcontrib><creatorcontrib>Tanabe, Wataru</creatorcontrib><creatorcontrib>Tomoike, Fumiaki</creatorcontrib><creatorcontrib>Hashiya, Fumitaka</creatorcontrib><creatorcontrib>Suzuki, Tetsuro</creatorcontrib><creatorcontrib>Hirota, Shuto</creatorcontrib><creatorcontrib>Saiki, Yuriko</creatorcontrib><creatorcontrib>Horii, Akira</creatorcontrib><creatorcontrib>Hirayama, Akiyoshi</creatorcontrib><creatorcontrib>Soga, Tomoyosi</creatorcontrib><creatorcontrib>Kimura, Yasuaki</creatorcontrib><creatorcontrib>Abe, Hiroshi</creatorcontrib><collection>CrossRef</collection><jtitle>ChemMedChem</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yoshida, Yuki</au><au>Zheng, Ti</au><au>Tanabe, Wataru</au><au>Tomoike, Fumiaki</au><au>Hashiya, Fumitaka</au><au>Suzuki, Tetsuro</au><au>Hirota, Shuto</au><au>Saiki, Yuriko</au><au>Horii, Akira</au><au>Hirayama, Akiyoshi</au><au>Soga, Tomoyosi</au><au>Kimura, Yasuaki</au><au>Abe, Hiroshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Front Cover: Development of Fluorophosphoramidate as a Biocompatibly Transformable Functional Group and its Application as a Phosphate Prodrug for Nucleoside Analogs (ChemMedChem 17/2022)</atitle><jtitle>ChemMedChem</jtitle><date>2022-09-05</date><risdate>2022</risdate><volume>17</volume><issue>17</issue><epage>n/a</epage><issn>1860-7179</issn><eissn>1860-7187</eissn><abstract>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.</abstract><doi>10.1002/cmdc.202200450</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-0440-6820</orcidid><orcidid>https://orcid.org/0000-0002-3967-3291</orcidid><orcidid>https://orcid.org/0000-0002-0663-2792</orcidid><orcidid>https://orcid.org/0000-0002-3754-789X</orcidid><orcidid>https://orcid.org/0000-0003-2724-2272</orcidid><orcidid>https://orcid.org/0000-0003-0048-3789</orcidid><orcidid>https://orcid.org/0000-0002-3609-602X</orcidid><orcidid>https://orcid.org/0000-0001-9502-2509</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1860-7179 |
ispartof | ChemMedChem, 2022-09, Vol.17 (17), p.n/a |
issn | 1860-7179 1860-7187 |
language | eng |
recordid | cdi_crossref_primary_10_1002_cmdc_202200450 |
source | Wiley-Blackwell Read & Publish Collection |
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) |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T17%3A42%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Front%20Cover:%20Development%20of%20Fluorophosphoramidate%20as%20a%20Biocompatibly%20Transformable%20Functional%20Group%20and%20its%20Application%20as%20a%20Phosphate%20Prodrug%20for%20Nucleoside%20Analogs%20(ChemMedChem%2017/2022)&rft.jtitle=ChemMedChem&rft.au=Yoshida,%20Yuki&rft.date=2022-09-05&rft.volume=17&rft.issue=17&rft.epage=n/a&rft.issn=1860-7179&rft.eissn=1860-7187&rft_id=info:doi/10.1002/cmdc.202200450&rft_dat=%3Cwiley_cross%3ECMDC202200450%3C/wiley_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c890-2bae6009385cc7550fd4744ad11d59c811b83bad9948475742dc98d6af20b7e53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |