摘要
A novel glucose-conjugated paclitaxel 5 was synthesized using succinic acid as linker between 2′-paclitaxel and methyl 2′-glucopyranose. 5 has not only improved the pharmaceutical properties of paclitaxel, such as solubility and stability, but also enhanced the specific target delivery to MCF-7 cells without the cytotoxicity against normal cells. Therefore, the glucose conjugation may be potentially used in the targeted delivery of other drugs into cells via glucose transporters (GLUTs) for cancer therapy.
原文 | 英語 |
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頁(從 - 到) | 617-620 |
頁數 | 4 |
期刊 | Bioorganic and Medicinal Chemistry Letters |
卷 | 17 |
發行號 | 3 |
DOIs | |
出版狀態 | 已發佈 - 2月 1 2007 |
ASJC Scopus subject areas
- 生物化學
- 分子醫學
- 分子生物學
- 藥學科學
- 藥物發現
- 臨床生物化學
- 有機化學