Design and synthesis a water-soluble group for ether-linkage of 10-hydroxycamptothecin prodrug

CNU IR > Pharmacy and Science > 2017 > Item 310902800/33571

Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/33571

Title:	Design and synthesis a water-soluble group for ether-linkage of 10-hydroxycamptothecin prodrug
Authors:	邱沛芳林偉琪陳國輝呂玉玲
Contributors:	藥學系
Date:	2017
Issue Date:	2022-01-25 14:44:35 (UTC+8)
Abstract:	For selective cancer chemotherapy, we previously designed and synthesized two β-glucuronidase-activated prodrugs of camptothecin (9-ACG and 10-HCG), which increased water solubility for camptothecins. In normal tissues, β-glucuronidase is localized primarily in lysosomes and thereby not available for activation of glucuronide prodrugs because these prodrugs are generally hydrophilic, thus rendering them impermeable to cell membranes. Therefore, glucuronide-based prodrugs can be used in prodrug monotherapy.9-ACG was more soluble than 10-HCG via oxycarbamate linkage, so 9-ACG was more low toxicity than 10-HCG. However, 10-HCG was a good substrate for β-glucuronidase, which has ether linkage. In order to increase the solubility of 10-HCG, we designed 10-HCPG, which creates a hydrophilic group in link of prodrug. We predict that 10-HCPG is soluble, low cytotoxicity and good a substrate for β-glucuronidase. We expect 10-HCPG, which is a good candidate for selective cancer chemotherapy.
Relation:	2017 第十一屆嘉南藥理大學藥理學院師生研究成果發表會，起迄日：2017/05/02-2017/05/04
Appears in Collections:	[Pharmacy and Science] 2017 [Dept. of Pharmacy] Proceedings

Files in This Item:

File	Size	Format
A01.pdf	742Kb	Adobe PDF	159	View/Open