The rôle of thymidine phosphorylase/PD-ECGF in cancer chemotherapy: a chemical perspective.

Anti-cancer drug design Pub Date : 1999-10-01
C Cole, A J Foster, S Freeman, M Jaffar, P E Murray, I J Strafford
{"title":"The rôle of thymidine phosphorylase/PD-ECGF in cancer chemotherapy: a chemical perspective.","authors":"C Cole,&nbsp;A J Foster,&nbsp;S Freeman,&nbsp;M Jaffar,&nbsp;P E Murray,&nbsp;I J Strafford","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The angiogenic growth factor thymidine phosphorylase/PD-ECGF has been identified as a potential target in the development of anti-cancer drugs. This review firstly discusses the biological rôle of TP/PD-ECGF and its importance in the activation of 5-fluorouracil and its prodrugs. The chemistry and chemotherapeutic potential of TP/PD-ECGF inhibitors are also discussed.</p>","PeriodicalId":7927,"journal":{"name":"Anti-cancer drug design","volume":"14 5","pages":"383-92"},"PeriodicalIF":0.0000,"publicationDate":"1999-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Anti-cancer drug design","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The angiogenic growth factor thymidine phosphorylase/PD-ECGF has been identified as a potential target in the development of anti-cancer drugs. This review firstly discusses the biological rôle of TP/PD-ECGF and its importance in the activation of 5-fluorouracil and its prodrugs. The chemistry and chemotherapeutic potential of TP/PD-ECGF inhibitors are also discussed.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
肿瘤化疗中胸苷磷酸化酶/PD-ECGF的rôle:化学观点。
血管生成生长因子胸苷磷酸化酶/PD-ECGF已被确定为抗癌药物开发的潜在靶点。本文首先综述了TP/PD-ECGF的生物学rôle及其在5-氟尿嘧啶及其前药活化中的重要作用。本文还讨论了TP/PD-ECGF抑制剂的化学和化疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Linker length in podophyllotoxin-acridine conjugates determines potency in vivo and in vitro as well as specificity against MDR cell lines. Topoisomerase I/II selectivity among derivatives of N-[2-(dimethylamino)ethyl]acridine-4-carboxamide (DACA). Synthesis and anticancer activity of nordihydroguaiaretic acid (NDGA) and analogues. Cyclohexylamino-demethoxy-hypocrellin B and photodynamic therapy decreases human cancer in vitro. Photokilling of cultured tumour cells by the porphyrin derivative CF3.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1